CORNEL L UNIV ERSITY THE 3\wmt tomnarg Sltbrar^ FOUNDED BY ROSWELL P- FLOWER for the use of the N. Y. State Veterinary College 1897 This Volume is the Gift of Dr. V. A. Moore. 356 QR 301.K6°r"""'"'"'""-"'"'^ Studies in the bacteriology & etiology o 3 1924 000 246 169 ■ Date Due HAY If 1961 MtF -^^ -H.^ r^^irrzrrr- ... — ^_^ I Library Burea Cat. No. 1137 Cornell University Library The original of tiiis book is in tine Cornell University Library. There are no known copyright restrictions in the United States on the use of the text. http://www.archive.org/details/cu31924000246169 STUDIES IN THE BACTERIOLOGY AND ETIOLOGY OF ORIENTAL PLAGUE STUDIES IN THE BACTEMOLOaY & ETIOLOGY OF ORIENTAL PLAGUE BY E. KLEIN, M.D., F.E.S. LECTURER ON ADVANCED BAOTERIOLOGT AT THE MEDICAL SCHOOL OF ST. Bartholomew's hospital, London WITH 89 PHOTOGRAMS MACMILLAN AND CO., Limited NEW YORK : THE MACMILLAN COMPANY 1906 All rights reserved CONTENTS PAGE Inteoddction . . . xiii CHAPTEE I The Bacillus pestis the Essential Cause of Omental Plague 1 CHAPTEE II Characters op the B. pestis . . . . 14 CHAPTEE III Analysis of Plague Materials . . .36 CHAPTEE IV Microbes simulating B. pestis ... 51 CHAPTEE V Plague in the Rat .... .84 CHAPTEE VI Plague induced in other Rodents 129 CHAPTEE VII Modes of Infection of Animals with Plague . 146 vii OEIENTAL PLAGUE CHAPTER VIII PAGE AO-aLUTINATION OF B. PESTIS . . 200 CHAPTEE IX Protective Inoctoation against Plague . . 244 CHAPTEE X Modes op Destruction op B. pestis . 279 ILLUSTEATIONS FIG, PAGE 1. Stained Film of the Juice of a Bubo — Bubonic Plague of Man 4-5 2. Stained Film of the Lung Juice in Fatal Pneumonic Plague of Man ....... 4-5 3. Stained Film of the Juice of a Bubo — Fatal Bubonic Plague . 4-5 4. Stained Film of Spleen Juice of a Eat dead of Natural Plague 4-5 5. Stained Film of the Inguinal Bubo of a Rat . 10-11 6. Stained Film of Inguinal Bubo of a Eat . 10-11 7. Stained Film of Lung Juice of a Monkey dead of Pneumonic Plague ...... 10-11 8. Stained Film of Liver Juice of same Monkey . . 10-11 9. Stained Film of Blood of a Guinea-pig dead of Plague . 14-15 10. Stained Film of the Blood of another Guinea-pig . . 14-15 11. Stained Film of Blood of a Mouse dead of Acute Plague . 14-15 12. Stained section through the Medullary part of the Inflamed Inguinal Lymph Gland of a Rat . . . 14-15 13. Same preparation as in Fig. 12 . . . . 14-15 14. Stained Film of Spleen Juice of a Guinea-pig dead of Acute Plague ....... 18-19 15. Stained Film of Spleen Juice of a Eat dead of Acute Plague . 18-19 16. Section through the Consolidated Lung of a Rat dead twelve days after Cutaneous Inoculation with Juice of Bubo . 18-19 17. Part of the Contents of the Bronchus of previous Figure . 18-19 18. Section through a Lobule of the Lung in Pneumonic Plague of a Guinea-pig ..... 20-21 19. The Exudation in one of the Infundibula of previous Figure . 20-21 20. From a section through the Lung of a Guinea-pig dead of Subacute Plague . . 20-21 ix X ORIENTAL PLAGUE FIG. PAGE 21. From a section through the Lung of a Guinea-pig dead of Subacute Plague ...... 20-21 22. From a section through the hardened Spleen . . . 24-25 23. One of the Bacillary masses of the previous Figure . . 24-25 24. One of the Bacillary (dark) masses of a Necrotic Nodule . 24-25 25. Film specimen of Peritoneal Exudation . . . 24-25 26. Stained Film of the Peritoneal Exudation . . . 24-25 27. Stained Film specimen of the Bubo Fluid . . .28-29 28. Young Colonies of B. pestis on the Surface of a Gelatine Plate 28-29 29. Young Colonies of B. pestis on the Surface of an Agar Plate . 28-29 30. Characteristic Colonies of B. pestis on Agar . . . 28-29 31. Streak Culture of B. pesiis on Gelatine . . . 32-33 32. Stab Culture of B. pestis in Gelatine . . . 32-33 33. The deeper part of the Stab of previous Figure magnified . 32-33 34. Colonies of Plague Bacilli on Gelatine "after some days' Incubation .... . 32-33 35. Colonies of Plague Bacilli on Gelatine after some days' Incubation . . 36-37 36. Colonies of B. pestis on Gelatine after many weeks' Incubation 36-37 37. Same Colonies as in previous Figure, more magnified . . 36-37 38. Film specimen of the growth of B. pestis from Agar Culture, twenty-four hours' Incubation. Virulent human type 1 . 36-37 39. Film specimen from a recent Agar Culture of the attenuated B. pestis (rat type or type 2) ... 42-43 40. Stained impression of a young Colony of B. pestis (virulent type) 42-43 41. Stained impression of an Atypical Colony — Filamentous Bacilli 42-43 42. Impression of a number of young Colonies of B. pestis on the surface of Gelatine . . . . 42-43 43. Stained impression of a recent Colony of B. pestis on Gelatine . 46-47 44 and 45. Two Ghee Broth Cultures of B. pestis . . 46-47 46. Bacterium Bristolense. — Growth on Potato . 46-47 47. Bacterium Bristolense. — Peritoneal Exudation of a Rat dead after Subcutaneous Injection with Culture . . 52-53 48. Bacterium Bristolense. — Film specimen of the Spleen Juice of a Guinea-pig ...... 52-53 49. Bacterium Bristolense. — Stained Film specimen of the swollen Inguinal Lymph Gland . . . 52-53 ILLUSTEATIONS xi FIG. 50. Stained Film specimen of the Subcutaneous Local Exudation of a Mouse ....-■• 52-53 51. From a section ttrough the Consolidated portion of the Lung of a Eat spontaneously dead . . . .56-57 5 2. The Exudation of an Alveolus of the Lung, as in previous Figure 56-57 53. A Gelatine Plate Culture of the Heart's Blood of the Eat spontaneously dead with Lung Disease . . ■ 56-57 54. Film specimen of a Gelatine Culture of the Tissue of Lung ofEat . . . . 56-57 55. Film specimen of same Culture as in previous Figure . 60-61 56. Film specimen of Blood from the Eight Ventricle of Nurse T. 60-61 57. Exudation at the seat of Inoculation in a Mouse . 60-61 58. Stained Film of Agar Plate of Blood of Nurse T. . . 60-61 59. Stab Culture in Gelatine of B. myxoides after a week's Incubation 64-65 60. From a Pure Culture of the B. wyxoides (from Nurse T.'s blood), showing a Zooglcea of the (Bipolar) Plague-like Bacilli 64-65 61. Film specimen of the Viscid Peritoneal Exudation of a Guinea- pig dead after Intraperitoneal Injection with B. myxoides . 64—65 62. Specimen of Heart's Blood of a Guinea-pig dead after Intra- peritoneal Injection with B. myxoides . . 64-65 63. Specimen of Heart's Blood of a Guinea-pig dead after Intra- peritoneal Injection with B. myxoides . . 66-67 64. From a section through the Liver of a Guinea-pig dead after Subcutaneous Injection with B. pseudo-tuherculosis . . 66-67 65. From a section of a similar Liver, showing the Liver Tissue per- vaded by the Nodules . . . .66-67 66. Section through a swollen Beyer's patch of the Ileum of a Guinea-pig infected by feeding with Culture of B. pseudo- tuberculosis . . . 66-67 67. A portion of Necrotic Lymph Follicle of a similar Peyer's patch as preceding Figure ..... 72-73 68. Film specimen of Purulent Caseous Matter of Inguinal Lymph Gland of a Guinea-pig dead of Pseudo-tuberculosis . . 72-73 69. Gelatine Surface Tla,te ahowing Colonies oi B. pseudo-tuberculosis 72-73 70. Same Colonies on Agar Plate, less magnified . . 72-73 71. Film specimen (stained) of B. pseudo-tuberculosis, from Agar Colonies. . . 76-77 xii OEIENTAL PLAGUE FIQ. PAGE 72. From an Unstained Broth Culture of B. pseudo-tuberculosis 76-77 73. From an Impression (Film) specimen of a young Colony on a Gelatine Plate of B. psevdo-tuberculosis . . 76-77 74. Stained Blood Film of B. equi from Rabbit's Heart Blood . 76-77 75. Section through the affected Beyer's patch of the Ileum of a Eat dead of Plague after feeding . . . 162-163 76. Large Blood-vessel of the Submucosa (3 of Fig. 75) . 162-163 77. Part of Fig. 76, more highly magnified . . . 162-163 78. Transverse section through Mesenteric Gland of a Rat dead of Acute Plague after feeding .... 162-163 79. From a section through the Testis of Rat mentioned in Fig. 75 ... . . 166-167 80. Section through the Ileum, at the site of Haemorrhage, of a Mouse dead of Acute Plague after feeding . . 166-167 81. Part of a similar Villus to that in Fig. 80, more highly magnified ...... 166-167 82. Transverse section through the affected part of the Ileum of a Rat dead after feeding with Plague material . . 166-167 83. A portion of the previous particle (Fig. 82), more highly magnified ...... 170-171 84. Part of previous Figure, more highly magnified . . 170—171 85. The same particle of Plague Spleen in Wheat as shown in Fig. 82 ..... . 170-171 86. Section through Mesenteric Gland of a Sewer Rat dead after feeding with semi-dried Plague organs . . . 170-171 87. Section through the Hsemorrhagic patch of the Ileum of a Guinea-pig dead of Subacute Plague . . 176-177 88. Section through the same portion of the Ileum at its Mesenteric attachment ...... 176-177 89. A Villus of Fig. 87, showing copious absorption of B. pestis 176-177 INTKODUCTION It is admitted on all sides that the Bacillus pestis is the real and essential cause of Oriental or bubonic plague, and consequently that the presence of this microbe in any material derived from a human or animal being denotes the disease plague in such a being. It is likewise ad- mitted that a patient, although exhibiting one or more symptoms suspicious of the disease plague — e.g. fever with swollen and inflamed subcutaneous lymph -glands in one or the other region of the body, cervical, axillary, inguinal, or femoral, — need not necessarily be affected with bubonic plague, notwithstanding that such person might have been indirectly exposed to plague infection. Should, however, in such swollen inflamed glands the B. pestis be demonstrated, epidemiologists and physicians would accept such a case unquestionably as true plague. It is obvious that should this be the case the relation of such a patient towards his surroundings would at once be vastly different from that in which a negative bacteriological result showed that the patient is not affected with that infectious disease, but is suffering from some other malady not requiring those stringent and costly measures that a case of plague requires. No greater misfortune, from a public health point of xiii xiv ORIENTAL PLAGUE view, could befall a community than an epidemic outbreak of bubonic plague in a large and crowded city. An epidemic might originate from a patient or patients who, while not exhibiting symptoms clinically typical of plague, nevertheless harbour the B. pestis, and this being over- looked might become a focus of further infection. If such be the case, the blame that an important step in the diagnosis of the disease, namely, the bacteriological evi- dence, had been omitted would rightly fall on those who relied solely on clinical evidence. The bacteriological examination of cases which, for one reason or another, are under suspicion of being affected with plague, and if undetected may be the means of introducing the disease into a new locality, is therefore of the greatest importance, since the clinician cannot venture to pro- nounce on the case with certainty. The same applies to rats in a ship coming from a plague -infected locality. It is established that ships have harboured plague rats without any one on board contracting the disease, but nevertheless such a ship if left to itself remains a real source of danger, not only to those who afterwards use it — as has actually occurred — but to the port of landing, where its plague-sick rats may carry infection to rats on shore, and further carry infection to human beings. The bacteriological diagnosis of plague in rats — the only ex- amination that is of scientific value — is from a public health point not less important than the examination of suspected human cases. In the following pages we shall have opportunity of giving an account of cases which, from a clinician's and epidemiologist's point of view, were under suspicion of being plague, and on bacteriological analyses were INTRODUCTION xv actually found to be so, while other similar cases were proved bacteriologically not to be cases of plague. Such cases, although clinically suspected to be plague, were, in confirmation of the negative bacteriological evidence, not followed by any further cases of the disease. The same applies to rats ; for while, on the one hand, bacteriological analysis confirmed the preliminary diagnosis made by the sanitary authority, viz. that mortality amongst rats on certain ships coming from infected ports was due to plague, it has, on the other hand, shown that mortality of rats on ships need not necessarily be due to plague, because rats are subject also to several forms of acute infectious maladies other than plague. During the last ten years I have had a good many opportunities of investigating bacteriologically materials of suspected and real cases of plague of human beings and of rats ; I have also made special studies of the B. pestis in its morphological, cultural, and physiological characters, and in the manner of its conveyance and action. Some of these studies have been published in the Annual Eeports of the Medical Officer of the Local Government Board, and are here reproduced, partially or wholly, by permission of the Controller of H.M. Stationery Office. It seems not out of place to collect the results of all these studies, carried on now for a succession of years, in a connected and easily accessible form. The following pages are devoted to this purpose.^ ^ With the exception of Fig. 1, all the illustrations are photograms made for me by Mr. Albert ISTorman, M.R.C.S., London. / CHAPTEE I THE BACILLUS PESTIS THE ESSENTIAL CAUSE OF ORIENTAL PLAGUE The literature of Plague, from the earliest historical periods, when the disease was recognised to be a com- municable disease, down to 1894, i.e. down to the outbreak of plague in Hong-Kong, contains a number of suggestions and assumptions as to the causation of the disease. But as is the case with other communicable diseases, before the . discovery of the actual contagium no scientific distinction was or could be made between the primary or essential cause, i.e. the causa causans, and those secondary conditions which contribute to, and which favour infection : terrestrial influences, peculiar atmospheric states, social defects, famine and want, crowded and ill - ventilated habitations, decomposing corpses, decomposed, insufficient, and unclean food-stuffs, and a number of other conditions which are apt to weaken and to influence in an unfavour- able sense the resistance of the individual ; that is to say, all conditions which in most infectious diseases play a part in facilitating and enhancing infection were formerly con- sidered as beiug of the nature of essentials. The discovery of the Bacillus pestis, however, as the true essence of the B 2 OEIENTAL PLAGUE chap. contagion, relegated all the above states to their proper place, viz. as being of the nature of secondary causes, and therefore of secondary importance. Yersin (Annales de V Institute Pasteur, viii. p. 662), and Kitasato {Lancet, 1894, ii. p. 428) showed that in all cases of bubonic plague the buboes, the spleen (and also the blood) contain in very large numbers minute bacUli, which in morphological and cultural respects possess definite characters ; that a trace of culture of the microbe inoculated into a rodent causes invariably the typical acute fatal disease, bubonic plague, with the same copious multi- plication of the same bacillus. These statements are easy of verification, and there can therefore remain no doubt that all postulates which a microbe has to fulfil in order to be regarded as specifically the causa causans has been complied with in the case of B. pestis. Moreover, the numerous cases of plague in man which, from time to time, have come under the notice of a large number of observers in various countries, in which plague has appeared since 1894, and the numerous rats dead in various plague- stricken countries that have been subjected to bacteriologi- cal examination, have all yielded the same result, viz. the inflamed lymph glands, the spleen, and other organs teemed with the same B. pestis. This bacUlus, as will be shown, is a well-characterised species — well characterised in morphology, in culture, and by experiment — so much so, that it has become an established fact that the identifica- tion in the glands, spleen, or other organs of any body is proof positive that that body is subject to and afiected with Oriental plague. Kitasato's earlier and later accounts of the B. pestis difier somewhat from the description given by Yersin, I THE ESSENTIAL CAUSE 3 inasmuch as Yersin's account is all throughout consistent, whereas Kitasato's earlier account appears somewhat at variance with his later statement, and it is for these reasons that an undesirable confusion has arisen in the minds of some later observers. Thus Aoyama ( Centralblatt f. Bahter. und Parasit. xix. 481), while confirming Yersin's B. pestis as the microbe of plague, denies to Kitasato's bacillus this same claim. We shall show that Kitasato's bacillus of his later account is the B. pestis, but under a modification, being a different type of the plague microbe. As mentioned just now, bacteriologists in all countries who have had the opportunity of becoming acquainted with, and who have carefully investigated the nature and character oi B. pestis in man, and in the rat, aflfected with plague, have confirmed Yersin's and Kitasato's discovery, that the B. pestis is the specific microbe of Oriental plague. The distribution of the B. pestis in the affected body, both of man and the rat, under natural conditions, is subject to certain slight variations, which are dependent, in a large measure, on the various forms under which plague declares itself. We proceed to consider in detail these variations. I. In Man (A) Pestis bubonica, — The most common form, as admitted on all sides, is the bubonic form, i.e. the one associated with conspicuous swelling and inflammation of the lymph glands, with oedema, haemorrhage, and inflamma- tion of the subcutaneous tissue around the glands ; both together forming a painful, large, more or less soft " bubo." 4 ORIENTAL PLAGUE chap. Whether the bubo occurs in the neck, the axilla, the inguinal or femoral region, in all instances the glands show haemorrhage in their substance with partially necrotised foci. A droplet of the gland juice, as also, but to a less degree, of the surrounding inflamed cellular tissue, shows in film specimens a conspicuously large number of B. pestis. The great number of bacilli, possessing the same charac- ters, aspect, staining power, and size, is alone sufficient to make diagnosis of plague highly probable, for there is no other acute disease known except plague which so affects the lymph glands, containing such vast numbers of this kind of bacQli, viz. non-motile, Gram-negative and bipolar in staining, i.e. a vacuole in the centre, or possessing a vacuole at one or both ends, and then appearing as if gnawed out at one or both ends. Unfortunately there are cases of bubonic plague in which a film specimen made of a droplet of the juice of the bubo of the living does not show great numbers of the B. pestis. This is, however, the exception, and is, in most instances, explicable by the fact that the material is not really derived from the interior of the gland, for when such glands after post mortem are dissected out and examined in film specimens, there is no difficulty in ascertaining that the B. pestis are really present in enormous numbers in the gland tissue ; in fact, such film specimens show that the gland tissue is densely packed with them. I have seen several such instances, in which the juice of the bubo, obtained by puncture of the bubo during life, showed in film specimens a comparatively limited number of bacilli — ^limited, that is, inasmuch as each field of the microscope under a magnifying power of 300 did not show more than a dozen or so; whereas the same bubo, having been removed after post mortem. . "k ' o ' - t ~ ^ I Fig. 1. Stained film of the juice of a bubo — bubonic plague of man. Magnification x 1000. Fig. 2. Stained film of the lung juice in fatal pneumonic plague of man. x 1000. Fig. 3. Stained film of the juice of a bubo — fatal bubonic plague of an Indian native, s.s. City of Perth. x 1000. Fig. 4. Stained film of spleen juice of a rat, dead of natural plague, Cardiff. x 1000. . f« ti'S' •■ *- V Fig. 3. :' ' ^ N ►•/ I THE ESSENTIAL CAUSE 5 when examined by film specimens, showed each field of the microscope literally crowded with the bacilli. While, then, in the acute cases, the microscopic ex- amination of the bubo material enables one to make the preliminary diagnosis " plague most probable," it is not so in the chronic cases, i.e. in pestis minor, or in ambulating plague, when the buboes suppurate and become converted into open discharging sores, for here the material in microscopic specimens may, and generally does, show a variety of microbes, (a) Foremost among these one finds cocci, which by culture are shown to be either Staphylo- coccus albus or aureus ; they are Gram-positive ; (&) next one finds streptococci ; they are Gram-positive ; these are less common ; (c) here and there a diphtheroid bacillus. Gram-positive, which by culture is shown to belong to the xerosis group ; (d) bacilli with round ends, and showing on staining more or less distinct bipolar character ; these may be B. proteus, B. coli, or B. pestis, all being Gram-negative. The culture test, however — surface agar plates at 37° C. incubated, — shows already in twenty -four hours the difi'erentiation in a marked manner ; these difierences will be dealt with fully later in a special chapter. I have in the course of the last nine years examined a large amount of material of inguinal, femoral, axillary, and cervical swellings which had been associated with febrile symptoms, and there being, on epidemiological grounds, a possibility of such disease being plague — the persons being either in a port or had arrived in a ship which had come fi:om or had touched an infected port — the material was subjected to careful bacteriological analysis, with the result that plague was negatived, and, as the further history proved, 6 OEIENTAL PLAGUE chap. the disease was not plague. Such materials in several instances showed in films no microbes, agar plates made with relatively large amounts remained quite free of growth. In other instances the microscopic examination showed abundance of cocci, chiefly diplococci in clusters in and amongst the leucocytes, and, as culture test proved, they were Staphylococcus pyogenes aureus ; in a few instances the microscopic examination, and particularly the culture test, showed streptococci — Gram-positive Streptococcus pyogenes ; in one case, in which suspicion was justified on clinical, less on epidemiological grounds, the suppurating bubo contained crowds of bipolar bacilli, which by culture were shown to be Proteus vulgaris. From all these facts it follows, that in cases of real bubonic plague great abundance of B. pestis, i.e. of Gram-negative, non-motile bacilli of the same aspect and size and staining power, in the tissue of the inflamed gland, and less so, but still sufficiently conspicuously, in the hsemorrhagic and oedematous tissues around the swollen lymph gland, is a fact, and therefore from the abundance of such bacilli in the gland juice of a person aff'ected with symptoms resembling those of plague — fever and bubo — the preliminary diagnosis of bubonic plague may be justifiably ventured upon. The bacteriologist need not, and generally does not in his preliminary diagnosis, i.e. microscopic examination, rely on or know of epidemiological evidence, if any, such as would point to plague. Moreover, there are cases, and I have had several such, where at first neither the epidemiologist nor the clinician knew of all the facts concerning the case ; in such instances the bacteriologist has, of necessity, to rely entirely on his own analysis. In such cases the micro- I THE ESSENTIAL CAUSE 7 scopic examination alone of tlie gland juice is sufficient to assert that the analysis is pointing in a distinct manner to plague, viz. great abundance of Grram-negative, bipolar- stained bacilli all of the same aspect ; subsequent culture and animal experiment should complement the analysis and definitely prove the case to be one of plague. Further inquiry by the epidemiologist leaves no doubt about the correctness of the diagnosis. Sections through the inflamed glands show, on micro- scopic examination, the following condition : — The tissue around the gland is highly oedematous, some lymph vessels containing leucocytes, red blood corpuscles, and numerous B. pestis ; the veins and capillaries are distended and filled with coagulated blood ; amongst the blood corpuscles are numerous B. pestis. The aff'erent lymph vessels are filled with coagulated lymph — leucocytes and fibrin — and crowds of B. pestis, some of the vessels showing thrombi almost entirely composed of B. p>estis. The cortical sinuses are distended and densely packed with B. pestis, so are many of the medullary lymph sinuses, besides containing blood corpuscles ; the lymphatic tissues of the cortical and medullary portions contain a large amount of extravasated blood ; in many parts the lymph tissue is broken down, necrotic, and is not easily stained ; numerous B. pestis are found in it. The efi'erent lymph vessels are distended by, and filled with, coagulated lymph, numerous blood cor- puscles, and masses of B. pestis. In a subsequent chapter we shall reproduce a photogram of a section through the inflamed lymph gland of a rat inoculated with plague bacilli cutaneously at the root of the tail ; the illustration may be taken likewise as a faithful representation of the bubo as it occurs in man. 8 OEIENTAL PLAGUE chap. The blood of the peripheral circulation in an acute case of bubonic plague contains very few B. pestis. A few hours before death they can be recognised already in film specimens, though on making a culture (plate or tube) with a drop of the blood at this stage, numerous colonies appear ; but in the early stages they are difHcult to find either in films or by culture, unless the blood is derived from the skin over or about the bubo. The lungs and kidneys, after post mortem, show the plague bacilli, in proportion to their distribution and presence in the general circulation. The liver, and particularly the spleen, are the organs which, next to the bubo, contain B. pestis in great numbers. Sections show that they are chiefly present in the spleen pulp ; in this the blood spaces are distended by blood in stasis with crowds of B. pestis ; in many places these occur in continuous masses, and are arranged more or less in reticulated fashion corresponding to the blood spaces and small veins ; the pulp tissue itself around and between these masses is in a state of necrosis. Fig. 24, taken from a section through a guinea-pig's spleen, gives a good representation of the state and condition of the spleen in bubonic plague in man. (B) Septiccemic Plague. — Just as in the acute form of plague caused by inoculation of animals — which is almost always of the septicsemic type — so also in the septicsemic plague in man, the B. pestis are copiously distributed throughout all the organs, notably in the blood-vessels. Amongst these organs, the spleen, lungs, kidneys, and suprarenals,as also the liver and intestines, show conspicuous changes. These consist essentially in capillary haemor- rhages with crowds of B. pestis in the capillaries and I THE ESSENTIAL CAUSE 9 veins. In the lungs there occur lobular patches of con- solidation, due to fibrinous exudation into the alveoli and infundibula, the capillaries being distended by blood ; haemorrhages occur in the peribronchial tissue with numerous B. pestis. In the kidney the capillaries of the glomeruli are distended by and filled with blood and B. pestis ; the blood-vessels in the cortex next the boundary layer are in many places surrounded by extravasated blood with numerous B. pestis. The vessels of the Malpighian pyramids are distended with blood, and some contain B. pestis. Plague bacilli can be recognised in the space of the Malpighian capsules, in the connective tissue around the extravasated blood, and also in some of the uriniferous tubules of the boundary layer. It is obvious that the blood of the general circulation readily yields positive result qud B. pestis on microscopic examination and in culture. The intestine shows, both in its small and large divi- sion, occasionally numerous punctiform haemorrhages, the contents being bloody mucus ; such mucus, even on microscopic examination, and, better, on culture and experiment on animals, reveals the presence of B. pestis in it. The spleen is Literally packed with B. pestis ; it is enlarged, and on section shows all parts of the pulp permeated by continuous masses of B. pestis. The number of B. pestis in the blood of the general circulation after death is, in some cases, so great that their number is not much inferior to that of the blood corpuscles. In the liver many interlobular capillaries show masses of B. pestis ; the liver cells around them in some places are full of fat globules, in other places they show coagulation necrosis. In the suprarenals the blood-vessels are dis- 10 ORIENTAL PLAGUE chap. tended by blood : in some of these vessels are seen con- tinuous masses of B. pestis ; particularly is this the case in the medullary part, in which extravasated blood is not uncommon. The description given here is taken from the examina- tion of the organs of animals (guinea-pig, rat, mouse) dead of acute plague, but on comparing with them sections through the hardened organs derived from a human subject dead of septicaemic plague, I have no doubt the above description is also correct for the human subject in general. (C) Pneumonic Plague. — I have had the opportunity of examining cases of acute pneumonic plague — two sailors who died in the port of Hull in 1902. Pieces of lung and spleen were submitted to bacteriological examination ; the microscopic examination of the juice of the inflamed lung was alone sufficient to make diagnosis certain. Figure 2 shows a film specimen of the lung of one case ; in the other case the appearances were exactly the same. The photo shows an almost uniform mass of beautifully stained bi- polar bacilli amongst blood corpuscles, and as there exists, except in plague, no pathological condition — no acute inflammation of the lung — in which a film specimen of the juice shows crowds of uniform bipolar bacilli, the diagnosis could be made at once. Culture and experiment fully confirmed the diagnosis. Also the spleen, in film specimens, showed abundance of bipolar bacilli like P. pestis, but they were not anything like so numerous as in the film specimens of the lung. The greater portion of the lung in these cases was in a state of red hepatisation — deeply red, almost purple, — and bits of it sank in water. -.;« Fkj. 5. Fio. H. Fig. 5. Stained film of the inguinal bubo of a rat, cutaneoualy infected with a trace of culture of B. pestis. x 1000. Fig. 6. Stained film of inguinal bubo of a rat, after being inoculated cutaneously at the root of tail with pharyngo-laryngeal miicus of a rat dead of plague with extensive pneumonia, x 1000. Fig. 7. Stained film of lung juice of a monkey dead of pneumonic plague after inoculation. x 1000. Fig. 8. Stained film of liver juice of same monkey. x 1000. * . ■/ -'='•■> ^■■-.•■■. ' -.'V . ' t -* ^•* Fli:. 7. V'' \ >■'«•, t ■) ' 1 i Fkj, S. I THE ESSENTIAL CAUSE 11 Sections were made and stained ; examined under the microscope the hepatised portions showed uniform and dense infiltration with leucocytes and red blood corpuscles, the alveolar septa indistinct, the infundibula and bronchi distended by and filled with red blood corpuscles, leuco- cytes, and fibrin. Everywhere in these parts the walls of the infundibula, bronchi, and alveoli were indistinct and more or less broken, and everywhere between the blood corpuscles and leucocytes there were B. pestis in con- tinuous streaks, so much so that they filled all spaces left by the cells ; some of the bronchioles were plugged with continuous masses of B. pestis. Haemorrhage was present in the peribronchial tissue. The rusty hsemorrhagic sputum of cases of plague pneumonia during life is described, by some observers, as showing, besides numerous normal bipolar plague bacilli, also some spindle-shaped and other swollen involution forms. I have not come across these either in the lung juice or lung sections of the above two cases, nor in the bronchial contents of the afiected lungs of animals which had died of subacute plague, in which the lungs showed larger or smaller, more or less necrotic patches, or were in the condition of red hepatisation ; whether these spindle forms occur naturally in the sputum or are artefacts, made when preparing the film specimens, I am unable to say. I have paid particular attention to this point in connection with the exudation which is invariably present in the larynx, trachea, and bronchi of animals (guinea-pigs and rats) which are aff'ected with subacute plague, and in which the lungs are the seat of severe inflammation and necrosis (pneumonic plague), but I have not been able to meet with these spindle forms, and, as mentioned above, I 12 ORIENTAL PLAGUE chap. have failed to find them either in the numerous film specimens or in the numerous sections which I have examined of the above two Hull cases of pneumonic plague ; all these showed everywhere only oval or cylindrical bipolar bacilli. 11. Plague in Animals The chief animal to be considered in this connec- tion is, of course, the rat, and of this species I have had the opportunity to examine in several instances rats naturally dead of plague, while in other instances dead rats were found to have been affected with another microbe, not B. pestis (see below). I will describe here the appearances in rats that had died of plague in docks and in warehouses in Cardiff. P.M. — The most strikingly affected organ was the spleen, this organ being dark red, firm, and at least twice its normal size ; when cut into, it showed a fairly dry cut surface ; cover-glass impressions made of the cut surface, stained and mounted, showed everywhere abundance of cylindrical bacilli with rounded ends and marked bipolar staining ; the liver, kidneys, and lungs were more or less congested, so were almost all lymph glands — film specimens of all these organs showing abundance of typical cylindri- cal bipolar B. pestis. The heart's blood contained likewise abundance of B. pestis. The small intestine — particularly the ileum — was relaxed and contained san- guineous mucus, in which numerous bipolar plague-like bacilli could be recognised. The bladder was in one case distended, and filled with blood-tinged urine ; in others it was collapsed and empty. In the blood-tinged urine, I THE ESSENTIAL CAUSE 13 kept for some minutes in a watcli -glass, bipolar bacilli could be found in the sediment. Cultures made of the spleen, lymph (inguinal) gland, kidney, liver, and lung, all produced a crop of typical colonies of B. pestis, most abundant in the case of the spleen and heart's blood. From this it follows that the form of plague of which these rats had died was the septicsemic form, viz. conges- tion of the viscera— particularly the spleen, lymph glands, and lungs — with general distribution of B. pestis in the circulation. The distribution in and effects of B. pestis on rodents infected with materials containing B. pestis are subject to certain variations, which will be considered fully later in connection with the experimental production in various ways of plague in these animals ; we proceed now to consider the morphology, cultural characters, and experimental effects of the B. pestis. CHAPTER II CHARACTERS OP THE BACILLUS PESTIS (A) Morphology. — The plague bacillus is a non-motile rod, of a short oval to cylindrical shape, possessed of rounded ends, and measuring in dried or stained film specimens of the tissues on an average from 0"8 /x to 1'6 yu. in length, 0'4 /x to 0"8 ya in thickness. Measurements which I made of various races show that the longest bacilli occur in the bubo of the rat spontaneously dead of the plague ; these bacilli are at the same time well rounded, almost slightly tapering at the ends. Next in size are those of the bubo of man affected with plague, presumably through the rat. The B. pestis stains readily with all the aniline dyes usually employed for staining bacteria ; the only special feature about the staining of the B. pestis is that when taken from tissues — film specimens — and subjected to particular staining, most individuals show within a deli- cately stained sheath a marked bipolar arrangement of the stained or chromatic substance, i.e. rods, short or long, with rounded ends, and showing a stained mass at each end, whereas the middle part is clear and not stained ; that is to say, the chromatic substance is limited to the 14 r S' S>i l-\r.. [>. Fill. 10. \'\r.. ]1. Fig. 9. Stained film of blood of a guinea-pig dead of plague after inoculation with B. pestis. Bipolar plague bacilli amongst blood discs, x 1000. Fig. 10. Stained film of the blood of another guinea-pig dead of inoculated plague. X 1000. Fig. 11. Stained film of blood of a mouse dead of acute plague after cutaneous inoculation. x 1000. Fig. 12. From a stained section through the medullary part of the inflamed inguinal lymph gland of a rat dead after cutaneous inoculation at the root of tail, same rat as Fig. 6. A mass of plague bacilli (dark) in the lymph space — the lighter part — filled with effused blood. x 300. Fig. 13. Same preparation as in Fig. 12. The lighter parts are the medullary lymph sinuses filled ivith effused blood ; the darker parts are the masses of adenoid tissue, of which only the densely aggregated nuclei are seen. X 300. w^^l ^^^'s,f-IJ' «vf^- L^^.A^-^-*' ^ rV Fig. 12. Fk;. la CH.II CHARACTBES OF THE B. PESTIS 15 ends of the rods, whereas the middle portion is occupied by a vacuole. Some observers (Fisher) maintain that this peculiar staining is observed only in dried (film) specimens ; but I cannot accept this interpretation as entirely satis- factory, because I find, on careful examination of B. pestis in the hanging drop, that some bacilli show a central vacuole already in the living and fi:esh state ; moreover, such a vacuole is also observed in many other bacteria in the fresh condition, as also in stained and dried specimens — e.g. B. coli, B. typhosus, Proteus vulgaris, — with this difference, however, that B. pestis shows the bipolar staining, both in dried film specimens of tissues as also of culture, in a more conspicuous manner and more constant than other bacteria. A further point to be mentioned in this connection is that in B. pestis taken from the tissues — and this applies notably to B. pestis in the bubo — a fair number of individuals show an unstained vacuole either at one or both ends, whereas the rest contains the stained chromatic substance. Plague bacilli of this kind appear at first sight to exhibit one or both ends truncated or concave, the former if the vacuole is at one end only, the latter if each end has a vacuole. Such forms do not occur in culture. The bipolar condition is always marked and easily demonstrated both in B. pestis of the tissues as also of recent culture, provided the film specimens are well stained and then well washed ; if the specimen is overstained and insufficiently washed, the whole bacillus appears either uniformly stained, or it shows in places slight differences in depth of colour. The best methods of staining to show the bipolar character are these : — 16 ORIENTAL PLAGUE chap. (a) Methylene blue and eosine, and (b) Dilute alcoholic fuchsin. As to (a) : a mixture is made according to Czinzinski's formula. It is this : — Concentrated aqueous solution of methylene blue, Griibler, 50 cc. Eosine (soluble in alcohol) . . . 0"5 gram. Absolute alcohol . . 70 cc. Distilled water . . 130 cc. This stain, if correctly made and properly used, is far preferable to any double stain that I know ; it is most useful for tissues (film specimens, as also sections of hardened tissues) not only containing bacteria or fungi, but for all histological and pathological purposes. Nuclei of cells, certain granules and bacteria assume a deep- blue colour ; cell substances, eosinophyle granules, red blood corpuscles appear bright pink. Film specimens are fixed, as usual, in the flame, then placed in absolute alcohol for about half a minute, dried, and placed, film downwards, over the stain contained in a watch-glass ; here they are heated, the watch-glass being held by forceps high over a small flame till the dye shows distinct steaming. Wash well in tap water, then in distilled water, dry, and mount in balsam. The plague bacilli appear deep blue (blue black) and distinctly bipolarly stained, the red blood corpuscles are pink, the nuclei of leucocytes and other cells more or less deep blue. Sections are placed first in absolute alcohol for several minutes, are then kept in the cold stain for several (six to twelve) hours, are then well washed in water, and passed in the usual manner through absolute alcohol, xylol, and finally mounted in balsam. In these sections the contrast II CHARACTERS OF THE B. PESTIS 17 between blood corpuscles and connective tissues — pink, — bacteria and nuclei — blue, — is very striking. I have extensively used this mixture both for film specimens of tissues and for sections for the last thirteen years, and do not consider any other mixture comparable to it in effecting strong contrasts and bringing out the different parts of the tissues, bacteria, fungi, etc., with admirable distinctness. (6) The ordinary Ziehl's carbolfuchsin is used ; a small quantity of it is diluted with an equal volume of absolute alcohol ; over this fluid in a watch-glass is placed the cover film specimen, having previously been kept for half a minute in absolute alcohol as above ; the film specimen remains in the dilute fuchsin for ^-f-1 minute, then it is well washed in tap water, then in distilled water, dried, and mounted in balsam. The plague bacilli both of tissues and of recent culture show polar staining very distinctly ; but it is essential that the films after staining should be well washed — that is, until no further discharge to the water of pink colour is noticed. These two methods suffice for all purposes ; in fact, the first-named double stain will practically be found quite efficient. B. pestis do not retain the stain after Gram solution, that is they are Gram-negative, and share there- fore this character with the microbes of the coli-typhoid and with those of the proteus group ; it is important to remember this, because it is just with these two groups {B. coli, B. Gaertner, proteus) that error in diagnosis may be, and as a matter of fact has been, in some instances, committed. Judging from the accounts given by different observers, " Gram staining " appears as a sort of variable quantity ; I will therefore state here the manner which c 18 OEIENTAL PLAGUE chap. from very long experience I consider as perfectly reliable for obtaining the necessary result. Film specimens fixed in the flame are placed in absolute alcohol for |- to 1 minute, then are placed, film downwards, on gentian violet anifine water contained in a watch-glass ; after one minute they are removed, well drained with blotting-paper, and then transferred to Gram solution (iodine dissolved in iodide of potassium), where they remain for two minutes ; they are then transferred to two successive lots of absolute alcohol, in each being washed for a few (two to five) seconds, then well washed in water, dried, and mounted. Gram-positive bacteria, like B. anthracis, B. diphtherice, Staphylococcus aureus, and others, appear of a deep-violet — almost black-violet colour ; Gram-negative bacteria, like those of the coli- typhoid group, proteus, gonococcus, B. pestis, are dis- coloured, in fact are not stained. A good result is obtained by using Gordon's modification, particularly when the material contains, or is supposed to contain, a mixture of Gram-positive and Gram-negative bacteria. This method is as follows : — The Gram staining is made in the same manner as above, with this difference, that the specimens remain in the gentian violet f to 1 minute, in the Gram solution for the same time (f to 1 minute), and after washing in alcohol, and then in water, are placed in 0"5 p.c. watery fuchsin solution for five to ten seconds, then washed in water, dried, and mounted. The result is that the Gram-positive bacteria, having retained the gentian violet stain, appear violet black, whereas the Gram-negative bacteria, having lost the first stain by the Gram solution, have taken up the second, viz. the fuchsin stain, and therefore appear bright pink. Film specimens of pus of a m ■f. V Fr(;, 14. ^ ;.» ^ ..«:>".••■ ■ ^ Fir,. 15. Pig. 14. Stained film of spleen juice of a guinea-pig dead of acute plague. Crowds of bipolar B. pestis amongst red blood discs and nuclei of leucocytes. X 1000. Fig. 15. Stained film of spleen juice of a rat dead of acute plague after inoculation. x 1000. Fig. 16. Section througli tlie consolidated lung of a rat dead twelve days after cutaneous inoculation with juice of bubo. The pbotogram shows on the upper left the consolidated lobule ; the rest is interlobular tissue containing on the right a bronchus in cross section and filled with exudation, on the left a blood-vessel in cross-section and filled with blood. x 30. FiQ. 17. Part of the contents of the bronchus of previous figure, showing crowds of B. pestis. x 1000. ''^^ -H. ^K , ^\ ^^^9«''^ *■ ^ N \ j^^a^kif* / J i -* ^ «. •1': 1 ? t 4 4 i. •1 «f», * i */- -•SJl. Ij'iu. IB. {,..«;£ 5..' .■.••7 j^**. J,. II CHARACTERS OF THE B. PESTIS 19 suppurating bubo stained after this method have, in several instances, yielded instructive specimens : Staphy- lococcus aureus. Streptococcus pyogenes, diphtheroid (xerosis) baciUi appeared deep violet ; B. pestis, proteus, coli-like microbes, bright pink. Plague bacilli are described by some observers as being possessed of a capsule. This I think is based on a misunderstanding : when film specimens, say of bubo or other diseased tissues, are fixed and then stained, and if the ground substance, owing to the thickness of the film, happens to be present in too thick a layer, or if the film has been insufiiciently heated, or if the specimen is insufficiently washed after staining, the deeply stained bacilli or cocci, as the case may be, appear surrounded by a clear space ; this is owing to the fact that the ground substance, which is also more or less stained, has during the drying process shrunk away from the bacilli, therefore the latter appear surrounded by an unstained clear area, which might be thus taken for a capsule surrounding each bacillus. But this is, of course, not a real capsule, such as surrounds the pneumococcus for instance, for this capsule can be actually stained ; whereas the other is merely a space, and cannot be stained. When the film specimen is thin, well heated, and the preparation after staining well washed, no capsule can be observed on the plague bacilli. I have paid particular attention to this point, and can speak confidently about film specimens made of bubo materials, of the spleen, the lung, and blood of human plague cases or of plague animals. Nor is there any trace of a capsule around the individual bacilli or the chains of bacilli which make up the characteristic powdery or floccular sediment of broth-cultures of B. pestis. 20 ORIENTAL PLAGUE chap. When a guinea-pig is injected intraperitoneally with a trace of virulent B. pestis, the animal is found dead within twenty -four to thirty hours ; the peritoneal cavity contains a quantity of grey slimy exudation, which, under the microscope, is made up of a sticky, viscid ground substance in which are embedded densely packed B. pestis, singly, in dumb-bells, and short chains. In stained film specimens the bacilli appear surrounded, though somewhat irregularly, by a faintly stained broader or narrower capsule ; this is the gelatinous ground in which the bacilli are suspended (see Fig. 26), but it is by no means comparable to a typical capsule such as surrounds the Diplococcus pneumonicB. As will be mentioned later, the B. pestis forms on the surface of solidified agar a slimy translucent layer ; when a particle of it is removed with a platinum needle it is viscid and is easily drawn out into threads ; it does not emulsify readily, because the plague bacilli are agglutinated together into larger or smaller masses by a viscid hyaline intercellular secretion ; stained film specimens show this intercellular substance faintly stained, but this is not comparable to a real capsule. In gelatine-surface cultures the growth of B. pestis is devoid of this slimy character, the plague bacilli emulsify more readily in salt solution, and there is in film specimens of such emulsion no capsule recognisable. From all this it follows that the B. pestis does not possess a real capsule such as is possessed by Diplococcus pneumonicB. (B) Cultural Characters. — The plague bacillus grows well at 37° C. ; it grows also well, but slower, below 37° C. down to 20° C. and less. There seems a misunderstanding on the part of Professor Simpson in saying, in his Treatise / Fig. 19. Fig. 18. Section througli a lobule of the lung in pneumonic plague of a guinea- pig. Most of infundibula and alveoli are filled with exudation ; in the centre several vessels filled with plague bacilli — dark in figure. x 85. Fig. 19. The exudation in one of the infundibula of previous figure more highly magnified ( x 1000), showing that the exudation is practically a continuous mass of B. pestis. x 1000. Fig. 20. From a section through the lung of a guinea-pig dead of subacute plague, showing a nodule with masses of plague baciUi (dark). x 85. Fia 21. From a section through the lung of a guinea-pig dead of subacute plague, showing a nodule the centre of which is the alveolar duct and corresponding alveoli, all filled with plague bacilli (dark). x 100. Fig. 20. , A •:.;•.» -l «. * "' >^' -^• Fig. 21. 11 CHARACTEKS OF THE B. PJESTIS 21 on Plague, that the plague bacillus grows better at the lower than at the higher temperature. I am confident it would considerably delay diagnosis in a given analysis of suspected material if the cultures were kept at a tem- perature lower than 37" C. Plague bacilli planted, for instance, on agar kept at 37° C. show their colonies well developed to the aided and unaided eye already after twenty-four hours, whereas when kept at the temperature of 20° to 25° C. for forty-eight hours would be only just discernible with a glass. I believe the statement of Simpson may be explained in the following manner : — As will presently be shown, plague bacilli grow well, but somewhat slow, in broth even at 37° C. In preparing Haffkine's prophylactic (see later) a broth is used, of which the top is more or less covered with clarified butter (ghee) ; now this was introduced by Hafi'kine in order to obtain copious masses of plague bacilli, for he made the observation that in connection with the ghee drops of the surface a rich crop of plague bacilli is continuously reproduced (stalactites), and the culture flask being shaken every twenty-four hours or so, these masses fall to the bottom, forming and accumulating here as a copious whitish, powdery, flaky sediment. Now, the most abundant crops of bacillary masses sprouting downwards from the surface or ghee layer are developed if the ghee layer is in a solid state — they are far less abundant if the ghee layer is in a fluid state. From this it follows that such a ghee broth flask shows far less abundance of masses (granules and flakes) of plague bacilli if incubated at 37° C. — at which temperature the ghee is fluid — than at 25° C. — at which temperature it is solidified. In order to obtain in such ghee broth the most abundant masses of plague 22 OEIENTAL PLAGUE chap. bacilli, the flasks are incubated at 25° C. or even down to 20° C. This seems to me the origin of Simpson's state- ment, viz. that B. pestis grows better at lower temperatures than at 37° C. I have made series of comparative experi- ments with B. pestis of different races derived from various sources, planting them on the surface of various solid media such as are generally used for culture of bacteria in the laboratory, e.g. nutrient gelatine (streak and stab), nutrient agar (streak and stab), solidified blood serum (streak), ascites agar (streak and stab), nutrose ascites agar (streak and stab), and there never was any difference in regard to the growth of the different races, for all showed the quickest and most abundant growth when the culture tubes were kept at 37° C. According to my experience, the best way to obtain rapid and reliable evidence of the growth of B. pestis is to plant the suspected material on the surface of the ordinary, i.e. faintly alkaline agar (beef broth, peptone, agar), set in a plate dish and kept at 37° C. Next day the colonies are visible already to the unaided eye — better, of course, with a magnifying-glass — as small, rounded, grey, translucent, watery, slightly raised droplets. Examining these carefully with a magnifying-glass, it is noticed that the edge of the colonies is not quite rounded, showing already now slight irregularities ; these become more pronounced after a further twenty-four hours. At this time the colony is thinner at the margin than in the centre, is therefore slightly conical ; this also becomes more pronounced later. In transmitted light, and viewed under a glass, the substance of the colony — particularly in the central portion — is finely granular. Now, I wish already here to state that a difference II CHAKACTERS OF THE B. PESTIS 23 can be noticed between the colonies of B. pestis derived from a virulent source (human or rat) and those derived from a slightly virulent source (human or rat), this difference being that the former, as incubation proceeds, show a gradually more pronounced angular margin, and are more conically raised in the centre than the latter. What, however, is very characteristic of colonies of B. pestis growing on the surface of an agar plate is the fact that when attempting to remove a particle of the growth with a platinum needle it is found that the sub- stance of the colony is very viscid, so much so that either the whole colony adheres to the point of the needle or that it is difficult to take up any part of the colony ; further, when the growth is deposited in a drop of fluid — e.g. saline solution, water, or broth — it is difficult to emulsify it, the growth remains in coherent threads and flakes ; under the microscope, therefore, connected masses of bacilli — small and large, according to the amount of mechanical force used in the attempt to emulsify — are met with, some of these masses drawn out into longer or shorter strings. On the surface of gelatine the colonies of the typical B. pestis as soon as they are discernible, i.e. soon after forty-eight hours, show themselves as grey, in transmitted light as somewhat opaque, distinctly granular, rounded or slightly angular points. Later on the distinction between an angular thin marginal and a conically raised thick middle part becomes very marked ; so also the granular character of the colony, so much so that when examining in transmitted light, with a magnifying - glass, a well- developed colony, i.e. after four to six days incubation at 20° to 21° C, its substance, particularly in the middle parts, 24 OEIENTAL PLAGUE chap. is coarsely granular, almost filamentous, and its margin irregular and much fringed, such as is shown in Figs. 34 and 36. Seen in reflected light under a glass it may truly be compared to a limpet -like mass stuck to the surface of the gelatine (Fig. 28). Eemoving a particle of a colony from the gelatine surface it will be found to be coherent, but less so than from agar, and further, that it emulsifies better in saline solution than one from agar, but there are nevertheless present larger or smaller aggregations of bacilli. When viewing a surface gelatine plate, i.e. one con- taining numerous surface colonies, it will be found that, while all are more or less angular with filmy margin and conically raised centre, there is a distinction to be drawn if of a recent plate, e.g. one only a few days old (21° C), an impression preparation is made. When after staining and mounting they are examined under the imicroscope with a low magnifying power, say 60 to 90, two kinds of colonies will be noticed : (a) the great majority are typical colonies — angular patches composed of rod-shaped bacilli fairly well separated from one another by clear interstitial substance ; (6) a small number of irregular colonies, which, however, are composed chiefly of more or less thready or long cylindrical bacilli ; these latter colonies represent what I have called atypical colonies, and both sets are well shown in Figs. 41 and 42.'' We shall have the opportunity of showing that as regards virulence two types of B. pestis may be dis- tinguished : the first type (type 1) — human type — is the one that is the more virulent, and is found in typical ' As to the filamentous modification of B. pestis in salted media, see a later page. >>-. u 5^, a^«; r^V % ' Fig. 23 A* f [G. 24. Fig. 22. From a section through the hardened spleen of the same guinea-pig as Fig. 21, showing above and below in the figure masses of Malpighian corpuscles ; the rest — the main part of the iigure — is spleen pulp with numerous necrotic nodules ; in these nodules are masses (dark) of bacilli. x40. Fig. 23. One of the bacillary masses of the previous figure more highly magni- fied. X 300. Fig. 24. One of the bacillary (dark) masses of a necrotic nodule of a guinea-pig dead of subacute plague; the bacillary masses show a reticulated arrangement, being contained in the blood spaces of the pulp. x 100. Fig. 25. Film specimen of peritoneal exudation of a guinea-pig dead after peritoneal injection with B. pestis of attenuated type 2. Chains of bipolar bacilli in a gelatinous matrix. x 1000. Fig. 26. Stained film of the peritoneal exudation of a guinea-pig dead after intra- peritoneal injection with B. pestis, showing the bipolar bacilli embedded in a gelatinous matrix, and simulating capsules. x 1000. V X s' 1m\ ■N. •»-■ \ '■Is 1 . V N Fig. 25, \' .. «» # .s m • V »v » » t'Ki. 26. II CHARACTERS OF THE B. PESTIS 25 human cases of plague ; the second type ('type 2) — rat type — is the one which is less virulent, and which is characteristic for the rat, that is when it has been pro- pagated through rats. These two types differ in the nature and aspect of their colonies during the early period of their growth on the surface of nutrient gelatine ; type 2 forming colonies distinctly more translucent and less granular than those of type 1, and at the same time those of the former are less angular, more rounded, than those of the latter or type 1. It will be understood that these differences, although distinct and easily ascertained in the early phases — two to five days at 20° to 21° C, — become lost as development proceeds ; after ten days or more the angular thinned margin, the granular opaque raised centre, appear the same in both sets. Microscopic specimens of the two types of colonies during the earlier phases show also a marked distinction, inasmuch as those of type 1 are distinctly more cylindrical than those of type 2 (see Figs. 38 and 39). In stab culture of B. pestis, both in gelatine and in agar, the stab becomes marked as a series of opaque granules, and after some progress has been made each granule shows a filmy projection at one side or the other (Fig. 33), at the same time the upper or free end of the stab being marked by a greyish-white filmy expansion of growth, which in cultures (agar) of some standing (two to three weeks) has the character of a rounded shield, showing distinct concentric and radial markings as shown in Fig. 30. This surface growth possesses the viscid nature of plague growth in a marked manner. Streak cultures of B. pestis on agar show a filmy, grey, translucent growth, which, as mentioned on a former page. 26 OEIENTAL PLAGUE chap. is of a characteristic viscid character. Streak cultures on serum and other agar compounds are of the same character. Later on the growth becomes thicker, less translucent, in reflected light of a slightly brownish tint, with numerous raised droplike round thickenings. On gelatine surface streak culture the streak becomes marked as an at first grey, then whitish, dry band, gradually thickening, and becoming more opaque and granular ; the centre of the streak is thicker than the margin, which latter is crenate, or, more correctly speaking, knobbed and with fine projections. The gelatine is not liquefied at any time. A gelatine streak culture of B. pestis, as also a gelatine surface culture containing isolated colonies of B. pestis, is, after several weeks' incubation, extremely characteristic : whitish, dry, thick, granular, opaque, thicker in centre than at margin ; in streak, knobbed margin ; in isolated colonies with filmy irregular margin and conically raised centre. In milk B. pestis grows well at 20° to 37° C. without causing any change of the milk either in aspect or its fluid character. In litmus milk a slow and gradual change of the at first blue colour into less blue, then violet, and ultimately slight red colour takes place, thus showing that the B. pestis is a slow acid producer. This can be proved also in this way, that if of a culture of B. pestis in alkaline glucose broth, incubated at 37° C. for two or three days, a few drops be added to a few cc. of a watery solution of litmus, this at once turns distinctly red. B. pestis grows on steamed potato but feebly, forming thereon a transparent film ; the growth is therefore invisible to the unaided eye, and only by taking a particle of the inoculated surface and examining it in a II CHARACTERS OF THE B. PESTIS 27 drop of fluid under the microscope can the actual presence of growth be ascertained. In neutral-red beef broth the growth is of the same character as in ordinary alkaline broth (see below), the normal cherry colour of the neutral-red broth remaining unaltered. B. pestis does not thrive in glucose taurocholate peptone water (MacConkey fluid), nor in lactose peptone water, nor in peptone salt water. B. pestis grows well at 37° C. in faintly alkaline beef- broth peptone ; the broth remains clear, but along the glass wall and at the bottom there appear whitish granules and flocculi, these being masses of the bacilli, many forming longer or shorter chains ; ^ as growth proceeds the amount of floccular sediment increases, but is inot at any time very copious. Pakes and Joseph (Transactions of the Pathological Society of London, vol. Ivi. p. 135) show that B. pestis grows in slightly acid broth, and by this means can be readily difierentiated from the pneumo- coccus present in the sputum of pneumonic plague. For the production in broth of greater amounts of bacillary masses, Hafi'kine hit upon the plan of covering the top of the broth with a layer of clarified butter or ghee. As mentioned above, when incubation takes place at a tem- perature at which the ghee remains solid, i.e. temperatures at or below 25° C, its (the ghee's) under surface becomes covered with masses of growth hanging down like shorter or longer whitish fringes (" stalactites ") ; these, on dis- turbing the fluid, e.g. by shaking, become detached and ^ The formation and the arrangement in chains is noticed in B. pestis whenever it gi-ows in fluid media — broth, fluid serum, condensation fluid of agar or serum and the like. The same is observed in the peritoneal fluid. These chains at first sight resemble streptococcus chains. 28 OEIENTAL PLAGUE chap. sink to the bottom of the fluid. This falling of copious flakes of growth from the surface to the bottom is graphi- cally compared by Hafi'kine to a fall of snowflakes. On further incubation new stalactites are developed, which in their turn, on shaking the culture, become detached, and fall to the bottom to increase the deposit. In this way — by rest and then shaking — in the course of four to six weeks a continuous re-formation of bacillary masses (stalactites) can be ensured, so that by this time consider- able amounts of bacillary sediment are obtained. A flask of slightly alkaline ghee broth infected with B. pestis, and kept for some weeks at 25° C, shows an almost com- plete pellicle of growth on the top of the fluid, and from it projects downwards into the fluid a dense forest of threads or stalactites, which on slight disturbance rapidly fall to the bottom (Figs. 44 and 45). The formation of stalactites in ghee broth kept in a perfectly quiet place is very characteristic for B. pestis ; but it has to be added that unless the culture is kept in a place where absence of all disturbance, vibration, etc., can be ensured, no visible stalactites are formed. I have shown that a strain of B. pestis after many transferences in artificial culture may lose the power to form stalactites altogether, but regains this power when passed through an animal. B. pestis obtained from a case of pneumonic plague in 1896, and kept up in the laboratory in sub- culture, failed completely to form stalactites in ghee broth in 1899, but at once regained this power when cultures were again started from the spleen and bubo of a guinea- pig dead of acute plague after subcutaneous injection with this same strain. For diagnostic purposes the formation of stalactites in ghee broth is of value, although in practice Fig. 27. /»' .'»,!) %*? 3" I :£) \i<^' ..^^^ Fig, 28. Fig. 27. Stained film specimen of the bubo fluid of a protected guinea-pig, the plague bacilli as involution forms. x 1000. Fig. 28. Young colonies of B. pestis on the surface of a gelatine plate, after several days' incubation ; the colonies are raised, conical in the centre, filmy and irregular at the margin, the centre granular or even filamentous. xl7. Fig. 29. Young colonies of B. pestis on tlie surface of an agar plate ; the colonies are thicker and granular in the centre, filmy and slightly irregular at their margin. x 50. Fig. 30. Characteristic colonies of B. pestis on agar after several weeks' incuba- tion ; the contrast between thickened centre and iilmy crenate margin is striking. x 2^. Fig. 29. Fig. 30. n CHARACTERS OF THE B. PESTIS 29 it need not, on account of the delay and the above difficulties, be considered as essential, and also because there are other quicker means of establishing positive diagnosis. Hankin describes a modification of the B. pestis when growing in salted media, viz. that the bacilli grow out into long filaments. I have many years ago^ described such filamentous modification occurring in many microbes (coli-typhoid group and others) when growing in media to which more than the normal amount of salt is added, and I cannot therefore accept either Hankin's priority (gener- ally attributed to him in this matter) nor that such filamentous change is characteristic for B. pestis. (C) Experimental. — B. pestis produces in rodents after cutaneous or subcutaneous injection definite disease. This wUl be considered in detail later on, here we wish merely to give a general account of its action. A loopful, or even a part of a loop, of a 24 h. culture on agar at 37° C, or a trace of plague material (bubo, spleen) containing a large number of B. pestis, injected into the peritoneal cavity of a young or half-grown guinea- pig, causes fatal results in twenty to thirty-six hours, if the B. pestis is of normal virulence ; if the dose is too small or the virulence subnormal, death may be considerably delayed. In the former case the abdominal organs are found much congested, with petechise on the serous covering of the intestine and on the parietal peritoneum ; in the peritoneal cavity is copious, sticky, viscid grey exudation ; under the microscope, besides red blood corpuscles and a few leucocytes — the number of the latter 1 Klein, Grouse Disease and Fowl Enteritis, 1892, p. 31 ; Micro-organisms and Disease, new edition, 1896, p. 93. 30 OEIENTAL PLAGUE chap. inversely proportional to the- duration of the disease — the fluid is densely packed with B. pestis embedded in a gelatinous ground substance, many of the B. pestis forming shorter or longer chains. Staining film specimens, the bipolar nature of the individual bacilli is well brought out, as also the gelatinous ground substance, which here and there may be mistaken for a special capsule enveloping the bacilli (see a former page). The viscid nature of the exudation together with the dense aggregation of bipolar bacilli, many of them in longer or shorter chains, may be considered as fairly characteristic for plague ; but it is not absolutely so, since we shall mention some other microbes which, under similar conditions, produce similar results. Cutaneous inoculation of mice, rats, and guinea-pigs causes the disease with certainty. The great value of cutaneous inoculation, which was practised by the Austrian Plague Commission, lies principally in this, that very small amounts can be used for infection with positive results ; leaving out malignant anthrax, and one or two others, B. pestis is one of the few microbes which cause acute disease in rodents when applied in minute doses to a scratch or a surface incision of the cutis, or is merely rubbed into the cutis. This shows that the B. pestis readily and rapidly multipHes in the skin ; at the same time, as far as mice, rats, and guinea-pigs are concerned, when inoculated into the skin the B. pestis does not lose anything of its virulence. As regards mice and rats I proceed in the following manner : — The hairs are cut off with scissors from the skin of the dorsum at the root of the tail ; with the point of a scalpel which is previously dipped into plague material II CHARACTERS OF THE B. PESTIS 31 (bubo, blood, spleen) or into an emulsion of a recent culture of B. pestis (twenty-four hours' agar culture at 37° C.) a few scratches or superficial scarifications are made, or the surface cuticle is scraped off from the place bared of the hairs and slightly scratched with the point of a knife ; then a particle of growth from an agar culture (twenty-four hours at 37" C), having been removed from the culture with a platinum loop, or a particle of plague tissue, is directly rubbed in by the platinum loop or the scalpel respectively into the scratched skin. Provided the culture be of medium virulence, I have in a very considerable number of experiments never failed by this method to obtain positive results m mice and rats — that is, acute plague with fatal issue. According to the virulence of the culture, fatal issue, both in mice and ia rats, follows in as short a time as 30-40-48 hours ; or, working with less virulent culture, death may be delayed up to four or five days. In mice such delay is, however, rare even with less virulent culture, since mice are highly susceptible and promptly answer even to plague materials which, when tested on rats, and particularly on guinea-pigs, appear only of moderate virulence. Subcutaneous injection of mice and rats with doses much larger than are required for cutaneous inoculation does not cause quicker or more virulent results than cutaneous inoculation. It is otherwise with guinea-pigs : subcutaneous injection, while permitting the application of larger doses than does the cutaneous inoculation, causes — if the virulence is not abnormally low — fatal issue in between two and three days ; material which acts thus may be considered of normal virulence. Death in less than forty-eight hours in a guinea-pig after su"bcutaneous injec- 32 OEIENTAL PLA.GUE chap. tion even of large doses is extremely rare. Death after three or even four days would not necessarily indicate virulence greatly inferior than normal. Cutaneous inocu- lation of guinea-pigs with virulent and moderately virulent material is followed by death after four days up to seven, nine, or even more days ; and this mode of inoculation distinguishes in a marked manner the guinea-pig from the rat, for in this latter animal the result of cutaneous inoculation with plague material of great or moderate virulence always causes acute fatal illness. In the guinea- pig, on the other hand, material which on subcutaneous injection in moderate doses causes death in two to three days, and which material is therefore of normal virulence, when administered cutaneously causes fatal issue always much later, and with pathological symptoms different from those found in animals dead in two or three days. When death ensues later (four to seven days or more) the bubo and spleen, also the hver and lungs, exhibit more or less necrotic changes in the form of nodules and patches of various sizes and in varying numbers. Such is generally the case with guinea-pigs inoculated cutaneously even with virulent material ; it is the same also in guinea-pigs injected subcutaneously with material of less than normal virulence. Cutaneous inoculation of guinea-pigs with ex- ceptionally virulent material may cause death occasionally, but not invariably, in two to three days with symptoms of acute plague — that is to say, before necrotic changes in the bubo or spleen or lung had had time to develop and to make their appearance. The necrotic changes — viz. whitish nodules in bubo, spleen, liver, and lung, — which require at least four days for their development, follow cutaneous inoculation of the guinea - pig with Fiu, 31. Fiu. 32. Fig. 31. Streak culture of B. pestis on gelatine after a few weeks' incubation. Natural size. Fig. 32. Stab culture of B. pestis in gelatine after a few weeks' incubation. Natural size. Fig. 33. Tlie deeper part of the stab of previous figure magnified. x 4. Fig. 34. Colonies of plague bacilli on gelatine after some days' incubation. Virulent type 1 (human). x 8. •■': Fk4. 33. Fio. 34. II CHARACTBES OF THE B. PESTIS 33 normally virulent material, or subcutaneous injection with material of less than normal virulence. This form of plague with delayed death and necrotic changes ia the bubo, spleen, liver, and lung, I have termed the " subacute form." The rabbit is not so well suited for plague experiments, because its susceptibility is not sufficiently high and not sufficiently constant, and therefore a fatal result with a given material cannot be depended on. Body weight seems to make no difference, since a subcutaneous dose may be productive of fatal issue in one rabbit, while the same dose of exactly the same material may cause nothing more than transitory illness in a rabbit of lesser body weight. Amongst rats the tame or white rat is the most susceptible, the common brown sewer rat is considerably less so, and therefore the former is for experimental purposes far preferable. Another reason which enables us to dispense with the sewer rat for laboratory purposes is the fact that between 25 to 30 per cent die when kept in captivity, and, further, the fact that they are unpleasant and unsafe to handle ; whereas the tame or white rat (all white, white-black, white-brown, white and plum-coloured) is born and bred in captivity, lives well in cages, and is easily and safely handled. Next in plague susceptibility to the white rat is the brown dock and ship rat ; about the same, but a little less perhaps, is the black or plum-coloured ship rat, and stUl lower in the scale is the brown rat with yellowish cream- coloured belly — the Norwegian rat (which we get from ships coming from Norway). The common sewer rat seems to compare as regards susceptibility with the Norway rat. 34 ORIENTAL PLAGUE chap. Statements have been made (Calmette) according to which, the virulence of a strain of B. pestis may become enhanced by its passage through a series of animals of the same species, but that while thus increasing in virulence for this species it does not follow that this same strain of B. pestis possesses also increased virulence for another species of animals — in fact the contrary generally is said to take place. Quite a different statement is made by Hankin and Colonel Skinner, viz. that, on the contrary, the virulence of B. pestis decreases on its passage through a series of animals of the same species, including man. I have had a considerable experience in testing these propositions and cannot agree with either. I have tested B. pestis derived from acute fatal human cases by injecting the plague material directly into guinea-pigs and rats, in the former subcutaneously, in the latter cutaneously, and have proceeded to do so from guinea-pig to guinea-pig and from rat to rat, both by using the material directly from the spleen of a previous animal, as also by using twenty- four hours' agar culture of the spleen of the previous animal, and as a result I have not noticed anything of an increase in virulence of the B. pestis in its passage through these series of animals. True, B. pestis, like other pathogenic microbes, lose in virulence by trans- mission in the laboratory through series of subcultures on artificial media, and, unless this decrease has become very great, become generally enhanced in virulence by passage through the suitable animal body ; but this has nothing to do with the above statement that a race of B. pestis derived from a particular source (human or animal) undergoes increase in virulence by passage through a II CHAEACTEES OF THE B. PESTIS 35 series of animals. Nor have I seen anything of a decrease in virulence either in the animals of the same species or when plague material (bubo or spleen of the dead animal) is taken from one species (guinea-pig or rat) and is used for infection of the other species (rat or guinea-pig). What I found in a very large number of experiments made for this object is that it does not matter whether the animal which yields or receives the material is a guinea-pig or a rat, so long as the bubo, or spleen, or blood of the plague giver contains the typical B. pestis in considerable numbers, the result of cutaneous inoculation of the rat or of the guinea-pig is followed by fatal plague, acute in the rat, subacute in the guinea-pig. A difference, however, which I have noticed to occur and which denotes some kind of difference iu virulence, refers to an altogether different circumstance, viz. to the race of the B. pestis itself With this we shall have to deal in a future chapter. Another difference which is to be mentioned in connection with the above is the fact that B. pestis when passed through the mouse (dead of plague after inoculation) is as a rule of lesser virulence towards the other rodents than when the same race of B. pestis is passed through the rat or the guinea-pig. All races of B. pestis act virulently on the mouse, this animal being highly susceptible and easily affected with acute fatal effect by cutaneous inoculation of almost any B. pestis. CHAPTER III ANALYSIS OP PLAGUE MATERIALS Since Oriental plague, wMcli appeared in Hong-Kong 1894, in India 1896, had become pandemic, amongst the many ships — passenger and cargo — constantly arriving at English ports, there must be, as a matter of course, always a considerable number which have started from one or another plague-infected country— India, the Argentine, the Levant, Egypt, and China ; it therefore behoves all port sanitary officers to be continually on the alert, both as regards possible infection of the crew as also of the cargo and rats of such vessels. While in several instances such ships have, on arrival, been found to have had on their voyage cases of plague in man or in rats, or in both ; others were, according to the captain's statement, free of suspicious illness both in man and the rat, but on closer inspection were found to harbour one or other of the crew affected with inguinal bubo ; further, ships which have started from an infected locality, although free of suspicious illness on the voyage, have, soon after arrival into a port, been found to harbour one or other of the crew affected with, or rather developing, suspicious illness ; in a further set of ships coming from infected localities the presence of dead 36 KlG. 3i Vw. 30. Fig. 35. Colonies of plague bacilli on gelatine after some days' incubation. Attenuated type 2 (rat type). x 8. Fig. 36. Oolonies of B. pestis on gelatine after many weeks' incubation. Attenuated type (rat type 2). x 5. Fig. 37. Same colonies as in previous figure, more magnified. x 10. Fig. 38. Film specimen of the growtli of B. pestis from agar culture, twenty-four hours' incubation. Virulent human type 1. x 1000. Fig. 37 -,*••* '^•^ '>,?'.■ ■^■^ ^l^^" ' Fii!. 38. cH.ni ANALYSIS OF PLAGUE MATEEIALS 37 rats, nay even highly suspicious illness amongst one or other member of the crew, had been, owing to the master's negatory statements or from some other cause, either overlooked or had been discovered only some time after landing crew or cargo, or both; and finally, ships have come into port which during the voyage and on landing had on board cases of suspicious illness, presumably plague, in man or in rats, or in both. Dr. Bruce Low, in Report and Papers on Bubonic Plague (Loc. Gov. Board, 1902), has dealt in detail with all such cases, and it is not my object to repeat what Dr. Low has already ably and fully described, but I wish merely to point out briefly some of the many occasions when the aid of the bacteriologist is called in to help to make, or to verify, diagnosis. In addition to these occasions — that is, when bacteriological diagnosis is wanted of cases directly con- nected with a ship arriving from an infected country — there are a good many other occasions when in times of threatened invasion cases of suspicious illness are brought to the notice of medical ojQElcers of health in different inland parts, which cases per se might be cases of Oriental plague, and which might be such on account of their having been in some indirect way in contact or in relation with men or goods coming from a ship that had been some time previously in contact with an infected country ; that is to say, now and again isolated indigenous cases of suspected or real plague may occur, and as a fact have occurred, e.g. such as suddenly appeared in an hotel in Glasgow in 1902, in Liverpool in 1904. It is unnecessary to emphasise the importance of early recognition of such indigenous cases in order to take at once the necessary preventive measures. It is equally obvious that in 38 OEIENTAL PLAGUE chap. times of pandemics such as we have had now for several years, cases simulating indigenous cases of plague may occur which are clinically indistinguishable from real plague, but on bacteriological analysis turn out not to be plague ; wherefore the bacteriological analysis of such cases is obviously of the first importance. During the last nine or ten years I have analysed for the medical department of the Local Government Board materials derived from a good many ports and also from inland places in considerable numbers. These materials were taken from cases — man or rat — which were either prima facie, i.e. epidemiologically, probably cases of plague, or which might have been plague both on clinical and on epidemiological grounds. Without wishing to give the details of these analyses I will restrict myself to giving a few instances of diflferent categories only, in order to show on what lines these analyses were carried out : — 1. The s.s. Simla.^ — " The Simla is a hospital ship, which had been conveying invalids from South Africa to Southampton. This vessel arrived at the latter port on March 13th, 1901, having touched at Plymouth on March 12th, where she had been given pratique by the Customs after all the usual questions had been satisfactorily answered. A case of enteric fever was landed at Plymouth and another at Southampton. It appears that two days after leaving Cape Town a Lascar member of the crew came under the ship's surgeon's care with a bubo in the groin. Though a natural suspicion of plague arose at once the idea was dismissed, and when the ship was boarded at Plymouth, and again at Southampton, and the usual questions were put as to plague, cholera, etc., no mention of this case was made in their replies by the master or the surgeon of the ship. On landing, the Lascar obtained admission to the South Hants Hospital for treatment of a large abscess pointing in his groin. Some time prior to this Dr. Wellesley Harris, the port medical ' Dr. R. Bruce Low's Report and Papers on Bubonio Plague, p. 18. m ANALYSIS OF PLAGUE MATEEIALS 39 oflBcer of health, in view of the importation of plague by anomalous, mild, or unrecognised cases, had requested the authorities of the hospital to inform him when any cases of glandular swelling were admitted for treatment. On March 17th the resident surgeon sent Dr. Harris intimation of the Lascar's case. The medical officer of health at once took material from the abscess in the groin and sent it to the Board for bacterioscopic examination." The pus sent was examined in stained film specimens ; it showed numerous microbes: cocci, singly and in clusters; streptococcus chains; some diphtheroid bacilli, and some oval rods showing distinct bipolar staining. Agar plates (surface inoculation) were made, and a guinea- pig was injected subcutaneously in the groin with a fair amount of the pus. Next day the plates showed, besides colonies of cocci (albus and aureus), a few colonies of streptococci, and a sprinkling of colonies resembling those of B. pestis, viz. small, grey, watery, raised in centre, with slightly irregular margin. When taken up with the point of a platinum needle they were found viscid, and placed in saline solution emulsified with difficulty. Examined in the hanging drop they were found non -motile rods in clumps and in streaks ; they showed in fuchsin staining (see above) distinct bipolar character and were Gram-negative. Subculture on gelatine and on agar produced typical growth of B. pestis. Patient recovered. The guinea-pig, injected in the groin, was quiet and slightly off feed after twenty-four hours ; it had distinct soft swelling in the groin, seemingly painful to the touch. With a pointed glass capillary pipette a drop of sanguineous fluid from the subcutaneous swelling was obtained ; examined under the microscope in stained film specimens it exhibited, besides a few leucocytes, a fair number of red blood corpuscles and a very large number of oval to cylindrical bacilli showing very marked bipolar staining ; they were non-motile and gave negative Gram staining. On account of the typical character of the plague-like colonies in the agar plates, and on account of the microscopic character of the bubo fluid of the guinea-pig, the diagnosis was made : Pestis hibonica. The subsequent subcultures on agar and gelatine of the bubo fluid of the guinea-pig and the death of the guinea-pig on the third to fourth day with all the typical appearances of plague in the groin and spleen — which organs were crowded with B. pestis — confirmed the correctness of the early diagnosis. 40 OEIENTAL PLAGUE chap. The subcultures obtained from the primary agar cultures, i.e. direct from the pus of the patient, as also those obtained from the bubo fluid of the guinea-pig during life, and those of the spleen of the animal after death, were, for some time afterwards, on several occasions used for experimental purposes on guinea-pigs and rats and found highly virulent. 2. " The s.s. Friary,^ from Alexandria, arrived at Hull on January 10th, 1901, having called at only one port on the return voyage, namely, Algiers. The usual inquiries on arrival were made by the Customs, who informed the port medical ofScer that on board there was the body of a sailor who died on January 10th, about twelve hours before the vessel reached Hull, from an illness then regarded as 'influenza.' The corpse was removed to the mortuary and after- wards buried. At the time of arrival no cases of sickness existed on board, but on January 12th two sailors sickened. They were seen by a private medical man as well as by Dr. Mason, the port medical officer of health, who made a provisional diagnosis of ' influenza with lung complications.' On January 15th two more members of the crew sickened, and subsequently two others also were attacked. All of these six cases proved fatal, and in all the diagnosis of plague was confirmed by bacterioscopic investigation." The materials submitted to me for bacterioscopic analysis were pieces of lung and spleen of two of the dead sailors. In both cases the lung pieces were deep purple red, solid, and sank in water. A film specimen (impression of a cut surface) made of the lung showed, besides a few leucocytes and red blood corpuscles, an almost continuous layer of oval bacilli with marked bipolar stain- ing in pure culture (Fig. 2) ; these bacilli were Gram-negative ; film specimens of the spleen likewise exhibited abundance of the same oval bipolar bacilli. Since these appearances of the lung juice do not occur in any other acute disease than pneumonic plague, the diagnosis of "plague" could be at once made. Cultures in agar plates and agar tubes, injection of guinea-pigs with lung juice and spleen juice of both cases, fully confirmed the diagnosis. 3. Manchester Case. — The second cook of a steamer which arrived at Middlesbrough had with other seamen been passed by the port sanitary authorities. He travelled to Manchester, where soon after arrival he was taken ill with fever and inguinal bubo, and admitted (June 10, 1905) to hospital. His illness was diagnosed as (1) pestis ■^ Dr. R. Bruce Low's Report, p. 14. Ill ANALYSIS OF PLAGUE MATERIALS 41 bubonica. He died on June 12. Capillary pipettes containing sanguineous fluid which had been taken by puncture from the inguinal bubo soon after the death of the patient were submitted for analysis. Film specimens showed numerous bipolar bacilli in size like B. pestis, Gram-negative. Diagnosis was made : " Probably plague." Agar surface plates were made with the material ; these brought forth in twenty-four hours (37° C.) pure cultures of colonies of typical B. pestis. A guinea-pig injected subcutaneously at the same time with a few drops of the original material showed, after twenty- four hours, a big soft swelling. A drop of the fluid was withdrawn from the swelling ; in stained film specimens it showed crowds of bipolar bacilli like B. pestis, Gram-negative, non-motile. Diagnosis was made : Pestis bubonica. Subcultures and further inoculations of guinea-pigs and rats, both from the original agar plate as also from the above guinea-pig, fully confirmed diagnosis of virulent plague. 4. A case of Plague at Tynemouth, September 1 904. — German sea- man of s.s. Bishopsgate, ill with bubo, suspicions of plague ; recovered. Juice of bubo, obtained by aspiration, was received in sealed capillary tubes. Film specimens showed no definite bacilli. With the bubo fluid agar surface plates were made, and a guinea-pig was injected subcutaneously in groin. After twenty-four hours one agar plate showed one, the other two colonies, which in aspect, character, and constitution (staining characters) were identical with those of B. pestis. The guinea-pig exhibited after twenty-four hours a soft distinct swelling, and was quiet and a little ofi' feed. A drop of fluid was withdrawn from the swelling by means of a pointed capillary pipette. This fluid in film specimens showed crowds of non-motile bipolar B. pestis. Diagnosis was now justified : " Plague." Inoculation of a further guinea-pig (subcutaneously) and a rat (cutaneously) with a colony from the agar plate, and a similar set with the juice of the bubo of the guinea-pig, (caused fatal plague in all the four animals inoculated. The two guinea-pigs as also the first guinea-pig (injected with the original material from the patient) died on the sixth day with post-mortem appearances of subacute plague : necrotic bubo, necrotic nodules of spleen. The cultures obtained from the spleen and bubo of the guinea-pig and of the rat inoculated with colonies from the original agar plate were subsequently used in the laboratory for experiments and study, and it was found that this 42 ORIENTAL PLAGUE chap. race of B. pestis exhibited the characters of our second or rat type, i.e. shorter rods than those of the human type, colonies more trans- lucent in gelatine, and of less virulence than the first or human type. It subsequently was elicited by Dr. Buchanan that this steamer had arrived from Hamburg, where a number of rats had been found on it, which rp.ts had been diagnosed to have died of plague ; the ship had been disinfected in Hamburg, and the seamen on leaving Hamburg were all well. But soon after arrival the seaman was taken ill and removed by the port medical officer to hospital as " being clinically very suspicious." 5. The notes of this case (5) are as follows : — " Purulent discharge from a suppurating bubo, most other groups of glands are enlarged " (May 28, 1904). "The patient is a sailor on a steamer just arrived from Rosario. One of the crew died suddenly on the voyage.'' The medical officer of health who forwarded the material added : " I think it is syphilitic, but I am sending the discharge in case it might by any chance happen to be plague." It has to be remembered that Rosario is an infected place, and several instances of plague on ships arriving from Rosario in English ports had been previously recorded. Film specimens showed amongst leucocytes and red blood discs numerous cocci, as diplococci, in fours and in small and large masses ; no bacilli. Agar surface plate was inoculated with the pus ; it showed, after twenty-four hours, crowds of colonies of typical Staphylococcus aureus in pure state. The guinea-pig that had been injected sub- cutaneously with a fair amount of the purulent matter showed no tumour twenty-four hours afterwards, nor later, and remained quite well. The diagnosis was therefore negative qua plague. Patient recovered. 6. Case at Plymouth.^ — Towards the end of February, Dr. Williams, the medical officer of health, reported to the Local Government Board a case as to which the medical attendant had been entertain- ing suspicion that the illness might be plague. The patient, a Jewish pawnbroker, became ill on February 16, with rigors, head- ache, and fever, attended with prostration. Painful glandular swell- ings developed in his armpit and groin. Material taken from this patient was submitted to bacterioscopic examination. What had added to the suspicion of the medical attendant was the fact that the pawnbroker had in the course of his business to handle a considerable amount of clothing that had already been ' From Dr. K. Bruce Low's Report, p. 32. ■•' „''^ :" • V • '"^ ." • • •" ' y ^. ' ., ;•; /'-.--■;•. '•.-•'.■.. •: •' ' ^•^''• * 1' * . --• ...... « , > •...*,•• * ..":'. ' f ^- •.-. •. % • * • • * #1 Fw. 39. V. ^'^ I'm. 40. Fig. 39. Film specimen from a recent agar OTilture of the attenuated B. pestis (rat type or type 2). x 1000. Fig. 40. Stained impression of a young colony of B. pestis (virulen t type) on gelatine. x 800. Fig. 41. Stained impression of an atypical colony — filamentous bacilli. x 800. Fig. 42. Impression of a number of young colonies of B. pestis on the surface of gelatine. x 80. One of these colonies was shown in Fig. 40 more magnified. Near the lower right margin and isolated the atypical colony shown in Fig. 41. "^^ Fig 41. ^ % m^ ^^i:-- Fig. 42. m ANALYSIS OF PLAGUE MATEEIALS 43 ^OTxi, and it was thought that possibly plague infection had been contracted through the instrumentality of infected clothing from some Unknown or concealed case. Sanguineous fluid taken from the glandular swelling of the armpit was submitted for examination ; film specimens showed amongst the red blood discs and pus cells numerous cocci (Gram- positive), either as diplococci or in small clusters : no bacilli. Agar surface plates yielded pure cultures of Staphylococcus pyogenes aureus ; a guinea-pig injected subcutaneously with a fair amount of the material showed no illness. Diagnosis : Infection with Staphylococcus pyogenes aureus. Case recovered. 7. Dr. Williams, port medical oflficer (port of London), informed the medical officer of the Local Government Board that two China- men (sailors, s.s. Dundas and s.s. Haselder) had died in the Seamen's Hospital at Greenwich of pneumonia. They had before admission been living at a lodging-house in Limehouse Causeway. One was admitted to hospital on the 19th December 1903, and died the same day ; the other was admitted on the 24th December at 1 P.M., and died at 4 p.m. on the same day. The house physician informed that " the cases were very suspicious," he believed them to be plague, and he was supported in this opinion by the visiting physician. At the post-mortem of the second patient material was obtained : pieces of lung and pieces of spleen. The lung was highly congested, in parts almost consolidated. Film specimens made of the spleen showed no bacteria. Film specimens of the juice of the inflamed lung showed abundance of very minute bacilli, singly, in chains, and particularly in large connected masses and streaks ; they resembled in staining and arrangement the typical influenza bacillus. Several drops of the sanguineous juice of the lung were rubbed over the surface of agar solidified in plates ; the same kind of plates were made of the san- guineous juice of the spleen. Guinea-pigs were injected sub- cutaneously with large amounts of the lung juice, as also of the spleen juice, one animal for each set. After twenty-four hours the agar plates of the spleen showed no colonies, those of the lung juice showed abundance of typical colonies of B. influenzce. Both guinea- pigs showed no tumour and remained unaffected. Diagnosis : Influenza pneumonia. From the above cases, which represent types of cases, of which materials were submitted for bacterioscopic 44 OEIENTAL PLAGUE chap. examination, the following conclusions may be drawn. According to this analysis we may group the cases in — (1) Cases which already on microscopic examination of stained film specimens alone may be pronounced to be most probably plague, and therefore the microscopic examination is able to justify the epidemiologist's and clinician's preliminary diagnosis of plague, or at any rate make it highly probable that the cases are true plague ; such are Case 2 (pneumonic plague) and Case 3 (bubonic plague). Culture in surface agar plates and experiment on guinea-pigs clinched the diagnosis in twenty-four hours. (2) Cases in which the microscopic examination of stained film specimens could not venture to make any diagnosis, but in which culture in agar surface plates and animal experiment enabled diagnosis of B. pestis to be made after twenty-four hours or later; such were Case 1 (abscess in groin) and Case 4 (bubo in groin). (3) Cases in which film specimens and twenty -four hours' agar culture could negative plague ; in some of these the glandular swelling, or the suppurating bubo, was clearly caused by infection with Staphylococcus pyogenes aureus, and in others (Case 7) the fatal pneumonia was caused by B. infiuenzoB. (4) There is a fourth category of cases, however, in which the microscopic examination and the culture of material taken from a glandular swelling (associated with fever) yielded no bacteria of any kind : cases, that is, which already on this evidence could be negatived as due to plague. I have had several such instances ; materials of these were submitted for analysis because, notwithstanding the want of epidemiological evidence, the medical officers of health quite laudably did not wish to incur any risk of Ill ANALYSIS OF PLAGUE MATEEIALS 45 possibly overlooking a case of plague at a time when occurrence of plague in their respective districts — after the numerous cases of plague that had landed in ports of these Islands — could not be excluded. Several points which ought to be here mentioned in connection with the culture test I consider of particular importance. The first point is this : surface plates on agar ought in all instances to be made with the materials submitted. A fair amount of the material, several drops of the juice of bubo or inflamed gland, of the lung, of the spleen when available, are rubbed over the surface of nutrient agar (beef broth, peptone, salt, agar), solidified in a plate dish of good size (three inches diameter). If B. pestis are contained in the submitted material they are sure to be discovered in twenty-four to thirty-six hours at 37° C. incubation. I have never failed to find them even in cases in which film specimens failed to give clear indica- tion of their presence. If film specimens already show B. pestis or bacilli like them in great numbers, agar tubes (slanting surface) will bring them forth, but such cases are not often submitted ; the materials generally sub- mitted are in the great majority of instances such as contain few B. pestis amongst other microbes, or contain few B. pestis only. In the former instance, if the inocula- tion has been made in a tube, the few colonies of B. pestis become generally overgrown or crowded out by other microbes (cocci, bacilli) ; in the latter, not enough material is used for development on the limited surface of the agar tube. The great importance of using at once plate cultures in preference to tube cultures of solid or fluid media cannot be sufficiently emphasised. If B. pestis is mixed in any 46 OEIENTAL PLAGUE chap. material with other microbes, the only way, in my experience, to identify it by culture is by plate cultures. And if it cannot be identified in this way, it is hardly to be expected that it will be identified by tube culture. Of course it is supposed that the observer is familiar with the appearances and nature of the colonies of B. pestis in their early stages. This conceded, I am confident, from a large experience, that there need be no difl&culty in identifying B. pestis in a mixture, such, for instance, as would occur in the sputum of some pneumonic cases, or in the purulent discharge of a suppurating bubo. The plates should be, of course, sufficiently large (three inches diameter), and several plates should be inoculated with the material. As regards the sputum, it should be re- membered that the Diplococcus pneumonice is a frequent microbe in expectorations, and except in acute cases of croupous pneumonia, in which this microbe occurs very numerously, it is present generally only in moderate numbers. But however scarce or however frequent, there ought to be no difficulty in identifying the B. pestis by plates, if this latter should be present in such sputum. Drs. Pakes and Joseph of Johannesburg have recommended to make the cultures of sputum of suspected lung cases in slightly acid broth, for in this medium the B. pestis grows well, whereas the Diplococcus pneumonice does not, and consequently the former is secured from being crowded out by the latter, which, according to Pakes and Joseph, does happen if the culture medium is ordinary broth. Without for a moment doubting that this modification, viz. using slightly acid broth as culture medium, may be very useful, I have likewise no doubt that plate cultiva- tion with proper nutrient beef-broth agar, such as I have ^^- Fic. 4:j. Fig. -11. Fig. 43. Stained impression of a recent colony of B. pestis on gelatine. x 1000. Figs. 44 and 45. Two ghee broth cultures of B. pestin, each holding 1500 cc. of culture fluid, showing developing surface pellicle with stalactites ; the broth is clear ; at the bottom masses of granular sediment — former stalactites that had become detached. Eeduced size. Fig. 46. Bacterium Bristolense. — Growth on potato, showing numerous gas bubbles in the growth. x 4. Fri;, 4S Fig. IQ. in ANALYSIS OF PLAGUE MATEKIALS 47 mentioned above, is for all practical purposes perfectly sufficient. Moreover, my experience leads me to suspect that failure by Dr. Pakes and liis colleague in identify- ing the B. pestis in the earlier cases of pneumonia in Johannesburg might have been due to the cultures not having been made by plates, but in tubes. The second point I wish to point out, and to insist on, is this : it ought to be remembered that in sputum of acute lung affections, besides the Diplococcus pneumonia there may be, and occasionally are present, coli - hke microbes, or microbes belonging to the proteus group ; both these microbes in film specimens of the sputum, well stained and well washed, appear as bipolar oval to cylindrical rods not unlike B. pestis. In these cases to make diagnosis " plague " or even " probably plague " from the microscopic examination alone would be quite unjustifiable, and might lead to extremely embarrassing results. Some observers appear to place, with Hankin, a certain diagnostic reliance on the capability of the plague microbe to grow into long threads in salted media. I have shown many years ago, i.e. long before Hankin, that a number of different bacteria (including B. coli and those of the coli group) when grown- in media containing excess of salt grow into long filaments ; it is therefore clear that this modification can be of no diagnostic help. Moreover, these lung B. coli and lung proteus, when injected into the groin of the guinea-pig in sufficient amounts, cause acute septicaemia : hgemorrhagic^effusions extending over the thigh, groin, abdomen, and even the chest wall ; the effusion is crowded with the bacilli, and these in film specimens show bipolar staining and are Gram- negative. Owing to this morphological and experimental 48 OKIENTAL PLAGUE chap. result, to conclude that the sputum which caused this state in the guinea-pig contained the B. pestis, and that the disease of the lung is due to plague, would be a grave error. The culture (plate) test with the sputum made at the same time as the animal experiment would at once check this possible error ; and, further, the examination of the hsemorrhagic exudation in the fresh and living state would show at once that the microbe, being motile, cannot be B. pestis. The culture of the exudation would also soon show that the microbe is not B. pestis. There occurred actually such a case of pneumonia, which was said to be due to B. pestis, but which was not due to B. pestis at all, but to a motile, highly pathogenic (for the guinea-pig), coli-like microbe. The premature dia- gnosis of plague on insufficient or on erroneous data is not only apt to discredit the great value and great importance of bacterioscopic analysis in respect of suspected cases — which of all others are those in which the bacteriologist's assistance is most needed, — but is liable to cause consider- able embarrassment and actual damage to the locality in which the case has occurred. For it has to be remembered that by international convention (Venice and Paris) the Foreign Office are bound to notify to the foreign Consuls the occurrence of any case of plague, and that our Foreign Office have always carried out this obligation both in the spirit and in the letter — different from some continental Foreign Offices. The loss liable to be inflicted on commerce and the damage done in other respects to the inhabitants and the locality in whose midst an indigenous case of plague suddenly occurs — or rather is said to have occurred — can easily be imagined. The diagnosis of such an indigenous Ill ANALYSIS OF PLAGUE MATERIALS 49 case of plague rests practically on the bacterioscopic dia- gnosis, and it therefore behoves the bacteriologist to have his data resting on a firm basis : the morphological, cultural, and experimental evidence must be clear and decisive. Such evidence is not difiicult to obtain if all the steps above detailed are taken with care and circum- spection, and not the least important part of the analysis is, or should be, the culture test and the cutaneous or sub- cutaneous inoculation of the mouse or rat or guinea-pig. A single colony which, in a plate cultivation, complies both in general aspect and constitution with the characters of a colony of the true B. pestis, and which, inoculated Gutaneously into the mouse or rat, subcutaneously into the guinea-pig, causes, as it should, an acutely fatal disease with the presence in great numbers of typical B. pestis in the bubo and spleen, is perfectly sufficient to ensure correct diagnosis of " plague." A third point which ought to be here mentioned is this : when plate cultivations are made of material which is obtained by puncture from a bubo, i.e. from a sub- cutaneous inflamed swelling, there occur not infrequently one or more colonies which appear as small, grey, trans- lucent, flat discs, with a central slight thickening due to an opaque granule ; these colonies are somewhat slow in their growth, and have a crenated or slightly angular margin. When touched with the point of a platinum needle they are found to be composed of a somewhat cohesive material, they do not well emulsify in saline solution, and when looked at under the microscope are composed of non-motile bacilli more or less connected in strings and masses. When stained they do not show bipolar character, moreover are in shape diphtheroid, i.e. E 50 OEIENTAL PLAGUE chap.iii conical, and some of them club-sliaped ; they are Gram- positive. In fact, they are non -pathogenic diphtheroid bacilli belonging to the group of B. xerosis. I am inclined to think that the "modified plague bacilli" which Dr. Cantley and Professor Hewlett described (Pathological Society, 1904), and which were found in a culture made from the juice of a punctured "climatic bubo" (Cantley), are nothing more or less than such xerosis bacilli belonging to the pathological skin over the " climatic bubo," and that therefore Dr. Cantley's contention that these climatic buboes which, according to him, are " not yet plague " but " may lead to plague," and which he wishes us to term " pestis minor," receives no confirmation from the above bacteriological fact, i.e. the presence of the xerosis bacilH. I have seen such xerosis colonies in several instances in plate cultivations made with material derived by puncture from buboes associated with fever, which buboes were connected not with plague, of which there was no history, and which led to no further occurrence of plague, but which were due to infection with Staphylococcus aureus or other microbe. CHAPTEE IV MICROBES SIMtFLATING IN ONE OR ANOTHER RESPECT THE B. PESTIS Although the B. pestis is, in respect of its morphological, cultural, and experimental characters, a well-defined species, and not easily overlooked or mistaken, yet there are in the nature of things occasions when either in cases of man under suspicion of plague, or in cases of rats dead under suspicious circumstances — in docks, on board ship, in houses and localities open to invasion or actually invaded by plague, — correct bacterioscopic diagnosis might be for one reason or another difficult, or, owing to inexperience of the analyst, might not be forthcoming. And for this reason we shall presently show there are microbic species which, in their pathogenic effect on some test animals, e.g. the guinea-pig, simulate plague ; or in their morphological and staining characters are not easy to distinguish from the true B. pestis, e.g. B. proteus or B. coli and other similar microbes ; or which in morphology and certain cultural characters bear a certain resemblance to B. pestis. Add to this that these simulating species may be found in man or in the rat under suspicious circumstances — that is, under circumstances which do not exclude plague — and no 61 52 ORIENTAL PLAGUE chap. apology is required to enter more fully into a description of these microbes. 1. Proteus vulgaris. — First in importance of frequency is the proteus vulgaris, and its varieties or races. Why I consider this microbe of first importance will be apparent if I describe two instances. In a large city situate at a port on the East Coast, in which port a case of plague had been landed the previous year, a woman, the owner of a small shop in the town, was suddenly taken ill with fever (T. 101 F.), swelling and inflammation of axillary and femoral lymph glands. After four days' illness the temperature fell and soon became normal. While the temperature was still ab- normal, a small amount of the sanguineous juice of the swollen axillary gland was obtained by puncture, and sub- mitted to bacterioscopic analysis. The suspicion of plague was justified, first, by the fact that without any visible external wound the woman suddenly showed clinically symptoms resembling plague, and, secondly, that this case occurred in a port in which a case of plague had occurred. According to the inquiry, instituted by the medical officer of health, a coloured man (sailor), himself quite well, had visited the shop, but besides having shaken hands with the woman, no other channel of possible infection could be established. The woman recovered. Microscopic examination of stained film specimens revealed a very small number of oval rods, some of which showed more or less distinctly bipolar staining. Agar plates were made, and a guinea-pig was injected sub- cutaneously with the whole of the remaining material. The agar plates showed next day a filmy, translucent, viscid growth, which, when examined under the microscope, Fig. 47. .* - .^:. :: X • ^ Mt •■ ** Fig. 47. Bacterium Bristolense. — Peritoneal exudation of a rat dead after sub- cutaneous injection with, culture. The stained film specimen here shown exhibits bipolarly-stained baciUi embedded in a gelatinous matrix like a zoogloea. x 1000. Fia. 48. Bacterium Bristolense. — Film specimen of the spleen juice of a guinea- pig dead after subcutaneous injection with culture, showing numerous bipolar-stained bacilli, x 1000. Fig. 49. Bacterium Bristolense. — Stained film specimen of the swollen inguinal lymph gland of a guinea-pig injected into the groin with culture of the microbe ; some of the bacilli are bipolar and oval, but many others seem swollen up like involution forms. x 1000. Fig. 50. Stained film specimen of the subcutaneous local exudation of a mouse injected with culture, showing numerous bipolar bacilli, some thicker than others. x 1000. ,'•■*•«. Fig. 49, ■A '. AV .. V .'S' ••j», Fig. 50. IT MICROBES SIMULATING THE B. PESTIS 53 m the hanging drop, was seen to consist of motile bacilli. The extent of the filmy growth — covering the greater part of the surface of the plate after twenty -four hours' incuba- tion — was alone sufficient to negative B. pestis ; add to this that the bacilli were motile. But a bacteriologist of insufficient experience — and the number of these who perform bacteriological analytical work has of late years greatly increased — might have been misled by the trans- lucent viscid growth (ground-glass-like) ; further, omitting to examine the growth in the living state — an omission not infrequent — and therefore not noticing the motility of the component bacilli, might (and generally does) at once proceed to prepare stained film specimens. In these he would notice that most of the bacilli show bipolar staining, just like B. pestis ; moreover, he would ascertain that they are Gram-negative, and he might well sustain and express what appears to him a justifiable suspicion, that he is dealing with B. pestis. The guinea-pig injected with the original material did not show after twenty -four hours any noticeable bubo, nor did it after forty-eight hours, but this might perhaps be thought to be due to the material containing only very few of the incriminated bacilli ; he therefore would proceed to inject subcutaneously a fresh guinea-pig in the groin with a larger — considerable — amount of the filmy growth from the agar plate. This second guinea-pig shows next day a decided gelatinous swelling about the groin, and the animal is quiet and a little off feed. If the guinea-pig is killed, the subcutaneous tissue of the thigh, groin, and flanks appears greatly congested and infiltrated with sanguineous fluid ; when a drop of this is examined in the fi-esh state it shows numerous actively motile bacilli ; but if, as not infrequently 54 ORIENTAL PLAGUE chap. happens, the analyst proceeds at once, without examina- tion of fresh specimens, to make stained film specimens, he would notice that the bacilli, at any rate some of them, show distinct bipolar staining, that they are Gram-negative, and that in shape and size they resemble the B. pestis. Diagnosis of "plague" under the conditions of analysis just detailed might seem justified, but aU the time the analyst was working with the common Proteus vulgaris. A gelatine plate or gelatine tube subcultured from the agar plate or from the subcutaneous exudation of the second guinea-pig would produce the typically liquefying Proteus vulgaris. I have in the foregoing described the results, not of an hypothetical, but of the actual analysis of the case. This proteus, as is highly probable, might have been picked up from the surface of the (dirty) skin of the axilla while gland juice was taken from the gland, or it might have been in the gland itself ; at any rate the microbe was undoubtedly Proteus vulgaris. Or take other instances. Eepe'atedly it occurred that dead rats found in the hold of a ship were sent for ex- amination. These ships had touched at or came from an infected country. Although no cases of plague had occurred on board ship, nor had any diseased or dead rats been found during the voyage, nevertheless when dis- charging cargo one or other dead rat had been found. In other cases, the ship having had a case of plague during the voyage, or a case of plague having occurred on landing, and the ship having been subjected to disinfection by the Clayton or other process, dead rats in numbers would then of course be found, and some submitted to analysis. IV MICROBES SIMULATING THE B. PESTIS 55 Rats are peculiar in this respect, that even a short time after death — in the warm part of the year, in less than twelve hours — the spleen may swarm with proteus, obviously derived from the intestine. Stained film specimens of such a spleen always show more or less numerously — particularly in the outer portions of the organ — oval bacilli with bipolar appearance. These bacilli under culture prove to be Proteus vulgaris : an agar surface plate shows already, after twenty-four hours and less, a filmy, translucent, rapidly spreading growth ; when examined in the hanging drop the growth is com- posed of actively motile bacilli ; when stained, many exhibit bipolar staining ; gelatine is liquefied by the growth. The bacilli of this growth are virulent for the guinea-pig : when an emulsion of the rat spleen — if con- taining abundance of these bacilli — or when a portion of the agar growth is injected subcutaneously into the groin of a guinea-pig, it will be found that the animal shows after twenty-four hours extensive hsemorrhagic infiltra- tion of the subcutaneous tissue, the exudation being crowded with Proteus vulgaris — actively motile rods. Gram-negative, bipolar in staining. The animal may be dead within thirty-six to forty -eight hours ; no bacilli are found in the blood or spleen, but they abound in the local infiltration. It is therefore obvious that, judging by mere stained film specimens of the original spleen, or by the fatal efiect on the experimental guinea-pig, showing hsemorrhagic tumour about the seat of injection, contain- ing abundance of bacilli which in stained films exhibit bipolar staining, an error in diagnosis may be easily committed. If a rat really had died of plague the bipolar bacilli seen in the film specimens of its spleen will yield on 56 OKIENTAL PLAGUE chap. agar plates the characteristic circumscribed small watery raised colonies, composed of non-motile bacilli, and when inoculated cutaneously into mice, rats, or guiuea-pigs, will produce the appearances and fatal results of plague. Sub- cutaneously injected into the guinea-pig the B. pestis produces marked swelling and inflammation of the lymphatic gland themselves, not merely a subcutaneous infiltration; after death the spleen is crowded with the non- motile. Gram-negative, bipolar bacilli. Proteus vulgaris, however virulent otherwise, when inoculated cutaneously into guinea-pigs, mice, or rats, produces no effect. The frequent occurrence of virulent Proteus vulgaris — that is, virulent on subcutaneous injection of fair amounts into the groin of the guinea-pig — particularly in the spleen of rats, in the lung of man some time after death (in the warm season in less than twenty -four hours), as also in the fluid of the mouth, and therefore in the expectoration, has to be carefully borne in mind. These microbes show, in properly stained film specimens, more or less marked bipolar staining ; wherefore, to make diagnosis by a mere stained film specimen is to be seriously avoided in such cases. 2. B. coli. — Next in importance are the pathogenic varieties of B. coli, or at any rate the microbic species which, by their general characters, belong to the group of B. coli and allies — that is, bacillary species which do not liquefy gelatine, which are Gram-negative, which ferment glucose (and some other sugars), which in surface plate cultivations (gelatine, agar) exhibit the character of colonies of B. coli and coli -like microbes, viz. rapidly growing, flat, dry, angular, grey expansions on gelatine,their bacilli motile. Obtained from diseased tissues — sputum, cystitis, perito- "^r"* 2 -■-''" ■%' y Til-*' ' ■AH "5? />• Fig. 52. Fia. 51. From a section through the consolidated portion of the lung of a rat spontaneously dead, showing the alveoli filled with exudation in which are masses (deeply stained) of the bacilli. x 85. Fig. 52. The exudation of an alveolus of the lung as in previous figure, but more highly magnified, showing the bacilli. x 1000. Fig. 63. A gelatine plate culture of tlie heart's blood of the rat spontaneously dead with lung disease. The culture is some few weeks old. x 30. Pig. 54. Film specimen of a gelatine culture of the tissue of lung of rat ; methylene- hlue staining, showing distinct metachromatismus. x 1000. Qj??' ''S Viij 6S. \ H Flu. 54. IV MICROBES SIMULATING THE B. PESTIS 57 nitis, suppurations — they prove virulent to the guinea-pig. There is one character by vs^hich these pathogenic coli-like microbes can be at once distinguished, viz. a particle of a colony examined in the hanging drop shows motile bacilli. Further, inoculated cutaneously into mice or rats or guinea-pigs they cause no effect, also subcutaneously into rats they are non-pathogenic ; but subcutaneously injected in fair amounts into the groin of guinea-pigs they cause gelatinous, often sanguineous, infiltration, leading in some instances to death of the animal within thirty to forty-eight hours. The bacilli of the culture as also of the subcutaneous infiltration show motility, and, after suitable staining in film specimens, more or less marked bipolar staining. I will here give an instance in which coli-like microbes present in diseased tissues (of man) had, on account of their bipolar staining in film specimens, and on account of their virulence for the guinea-pig, been erroneously declared as B. pestis. A case of acute broncho-pneumonia occurred in hospital in a certain city — A. In the routine work of the patho- logist of the hospital the sputum of the case showed in stained film specimens a large number of bacilli with marked bipolar appearance. This occurred at a time when not only in several ports of England single cases of plague had been imported, but there had also occurred several cases of plague in a port B. in fairly close and frequent communication with A. Cultures of the sputum and also injection of a guinea-pig were made. The guinea-pig died after a few days with sanguineous tumour. In this sanguineous exudation were crowds of bacilli, which in film specimens showed bipolar staining. Diagnosis was made : Plague pneumonia. 58 OEIENTAL PLAGUE chap. Now, the above sputum, as also its cultures, and tlie cultures obtained from tbe injected dead guinea-pig, were submitted through the Local Government Board to analysis, and it was at once seen that there was no justifi- cation for the above diagnosis, because the cultures all showed that the bacilli, when examined in the hanging drop, were actively motile. Subcultures and experiment proved them to be B. coli of a pathogenic kind. The above case of pneumonia recovered, and no further cases occurred. Unfortunately the case had been already notified as plague at A. on the basis of the local evidence, and it required a considerable amount of effort, not of the most desirable kind, to negative the first impression and to retract the erroneous diagnosis of plague. Another instance : a ship coming into port was at first thought probably to harbour plague rats owing to mortality of these rodents on board ; but on careful bacterioscopic analysis the mortality was shown not to be due to B. pestis, but to an altogether different microbe, as the following description will show : — 3. Bacterium Bristolense} — In a cargo vessel, s.s. George Royle, which was being unloaded at Bristol, a number of dead rats were found. One of these was for- warded by Dr. Davies, medical officer of health, to the Board for bacterioscopic examination. Owing to the steamer having come from Smyrna, which was then plague-infected, it was thought probable that the rats in question had died of plague. No case of plague in man had occurred on board the vessel. ^ Report of the Medical Officer of the Local GoYernment Board, 1902-1903, p. 414 and passim. IV MICROBES SIMULATING THE B. PESTIS 59 The post-mortem examination of the above rat showed the following condition : — The inguinal glands were not enlarged. The spleen was enlarged, dark, and very juicy. Both lungs were very congested, showing in addition patches of consolidation. In the spleen and in the in- flamed parts of the lung a variety of microbes were found in stained film specimens, and amongst them some which owing to bipolar staining might have passed for B. pestis. In the film specimens of the spleen in particular the great majority of the microbes were shorter or longer oval bacilli showing bipolar staining. Subcutaneous injection of a few drops of the inflamed lung juice into a guinea-pig (No. 1) caused illness within twenty -four hours, viz. the animal became quiet and developed local tumour. It was found dead on the second day. The post-mortem examination showed the following condition : — The subcutaneous tissue of the groin, abdomen, and chest of the injected side — the injection having been made in the groin — was much infiltrated with sanguineous fluid. In this fluid crowds of bacilli were present, of the same size and staining as those mentioned above as present in the lung juice of the rat. The inguinal glands on the injected side were swollen and firm ; and in them were much blood and numerous bacilli of the same character as those already mentioned. Both lungs were hypersemic ; sanguineous exudation was present in the pericardium ; the spleen was not enlarged ; the suprarenals were deeply congested. Cultures were made, not only from this animal, but also from a large number of other animals, both guinea-pigs and rats, inoculated in series from it ; so that the morpho- logical, cultural, and physiological characters of the microbe 60 OEIENTAL PLAGUE chap. could be studied in every detail. As a result it was definitely ascertained that the microbe was not B. pestis, but a microbe related partly to Bacillus coli and partly to the Bacterium lactis aerogenes. In some of its physio- logical and also in its morphological characters it re- sembles to a considerable degree B. pestis ; indeed, if the microbe were insufficiently examined, i.e. by these tests alone, the mistake that it was B. pestis might easily have been made, as will appear from the details of my observations. From the first experimental guinea - pig. No. 1 , a guinea-pig. No. 2, was injected intraperitoneally with a few drops of the sanguineous subcutaneous exudation, while another guinea-pig, No. 3, received a similar dose subcutaneously. The latter (No. 3) died within forty -eight hours ; the former (No. 2), which in forty-eight hours was in a dying condition, was killed. The post-mortem of the subcutaneously injected guinea-pig (No. 3) was exactly similar to that of guinea-pig No. 1. Guinea-pig No. 2 showed copious exudation in the peritoneum, and in the exudation purulent flocculi and pseudomembranes. These materials contained dense crowds of the same bipolar- stained bacilli as in guinea-pig No. 1 ; the bacilli appeared embedded in a viscid, gelatinous matrix. Of a single colony of an agar plate (twenty-four hours old) of the peritoneal exudation of guinea-pig No. 2, a small amount was injected intraperitoneally into a guinea-pig No. 4. This animal was found dead in twenty hours. Its post-mortem appearances showed copious viscid grey exudation in the peritoneal cavity ; the spleen was small ; the liver was covered with grey pseudomembranes ; both lungs appeared injected ; the pleural cavity contained ,5C> / Fig, 55 Fig, 56 Fig. 55. Film specimen of same culture as in previous figure, stained after Gram, x 1000. Fig. 56. Film specimen of blood from the right ventricle of Nurse T., dead Decem- ber 9, showing numerous capsulated diplococci. x 1000. Fig. 57. Exudation at the seat of inoculation in a mouse dead after subcutaneous inoculation with, culture of the above capsulated diplococcus. x 1000. FiGf. 58. Stained film of agar plate of blood of Nurse T., showing the Diplococcus pneumonicB, chiefly in chains, as also the bipolar-stained B. X 1000. * • i * Fio. 57. IV MICEOBES SIMULATING THE B. PESTIS 61 viscid grey exudation. Both the peritoneal and the pleural exudations contained in a gelatinous matrix crowds of beautifully bipolar-stained oval bacilli. The result of the injection, the nature of the peritoneal exudation, and the aspect and staining of the bacilli in this exudation, were such that a mistake for B. pestis could easily have been made. One further experiment only need be here detailed. Of the viscid peritoneal exudation of guinea-pig 4 a few drops were injected into the groin of two rats (Nos. 5 and 6) on April 12. On April 14 both animals seemed affected ; they were quiet, their coats rough, their breath- ing accelerated, and they did not feed normally. On April 15 the animals seemed a little better, though not quite well. On April 16 one of the two rats appeared much worse, and on April 17 it was found dead. Post mortem there was in the groin a large tumour which involved the subcutaneous tissue and the inguinal lymph glands, which were infiltrated with sanguineous fluid. In this fluid were crowds of bacilli, which in size and bipolar staining resembled B. pestis. The peritoneum contained slimy grey pseudomembranes covering the surface of the liver, the spleen, and the parietes. These pseudomem- branes consisted of an interstitial gelatinous matrix, em- bedded in which were bacilli of the size of B. pestis, showing (in stained films) exquisite bipolar staining. In the omentum were hsemorrhagic spots. The small intes- tines were found much congested, relaxed, and contain- ing sanguineous mucus. Both lungs were much inflamed. From this post-mortem examination, therefore, a diagnosis of " plague " might have been justified. But cultures of the peritoneal exudation, of the tissue and 62 ORIENTAL PLAGUE chap. juices of the bubo, and of the heart-blood, proved conclu- sively that the microbe was not B. pestis. All these cultures were pure growths of one and the same species — which was not B. pestis. Numerous other experiments with the same material gave like positive results. To sum up the facts so far with reference to the George Royle rat : there was obtained by experiment on the guinea-pig, as also by culture, with the inflamed lung of the rat in question, a microbe which acted pathogeni- cally in the guinea-pig, both subcutaneously and intraperi- toneally, and on the rat when injected subcutaneously. The result of the inoculation of these animals was pro- duction in them of a hsemorrhagic septicaemia, with the copious presence, in the exudations of the inflamed parts and tissues, of a single definite species of bacillus. The post-mortem appearances were in their character not un- like those of plague, except that the spleen was not much enlarged, or at least not so distinctly as in plague. The microbe recovered from the tissues of the dead animals showed in its general morphology and staining power a remarkable similarity to B. pestis ; so much so that film specimens, such as are shown, would no doubt justify the provisional diagnosis of B. pestis. I refer here particularly to the stained film specimen of the peritoneal exudation of a guinea-pig dead after intraperitoneal injection, shown, and to the film specimen of the spleen juice of a guinea- pig dead after injection subcutaneously with culture (Figs. 47 and 48). Another point which it is necessary to insist on is the important one that neither in the guinea-pig nor in the rat have I been able to produce with this bacillus, whether using the animal tissues or culture, any positive result IV MICKOBES SIMULATING THE B. PESTIS 63 by cutaneous inoculation, thougL. that method ensures always characteristic and positive result with B. pestis and with plague material. In order the more effectively to discuss the nature of the microbe in question, I propose to describe it under the name of Bacterium Bristolense ; " bacterium " because following Migula's nomenclature the microbe is non-motile, and " Bristolense " because it was derived from a vessel in the Port of Bristol and was not B. pestis. The Bacterium Bristolense is a non-motile rod, vary- ing in length just as does B. pestis ; similarly it varies in shape from a short oval to a cylindrical bacillus, and is of about the same thickness as B. pestis. The character of the microbe on gelatine, on agar, on serum, and in broth is altogether similar to that of some varieties of B. coli communis, and different therefore from that of B. pestis. The colonies on gelatine are round, raised, and moist-looking. B. Bristolense, like B. coli com,munis, produces indol in broth ; it gives positive neutral-red test ; it " bubbles " (i.e. forms gas) in glucose gelatine shake culture ; it forms acid in milk, and curdles this medium in a few days. In these characters the microbe therefore corresponds closely with B. coli, and in particu- lar to a definite variety of B. coli communis. But it differs from B. coli by the more rounded, thicker, and whiter aspect of its colonies in gelatine plates, and its thicker, whiter, and less expansive growth in gelatine streak culture. After some weeks' culture on gelatine there is just an indication of liquefaction, but it never becomes marked. In these respects the microbe resembles more the B. lactis aerogenes. B. lactis aerogenes, how- ever, does not produce indol in broth, and does not give 64 OEIENTAL PLAGUE chap. a positive reaction in neutral-red broth. On potato at 37° C. the microbe forms a thick, moist, whitish cream- coloured growth in which copious gas bubbles appear : this condition obtains when the surface of potato of some age is inoculated ; on recently prepared potato the gas bubbles are not evident. Fig. 46 is an accurate illustra- tion of this appearance, and the character in question conclusively eliminates this microbe from the B. coli communis, and places it amongst the group of B. lactis aerogenes. Culturally, then, the B. Bristolense stands somewhere between B. coli communis and B. lactis aerogenes. As already mentioned, B. Bristolense is pathogenic to rats and to guinea - pigs both by subcutaneous and by intraperitoneal injection ; and, further, the pathological appearances induced by it in the infected animals — particu- larly the distribution, aspect, and staining power of the microbe in the tissues of these animals — might be easily mistaken for those oipestis huhonica. In this connection it is necessary to insist on what has been already said as to the nature of the tumour at the seat of injection and as to the bipolar-stained numerous bacilli in the tissue of the tumour, in the peritoneal exudation, and in the spleen of the experimental animals ; for a diagnosis made from the morphological appearances alone or from the results of intraperitoneal and subcutaneous injections of rats and guinea-pigs might lead to serious mistakes. The culture test is, however, in this instance decisive against B.pestis. But, as already noted, neither a culture nor the patho- logical products of the experimental animals can repro- duce the disease in other animals by cutaneous inoculation alone ; and this fact is an important help towards a correct Fig. 59. Fig. 59. Stab culture in gelatine of B. myxoides after a week's incubation. Natural size. Fig. 60. From a pure culture of tlie B. myxoides (from Nurse T.'s blood), showing a zoogloea of tbe (bipolar) plague-like bacilli. x 1000. Fig. 61. Film specimen of the viscid peritoneal exudation of a guinea-pig dead after intraperitoneal injection with B. myxoides. x 1000. Fig. 62. Specimen of heart's blood of a guinea-pig dead after intraperitoneal injection with B. myxoides, showing great numbers of the bipolar bacilli. X 1000. .^?;^; /Ai " <^y Fir,. 61 -^' > / 4 €A Jm; Fig, t)2. IV MICROBES SIMULATING THE B. PESTIS 65 diagnosis, since the plague bacillus reacts positively, caeteris paribus, by cutaneous inoculation. Though B. Bristolense possesses, as already shown, pathogenic action for rodents, the statement requires certain qualifications. Rabbits, for instance, appear in- susceptible. Moreover, the virulence of the subcultures rapidly decreases even for the susceptible aninaals ; a comparatively small number of transferences in culture sufl&ce to diminish its pathogenicity. Feeding with culture produces^ no effect either in guinea-pigs or in rats. Mice are killed by the culture in thirty to forty-eight hours on subcutaneous injection. They show oedema at the seat of injection ; the bacilli which are numerously present in their spleens and blood exhibit good polar staining, but are decidedly thicker than B. pestis. Dunbar and Kister {Centralblatt f. BaJct. und Para- sitenk. Bd. xxxvi. p. 127) found in the organs of some rats dead on board ship, which were submitted to them, bacteria of various kinds, not B. pestis. Some of those figured by them, showing bipolar staining, clearly belong to the tribe of proteus, others may have been B. Bristolense. 4. Bacterium myxoides.^ — A particular case of a hsemorrhagic acute febrile disease which by most clinicians would be, and as a matter of fact has been, classed as hsemorrhagic small-pox may be here quoted. This is a case of a nurse, T., who was under the care of Sir Hugh Beevor. She was taken ill on December 4, and she died on December 9. The post mortem was ordered by the medical ofl&cer of the London County Council, Sir Shirley Murphy, to whom one of the attending physicians had notified the case as possibly one of septicsemic plague. ^ Report of the Medical Officer, 1901-1902, p. 549 and passim. P 66 ORIENTAL PLAGUE chap. " Post mortem on 9tli. On exposing the surface of the abdomen, the lower part was found to be covered with a purpuric eruption, con- sisting of thickly-set pin-point petechise with larger blotches, some of which were the size of a split pea. The eruption was especially marked, roughly speaking, in a triangular area included between a transverse line drawn through the umbilicus and bounded below by two lines drawn across the front of the thighs parallel to and a few inches below Poupart's ligaments. Two chains of more scattered petechise extended from the main area of eruption upwards towards the arm- pits. On the arms and lower legs there were purpuric blotches here and there, but the main development of the eruption was in the situation already defined. There were conjunctival hsemorrhages and minute petechise on the pericardium. The pericardial sac con- tained several ounces of fluid. The appearances of the eruption and of the conjunctivse were those characteristic of hsemorrhagic small- pox. The lungs had a few petechise, but otherwise seemed healthy.'' Material was obtained from this body : blood which had been withdrawn aseptically from the right ventricle by means of freshly drawn-out glass capillary pipettes, afterwards sealed ; and pieces of lung and pieces of skin of the abdominal and femoral region, which had been cut out under all necessary precautions. In the laboratory these samples were used for cultivation and experiment, pieces of the lung and of the skin being also placed into Muller's fluid for hardening. The heart's blood was used thus : — 1 . Film specimens were made and stained ; 2. Agar surface plates were inoculated and incubated at 37° C. ; 3. Guinea-pigs were subcutaneously injected. The above proceedings were undertaken for demonstration of the presence of plague bacilli, the case having, as already mentioned, been notified as possibly plague. Examination of specimens of the heart's blood yielded the follow- ing results : — Microscopic film specimens, stained, showed numerous capsulated diplococci — each diplococcus consisting of two demilunes closely facing each other and invested in a distinct capsule. They were arranged either as single diplococci or more commonly as short (two diplococci) and longer chains (four diplococci). Fig. 56 shows a specimen of this kind. Not every microscopic field of the specimen contained these capsulated diplococci in such numbers as is shown in Fig. 56 ; never- X % ^' > ^i «s.,. Jl^..^^ C^i^.;""' Fig. 63. a* -» Fig. 63. Specimen of heart's blood of a guinea-pig dead after intraperitoneal injection with B. myxoides, showing great numbers of the bipolar bacilli. X 1000. Fig. 64. From a section through the liver of a guinea-pig dead after subcutaneous injection with B. pseudo-tuberculosis. The liver was pervaded by nodules, some in the early stage (round cell masses), others already necrotised, near the surface of the liver (upper part of the iigure) ; one such necrotic mass is shown, in which large and small aggregations (deeply stained masses) of the bacilli are recognisable. x 50. Fig. 65. From a section of a similar liver, showing the liver tissue pervaded by the nodules. x 23. Fig. 66. Section through a swollen Peyer's patch of the ileum of a guinea-pig infected by feeding with culture of B. pseudo-tuberculosis. The lymph follicles of the Peyer's patch are enlarged and necrotic. x 1 8. 'h ■- . J^-Ti* ■i ft^" Fig. 65. Fig. 60. IV MICROBES SIMULATING THE B. PESTIS 67 theless the microbe was on the whole very abundant, and it was obvious from microscopic examination alone that the case was dis- tinctly one of blood infection — infection due, that is, to a Diplococcus capsulatus, the exact nature of which could, of course, only be deter- mined by culture and by animal experiment. The agar surface plate made from the original blood showed next day (but better still after forty-eight hours) an uncountable number of translucent grey colonies, in many places confltient into a grey filmy layer. These colonies in their general aspect were identical with those of Diplococcus pneumonim, and, like the latter, were made up of diplococci, either altogether wanting in capsule or possessed only of an indication of it. So, too, they were chiefly arranged as chains, some of these chains being composed of as many as eighteen to twenty diplococci. A small amount of the growth, a few colonies only, was used for making an emulsion, and with this emulsion mice and guinea-pigs were injected subcutaneously. The result was perfectly distinct and uniform ; the guinea-pigs showed no illness, while the mice died. The post-mortem appearances in the latter case were those found in mice after infection with the Diplococcus pnevMwnim ; the oedematous fluid of the seat of inoculation was found crowded with the capsulated diplococcus, either as single diplococci or as short chains of two elements. Fig. 57 is a char- acteristic specimen of this kind, the capsules being shown with great distinctness. There can, then, be no question as to the identity of this microbe. It was the Diplococcus pneumonicc, and it was present in the blood of the patient T. in very large numbers. As already mentioned, this patient had no pneumonia, while at the post-mortem examination only a few petechise were found in the lung. The case, therefore, was undoubtedly one of general blood infection with the Diplococcus pneumonice. That such a general infection — viz. copious presence of the microbe in the blood — existed in this case ante mortem may be taken as certain : cold weather prevailed at the time (December 9) ; moreover, the blood was obtained within twelve hours of death. It is altogether improbable, therefore, that an appreciable multiplication of the microbe had taken place after death, since the Diplococcus pneumonim requires for its growth and multiplication higher tempera- tures than could have obtained here. Below 25° C. the growth of this microbe in the laboratory is either nil or very delayed and slow. 68 ORIENTAL PLAGUE chap. The abundant presence in the circulation of a virulent microbe like the Diplococcus pneumonim must needs be of considerable im- portance, and in the particular instance may well have caused the severe constitutional illness and death. As will presently be seen, the microbe was present also in the skin in the hsemorrhagic spots, and although it may have been so present as a result of blood effusion, it might, on the other hand, by its intravascular toxin have been the primary cause of the destructive (chemical) vascular change leading to the haemorrhage. It is well known that many microbes have such an (vascular) angiolytic action ; as, for instance, all the pathogenic microbes which grow and multiply within the circulation, such as the whole group of bacilli causing hsemorrhagic septicsemia. To these must be added the Bacillus pestis, the B. anthracis, the Diplococcus (lanceolatus) pneumonim (when injected into the vascular system ^), and as well some species of streptococcus and some virulent species of Bacillus coli (e.g. bacillus of aerobic malignant cedema, bacillus of G-sertner, bacillus of Danysz, and others). The destruction (chemical solution) of the wall of minute blood-vessels by the toxins of many microbes growing and multiplying within the circulation is indeed a well-known fact, and accordingly the haemorrhage in the skin of Nurse T. may have been due to the copious presence of the Diplococcus pneumonim within the circulation. The questions, therefore, that arise in connection with this case are these : If this was really a case of small-pox, was the presence of the Diplococcus pneumonim the cause of the hsemorrhagic condition ? and is it also the cause of the hsemorrhagic condition in other cases of small-pox ? Before proceeding to seek for an answer to these questions it is necessary first to supplement the bacterioscopic analysis of the case of Nurse T. The Diplococcus pneumonim present in this case in the blood (see film specimens and culture plate) in enormous numbers was not the only microbe found therein. In the film specimens of the blood now and again, but on the whole very sparsely, there were found single microbes without capsule, which on more careful examination were recognised as oval bacilli. On the agar plate, too, above mentioned, which had uncountable translucent small grey colonies ■^ The Diplococcus pneumoniae seems to be capable of causing vascular disruption, even when growing outside, but close to, capillaries, e.g. the haemorrhage into the exudation of the alveoli of the lung in acute croupous pneumonia causing the "rusty sputum." IV MICROBES SIMULATING THE B. PESTIS 69 of the Diplococcus pmv/monm, there were present in addition, after twenty -four hours' incubation, eight to twelve colonies of an altogether different character. These were heaped -up whitish -grey round to irregular colonies several times larger than those of the Diplococcus pneumonicB. Such colonies were composed of a viscid slimy material which under the microscope was seen to be made up of a hyaline transparent viscid interstitial or ground substance in which were embedded in close juxtaposition oval to cylindrical non-motile rods, thus representing a typical zoogloea mass. In stained films the bipolar staining of the rods was very distinct ; so that these bacilli are not dissimilar to those of Bacillus pestis. Subcultures were made from the primary colonies in the different media, and in these the characters of the microbe were found similar to those of microbes constituting the group of bacillus of Friedlander, but with this difference, namely, that the growth of the microbe in question was quicker, and that it formed more pronounced viscid slimy masses. Another point which distinguishes it from the B. Friedlander is that in culture it formed distinct zoogloea ; that is to say, the individual bacilli are barren of a separate capsule like the typical bacillus of Friedlander, but, unlike that microbe, are embedded in, and held together by, a slimy interstitial substance. The character, aspect, and rapid growth of the colonies, as well as their mode of growth in the different media, seem in general to distinguish this microbe from the B. pestis, which it closely resembles as regards polar staining, and also as regards length and thickness. Owing to the conspicuously slimy character of the growth of this microbe I propose calling it Bacterium myxoides. For the rest, in a general way it presents the characters of the microbes belonging to the group of Bacillus Friedlander ; like these, it does not stain by Gram's method, and does not liquefy gelatine. A point of constant difference between this Bacterium myxoides and Bacillus Friedlander is that the former, taken from the animal tissues, does not under any circumstances show a capsule. This, of course, can be demonstrated readily in the tissues after inoculation into animals. Guinea-pigs and rats were, with the pure culture of B. myxoides, injected cutaneously and subcutaneously. But no effect whatever was hereby produced ; the animals remained well. This of course proved also experimentally that the microbe was not B. pestis. Intraperitoneal injection of the microbe into guinea-pigs, how- 70 ORIENTAL PLAGUE chap. ever, even in small doses, caused invariably a fatal result in twenty to thirty hours. The post-mortem appearances were as follows : — Copious grey viscid peritoneal exudation ; intestines much inflamed ; liver, spleen, and kidneys highly congested. The peritoneal exudation of these guinea-pigs in stained film specimens showed crowds of oval to cylindrical bacilli, often in couples end to end. The conspicuous thing about them was their exquisite bipolar staining; no leucocytes and no other microbes were present. Plate cultures proved that the exudation was a pure culture of Bacterium myxoides. There was nowhere any indication of a capsule around individual bacilli, but the matrix in which the bacilli were embedded was a homogeneous viscid stainable substance, similar to that mentioned in regard of the zooglcea matrix of the culture. The blood of these guinea-pigs contained a very large number of the same microbes, viz. the £. myxoides ; so much so that in a dried and stained film specimen of the heart's blood every field of the microscope contained great numbers of the bacilli ; some fields, indeed, appeared crowded. The bacilli showed no trace of a capsule, but they all showed very distinct bipolar staining. The majority of the bacilli in the blood were rounded at both ends, but some showed one end, seldom both, as if cut away. The bacilli in the blood were distinctly thicker than those of plague. The subcutaneous injection of culture of the microbe into mice always produced acute disease and death in three to four days. At the seat of inoculation inflammation and gangrene were apparent ; the spleen was found enlarged, congested ; the peritoneum inflamed ; all the viscera were hypersemic. The bacilli {£. myxoides) were readily demonstrated by film specimens and in culture, being very numerously present at the seat of injection, in the blood, in the spleen, and particularly in the peritoneal exudation ; the latter appeared densely crowded with them. Rabbits are unsusceptible alike to subcutaneous and intravenous injection of large doses of culture. It has been shown, then, that in the blood of Nurse T. there were present two virulent species of microbes, — the one, the Biplo- coccus pneumonice, in enormous numbers, so much so that its presence in the blood would be quite sufficient to account for the severe illness and death with haemorrhages ; the other microbe, the Bacterium myxoides, although not present in large numbers, is nevertheless a IV MICROBES SIMULATING THE B. PESTIS 71 microbe pathogenic for certain rodents. This J5. myxoides, which morphologically and in staining presents a certain resemblance to Bacillus pedis, has cultural characters sufficiently distinct to differ- entiate it from the plague bacillus. 5. Bacterium muris} — For some time back I have kept white rats — half-grown and adult — in my laboratory. They are generally in couples in clean and specially made cages. On July 21 one of a couple of such rats was found dead. It had been observed to be ailing some days previously : its coat being rough, its breathing rapid, and the animal showing somnolence. On post-mortem examination the following condition was found : — A portion of the left and the whole of the right lung were dark red. These portions were consolidated and sank in water ; when cut into they appeared solid ; there was caseous matter in the bronchi. The spleen was not enlarged. No swollen lymph glands could be found. The small intestine was congested, relaxed, and contained mucus and numerous gas bubbles. Film specimens made from the inflamed portions of the lungs showed numerous large and small masses of cylindrical and even filamentous bacilli. These when stained in methylene-blue exhibited pronounced meta- chromatism just like the diphtheria bacilli. Sections through the hardened lungs showed that the consohda- tion was due to distension of the alveoli, infundibula, and bronchi by fibrinous exudation ; the latter containing numerous leucocytes and coloured blood corpuscles, and, as well, connected masses of the above bacilli. Cultiva- tions made of the inflamed lung tissue yielded pure ' Eeport of Medical Officer, ] 902-1903, p. 418 and passim. 72 ORIENTAL PLAGUE chap. cultures of one and the same bacillus, as also did the blood of the heart. The companion rat died eighteen days later, and on post mortem showed precisely the same pathological con- dition and the same bacteria. As far as the morphological characters were concerned, the bacterium in question appeared identical with Klebs- Loffler's Bacillus diphtherice, not only in regard of shape and non-motility, but also as regards staining characters. The microbe stains well by Gram's method ; indeed gives positive Neisser staining ; and shows, as mentioned already, distinct metachromatism in methyl- blue staining. Culturally, also, it resembles the diph- theria bacillus : on agar, on gelatine, on serum, and in broth the character of the growth is very much the same in both cases ; like the diphtheria bacillus this microbe produces acid reaction in glucose broth. As regards its effect on animals, it is distinctly pathogenic for rats and for guinea-pigs. In both these animals it causes on subcutaneous injection a local tumour. Sub- cutaneous injection into the groin of a small or large dose of culture causes the formation of a gradually en- larging firm tumour, which in the course of ten to twelve days attains a very considerable size. The fate of the tumour is either a gradual resolution and absorption, or it becomes converted into an abscess which contains thick pus. In either case complete recovery takes place. The tissue of the tumour, and the pus of the abscess at all stages, contain the bacilli in abundance. I have not been able hitherto to produce any but a local result, be the injected dose small or large. Several other rats dead since with the same lung disease due to the same riP^-iJi Vie. fi7 ^ KiG fi8. Fig. 67. A portion of necrotic lymph follicle of a similar Peyer's patch as preceding figure, more magnified, showing deeply stained masses of the bacilli around it. x 65. Fig. 68. Film specimen of purulent caseous matter of inguinal lymph gland of a guinea-pig dead of pseudo-tuberculosis after injection into the groin. Leucocytes swollen and disintegi'ating, containing the bacilli. x 1000. Fig. 69. Gelatine surface plate showing colonies of B. pseudo-tuberculosis, after forty -eight hours' incubation. x 18. Fig. 70. Same colonies on agar plate, less magnified. x 6. i'lG. 69. l-'ic 70. rv MICEOBES SIMULATING THE B. PESTIS 73 microbe, would suggest that the disease is naturally contracted by way of the respiratory organs. It might be inferred from the foregoing description that this microbe is the diphtheria bacillus in an attenuated state of virulence. Against such conclusion there are, however, some very valid reasons : {a) the microbe acts well on adult rats, animals which are refractory towards even virulent diphtheria cultures ; (6) diphtheria anti-toxin has no effect whatever in neutralising the action of even a small dose of this microbe. In this direction I have made a number of experiments. A dose in each instance of a recent culture of the microbe was subcutaneously injected into certain control guinea-pigs, while a similar dose of the same cul- ture mixed with 400, 500, and even 600 units of diph- theria anti-toxin (obtained of Burroughs and Wellcome, as also of Allen and Hanbury) was injected into each of several other guinea-pigs. At the same time a dose of diphtheria an ti- toxin (100 and 200 units) mixed with a lethal dose of culture of the true diphtheria bacilli was injected into each of another series of guinea-pigs. These latter remained without any disease, but the control animals and those injected with mixture of culture of the microbe which is in question and diphtheria anti- toxin developed the characteristic tumour. It is quite clear, then, that this microbe is in no way affected by the diphtheria anti-toxin, and that it is, therefore, not the true diphtheria bacillus, though it is a pathogenic microbe belonging to the group of diphtheroid bacilli. On account of its having been found in the rat I have named it Bacterium muris. During the last twelve months I have had the oppor- 74 ORIENTAL PLAGUE chap. tunity of experimenting for purposes of studying the new plague prophylactic (which I described in a pre- liminary report to the Local Government Board, December 19, 1905) on a large number of white rats. Amongst these (two hundred odd), I have seen at diiOferent times spontaneous deaths in about half - a - dozen ; on post-mortem examination they exhibited the caseous necrotic patches in the lungs (chiefly of the upper lobes), due to the presence of masses of the B. muris. 6. Baderimn diphtheroides of Mice. — For completeness' sake I add here the description of a microbe which distinctly belongs to the group of diphtheroid bacilli, is indeed closely related, if not identical, with the preceding B. muris, and therefore in morphology and by positive Gram staining can be readily distinguished from B. pestis ; as on several occasions 1 have met with it in mice, it might not be out of place to mention this microbe here, as it is pathogenic to mice, and as these animals are very useful and often used in experimental and diagnostic work for plague. The history of this pathogenic diphtheroid microbe is as follows : — A guinea-pig had been inoculated cutaneously on February 18, 1 905, with a trace of an agar culture (forty - eight hours old) of B. pestis derived originally from the spleen of a rat dead of plague. The guinea - pig was found dead on February 22 (fifth day). On post-mortem examination it showed large haemorrhagic bubo crowded with B. pestis; almost the whole of the intestine showed numerous petechise in the serous coat ; both testes showed the superficial lymphatics injected with blood; the pelvic lymph gland was enlarged and hemorrhagic ; the spleen was large, mottled with grey nodules and crowded with B. pestis; the liver was pervaded by whitish punctiform nodules ; the suprarenals were haemorrhagic. From this it follows that the guinea-pig had died of typical subacute plague. The spleen and the bubo of this guinea-pig were finely minced, and a small amount of this material was placed on bits of cloth, which were then kept under a bell jar and left to dry at the temperature of the laboratory. On March 8, i.e. after fourteen days' drying, some of the dry particles were taken off the cloth and rubbed down in sterile distilled water, and from this emulsion IV MICROBES SIMULATING THE B. PESTIS 75 a few minims were injected subcutaneously into the dorsum of two mice. One of these mice was found dead next morning, i.e. within twenty hours. The second mouse was very ill — lumpy, coat rough, eyes closed, breathing very rapid; it was found dead the next morning, i.e. within forty hours. At the post-mortem examination both mice showed the following appearances : — At the seat of inoculation the subcutaneous tissue was inflamed, oedematous, and with haemorrhagic spots; the intestines and lungs were very hypersemic and showed haemorrhagic spots ; the spleen was large and dark. Neither in the subcutaneous exudation nor in the spleen or lungs could any B. pestis be discovered, either in stained film specimens or by culture.^ But in the subcutaneous exudation were numerous bacilli in clumps and in streaks which could at once be recognised as diphtheroid : small bacilli pointed at one end, some with clubs and showing segregation of their chromatic substance ; they stained positive in Gram. Cultures on agar surface and on agar plate were made, and in these came up in pure state numerous colonies of the same diphtheroid bacilli. Subcutaneous injections with these cultures were made into mice and guinea-pigs, and thereby it was shown that the microbe was possessed of distinct pathogenic action : in the guinea-pigs the subcutaneous injection into the groin of a moderate dose of culture — several drops of turbid emulsion — caused after forty-eight hours slight but firm enlargement of the inguinal glands ; this enlargement gradually increased, till in about ten days the tumour was of the size of a filbert, changing at the same time from a firm tumour into a tumour containing thick pus. The pus contained crowds of the same diphtheroid bacilli, many in small and large masses. None of the guinea-pigs died, and the animals remained the whole time apparently lively and feeding. The mice showed constitutional disturbance for two or three days, being quiet and off feed, but they soon recovered and showed tumour at the seat of injection. This tumour about the end of a week or ten days began to ulcerate, and became covered with a dry scab about |- to l inch in diameter. The mice recovered, and after about three weeks the place was healed up. Several other experiments were made with the culture in guinea-pigs and mice with the same result. ' In a subsequent chapter it will be shown that death was due to plague toxin present in the dried plague tissues. 76 ORIENTAL PLAGUE chap. The microbe in question shows the morphological characters of the B. diphtherim of the short variety, it gives but feeble Neisser granules, and it does not act fatally on guinea-pigs or mice, be the injected dose large or small. The microbe, as stated just now, is strongly Gram -positive, it produces acid in glucose broth after forty-eight hours' incubation at 37° C. On gelatine at 21° C. its growth is extremely retarded, not before the fourth day is there a noticeable growth to be detected, and when it has started, the colonies are and remain very minute and very translucent. In this respect it differs both from the true B. diphtherim and from the B. mwis. On account of its action on the guinea-pig being similar to that of B. muris — causing the gradual formation of abscess — and on account of its having been obtained from the mouse, I conclude that it is the B. mwris, or a variety of the microbe obtained from the lung of rats (see previous pages) ; but the diphtheroid microbe of the mouse is shorter, gives but feeble Neisser, and grows much more slowly on gelatine than the typical B. mwris of the rat. I do not think the two are quite identical, although it must be inferred that they are clearly different varieties closely related to one another. I am confirmed in this by the result of their culture in different sugar media. Dr. Gordon informs me that both the B. muris of the rat and the diphtheroid bacillus of the mouse exhibit exactly the same reactions in the different sugared media — -reactions which not only prove their mutual relation, but distinguish them from the B. diphtherim. B. dipMTierice. B. muris. Bacillus of Mouse. Glucose . . -I- + + Saccharose . . - + + Salicin . — + + + means acid in two days. — means no acid in two days. The question of interest is, Whence is derived the diphtheroid microbe — B. muris — of the mouse ? Was it present in the organs (bubo and spleen) of the guinea-pig dead of subacute plague ; was it present in the cloth on which the particles of those plague organs had been dried ; or was it present in the skin of the experimented mice, and carried during the subcutaneous injection of the emulsion into the subcutaneous tissue, where, owing to the inflammatory effect of the plague toxin, it multiplied ? '^h" Fii n. rv^ 1; ,w Fig. 72. % --^■^^ U Fig. 71. Film specimen (stained) of B. pseudo-tuberculosis, from agar colonies twenty-four hours old. x 1000. Fig. 72. From an unstained broth culture of B. pseudo-tuberculosis, incubated twenty -four hours at 37° C. ; showing a "granule" or flocculus composed of chains of the bacilli. x 400. Fig. 73. From an impression (film) specimen of a young colony on a gelatine plate of B. pseudo-tuberculosis. x 1000. Fig. 74. Stained blood film of B. equi from rabbit's heart blood. x 1000. i --V \ ' ■ '. ^ •* /I, '^ 5 3 'VT^y'J^WfF Fk;. 7H. Fia. 75. Reproduced from a section through the affected Payer's patch of the ileum of a rat dead of plague after feeding ; seen under a low magnifying power. At 1. Piece of " food " (crowded with B. pestis) wedged in and fastened at the pit of the mucous membrane corresponding to the internal portion of the Peyer's gland. At 2. A swollen and partially necrotic lymph follicle. At 3. Lymph spaces surrounding a large blood-vessel and filled with continuous masses of B. pestis. At 4. Lymph vessels filled with B. pestis between the layers of the outer muscular coat. At 5. Necrotic mucous membrane filled with extravasated blood and masses of B. pestis. x 25. Fig. 76. Large blood-vessel of the submucosa (3 of Fig. 75) containing numerous B. pestis amongst the blood corpuscles, surrounded by lymph space filled with B. pestis. x 300. Fig. 77. Part of Fig. 76, more liighly magnified. A, Blood corpuscles within the blood-vessel. B, B. pestis in surrounding lymph spaces. x 1000. Fig. 78. Transverse section through mesenteric gland of a rat dead of acute plague after feeding. A, An afferent lymph vessel filled with B. pestis. B, Cortical lymph sinuses filled with B. pestis. All the light areas of the figure are the parts containing extravasated blood, the dark parts are masses of B. pestis. In the actual preparation, which was stained with methylene blue and eosin, the contrast between the masses of B. pestis (blue) and the extravasated blood (pink) was particularly striking. x 20. % -^^ ^ ^v ? ^^ c% -B ^'•C- Lfer," \->3)*^We', ,^^>**w«a(* B Til INFECTION OF ANIMA.LS WITH PLAGUE 163 m tlie submucous tissue, is a large blood-vessel distended by blood, and surrounding it is a lymph space densely filled with a continuous mass of B. pestis. Similarly at 4, lymph vessels situated between the inner circular and outer longitudinal layer of the muscular coat are filled with continuous masses of B. pestis. In the figure these lymph spaces at 3 and 4 appear dark ; but in the actual specimen stained with methyl-blue and eosin these parts are deeply blue, while the blood of the blood-vessels is pink. Under a sufficiently high magnification the fact that the masses are composed of B. pestis is easily recognised. In this animal, as also in others yet to be described — rats, guinea-pigs, and mice — sections through the hsemor- rhagic patches of the mucous membrane over and around the affected Peyer's glands show some villi which present a remarkable appearance. Continuous streaks and masses of 5. pestis (Figs. 80, 81, 87, and 89) not only cover the surface of the villi denuded of their epithelium, but extend between the tissue elements in the same reticular fashion as chyle does during absorption ; moreover, in some instances the central chyle vessel appears distended and filled with the B. pestis. In particular villi the tissue is completely deranged by effused blood in which appear numerous B. pestis. Continuous masses of B. pestis are found also around the fundus of the Lieber- kiihn crypts, surrounding these like lymph spaces, as also within the cavities of the crypts. In Fig. 7G the blood-vessels mentioned at 3 (Fig. 75) are shown somewhat more magnified ( x 300). They are filled with blood in which abundance of small and large masses of B. pestis can be seen (dark in the figure) ; the 164 OEIENTAL PLAGUE chap. blood-vessels are surrounded (perivascular lymph spaces) by tbe continuous masses of B. pestis mentioned above. This is specially shown in Fig. 77 {x 1000) from a point where the B. pestis are less densely packed, and therefore recognisable as such. Fig. 78 represents a section through the hsemorrhagic mesenteric gland, photographed under a low magnification ( X 20). The gland is seen surrounded by fat tissue. Near the middle of the upper part, close to the capsule, is an afferent lymphatic (dark) densely packed with B. pestis. At the right upper angle, within the fat tissue, is a blood-vessel containing masses of B. pestis (dark). In several places on the inside of the capsule, in situations correspondtag to cortical lymph sinuses, are continuous masses (dark) of B. pestis; so also in the medullary part. A good deal of the cortical part is more or less necrotic, and contains effused blood (light). In the actual specimens, stained double with methyl -blue and eosin, the contrast between the masses of B. pestis (blue) and those of blood corpuscles (pink) is very striking. Sections through the spleen, kidney, liver, and lung show not only that the blood-vessels up to their finest branches are distended with blood, and contain large numbers of B. pestis, but that in many places there is blood effused outside the vessels between the elements of the parenchyma, in which blood a great many B. pestis in small and large masses are seen. The spleen pulp is in many places literally packed with continuous masses of B. pestis in streaks and patches. Sections through the testis show the intertubular lymph spaces filled with blood, and amongst this continuous streaks and irregular VII INFECTION OF ANIMALS WITH PLAGUE 165 clumps of B. pestis (see Fig. 79). In tlie liver the capillary blood-vessels within the acini appear in some places almost as if injected with B. pestis, while the liver cells appear shrunk or full of fat globules. Sections through the lungs show, besides B. pestis present in some parts in the distended veins and capillaries of the minute bronchi and alveolar waUs, that the alveoli contain blood and homogeneous exudation. Extravasation of blood en masse occurs in many parts of the peribronchial and inter- lobular connective tissue. Similar extravasations of blood en masse, containing numerous B. pestis, are met with in many places in the connective tissue between the cortex and medulla of the kidney. And small branches of veins in the cortex of the kidney, as also the capillaries of the glomeruli, contain numbers of B. pestis, forming in many capillaries continuous blocks. [As mentioned above, the naked-eye appearances and cultural results of rat 2 were the same as those of rat 1, and it is not necessary to describe again the appearances of the sections made through the hsemorrhagic swollen Peyer's patch, the mesenteric glands, the spleen, the liver, and the kidney. They showed the same copious distribu- tion of B. pestis in the blood-vessels, in the lymphatics, and in the parenchyma.] From these observations it is seen that out of three rats fed, two succumbed to plague ; that they showed not only definite changes of the intestine, but in unmis- takable manner the exact spot or portal of the infection. Further, it is seen that not only was there abundance of B. pestis in the interior cavity of the aflfected intestine, but also that the lymphatics of the affected part of the intestine (villi, mucosa, submucosa, and muscular coat), 166 ORIENTAL PLAGUE chap. the mesenteric glands, and the vascular system in general, had become literally crowded with the B. pestis. This is a result more intensive in respect of the distribution of the B. pestis in the aflfected animal than that which occurred after subcutaneous or cutaneous injection. Experiment 3. — Four rats, Nos. 4, 5, 6, and 7 (kept in couples in cages), were fed on May 10 with bread mixed with gelatine cultures of B. pestis. The cultures were six weeks old and contained abundance of typical colonies ; but the gelatine around them was almost dry, and the colonies themselves were dry -looking and shrivelled. Rat No. 4 was found dead on May 13; rats Nos. 5 and 6 on May 14. Rat No. 7 appeared quiet at this date, but by May 17 had become quite normal, and it remained so. The post-mortem examination of rat No. 4 showed the following appearances : — Both mammary glands much congested and showing streaky haemorrhages ; sections through the hardened tissue showed a great deal of eflfused blood in the alveolar tissue, with numerous B. pestis. The omentum was congested, and there were numerous petechise in the ileum ; a distinct patch of haemorrhage was seen around a swollen Peyer's gland ; the mesenteric glands were swollen and hsemorrhagic ; the spleen was typically enlarged, dark, and firm ; the other viscera were congested. Cultures and film specimens of the mesenteric glands, of the interior of the intestine at the seat of haemorrhage, of the spleen, and of the heart's blood showed copious presence of B. pestis. Rat No. 5. — The whole of the lower ileum was relaxed and filled with a sanguineous mucus ; several Peyer's ll.3C Fig. 79. From a section through the testis of rat mentioned in Fig. 75. 1. A small arteriole showing a rupture (at its upper end). The tissue around it and the lymph spaces between the seminal tubules, seen here in cross section, are filled with the extravasated blood. 2. Masses of B. pestis in this extravasated blood. x 120. Fig. 80. Reproduced from a section through the ileum, at the site of haemorrhage, of a mouse dead of acute plague after feeding. 1. A villus containing a large amount of extravasated blood ; its central lymph vessel, 3, seen in section, is filled with B. pestis ; the same appears at 2A and 3B. 2. A villus denuded of its epithelium and permeated in reticular form by masses of B. pestis ; the same as during absorption with chyle. x 165. Fig, 81. Part of a similar villus to that in Fig. 80, more liighly magnified. At 1. Surface of villus covered with continuous masses of B. pestis, which extend (2) in reticular formation between the tissue elements of the villus ; exactly the same appearances as are shown by a villus in an active state of an ordinary absorption with chyle, with the difference that in this particular case the chyle globules are replaced by jB. pestis. x 1000. Fig. 82. Transverse section through the affected part of the ileum of a rat dead after feeding with plague material, i.e. with plague spleen dried in wheat. In the interior of the gut is a particle of material fixed a little above the section to the inflamed and necrotic Peyer's gland. This particle con- sists of a central mass of spleen tissue full of B. pestis, surrounded by semi- digested wheat. The villi contain abundance of B. pestis similar to what was shown iu Figs. 80 and 81. x 25. Fli:. Nl. ■hie- is.'.' . .>'! Fig. sa. VII INFECTION OF ANIMALS WITH PLAGUE 167 glands were swollen and showed punctiform hsemorrliages ; the mesenteric glands were swollen and showed haemor- rhages ; the spleen and kidney were large and dark ; the testes showed several hsemorrhagic patches, and their lymph vessels were injected with blood. Cultures, film specimens, and sections of the hardened organs showed the same copious presence of B. pestis as mentioned in regard of the former animals. Sections through the various organs showed the same appearances of distended vessels and haemorrhage, along with copious presence of B. pestis, as was described in the case of rat No. 1. Eat No. 6. — Several of the Peyer's glands of the ileum were enlarged and showed haemorrhages ; mesenteric glands slightly enlarged, congested ; both testes showed lymph spaces and lymph vessels injected with blood ; the spleen was large and dark. Cultures and film specimens of the Peyer's glands, of the mesenteric glands, of the spleen, and of heart's blood proved to be crowded with B. pestis. Sections through the various organs showed appearances as in the former case. Here, then, there was positive result in three out of four cases ; definite pathological changes of the intestine with intensive and extensive distribution of B. pestis. Experiment 4. — Two guinea-pigs, Nos. 8 and 9, were fed at the same time (May 10) and with the same stock of gelatine cultures as were the rats of the previous experiment ; with this difierence only, that for the guinea-pigs the gelatine cultures were mixed with soft green food — cabbage leaves finely cut up. In all these feeding experiments it was of course essential that no pointed particles should be in the food, in order to obviate 168 OEIENTAL PLAGUE chap. the possibility of inoculation of the fed animal by pricks of its skin or mucous membrane. As a matter of fact, in no case was any such accident noticed — the animals either succumbed with definite lesions of the ileum, denoting the place of entrance of infection, or they remained alive. Guinea-pig No. 8 was found dead on May 16. The post-mortem examination showed a considerable portion of the lower ileum swollen, deep purple in colour, and hsemorrhagic ; several Peyer's glands swollen and necrotic ; the interior of this part of the Ueum, as also of the adjoining portions, appeared filled with sanguineous matter, which in film specimens yielded B. pestis in pure culture. The mesenteric glands were swollen and hsemorrhagic, showing also several whitish-grey necrotic foci. The liver and spleen were crowded with grey punctiform nodules. Cultures were made of the intestinal contents, of the heart's blood, and of the spleen. As a result, in all cases pure cultures of B. pestis were obtained, except as regards cultures of the intestinal contents, which contained a small number of B. coli in addition. Two mice were inoculated cutaneously with a trace of the sanguineous intestinal contents of guinea-pig No. 8. One of these mice was found dead on the third day, the other on the fourth day. Both showed all the appear- ances of typical acute plague ; the spleen and heart's blood were literally packed with B. pestis. Sections were made through the hardened intestine, the mesenteric glands, the spleen, and the liver of the above guinea-pig. No. 8, and the results were practically the same as were described in regard of previous rats. In the swollen Peyer's patches the blood-vessels were dis- VII INFECTION OF ANIMALS WITH PLAGUE 169 tended, with extravasation of blood en masse, and with B. pestis everywhere ; the mucosa over and around the lymph follicles was filled with extravasated blood. Both the tissue of the mucosa and that of the lymph follicles were necrotic ; the lymph vessels and sinuses in the mucosa and submucosa were distended and filled with continuous masses of B. pestis. Necrotic patches were found in the mesenteric glands, in the liver and in the spleen asso- ciated with masses of B. pestis. Guinea-pig No. 9, which had been kept in the same cage as guinea-pig No. 8, remained alive. On May 30 it was injected subcutaneously with a trace of gelatine culture of the heart's blood of its dead companion, guinea- pig No. 8. It died on the seventh day with all appear- ances of subacute plague : necrotic bubo ; liver and spleen full of minute necrotic points ; lungs congested with necrotic patches. Film specimens and cultures were made of the bubo, the spleen, and the lung, and these showed copious presence of B. pestis. This experiment is instructive in that it bears out a fact on which in former reports I have repeatedly insisted, viz. that of two animals kept together in one cage, one may succumb to plague — its intestine, kidney, spleen, and blood in general literally swarming with B. pestis, — whereas its companion may remain, and this notwith- standing blood-sucking insects with which guinea-pigs are well provided, quite unafiected. If after twenty days the animal which has thus escaped illness be inoculated with B. pestis derived from its dead companion, it promptly succumbs to plague. Experiment 5. — Two mice, Nos. 1 and 2, were fed on 170 ORIENTAL PLAGUE chap. May 4 with bread mixed with minced fresh spleen of a rat which had died of typical plague after cutaneous inoculation. The spleen in question was typical of plague : large, dark, and crowded with B. pestis. These mice remained unaffected. On May 16 they were inoculated cutaneously with a trace of a gelatine culture derived from the rat-spleen with which they had been fed. Both were dead of typical plague on the third and fourth days respectively. Experiment 6. — Two mice, Nos. 3 and 4, were fed on May 20 with gelatine cultures of B. pestis. These gelatine cultures were sixteen days old, and showed on their sloped surface crowds of typical colonies, somewhat dry at the margin. Both mice were found dead in the morning of May 24. One of them must have been dead for some hours as its abdomen was in an advanced state of putrefaction. But the other, which was in a good state of preservation, showed the following interesting appearances on post- mortem examination : — In the ileum a number of hsemor- rhagic patches surrounding injected Beyer's glands ; mesenteric glands swollen and hsemorrhagic ; liver pale ; spleen large, dark, and firm ; kidneys much injected. Film specimens and cultures showed that the heart's blood and spleen were packed with B. pestis. Sections through the heemorrhagic parts of the intestine showed appearances similar to those already described in regard of rats fed in like manner. Not only was the actual infecting particle (full of B. pestis) found fixed to the intestinal mucosa, that is within the lumen, but the surface of the mucosa (villi) was denuded of its epithelium and covered with a continuous layer of '*;■ ^l^..*'iJm Fl.i. S4. Fig. 83. A portion of the previous particle (Fig. 82) more highly raagnifled. A, Gluten bodies and separating membranes. B, The same, but permeated by masses of B. pesiis. Cl-G, Bit of plague spleen with numerous B. pestis. x 300. Fig. 84. Part of previous figure more highly magnified. A- A, Semi-digested wheat permeated by masses of B. pestis. B, Piece of plague spleen (blood corpuscles are well shown) with numerous B. pestis forming aggregations at the margin of spleen and wheat. This tends to indicate that the wheat does not offer any antagonism or inhibition to the multiplication of B. pestis brought in contact with it. xVOO. Fie. 85. The same particle of plague spleen in wheat as shown in Fig. 82. The middle portion corresponds to the particle of plague spleen, surrounded by remains of wheat. x 85. Fig. 86. Section through mesenteric gland of a sewer rat dead after feeding with semi-dried plague organs. The light parts are filled with extravasated blood, the dark parts contain masses of B. pestis filling the cortical and medullary sinuses. 1. Two efferent lymph vessels in section filled with B. pestis ; there is een at the hilum (2) an efferent lymph vessel filled with B. pestis, just merging from the gland. lA. An afferent lymph vessel fiUed with B. pestis. x 45. »«. ir''; , ■■■■;-■■ Fic. Sfi v;^^^ # /A Fig. 86. VII INFECTION OF ANIMALS WITH PLAGUE 171 B. pestis. These baciUi could be traced in almost con- tinuous masses (see Figs. 80 and 81) into the villi, into the lymph spaces of the mucosa around the Lieberkiihn crypts, and into the lymph vessels of the submucosa around and between the lymph follicles. The mesenteric glands were literally crammed with B. pestis forming denser masses corresponding to the subcapsular and medullary lymph sinuses. Experiment 7. — Having thus satisfied myself that rats, mice, and guinea-pigs can be infected with plague by feeding them on old and drying gelatine and agar cultures, and that the intestines (ileum and Peyer's glands) of the experimental animals demonstrate in unmistakable manner the exact place where infection occurred, I directed my attention to similar feeding experiments with grain, i.e. with wheat and rice, which, having been mixed with minced plague organs of guinea-pigs or rats, or with gelatine cultures, had been allowed to dry. It is obvious that these further experiments more nearly represent con- ditions to which rats may become subjected as it were naturally. The bubo, spleen, liver, and lung of a guinea-pig that had died of plague after subcutaneous injection (guinea- pig No. 9 of experiment 4) were, on June 6, finely minced, and then well mixed in separate plate dishes, partly with wheat, partly with rice. The two lots were placed over sulphuric acid to dry. On June 7, i.e. after twenty -four hours, the materials were found well dried, and were now used for feeding. One dish (wheat and organs) was supplied to two rats in one cage, the other dish (rice and organs) to two other rats in a separate cage. Thus : — 172 ORIENTAL PLAGUE chap. Eats Nos. 10 and 11 were fed on June 7 with plague organs dried with rice. These two animals were distinctly affected on June 10, and they were found dead on the morning of June 11. On post-mortem examination the lower ileum in both animals was found intensely inflamed and showed haemorrhages ; the mesenteric glands were swollen and hsemorrhagic ; spleen typical, large, dark, firm, and crowded with B. pestis. Rats Nos. 12 and 13 were fed on June 7 with plague organs dried with wheat. One was found dead in the morning of June 10, the other remained unaffected. The post-mortem examination of the dead rat showed in the ileum five different spots where haemorrhage had taken place over and in the neighbourhood of Peyer's glands ; within the cavity of the ileum was a good deal of blood, and mingled with it crowds of typical B. pestis ; in the mesentery around the mesenteric glands was a big hsemor- rhagic patch, while the mesenteric glands themselves were swollen and exhibited petechise. The spleen was large, dark, firm, and crowded with B. pestis ; both kidneys, which were twice the normal size, were deeply congested in all parts ; both lungs were congested with numerous hsemorrhagic spots. Film specimens and cultures of the intestinal sanguineous contents of the spleen and of the heart's blood yielded B. pestis. Sections were made of the hardened intestine through the haemorrhagic spots, and Figs. 82, 83, 84, and 85 show the appearances observed. Fig. 82 is from a transverse section through a hsemor- rhagic part of the intestine close to a swollen Peyer's gland ( X 25). In the lumen of the intestine is seen a mass which is only the outlier of a larger mass attached to the inner portion of the Peyer's patch. Part of this VII INFECTION OF ANIMALS WITH PLAGUE 173 central mass is shown more highly magnified ( x 300) in Fig. 83. Here may be recognised between two masses of wheat A and B — or what is left of wheat undigested — a streak of tissue CCi, which, examined under a higher power, X 1000 (as in Fig. 84), shows itself to be a mass of tissue, most probably a piece of spleen ; and, further, there is seen in this tissue, as also in the part of wheat next to it, at B, continuous masses and clumps oiB.pestis which appear dark in the figure. Likewise there is seen in Fig. 83 at Cj a dense mass of B. pestis surrounded by what under high power is recognisable as a necrotic portion of tissue, probably spleen. At A in Fig. 83 there are gluten globules and septa between them. Here, then, is demonstration of a striking fact. In the lumen of the intestine, exactly at a hsemorrhagic spot and next an inflamed Peyer's gland, is a piece of the infected food — i.e. plague tissue wedged in between two portions of wheat — which would seem to have become attached to a Peyer's patch during the life of the animal. In this food particle there are recognisable more or less undigested parts of wheat (gluten portions) and part of the original plague organ that was dried with it. Further, it would appear there had been active multiplication of plague bacilli in the adjoining loosened wheat particle.^ Fig. 84 shows under a high power these streaks and masses of B. pestis between the layers of the remains of the wheat A A, B being the original plague material dried in the wheat. It remains to be noted that many vilh of Fig. 82 showed, when examined with a high power, crowds of B. pestis on the surface (denuded of epithelium) ^ This observation does not lend support to Hankin's contention that the wheat ofifeis antagonism and inhibition to the life and multiplication of B. pestis brought in contact with it. 174 OEIBNTAL PLAGUE chap. and in the tissue of the villi. Sections through the affected swollen Peyer's glands showed appearances like those previously described (Fig. 75). Particularly some villi showed haemorrhages with numerous B. pestis, and others were crammed with B. pestis in the manner re- presented in Fig. 80. Sections through the hardened kidney showed appear- ances already described, but more pronounced, in respect of numerous hsemorrhages in the cortex and at the boundary layer. Almost all glomeruli showed some capillaries degenerated, others blocked with B. pestis ; in many of the Malpighian corpuscles the cavity of the capsules contained blood and B. pestis. A like appear- ance was observed in many of the convoluted tubules. It should be mentioned here that while in the actual specimens double staiued with methylene-blue and eosin the distribution of the B. pestis in the tissues is at once strikingly apparent owing to the contrast between the bacilli staiued blue and the blood corpuscles red, iu the figures submitted this contrast is lost ; owing to the low magnifying power and to dense packing of the B. pestis these collections are only indicated as dark masses. In addition to the above experiments, I have obtained a number of other positive results from feeding rats with wheat and rice mixed with finely minced plague organs and dried over sulphuric acid for two or even three days. It is, however, unnecessary to describe all of them in detail ; they fully confirm the above observations. Experiment 8. — Parts of the organs (spleen and hver) of plague rat No. 12 were finely cut up and mixed in separate dishes, with wheat and rice, and placed on June 11 over sulphuric acid. After forty-eight hours (June 13) VII INFECTION OF ANIMALS WITH PLAGUE 175 the materials were found quite dry and extremely hard and brittle. They were now given as food to two white mice, Nos. 5 and 6 (rice plague organs), and to three wild mice, Nos. 7, 8, and 9 (wheat plague organs). The animals ate all the food within twenty-four hours. One of the white mice was found dead on June 16. It had extensive skin disease and a big worm in the hver, but its intestine and spleen were not affected. The other white mouse and the three wild mice remained alive and un- affected. From this it would seem that the material had been dried too much, and that probably all plague bacilli in them had been killed. Experiment 9. — This experiment was made in repeti- tion of experiment 3. Wheat and rice were mixed with old gelatine cultures of B. pestis (derived from blood and spleen of rats and mice dead of plague after feeding), and the mixed materials dried over sulphuric acid for twenty- four hours. The materials were then, June 21, given to rats, two for each lot. One of the rats, No. 14, fed with wheat gelatine culture was found dead in the morning of June 25 ; the companion, No. 15, pregnant, was very ill and was killed. On post-mortem examination this animal (15) contained seven dead foetuses, nearly full time ; there was a great deal of peritonitis ; the spleen was small and had no plague bacilli ; there was no appear- ance of plague. But the post-mortem examination of rat No. 17 showed lesions in the ileum and Peyer's glands, mesenteric glands, and spleen, identical with those already described. It is not necessary, therefore, to further refer to them beyond saying that film specimens and cultures of the hsemorrhagic mesenteric glands, of the spleen, and of the 176 ORIENTAL PLAGUE chap. heart's blood showed abundance of B. pestis. The rice- fed rats both remained alive, and showed no alteration in their condition. Experiment 10. — A guinea-pig which had been inocu- lated with plague having died, its organs — bubo, spleen (full of B. pestis) — were finely minced, and then mixed well with wheat and flour, and placed over sulphuric acid. After twenty -four hours the material, which was now perfectly dry and hard, was given (June 28) as food to three white and to three wild mice. On July 1 one of these wild mice was found dead. The ileum was relaxed and full of sanguineous mucus ; petechias in the mucous membrane ; mesenteric glands much injected and swollen ; spleen literally packed with B. pestis. The kidneys, lungs, and the liver were hardened, and sections were made. In all these organs great con- gestion of the blood-vessels was found, and iu the large and small vessels numerous B. pestis ; in the kidney some of the capillaries of the Malpighian tufts were quite blocked with them. The other two wild mice remained alive. Of the three white mice one was found dead on July 11, i.e. after thirteen days, and post-mortem examination showed the following conditions : — Ileum much congested ; at one spot, around a swollen more or less necrotic Peyer's gland, the mucous membrane was hsemorrhagic ; the mesen- teric glands swollen and hsemorrhagic ; the spleen much enlarged, dark, and firm. Sections through the swollen Peyer's gland and sur- rounding membrane showed almost complete necrosis, the tissues being permeated with efi'used blood, and the lymphatic vessels blocked with continuous masses of B. Fic. 87 « Cij .,; o ■"'^-' ^^>' Fig. SS. Fig. 87. Section througli the haemorrliagic patck of the ileum of a guinea-pig dead of subacute plague. The figure shows the mucosa and part of the submucosa ; on the top of the mucosa is a mass of blood-clot pervaded by B. pestis (dark). The villi and the rest of the mucosa are crowded with B. pestis (dark). x 65. Fig. 88. Section through the same portion of the ileum at its mesenteric attach- ment, shown in the lower part of the figure. In this attachment ai'e seen (about the middle) two blood-vessels in section fiUed with blood ; in the upper left and lower right of the mesentery are chyle vessels filled with B. pestis. X 30. Fig. 89. A villus of Fig. 87, showing copious absorption of B. pestis (dark). The epithelium of the surface of the villus is detached both on right and left. x300. VII INFECTION OF ANIMALS WITH PLAGUE 177 pestis. The mesenteric glands were necrotic, the lymph- atics here being filled and distended with masses of B. pestis. The two other white mice remained alive. In a number of other experiments old gelatine cultures of plague bacillus or actual particles of plague organs were mixed with wheat, rice, and flour, and were then left over sulphuric acid for more than three days. As a result the materials became thoroughly dry ; too dry, in fact, as negative result of feeding rats and mice with them showed — the animals remaining unaffected. More than forty- eight hours drying over sulphuric acid appears to preclude expectation of B. pestis remaining present in the material in a living state. From these experiments it appears : — (1) That irats, mice, and guinea-pigs are capable of infection with plague by feeding them with old ^ and drying gelatine cultures alone ; with old gelatine cultures mixed with wheat or rice and well dried previously ; and with pieces of plague organs mixed with wheat or rice or flour and dried previously. (2) That of animals thus fed a considerable percentage become infected ; that the infection takes place in the ileum at or about the Peyer's glands ; and that the in- fected animals die between the fourth and sixth days. (3) That haemorrhage with great multiplication of plague bacilli occurs in the ileum at the point of infection, and this not only in the cavity of the intestine and on the free surface of the mucous membrane, but also wittiin the villi themselves, in the absorbents of the villi and of all ' By old I do not mean gelatine cultures whicli aie practically dead and have lost all virulence, but gelatine cultures from two weeks to two months old and which yield active and living subcultures. N 178 ORIENTAL PLAGUE chap. parts of the intestinal wall ; and further, in the mesenteric glands, whence the vascular system of the other viscera become crowded with the bacUli. (4) That the positive results obtained by feeding with semi-dried or more completely dried gelatinous plague materials — e.g. gelatine cultures and plague organs dried by themselves or mixed with food-stuflfs (wheat, rice, flour) — are in marked contrast to the negative results of feeding with fresh plague materials — e.g. fresh milk cultures, broth cultures, watery emulsions of cultures of B. pestis and fresh plague organs. (5) That it is, therefore, justifiable to assume that the positive results in the former cases are due to the gastric juice failing to reach the central portions of the infective food particles, the plague bacilli in these central portions being left undisturbed and unaffected owing to the pro- tection afforded them by the outer dried shell of material. In a word, I am inferring that on their passage through the stomach the infective materials would retain some of the plague bacilli protected and living ; that on reaching the ileum the infective particles would, by the absorptive tendency of the Peyer's glands, become fixed, as it were, on these glands, and that the living plague bacilli within the material thus affixed to the mucous membrane would at once commence to multiply in situ, causing thereby the changes which were actually found, viz. haemorrhage and necrosis and charging of the absorbents with B. pestis, with the result of general infection of the rest of the body.i' 1 As direct evidence bearing on this point, the following observation deserves to be mentioned : — A guinea-pig was inoculated cutaneously, on April 11, with a particle of the spleen of a rat dead of acute plague. This guinea-pig was found dead on April 17, showing the following post-mortem appearances : large necrotic bubo with haemorrhage around it, while the spleen, liver, and lung contained numerous Til INFECTION OF ANIMALS WITH PLAGUE 179 Similarly I am inferring that the negative results of feed- ing with fresh materials are due to aU the ingested plague bacilli becoming readily exposed to the action of the gastric juice, so that no living plague bacilli are capable of reach- ing the ileum, and that the animal therefore escapes. It must be obvious from the above description that the discharges of the intestine and the secretion of the kidney in animals (rats, mice, or guinea-pigs) affected with plague by feeding, in all probability contain abundance of plague bacilli. It has been seen that the materials within the cavity of the ileum of such animals swarm with B. necrotic nodules crowded with the B. pestis ; that is to say, the animal presented the appearance of subacute plague which follows the cutaneous inoculation. But in addition a portion of the lower ileum of this guinea-pig showed great hasmorrhage with a blood -clot in its cavity firmly adhering to the mucous membrane, while the mesenteric glands were enlarged and showed haemorrhages ; there were haemorrhages also — besides those mentioned — in the subcutaneous tissue surrounding the inguinal bubo, also in the testis and omentum. Sections were made of the hemorrhagic portion of the ileum and of the mesenteric glands. These showed : (a) in the ileum and firmly adhering to the mucosa (villi) a mass of blood, in which were large numbers of nests of £. pestis ; the tissue of the villi was full of B. pestis, forming reticulated masses, as described and figured of former cases, in which infection had started from the intestine ; the central chyle vessel, as also the lymph vessels of the mucosa, were literally crowded and injected with B. pestis, as were also the lymph vessels of the sub- mucosa and of the outer muscular coat ; in the mesenteric margin of this part of the intestine the efferent chyle vessels were distended and filled with blood and with masses of B. pestis ; the large blood-vessels of the same parts were also filled with blood, amongst which some B. pestis could be recognised. (6) The mesenteric glands showed the same appearances as were described on a former page, viz. the afferent and efferent lymph vessels were distended and filled with B. pestis, so also were the cortical and medullary lymph sinuses ; a great deal of haemorrhage was noticeable in the cortical lymph follicles. The appearances above described appear to me to admit of one interpretation only, viz. this : in the ileum haemorrhage had taken place, witness the presence of a blood-clot in the cavity ; the B. pestis in this clot being in a suitable place — the ileum — had multiplied and had become readily absorbed by the villi in which indeed they abounded ; the same process had followed in all the absorbents of the intestinal wall and mesenteric glands. This was evidently made possible by the duration of the disease (six days). So that a direct lodgment of B. pestis in the intestinal cavity having occurred while the animal continued to live, time was given for a secondary infection of this part of the ileum of the same character as that observed in the other cases in which the B. pestis had reached the ileum by way of the food. 180 ORIENTAL PLAGUE chap. pestis, and that these materials on inoculation promptly produce plague. Likewise it appears that plague bacilli are abundant in the Malpighian corpuscles (glomeruli and capsules) and in the uriniferous tubules.^ These facts in no way support a contention such as that put forward by Hankin in the Journal of Hygiene, to the effect that the intestinal or renal discharges of the plague rat are not to be regarded as materials capable of causing infection. On the contrary, the observations I have recorded go to justify a contention that, as regards rats which have contracted plague by feeding, the dejecta in question, teeming as they needs must with B. pestis, are to be regarded as in all probability infective. Indeed, in view of the ready transmission of plague to the rat by means of feeding with infected grain, rice, flour, and the like, the foregoing experiments afford strong suggestion that the excreta of a plague rat becoming mixed and dried along with food-stuffs may be the starting of extensive plague infection of the rats feeding on these substances contaminated by stale plague dejecta. In connection with the above propositions, it has to be borne in mind that the anatomical lesions in the ileum which I have described cannot be of a single day's dura- tion ; that the necrotic changes in the mucous membrane and in Peyer's glands caused by the multiplication of B. pestis within the cavity of the ileum must have occu- pied time in development, and that accordingly there ^ As a matter of fact I have made a number of experiments ( wHch need not be described in detail) in which the sanguineous mucus of the inflamed intestine of animals (rat and guinea-pig) dead of plague after inoculation was used for cutaneous as also subcutaneous injection, and by which fatal plague of the animals so inoculated (guinea-pigs and rats) was the result. I have also made inoculation experiments (subcutaneous) of guinea-pigs, employing the urine drawn from the bladder of guinea-pigs or of rats which had succumbed to (haemorrhagio) plague, and the result was positive in the majority of instances. VII INFECTION OF ANIMALS WITH PLAGUE 181 must have arisen ample opportunity for B. pestis to pass into and out from the large intestine with the alvine evacuations of the infected animal. It is not possible to deny that similar conditions might occur in respect of human beings ; that food-stuffs having become polluted with, say, excreta of plague rats preserved in a semi-dried or dried condition, might cause plague in persons ingesting them, the point of infection in such case being the intestine itself Simpson's contention (Eeport on Plague in Hong- Kong) that the septicsemic form of plague in man (in which the whole blood system and all organs contain abundance of B. pestis) may be caused by infection of man's intestine by means of food, was based on experi- ments in which wild rats were fed with fresh plague organs ; these rats, or some of them, having died, plague was considered to have been induced in them by way of the intestine. This inference seems to me, however, not justified, or at least not proven, and for two reasons : — (1) The fact that the rats in question died, as is said by Simpson, from the septicsemic form of plague does not afford presumption that they were infected by ingestion ; the septicsemic form of plague being that under which both rats and mice and also guinea-pigs commonly die after inoculation. (2) No indication is given by Simpson of any such conspicuous and definite local infection (hsemorrhage) in the ileum and in Peyer's glands as that described by me as resulting in those of my feeding experiments which proved positive. The general congestion of the small intestine mentioned by him (in addition to sanguineous mucus in the intestinal 1.82 ORIENTAL PLAGUE chap. cavity) is not, be it observed, an uncommon feature in the rat and mouse dead of plague contracted otherwise than by feeding ; it is not uncommon too in rodents which have died of septicsemic diseases other than plague. In the guinea-pig, dead of plague after subcutaneous injection, I have not unfrequently found the whole of the intestine showing punctiform haemorrhages. Also I have observed haemorrhage in the testis, whence the effused blood could be traced by the absorbents of the spermatic cord into the pelvic lymph gland. On the other hand, it is possible, in view of the experi- ments I have been describing, that Dr. Simpson's view may prove on the whole to be correct, and this mainly for the reason that in the septicaemic form of plague of the human subject the blood and the organs appear crowded with B. pestis, as also in the animals of my feeding experiments. Before, however, definitely pronouncing on this point, it would be necessary to make careful post-mortem examina- tion of septicaemic plague in man for the purpose of ascertaining whether local infection (ileum and Peyer's gland) and changes of the mesenteric glands similar to the conditions described here in regard of experimental animals, has actually occurred. Among the many interesting facts concerning the spread of plague in India ascertained by the Indian Plague Commission are those pointing to persistence for some considerable time of the contagium of plague in rooms and streets from which all plague cases had been removed; rooms or streets, for instance, are cited in which plague broke out afresh on the return to them of the inhabitants. Hankin, however, it appears (see also Eeport of Indian Plague Commission) had made experiments on the vitality VII INFECTION OF ANIMALS WITH PLAGUE 183 of the B. pestis in soil, and had found this to be of very short duration. These experiments of Hankin have been relied on by commentators as justifying the view that the observed persistence of infectivity in rooms and streets after removal therefrom of infected persons might have been due to retention of the contagium by rats or by fleas ; in a word, to the contagium having been kept alive as it were by these means. Before, however, accepting such interpretation of the facts it seemed to me necessary to ascertain whether the vitality of B. pestis in soil is really of short duration ; whether the result might not have been difierent if, instead of distributing B. pestis in the soil, as practised by Hankin, in the form of a broth culture, it had been applied under conditions more nearly approaching those in which it would naturally find access to soil, e.g. in blood, in discharges of a suppurating bubo, in mucous expectorations, in the mucoid discharges from the bowels of a plague rat, in the juices of plague organs, or in similar viscid or slimy materials. Accordingly I have made a series of experiments in this direction, and have thereby ascertained that B. pestis planted in or mixed with soil in the above manner has considerable power of persistence. Also I have made experiments with wheat and rice on the same lines ; that is, I have sought to ascertain for what length of time the bacilli in plague material (cultures or organs) mixed with wheat or with rice can retain their vitality. Gelatine cultures, about six weeks old, were melted in warm water and poured over fine earth (gravel) contained in a glass dish (July 2), and over fine sand (July 1) con- tained in a separate glass dish. The earth and the sand were 184 OEIENTAL PLAGUE chap. in each instance thoroughly mixed with the gelatine and then placed over sulphuric acid, of course in a hermetically closed space. The earth as also the sand were (after being kept not more than twenty-four hours over sulphuric acid) found perfectly dry and hard. After having been thus dried during one, two, three, or more days, a small amount (about ^ to 1 gramme) of the infected earth or sand was in each instance taken out, placed in a sterile watch-glass and distributed (rubbed down) in a few cubic centimetres of warm sterile water so as to form a turbid emulsion. Of these turbid emulsions small quantities in each instance (about ^, ^, ^ cc.) were injected subcutaneously into guinea-pigs. This method of procedure was chosen in preference to mere cutaneous inoculation of rats, for the reason that the object was to ascertain not whether living plague bacilli were present in a small droplet (the quantity that could be introduced by cutaneous inoculation) but whether any living plague bacilli were left in fair quantities of the materials. Experiment 1. — Guinea-pig No. 1 injected with " sand - gelatine," after '■ twenty - four hours' drying, on July 2. Guinea-pig No. 2 injected with " earth-gelatine," after forty-eight hours' drying, on July 4. Guiaea-pig No. 1 developed a big bubo and died on July 7 with typical subacute plague. Post-mortem examination showed a necrotic bubo with crowds of B. pestis ; spleen and liver dotted all through with white nodules full of B. pestis} ' It may not be unnecessary to state that in all experiments mentioned here, inclusive of all animals without exception deader killed after plague infection, stained film specimens of all afifected organs, and culture on gelatine from the bubo (when present), from the intestine (when affected), from the spleen and from the heart's blood, were made invariably and as a matter of ordinary routine. Yii INFECTION OF ANIMALS WITH PLAGUE 185 Guinea-pig No. 2 developed a bubo slowly ; it was found dead on July 11. Post-mortem examination showed typical subacute plague. Experiment 2. — Guinea-pig No. 3 was injected (on July 4) with " sand - gelatine," dried for three days. Guinea-pig No. 4 was injected on July 5 with " earth- gelatine," dried for three days. Guinea-pig No. 3 developed bubo slowly ; this became a big abscess by July 13. The same condition was observed with guinea-pig No. 4. But both animals appeared otherwise lively. Both were killed, and on post - mortem examination the pus of the buboes was found to contain, amongst cocci, crowds of B. pestis. The viscera appeared unaffected. Experiment 3. — Both the dishes containing "sand- gelatine " and " earth-gelatine " were removed from over the sulphuric acid after lapse of three days and were then kept under simple glass cover (raised about half an inch at one side) at the temperature of the laboratory. Six days after withdrawal from the influence of the sulphuric acid, the "sand-gelatine" was used for sub- cutaneous injection (on July 9) of guinea - pig No. 5 ; and five days after withdrawal the " earth-gelatine " was used in similar manner for injection (on July 9) of guinea-pig No. 6. Guinea-pig No. 5 was on July 15 without tumour and quite lively ; and it remained so. Guinea-pig No. 6 died on this day (July 15). On post-mortem examina- tion there was evidence of typical subacute plague : big necrotic bubo with crowds of plague bacilli, liver and spleen permeated with minute white nodules containing numerous B. pestis. 186 OEIENTAL PLAGUE chap. Experiment 4. — After a further week's (July 16) ■withdrawal from sulphuric acid, the samples having been kept meanwhile at the room temperature and in the air of the laboratory, the same " sand-gelatine " and " earth- gelatine" were used for injection of guinea-pigs Nos. 7 and 8 respectively. The " earth-gelatine " appeared now as dry and hard as brick. The " sand-gelatine " guinea- pig. No. 7, remained without swelling and quite well; whereas the " earth - gelatine " guinea-pig, No. 8, de- veloped a small firm nodule at the seat of inoculation. This, however, almost entirely disappeared in the course of a fortnight, the animal remaining lively and well. From these experiments it appears that gelatine cultures mixed with sand and earth can be dried over sulphuric acid for three days, until, for instance, the material becomes distinctly hard and dry, without the plague microbes losing their vitality ; and, further, it appears that the " earth -gelatine" kept for additional five days, till it had become as hard as brick, still retained living and active B. pestis. Experiment 5. — In this experiment gelatine cultures about six weeks old were (June 30) melted in warm water and poured over wheat and rice in separate glass dishes. After being well mixed in each instance the materials were placed over sulphuric acid, of course in a hermetically closed space. On July 1, i.e. after twenty-four hours, the materials being now quite dry, a little of each sample was placed in warm water and a guinea-pig was injected subcutaneously with the emulsion thus obtained ; viz. guinea-pig No. 9, with " rice-gelatine," and guinea-pig No. 10 with " wheat- gelatine." Both animals developed big tumours in the VII INFECTION OF ANIMALS WITH PLAGUE 187 groin. Guinea-pig No. 10, which appeared otherwise lively on July 5, was killed on that date, and on post- mortem examination showed the following conditions : — Extensive oedema over abdomen and chest ; about the place of inoculation a big cavity filled with grumous fluid. Spleen not enlarged, no bacilli in it. In the inguinal fluid were crowds of diplococci and streptococci ; as also numerous bipolar bacilli like B. pestis. With a dilution of the inguinal fluid an agar plate was made, and this brought forth crowds of colonies just like those of B. pestis. A guinea-pig, No. 11, was injected with one of these plague-like colonies. This animal was found dead on the fifth day, and gave evidence of typical plague with the typical distribution of B. pestis in the bubo and spleen. Guinea-pig No. 9, which had been injected with the " rice-gelatine," developed a big abscess in the groin and thigh ; on the eighth day it was quiet and ofi" its feed, and the bubo having opened spontaneously was discharg- ing pus. This animal, which was better and fairly lively again on the thirteenth day, was now killed, and showed the following post-mortem appearances : — In the inguinal region and about the thigh was a big cavity containing grumous creamy pus ; spleen and liver and also lungs showed numerous minute white nodules. In the pus of the inguinal abscess were numerous clumps of B. pestis. In the next series a number of animals were inoculated with earth and with sand which, after addition of small particles of plague organs, had been dried for various periods at the ordinary temperature of the laboratory. Experiment 6. — Of a guinea - pig dead on July 7 188 OEIENTAL PLAGUE chap. with typical subacute plague, bits of the necrotic bubo, and pieces of the spleen and liver (full of minute nodules), were finely minced and mixed separately in glass dishes with earth (fine gravel) and fine sand. These materials were then so placed as to obtain fairly free access of air,^ and were left to dry spontaneously. On July 14, i.e. after one week, a small amount in each case of the dry material was emulsified in warm water, and of each emulsion about i to ^ cc. was sub- cutaneously injected into a guinea-pig. These guinea-pigs will be designated : — No. 12. — "Sand-plague" guinea-pig. No. 13. — "Earth-plague" guinea-pig. Guinea-pig No. 12 was found dead on July 18, i.e. after four days; it had, however, been dead for some time, July 17 being a Sunday. The post-mortem examination showed typical plague (early stage of sub- acute), viz. necrotic bubo, and few minute nodules in spleen and liver. Bubo and spleen were crowded with B. pestis, as shown by film specimens and by cultures. Guinea-pig No. 13 was dying on July 21. On post- mortem examination there was found a big necrotic bubo crowded with B. pestis ; the spleen, liver, and the lungs were crowded with necrotic I [nodules and -patches ; film specimens and cultures yielded pure cultures of B. pestis.^ Experiment 7. — The materials of experiment 6 were used for inoculation of guinea-pigs after a further week of drying, viz. on July 21. By this date the materials appeared perfectly dry and hard as bricks. ^ The dishea were kept under a bell glass, raised all round about J to 1 inch and placed by the open window. VII INFECTION OP ANIMALS WITH PLAGUE 189 Guinea-pig No. 14 was injected with emulsion of the " sand-plague " organs. Guinea-pig No. 15 was injected with emulsion of the " earth-plague " organs. Guinea-pig No. 14 remained without swelling, and was altogether unaffected ; it was killed on August 2, and gave totally negative result as regards plague. But guinea-pig No. 15 was distinctly ill on July 26 and had bubo. It was killed on the same day, and showed the following appearances : necrotic bubo ; spleen, liver, and lungs crowded with necrotic nodules and patches. Pilm specimens and cultures of the bubo, spleen, and lung yielded crowds of B. pestis. Pig. 24 shows, in a section under a low power, a necrotic nodule of the spleen containing aggregations (dark) of B. pestis ; these aggregations being in reality networks of blood spaces of the pulp tissue. Fig. 21 shows, in a section (x 100) through the lung, one of the nodules (this being in reality an infundibulum with its alveoli) all blocked with masses (dark) of B. pestis. From this experiment it appears, therefore, that while " sand-plague " material dried for fourteen days at the ordinary temperature was barren of infective power, "earth-plague" material still retained its efficacy. The former was therefore discarded, but the latter was retained for further experiment. Experiment 8. — With emulsion of the same " earth- plague" material now dried for three weeks, guinea-pig No. 16 was injected on July 28. This animal appeared unaffected on August 3, i.e. after six days. It was killed and found in all respects normal. 190 ORIENTAL PLAGUE chap. Thus, earth subjected to admixture with the juice and particles of plague organs, and allowed to dry, retained its infective power for a fortnight, but after lapse of three weeks proved barren of infectivity. It is to be noted that these experiments were carried out during the hottest part of the year, when the drying was fairly rapid and thorough. Experiment 9. — The blood, bubo, spleen, and liver of a rat dead of acute (inoculated) plague were, on July 8, finely minced and mixed with sand and earth ; these materials being then put away to dry spontaneously, a fair amount of ventilation being in each instance allowed. In this condition the materials were kept for eight days (July 16); they were then placed over sulphuric acid for three days (July 19), by which time they were quite dry and as hard as bricks. On this date, i.e. July 19, emulsions were made and used for the subcutaneous injection of guinea-pigs. Guinea-pig No. 17 was injected with "sand-plague" organs. Guinea-pig No. 18 was injected with "earth-plague" organs. Guinea-pig No. 17 developed a small abscess on the abdomen, but otherwise remained lively. Guinea-pig No. 18 showed a gradually increasing soft tumour (abscess) in the groin, which by the end of the week (July 26) had reached the size of a pigeon's egg ; the animal, however, appeared otherwise lively. Both were killed on July 27, but with negative result qua B. pestis. Guinea-pigs injected with the pus of guinea- pig No. 17, as also with the pus of guinea-pig No. 18, remained unaffected. VII INFECTION OF ANIMALS WITH PLAGUE 191 Experiment 10. — Rice and wheat were in each instance mixed, on July 11, with finely minced bits of spleen and lung of a guinea-pig dead of typical subacute plague, and placed to dry spontaneously in the same manner and under the same arrangement as in the previous experiment. On July 21, that is after ten days, the materials were found quite dry, and were used for making emulsions in warm water for injection subcutaneously of two guinea- pigs :— Guinea-pig No. 19. — " Eice-plague " organs. Guinea-pig No. 20. — "Wheat-plague" organs. Both animals remained without tumour and lively. They were killed after one week and were found quite normal. Experiment 11. — A guinea-pig died on September 27 from typical subacute plague. Its organs (bubo, spleen, liver, and lungs) were finely minced, mixed with sand and with earth respectively, and placed to dry spontaneously in the laboratory under the same conditions as in previous experiments. By the end of a week (October 4) the materials seemed fairly dry, and were used to inject guinea-pigs : — Guinea-pig No. 21. — " Sand-plague " organs. Guinea-pig No. 22. — " Earth-plague " organs. Guinea-pig No. 22 was found dead on October 7 with very intensive acute plague ; guinea-pig No. 21 was found dead on October 10 with typical subacute plague. Experiment 12. — The same "sand" and "earth" plague materials were used for injection of guinea-pigs on October 11, that is after a fortnight's drying : — Guinea-pig No. 23. — " Sand-plague " organs. 192 ORIENTAL PLAGUE chap. Guinea-pig No. 24. — "Earth-plague" organs. Both animals were found dead on October 17 with typical subacute plague. Experiment 13. — The materials of September 27 were used for experiment on guinea-pigs on October 20, i.e. after twenty -three days' drying : — Guinea-pig No. 25. — " Sand-plague " organs. Guinea-pig No. 26. — " Earth-plague " organs. Both animals remained alive and unaffected. Experiment 14. — Gelatine cultures oiB.pestis, directly derived from rats and mice dead of plague after feeding and about fourteen weeks old, were on October 8 melted in warm water, mixed with sand and with earth, and left spon- taneously to dry in the laboratory in the manner described in previous experiments. Nine days later (October 17) these materials were used for injection of guinea-pigs : — Guinea-pig No. 27. — " Sand-gelatine " plague. Guinea-pig No. 28. — " Earth-gelatine " plague. Guinea-pig No. 28 was found dead on October 24 with typical subacute plague. Guinea-pig No. 27 was found dead on October 26 with typical subacute plague. Experiment 15. — The above materials were used again for injection of guinea-pigs on October 26, i.e. after eighteen days' drying : — Guinea-pig No. 29. — " Sand-gelatine " plague. Guinea-pig No. 30. — " Earth-gelatine " plague. Guinea-pig No. 29 died November 1 with typical subacute plague. Guinea-pig No. 30 was found dead on November 2 with typical subacute plague. Experiment 16. — These materials were again used on vn INFECTION OF ANIMALS WITH PLAGUE 193 November 7, i.e. after thirty days' drying, for injection of guinea-pigs : — Gruinea-pig No. 31. — " Sand-gelatine" plague. Guinea-pig No. 32. — " Earth-gelatine " plague. Guinea-pig No. 31 was found dead on November 16 with typical subacute plague. Guinea-pig No. 32 was found dead on November 14 with typical subacute plague. Experiment 17. — The materials were again used for injection of guinea-pigs on November 22, i.e. after six weeks and three days' drying : — Guinea-pig No. 33. — " Sand-gelatine " plague. Guinea-pig No. 34. — " Earth-gelatine " plague. Guinea-pig No. 34 was found dead on November 26 with typical subacute plague. Guinea-pig No. 33 remained unaffected. It was tested after a fortnight by the subcutaneous injection with plague culture and was found fully susceptible. Experiment 18. — The same "earth-gelatine" plague was again used on November 29, i.e. after seven weeks and three days' drying, one guinea-pig, No. 25, being injected with it. The animal was found dead with typical sub- acute plague. Experiment 19. — The last experiment with this same material, viz. " earth - gelatine " plague, was made on December 14, that is after nine weeks and four days' dry- ing, one guinea-pig, No. 36, being injected subcutaneously with turbid emulsion. The animal remained unaffected. This animal a fortnight later was injected with B. pestis of culture and promptly succumbed to plague. From this series it appears that the vitaUty of B. pestis in earth and in sand to which the micro-organism 194 OEIENTAL PLAGUE chap. had been added in the form of gelatine culture remained, during the autumn months, for a long period unimpaired. Indeed, B. pestis was present in a liviag state in the earth even after seven and a half weeks ; in the sand for six weeks and three days. These are periods of consider- able duration, much longer than were found in the previous experiments (experiment 7) in which the infective materials were exposed to drying during the summer months. In these later experiments of early winter the infective materials were old gelatine cultures, not plague organs, and they were left to dry spontaneously under conditions such as might occur naturally. The fact that plague contagium is, under gelatinous or viscid conditions and during the cooler months of the year, capable of retaining its vitality in sand, and particularly in earth, for a considerable time, is a circumstance having no small importance, seeing that under natural conditions during plague seasons plague expectoration and intestinal mucus charged with masses of the B. pestis cast upon the earth may very possibly in like manner long retain dangerous infective property. As a last series I have to mention some experiments in which plague organs were, by themselves, without ad- mixture with other material, exposed to drying, and were then used for feeding rats, both tame and wUd. The organs in question — bubo, spleen, lung, and liver, contain- ing abundance of B. pestis — were obtained from animals (guinea-pig and rat) dead of typical acute plague. These organs, after having been cut into fair-sized pieces, were put to dry over sulphuric acid. Experiment 20. — The organs of a guinea-pig dead of VII INFECTION OF ANIMALS WITH PLAGUE 195 subacute plague whicli had been cut up in small bits and kept over sulphuric acid for seven days were by this time perfectly dry and hard. Two rats were fed with this material. Both animals remained unaffected ; so they were at the end of a week injected cutaneously with agar culture (twenty -four hours old) of B. pestis derived from a recent case of plague in man (case from s.s. Weyhridge) which had been landed at Denton in December 1904. Both were dead of acute plague in three days. Experiment 21. — The organs (bubo, spleen, liver, and lungs) of two rats, dead of plague after having been in- oculated cutaneously with the blood of a guinea-pig dead of acute plague, were cut up into small bits and dried over sulphuric acid for eight days. With this material, by this time quite dry and hard, two wild rats were fed. Both animals remained unaffected. Experiment 22. — The organs of a guinea-pig dead on February 22 of acute plague were cut up into bits and dried over sulphuric acid for forty-eight hours. By this time the outside of the material was well dried, though the inside remained stiU moist. With this material two tame rats in one cage, and two wild or sewer rats in a second cage, were fed on February 24. One of the sewer ^ rats was found dead on February 28, the other remaining, by then and afterward, seemingly unaffected. Both tame rats at this date seemed ill, and showed rough coats. The post - mortem examination of the dead sewer rat showed the following condi- tions : — The greater part of the lower ileum congested, ' The wild rats used in these experiments were all of the common brown sewer rat type. 196 ORIENTAL PLAGUE chap. relaxed, and filled with blood and mucus ; at one point of the congested ileum a Peyer's gland appeared swollen, much projecting, and necrotic, the membrane forming around it a well-marked ring of haemorrhage; the mes- enteric glands were enlarged and hsemorrhagic (Fig. 86) ; the spleen large, dark, and firm ; the lungs of both sides were much congested and showed haemorrhages. The sanguineous mucus of the ileum, the mesenteric glands, the spleen, and the lungs were crowded with B. pestis (as was proved by film specimens and cultures) ; the blood also contained abundance of B. pestis. In this case, therefore, there was distinct and direct evidence that plague had been contracted by the feeding ; for here, as in former positive cases, the point of infection was anatomically easily located in the ileum at a Peyer's gland. Sections made through these parts fully confirmed this inference. A small particle of the sanguineous mucus from the ileum of the dead sewer rat was injected subcutaneously into a guinea-pig, and the rest of the mucus was mixed with bran and oats, dried over sulphuric acid, and then given as food to two wild rats. As a result, the two rats thus fed remained unafiected, whereas the inoculated guinea-pig sickened and became afi"ected with typical sub- acute plague, the subcutaneous injection causing a huge hsemorrhagic and necrotic bubo in which was abundance of B. pestis. It is of interest to notice in regard of this experiment 22, that a plague rat had been in the same cage with another rat which remained unaffected, though fed with plague material like its fellow — as indeed had happened in previous experiments, Series I. and II. In these condi- VII INFECTION OF ANIMALS WITH PLAGUE 197 tions, therefore, there was abundant opportunity for transmission of plague by fleas or other blood -sucking insects, such as lice, from the affected animal to its companion living with it in the same small cage ; more- over, ithe animal that sickened with and died of acute plague about the fourth or fifth day had plenty of B. pestis in its blood. It is not to be supposed that common sewer rats such as were used in these experiments were without fleas or lice, nor can it be supposed that the fleas of the rat that died did not leave this rat for the living rat, a practice of fleas noticed and recorded by several observers. On making the post-mortem examination no fleas but only lice could be found on this dead rat,^ though during life the animal was frequently observed to scratch itself in the manner customary with rats. Notwith- standing, therefore, all these circumstances specially favourable for the transmission of plague, the companion rat remained unaffected. Here was a rat the blood of which was teeming with B. pestis ; further, close at hand was a companion rat ready for any supposed fleas or lice to migrate to, and yet this companion rat remained un- affected by plague. Nevertheless this companion rat, when later on (after lapse of a week) it was cutaneously inoculated into the skin of the root of the tail with a trace of gelatine culture directly made of the blood of its former dead companion, died on the third to fourth day with acute plague (just like other rats after cutaneous inoculation), showing hsemorrhagic swollen glands in the groin with dense crowds of B. pestis, the spleen large, dark, and flrm, ^ It should be here added that I have not been able as yet to find " fleas " on sewer rats examined after death — caused spontaneously by plague or after killing them by chloroform ; lice alone, but these in abundance, have been hitherto found on their dead bodies. 198 OEIENTAL PLAGUE chap. crowded with B. pestis ; that is to say, with the appear- ances described in detail on a former page. This failure of transmission of plague from a plague rat to a healthy rat living amicably in the same or in an adjoining open wire cage is not an isolated instance.^ In my reports to the Medical Officer of the Local Government Board for 1902-1903 and 1903-1904 I have mentioned a good many such instances ; and in the present chapter I have recorded several in addition where only one of two animals (rats, mice) contracted and died of plague, be it by inoculation or by feeding, the companion remainiQg unaflfected, though highly susceptible, as proved afterwards by inoculation with active plague material. While, then, the transmission of plague from animal to animal is experimentally established both as regards cutaneous inoculation and feeding with semi-dry infective material, there is a distinct failure of evidence that trans- mission of the disease is effected by fleas or lice from an in- fected animal to a healthy one. It is not, therefore, in my view, justifiable to regard this mode of transmission, if, in- deed, it happens at all under natural conditions, as anything but exceptional, at any rate as far as the sewer rat and the tame white rat are concerned. Theoretically, such a trans- mission is possible and easily imaginable, as I have discussed on a former page ; it is possible, I mean, that a flea or louse which has just sucked from a rat blood well charged with B. pestis may, by biting a neighbouring rat, directly inocu- ' Hitherto I have searched in vain during autumn, winter, and spring for fleas on sewer rats and on the tame or white rats. I have been able to discover only lice. I would further point out that, as mentioned on a, former page, the above experiment is not altogether satisfactory, since the sewer rat is not an animal with high susceptibility for plague. It is probable that in these respects an important distinction may have to be drawn between this species and the Oriental rat or Mus rattus. vn INFECTION OF ANIMALS WITH PLAGUE 199 late this latter. But wliat I wish to insist on is, that such an occurrence is not likely under natural conditions to be anything but exceptional ; there is no direct evidence that this has happened, and in cases where it might have been expected to happen — e.g. in many experiments recorded by me — it certainly did not do so. As already mentioned, Hankia (I.e.) does not favour direct transmission of plague by fleas. He regards the flea as a true host, a living body in which the B. pestis multiplies and in which it acquires virulence, beheving, it would seem, that not until these further phases have been accomplished is the flea capable of transmitting plague to a new individual (rat or man). From what I have already said in this chapter it is, however, clear that definite support of proof for this view of Hankin's has yet to be furnished. CHAPTER VIII AGGLUTINATION OF BACILLUS PJESTIS The Physiological Action of Solid Sterilised Masses of Plague Bacilli. — AlP observers who, as regards plague, have worked with the bacillary growth en masse have found that the injection into the animal body of the sterilised material in sufficient amounts has a protective action. Haffkine himself {cf the evidence before the Plague Commission) laid stress on this. It is, in his view, the amount of the bacillary sediment in the prophylactic fluid which determines the dose, the amount of precipitate and the size of the dose standing in inverse proportion. Calmette (Harben Lectures, London, 1900) also relies almost entirely on the bacillary bodies (sterilised) as being the essence of the prophylactic material. The same applies to the German Plague Commission's recommendation. In my Plague Keport for 1896 (Report of the Medical Officer for 1896-1897) I had already described (p. 297) a number of experiments in which the bodies of plague bacilli, scraped from the agar surface and sterilised by heat, were injected in repeated doses subcutaneously and intraperitoneally into guinea-pigs and rabbits. I there 1 Report of the Medical Officer of the Loo. Gov. Board for 1901-1902, p. 360 and passim. 200 cH.Tni AGGLUTINATION OF B. PESTIS 201 showed that sterilised cultures (solid growth on gelatine and agar broth cultures) repeatedly injected, in large doses, subcutaneously or intraperitoneally, into guinea- pigs, do not confer absolute protection on the guinea-pigs against further infection any more than does repeated injection of sub-fatal doses of living plague baciUi. In fact, I showed in an unmistakable manner that the guinea- pig is an animal which it is extremely difficult to immunise against plague. This fact was subsequently verified in a series of experiments which Professor Hafi'kine and I together carried out in my laboratory with his plague prophylactic. We found that even injection of enor- mous doses of Hafi^kine's plague prophylactic, such as yielded positive results in protection of rats, did not confer absolute protection on the guinea-pigs against subsequent infection. In the same report I have also described experiments which conclusively show that, as was to be anticipated from the above negative results, the blood of guinea-pigs which had recovered from induced plague (produced by injection of sub -fatal doses of living plague bacilli) is devoid of immunising or germicidal substances in appreciable amounts. I have in further experiments sought to ascertain whether the blood of guinea-pigs previously prepared, either by repeated injection of sub- fatal doses of living cultures or by repeated injection of large doses of sterile cultures, possesses any agglutinating action on emulsion of plague bacilli ; and it is these experiments which I propose here to describe. It is now well established that by repeated injections of an animal with a particular microbe the blood and tissues of this prepared animal undergo certain changes 202 OEIENTAL PLAGUE chap. the result of which is the development in them of various new substances. Amongst these, two at any rate have been studied carefully : (a) agglutinins ; and (b) lysins, or germicidal or immunising substances. I do not discuss here — the matter being outside this treatise — ^the different theories that have been put forward as to the probable nature of these substances, viz. whether they are ferments (Roux, Emmerich) or are some highly and complexly constituted organic bodies other than ferments (R. Pfeiffer, Ehrlich, and others). I am content to give consideration to their mode of action as observed in actual experiment. The Agglutinins. — Bordet and Gruber were the first to show that the blood serum of an animal subjected to repeated injections with the typhoid or cholera microbe sooner or later (usually in about a fortnight) acquires a new property : that when a small quantity of the serum is added to an emulsion of the typhoid or the cholera microbe respectively the microbes soon lose their motility, are (attracted together, and become at the same time " agglutinated " or " clumped," so as to form smaller or larger masses. These, on account of their weight, gradually sink to the bottom of the tube in which the emulsion is contained, and the previously turbid fluid thus becomes clear. This process of "clumping" or "agglutinating" has been also studied in other cases besides those of the typhoid bacillus or the cholera vibrio, and it has been shown that the phenomenon is of a fairly general nature ; that the blood of an animal which has been repeatedly injected with a given microbe — pathogenic or non-pathogenic — acquires the power to " agglutinate " an emulsion of the particular microbe with which it has been, so to speak, " prepared," It had been further shown that the degree VIII AGGLUTINATION OF B. PESTIS 203 to whicli the agglutinating power of the blood can be raised differs, cceteris paribus, in the different animals for the different microbes ; that it differs also in regard to diverse methods of administration, and again as to the time at which the agglutinating power makes its appear- ance. A few instances may be mentioned in illustration. After intraperitoneal injection into guinea-pigs of sub-fatal doses of living culture of cholera vibrio, the blood serum of the animal shows some weeks later (two to three) distinct agglutinating power with an emulsion of cholera vibrios in the proportion of 1 : 20 or even 1 : 40. By- repeated (three) intraperitoneal injection of culture of living cholera vibrios this agglutinating power of the blood serum may be raised to 1 : 100 or even 200. I have, hke other persons, obtained a high degree of agglutinating action by injecting subcutaneously first a large dose of sterilised and then, from week to week, gradually increas- ing doses of living cholera culture. A fortnight after the last (fifth) injection the blood serum of the guinea-pig possessed so strong an agglutinating power that one part of the serum agglutinated completely, and within a few minutes 200 parts of bouillon emulsion of living (recent) agar culture, or, better still, a twenty-four hours old peptone salt solution culture of the vibrio. As regards the typhoid bacillus, a high agglutinating action of the blood serum of guinea-pigs can be produced in just the same way. After a fifth injection the blood serum agglutinates completely in the proportion of 1 in 400, within a few minutes, the bouillon emulsion of the typhoid bacillus being made from a forty-eight to seventy- two hours old gelatine culture. There is, however, a difference betwe.en the two 204 ORIENTAL PLAGUE chap. microbes, the vibrio of cholera and B. typhosus, as regards the above reaction. The agglutinating action of the blood serum of a cholera-prepared animal does not ensue immediately, say within a> )j 6th „ 18 It )) » )> 7th „ 31 . )) )) )j )) 8th August 27 . jj >j » J) 9th September 16 ») it >> tt The blood serum was tested (dilution 1 : 20) on tlie following dates, and with the following results in one hour : — No. Date. Result. 1st June 4 Negative. 2nd „ 13 . JJ 3rd „ 26 . Positive (?). 4th July 9 Rapid agglutination within 10 minutes. 5th ,, 29 . Distinct clumping in 10 minutes. 6th August 9 . Complete agglutination in 10 minutes. 7th September 12 Positive in 5 minutes. 8th October 1 . Indication of agglutination in 10 minutes, but not better in 30 minutes nor in 1 hour. 218 OEIENTAL PLAGUE CHAP. It is seen from this series that the triple intraperitoneal injection of sterile culture was less effective as to the production of agglutinins than had been subcutaneous injection of like material ; that the subsequent two intra- peritoneal injections of small doses of living culture brought about distinct presence in the blood of agglutinins; and that while further similar injections continued to enhance the agglutinating power of the blood, the ninth injection was followed by a distinct decrease of this power. 3. Guinea-pigs Nos. 5 and 6. — These two animals (half-grown) were repeatedly injected subcutaneously with Haffkine prophylactic. The animals were injected on the following dates, and with the following amounts : — No. Date of Injection. Method of Injection. Material (and Amount) Injected. 1st June 27 Subcutaneous . 10 oc. of Haffkine's prophylactic. 2nd July 3 5J 5 11 !) >- 3rd „ 18 )> 10 „ 4th August 1 J) 10 „ 5th „ 29 . J) 10 „ 6th September 17 )» 10 „ 7th October 21 » 10 „ The blood serum was tested (dilution 1 : 20) on the following dates, and with the following results : — vni AGGLUTINATION OF B. PESTIS 219 No. Date. Kesult. 1st July 8 Agglutination doubtful in 1 hour. 2nd „ 15 Negative'in 1 hour. 3rd „ 30 . 5? )) 4th August 28 5) ») 5 th September 13 J) 5» 6 th November 19 )) » The subcutaneous administration, many times repeated, of Haflfkine's prophylactic had therefore no result in producing agglutinin such as was demonstrable after repeated injection of small doses of living culture. 4. Guinea-pigs Nos. 7 and 8. — These, which were half-grown, were injected intraperitoneally on the foUowiug dates, and with the following results : — No. Date of Injection. Method of Injection. Material (and Amount) Injected. 1st 2nd 3rd 4th 5th 6th 7th 8th June 17 „ 27 . July 11 „ 18 . August 1 „ 29 . September 17 October 21 . Intraperitoneal 5 cc. of Haffkine's prophylactic. 5 „ 5 „ 5 „ 5 „ 6 „ 10 „ 10 „ 220 OKIENTAL PLAGUE CHAP. The blood serum was tested (dilution 1 : 20) on the following dates, with the following results : — No. Date. Result. 1st June 27 Indication of agglutination in 1 5 minutes. 2iid July 8 . Complete clumping in 10 minutes. 3rd „ 30 Slight clumping in 20 minutes. 4th August 8 Negative in 1 hour. 5tli September 9 . J) » eth November 1 9 » t> These experiments are in accord with those in which the blood after repeated injections acquired a gradually increasing agglutinating power, and later on, notwithstanding continued injection, again lost it. They, moreover, tend to show that the intraperitoneal injection of small doses of Haffkine's prophylactic into guinea- pigs is more conducive to the formation of agglutinin than the subcutaneous administration of doses twice as large. II. — Experiments op Agglutination with Blood OF Rabbits In this series rabbits were substituted for guinea-pigs, and, as will be shown, the rabbit proved very much more satisfactory. 5. One half-grown rabbit, No. 1, was injected intra- venously (ear vein) repeatedly with at first sterile and then living plague culture : — VIII AGGLUTINATION OF B. PESTIS 221 No. Date of Injection. Method of Injection. Material (and Amount) Injected. 1st 2nd 3rd 4th 5th May 6 „ 28 . June 13 July 9 „ 18 . Intravenous . Salt emulsion of plague gi-owth scraped from the surface of a gelatine cul- ture and sterilised for 15 minutes at 70° C. The amoxmt used for each animal was about | of a culture (6 centimetres by 2 centimetres). Same amount and same kind of material. Small amount of emulsion of living culture. This rabbit was found dead on July 20. On post-mortem examination the spleen was seen to be permeated by small grey nodules, which on microscopic and cultural examination proved to be of the nature of pseudo-tubercle. No plague bacilli were demonstrable either in the blood or the organs. The blood of the rabbit was, however, tested for its agglutination (dilution 1 : 20) on various occasions, with the following interesting results : — No. Date. Result. 1st 2nd 3rd 4th May 24 . June 5 July 7 „ 16 . Negative. Distinct agglutination in 30 minutes. Complete agglutination in 10 minutes. „ „ within 5 minutes. From this it appears that after the first intravenous in- jection of sterile culture no agglutinin had yet been formed, but that after the second such injection there was, eight 222 OEIENTAL PLAGUE CHAP. days later, distinct agglutinin present ; further, that this became enhanced by a similar third injection, and was still more distinct after a fourth injection with living culture. 6. One half- grown rabbit, No. 2, was injected into the ear vein in precisely the same manner and at the same time as the rabbit of the previous experiment. A fortnight after the third injection with sterile culture (first injection May 6, second injection May 28, third injection June 13), i.e. June 27, the animal's blood serum was tested (dilution 1 : 20) and was found to pro- duce complete agglutination in ten minutes ; the same result as was observed in the previous experiment. The animal, unfortunately, was found dead on July 8. The post-mortem examination showed extensive cysticercus disease of the omentum. 7. A half- grown rabbit, No. 3, was injected sub- cutaneously with Haffkine's prophylactic at the following times : — No. Date of Injection. Method of Injection. Material (and Amount) Injected. 1st and 3rd 4th 5th 6th 7th 8th June 17 . July 3 „ 18 . August 1 „ 29 September 17 . October 21 November 21 . Subcutaneous 10 CO. of Haffkine's prophylactic. 10 „ 10 „ 10 „ 10 „ 10 „ 20 „ 20 „ vin AGGLUTINATION OF B. PESTIS 223 The results of the testing of this rabbit's blood serum on emulsion of B. pestis (dilution 1 : 20) were the follow- ing :— No. Date. Result. 1st June 27 Negative in 1 hour. 2nd July 2 . a » 3rd „ 8 . ») »j 4tli „ 31 . . ) 3) 5tli August 26 • Positive in 10 minutes. eth September 13 . Negative in 1 hour. 7tli October 2 5) JJ 8th „ 15 M » 9th January 16 Positive and distinct in 15 minutes. This experiment in its early stages contrasts markedly with similar stages of experiment 5 ; for it shows that the subcutaneous injection of Haffkine's prophylactic, even after repeated (three) administration of considerable amounts (10 cc. each time), did not succeed in producing agglutinin in the animal's blood. 8. Rabbits Nos. 5 and 6.— In this experiment the administration of Haffkine's prophylactic was effected in two rabbits by intravenous followed by subcutaneous injection. As regards rabbit No. 5 : — [Table 224 ORIENTAL PLAGUE CHAP. No. Date of Injection. Method of Injection. Material (and Amount) Injected. 1st 2nd 3rd 4tlx 5th eth 7th July 1 . „ 11 „ 18 August 1 . „ 29 . September 17 . October 21 Intravenous . )) Subcutaneous 5 cc. of Haffkine's prophylactic. 10 „ 10 „ 10 „ 10 „ 20 „ The animal died on November 4. On post-mortem examination the liver was found atrophied, fatty ; the stomach was much distended, showing few hsemorrhagic patches in the serous covering ; in the abdominal cavity- were numerous cysticerci. The blood serum of this animal (rabbit No. 5) had been tested for agglutination on the following dates, and with the following results : — No. Date. Result. 1st July 8 Negative. 2nd „ 16 Complete agglutination in 15 minutes. 3rd „ 31 . . . Negative in 1 hour. 4th August 26 Positive in 10 minutes. 5th September 9 Negative in 1 hour. VIII AGGLUTINATION OF B. PESTIS As to rabbit No. 6 : — 225 No. Ist Date of Injection. Method of Injection. Material (and Amount) Injected. July 1 . Intravenous . 5 CO. of Haffkine's prophylactic. and „ 11 . » 5 „ Srd „ 18 . Subcutaneous 10 „ 4th August 1. 10 „ 5th „ 29 . 10 „ 6th September 17 . 10 „ 7th October 21 18 „ 8th November 21 . 20 „ The blood serum of this animal was tested (dilution 1 : 20) :— No. Date. Result. 1st July 16 . Positive in 20 minutes. 2nd „ 31 . Negative in 1 hour. Srd November 14 Indication in 15 minutes. 4th January 1 Distinct agglutination 10- 15 minutes. 5 th „ 16 ?j >» » This experiment is confirmatory of that with the previous animal, No. 5, A twofold intravenous iujection of HafiPkioe's prophylactic brought about production of agglutinias. But at this stage a single subcutaneous injection of 10 cc. not only did not enhance the aggluti- 226 ORIENTAL PLAGUE CHAP. nating power, but, on the contrary, seemed to destroy it, though it reappeared after several further subcutaneous injections. Another important fact is brought to light in this as in experiment No. 7, viz. the distinct agglutina- tion possessed by the blood serum nearly two months after the last injection. I shall have to reconsider later on other points con- cerning these animals, but at present I proceed with the examination by further experiments of the agglutination phenomenon. III. — Experiments in Agglutination after Injection OP Filtrate of Haffkine's Prophylactic 9. In this experiment two half-grown guinea-pigs were injected subcutaneously with the cleax filtrate of Haffkine's prophylactic. This was obtained by simply opening some of the sealed tubes in which the prophylactic had been preserved, decanting the clear fluid and passing it through a Pasteur-Chamberland filter. The filtrate was of course perfectly limpid. Guinea-pigs Nos. 9 and 10 (half-grown) were injected subcutaneously, each receiving 10 cc. of the above fil- trate : — No. Date of Injection. Method of Injection. Material (and Amount) Injected. 1st 2nd 3rd September 10 . 17 . October 21 . Subcutaneous . 10 cc. of the filtrate. » » VIII AGGLUTINATION OF B. PESTIS 227 One of these guinea-pigs died December 23. The animal was extremely emaciated, but no cause for its death could be found. The blood serum was tested (dilution 1 : 20) : — No. Date. Result. 1st 2nd 3rd September 29 October 12 . November 21 . Negative. 10. The half-grown guinea-pigs Nos. H and 12 were injected intraperitoneally, each receiving 10 cc. of the filtrate : — No. Date of Injection. Method of Injection. Material (and Amount) Injected. 1st 2nd 3rd September 10 . 17 . October 21 . Intraperitoneal 10 cc. of the filtrate. The tests with the blood serum were made as above, but with completely negative result. 11. Two half -grown rabbits, Nos. 7 and 8, were subcutaneously injected with the same filtrate, each animal receiving 20 cc. : — [Table 228 ORIENTAL PLAGUE CHAP. No. D^te of Injection. Method of Injection. Material (and Amount) Injected. 1st 2nd Srd 4th 5th September 10 . „ 17 . October 21 . November 21 . January 2 . Subcutaneous . J) 20 cc. of the filtrate. 91 fl The blood serum of both animals was tested (dilutions 1 : 20 and 1 : 10 in each instance) : — No. Date. Result. 1st 2nd 3rd October 2 . . . November 20 . January 1 . . . Negative. From this it appears that neither in the rabbit nor in the guinea-pig was there any agglutinin formed after repeated injection of the filtrate alone of Haffkine's prophylactic. It was altogether unexpected that half- grown rabbits should, after receiving a total of 100 cc. of this filtrate, yield blood serum which showed no sign of agglutinin even in dilution of 1 in 10. IV. — Experiments with Blood Serttm of Eats I have already mentioned that rats which had passed through the disease (rats which had first been prepared by VIII AGGLUTINATION OF B. PESTIS 229 Haffkine's propliy lactic, 10 cc. subcutaneously injected) and were tlien injected with more than an ordinary fatal dose of living culture of the plague bacillus, developed a distinct bubo which suppurated. This after some days healed completely, and the animals' blood tested along with salt emulsion of gelatine culture showed in a con- spicuous degree agglutination (dilutions 1 : 20 and 1 : 40) in ten minutes. I have had occasion to repeat this experiment on other rats which had passed through a non-fatal attack of plague, and have been able fully to confirm it. 12. In this experiment three rats were injected sub- cutaneously with Haffkine's prophylactic, each animal receiving 10 cc. : — No. Date of Injection. Method of Injection. Material (and Amount) Injected. 1st 2nd November 21 . December 31 . Subcataneous . I Occ. of Haffkine's prophylactic. 5) » »» As was ascertained from the experiments carried out in conjunction with Prof Haffkine in 1899, a single injection of 10 cc. of this prophylactic into rats suflfices to give them protection against an otherwise fatal dose of living plague. In the present instance no further injection beyond the above 20 cc. was employed. The blood serum of one of the rats (after the animal had been killed) was tested (dilution 1 : 20) on January 30, and it showed no distinct agglutination within one hour. 13. Four rats were injected on December 31 sub- cutaneously with Haffkine's prophylactic, each animal 230 ORIENTAL PLAGUE chap. receiving 8 or 10 cc. ; that is to say, two full-grown animals received each 10 cc, other two half-grown 8 cc. in each instance. On February 5 one of the small animals was killed and its blood serum tested (dilutions 1 : 20 and 1 : 10), with negative result in one hour. It follows from these experiments that injection into rats of Haffkine's prophylactic in amount more than sufficient to protect them against a fatal dose does not cause the production in their blood of any agglutinins. 14. In this experiment three rats were subcutaneously injected with the filtrate of Haffkine's prophylactic, each animal receiving 10 cc. on November 21 and other 10 cc. on December 31. Their blood serum was tested on February 2 (dilu- tion 1:20 and 1:10), with completely negative result. This result was to be expected, considering that the injection of the prophylactic as such did not in previous experiments produce agglutinins. The results, then, of the numerous experiments here described can be thus summarised : — 1. The blood of rodents (guinea-pigs, rabbits, rats) which have been repeatedly injected with large masses of the sterilised bodies of B. pestis possesses the power of agglutinating a duly prepared emulsion of the B. pestis. Especially in rabbits is this manifest. 2. The same' ^agglutinating action is observed with respect to the blood of rodents which having been injected with sub -fatal doses of living plague bacilli had as a consequence been affected with the disease and recovered from it. 3. The increase in agglutinating action of the blood of Tin AGGLUTINATION OF B. PESTIS 231 these " prepared " animals is not in a direct ratio to the amount of material injected, or to the number of the different injections. It appears to go on increasing up to a certain degree, and then to decrease or be lost entirely. 4. The repeated administration of Haffkine's pro- phylactic into guinea-pigs, when injected subcutaneously , produced no agglutinin in the blood; whereas the repeated intraperitoneal injection of the prophylactic into guinea-pigs appears to have produced agglutinin which, however, was soon lost, even during continuance of " treatment." 5. In the rabbit, on the other hand, the repeated injection (intravenous, less when subcutaneous) of Haffkine's prophylactic did produce agglutinins at one or another stage, although on the whole such production was uncertain. 6. In the rat the repeated injection subcutaneously of Haffkine's prophylactic failed to produce agglutinin. 7. The repeated injection (in whatever way) of the filtrate of Haffkine's prophylactic into rodents (guinea- pigs, rabbits, rats) failed to produce agglutinias. Besides the experiments on agglutinins above sum- marised, investigation has been made of the power of the blood serum of guinea-pigs and rabbits, and in a few instances also of rats, previously immunised in various ways, in inhibiting the action of the living B. pestis, when such serum along with a lethal dose of plague was injected into a susceptible or unprepared animal. In other words, account having been given of the agglutina- tion or test in vitro, what follows will deal with Pfeiffer's test or the test in corpore. 232 OEIENTAL PLAGUE CHAP. V. — Experiments in Testing Blood of Prepared Animals for the Presence of Germicidal Substance. (a) Guinea-pigs. — With reference to the guinea-pig of experiment 1, guinea-pig No. 1, referred to at page 212, it will be convenient here to restate, in tabular form, the several occasions on which this animal had been injected, and the material used for injection in each instance : — No. Date of Injection. Method of Injection. Material Injected. 1st 2nd 3rd 4tli 5th 6th 7th 8th 9th 10th 11th 12th 13th February 18 . „ 28 . March 11 „ 27 AprU 22 May 2 . „ 28 . June 17 . July 9 . „ 18 . . ,, 31 . August 26 September 16 . Subcutaneous . Sterile agar culture. » » Living agar culture. Living gelatine culture. " » J) » Test in corpore of the blood of this animal was performed as follows : — Blood serum of the animal was mixed with living plague emulsion, and the mixture injected subcutaneously into the groin of a guinea-pig, a like amount of living plague emulsion being at the same time injected into a control guinea-pig. The two animals were of about the same body -weight. Thus : — (1) July 16. — Guinea-pig No. 11 was injected with 100 cubic millimetres, 1000 cubic millimetres being equal to 1 cubic centimetre, of plague emulsion, plus 25-30 viii AGGLUTINATION OF B. PESTIS 233 cubic millimetres of blood serum. At the same time 100 cubic millimetres of plague emulsion were injected into control guinea-pig No. 12. Both guinea-pigs developed big buboes. The control guinea-pig died on the thirteenth day, the other guinea- pig which had received plague culture plus blood serum died on the seventh day, both of plague ; that is to say, the control animal died later than the other. The blood serum had therefore had no effect whatever of neutralising the fatal dose of plague culture. (2) July 29. — Guinea-pig No. 17 was injected with a mixture of 100 cubic milUmetres of plague emulsion and 50 cubic millimetres of blood serum. At the same time a control guinea-pig No. 18 was injected with 100 cubic millimetres of plague emulsion alone. Guinea-pig No. 17 developed no bubo, and remained quite lively and well. Guinea-pig No. 18, on the other hand, showed distinct bubo on the third day ; this en- larged tUl the eighth day, then gradually diminished and disappeared, the animal quite recovering. This experi- ment is therefore faulty in this, that the control animal did not succumb to plague, the dose injected not proving a fatal dose. But the experiment apparently indicates that some inhibiting effect was produced by mixing the blood of the prepared guinea-pig with a dose of plague culture that served in a control animal to cause a distinct bubo. Referring to the table, it will be seen that at the date on which the blood serum was obtained from the guinea-pig No. 1 this animal had been injected three times with sterile culture, and seven times with small doses of living culture of plague bacillus, and that therefore by this time its blood seemed to contain 234 ORIENTAL PLAGUE chap. some active germicidal substance, although in a small amount. (3) August 10. — Guinea-pig No. 26 was injected with a mixture of 100 cubic millimetres of emulsion and 100 cubic millimetres of blood serum. At the same time guinea-pig No. 27 was injected with 100 cubic milli- metres of emulsion alone. The control guinea-pig No. 27 died of plague on the sixth day, the other guinea-pig. No. 26, died of plague on the seventh day. This experiment does not denote the presence of germicidal substance in the blood of guinea-pig No. 1, even when serum and plague emulsion have been injected in equal amount. The guinea-pig No. 1 had been injected on September 16, a thirteenth time, this time with a double dose of living gelatine culture. On October 17 the animal was killed, and it showed nowhere any pathological appear- ances. As already mentioned, its blood serum at this stage gave on agglutination test (dilution 1 : 20) completely positive result in ten minutes. Its blood serum, as also a salt extract of the spleen (this organ looked quite normal), were now used in the following manner : — (1) 200 cubic millimetres of plague emulsion were mixed with 200 cubic millimetres of blood serum, and the mixture injected into guinea-pig No. 40. (2) 200 cubic millimetres of plague emulsion were mixed with 50 cubic millimetres of blood serum, and the mixture injected into guinea-pig No. 39. (3) 200 cubic millimetres of plague emulsion were mixed with 200 cubic millimetres of thick spleen emulsion, and the mixture injected into guinea-pig No. 41. VIII AGGLUTINATION OF B. PESTIS 235 (4) 200 cubic millimetres of plague emulsion were injected into control guinea-pig No. 42. The result was this : — Guinea-pigs 42, 39, and 41 died of plague on the fifth day ; guinea-pig 40 died of plague on the sixth day. All the animals had typical bubo and enlarged spleen crowded with plague bacilli. From this it appears that neither the blood nor the spleen of guinea- pig No. 1 were capable of exerting any appreciable germicidal action. That the guinea-pig No. 1 was dis- tinctly protected by September 16 is proved by the fact that an injection on that day of a considerable dose (certainly more than double the ordinary fatal dose) did not cause any illness whatever in this animal. As a matter of fact, some time previous to the above date the guinea-pig did not react on the injection of an otherwise fatal dose of living plague culture. And yet the last- named experiments prove that this animal possessed neither in its blood nor in its spleen those substances (antitoxins, germicidal substances, etc. ) which we associate with protection, i.e. substances produced by repeated injections of the microbe, as in diphtheria protection and cholera protection. It is justifiable, therefore, to conclude from the above very striking experiment that, as regards the guinea-pig, the injection (thirteen times) of the plague microbe does not result in the production of demonstrable amounts of anti-bodies — germicidal substances, Pfeiff"er's lysins — in the experimental animal. The second guinea-pig used for experiment was that already referred to as guinea-pig No. 4, p. 216. This animal had been injected at the following periods : — 236 OEIENTAL PLAGUE CHAP. No. 1st Snd 3rd 4th 5th 6th 7th 8th 9th Date of Injection, May 6 . „ 22 . June 5 . „ 14. July 9 . „ 18. „ 31. August 27 September 16 Method of Injection, Intraperitoneal Material (and Amount) Injected. Large dose of sterile gelatine culture. Small dose of living gelatine culture, The test in corpore was made as follows : — (1) July 29. — Guinea-pig No. 19 was subcutaneously injected with 100 cubic millimetres of living plague emulsion mixed with 50 cubic millimetres of blood serum. At the same time 100 cubic millimetres of the emulsion was injected into a control animal. Both these animals remained alive. The experiment is therefore useless, the amount of living culture injected having been insufficient to cause death in the control animal. (2) August 9. — The experiment was repeated. Guinea- pig No. 28 was subcutaneously injected with 100 cubic millimetres of living plague emulsion mixed with 100 cubic millimetres of blood serum of guinea-pig No. 4. At the same time 100 cubic millimetres of the emulsion were injected into a control animal. The control guinea-pig died of plague on the sixth Tin AGGLUTINATION OF B. PESTIS 237 day ; the other, No. 28, died of plague on the ninth day. (3) September 12. — Guinea-pig No. 35 was sub- cutaneously injected with 100 cubic millimetres of living plague emulsion mixed with 100 cubic millimetres of blood serum. At the same time 100 cubic millimetres of the same emulsion were iujected into a control guinea- Pig- The guinea-pig No. 35 died of plague on the fifth day ; the control guinea - pig died of plague on the seventh day. From this series confirmation of the previous result is obtained, viz. that even after several injections of living cultures into the peritoneum of the guinea-pig no appreci- able amounts of germicidal substances are present in the blood of the protected animal. Seeing, then, that no germicidal effect can be produced with the blood serum of guinea-pigs repeatedly injected with living culture, it was not to be expected that a positive effect could be produced with the blood serum of guinea-pigs repeatedly injected with the Haff"kine pro- phylactic. But, nevertheless, experiments as to this were actually made, as follows : — Guinea-pig No. 5, already mentioned (p. 218) as having been injected subcutaneously with Haffkine's pro- phylactic on seven separate occasions, furnished blood serum which was tested for the presence of germicidal substance twelve days after the fourth injection, and again fourteen days after the sixth injection. The result in both instances was negative. Guinea-pig No. 7, referred to at p. 219 as having been injected intraperitoneally on eight separate occasions 238 OEIENTAL PLAGUE chap. with Haflfkine's prophylactic, furnished blood serum which was tested for germicidal eflfects after the fourth and again after the seventh injection. The result was in both instances quite negative. In J the face of these results I have not thought it expedient to test the blood serum of the guinea-pigs which had been injected with the filtrate alone of Haffkine's prophylactic. (&) Rabbits. — The blood serum of the following three protected rabbits was submitted to the germicidal test, namely : — Kabbit No. 1, referred to at p. 220 as having been intravenously injected at first (three times) with sterile, then (twice) with small doses of living culture ; rabbit No. 3, referred to at p. 222 as having been repeatedly injected subcutaneously with Haffkine's prophylactic ; and rabbit No. 5, referred to at p. 223 as having been repeatedly injected, first intravenously and then sub- cutaneously, with Haffkine's prophylactic. Rabbit No. 1. — Test of this rabbit's serum was made on July 16, that is to say, one week after the fourth intravenous injection. (1) 100 cubic millimetres of plague emulsion mixed with 50 cubic millimetres of the blood serum were injected into guinea-pig No. 13. (2) 100 cubic millimetres of plague emulsion mixed with 100 cubic millimetres of the blood serum were in- jected into guinea-pig No. 14, The result was negative ; both animals died of plague. No. 13 on the sixth day. No. 14 on the seventh day. Rabbit No. 3. — The blood serum of this rabbit was vm AGGLUTINATION OF B. PESTIS 239 tested on July 15, i.e. after the second subcutaneous injection witli Haflfkine's prophylactic. 100 cubic millimetres of plague emulsion mixed with 100 cubic millimetres of its blood serum |were injected into guinea-pig No. 9. This animal, No. 9, died on the fourth day of typical plague. The test was repeated on July 31, i.e. thirteen days after the third injection of 10 cc. of HafFkine's prophylactic. 100 cubic millimetres of plague emulsion mixed with 100 cubic millimetres of the blood serum were injected into guinea-pig No. 23 ; and at the same time 100 cubic millimetres of the emulsion alone were injected into control guinea-pig No. 24. The control, No. 24, died on the eighth day, the other guinea-pig. No. 23, died on the twelfth day. The test was repeated on August 26, again with negative result. Rabbit No. 5. — The blood serum of this rabbit was tested on three diflferent occasions — July 16, July 31, and August 26. But, as was the case with rabbit No. 3, the result proved negative in all three instances. As regards rabbits Nos. 3 and 5, the test on the last occasion, viz. August 26, was altered in this way. In- stead of mixing equal parts of plague emulsion and blood serum, a double volume of blood serum was used, viz. 100 cubic millimetres of plague emulsion were mixed with 200 cubic millimetres of blood serum. The guinea-pigs injected with the mixture died, notwithstanding, of typical plague. From these experiments it follows that, as with the guinea-pig so with the rabbit, neither repeated intra- 240 ORIENTAL PLAGUE chap. venous or subcutaneous injection, first of sterile and then of living culture, nor repeated subcutaneous or intravenous injection of Haffkine's prophylactic, pro- duces germicidal substances in the blood of this animal in appreciable amount and in a way to render its serum serviceable for neutralising the fatal efiect upon the guinea-pig of a dose of living culture of plague bacillus. It will have been noticed from the above control experiments that the dose of plague emulsion, viz. 100 cubic millimetres, generally used, was by no means a large dose, since some of the control guinea-pigs did not die, while in most instances death was delayed. It will be remembered from my Eeport 1896-1897 that the normal fatal dose for a guinea-pig is the one that kills a half-grown animal between forty- eight and seventy -two hours. In the cases now in question some of the (control) animals die as late as the seventh or eighth day. (c) Rats. — One rat, which had been twice suhcuta- neously injected with Haffkine's prophylactic, November 21 and December 31, was killed on January 30. 250 cubic millimetres of plague emulsion mixed with 250 cubic millimetres of blood serum of above rat were injected into one rat, No. 1, and 250 cubic millimetres of emulsion only into a control rat. No. 2. Both animals died of plague, No. 1 on the fifth, No. 2 on the fourth day. A further experiment was the following : — A rat which had been protected by a first injection of 10 cc. of Haffkine's prophylactic was a week later injected with an ordinarily fatal dose of living plague culture. viir AGGLUTINATION OF B. PESTIS 241 The animal developed a bubo that suppurated and which in the course of two weeks had completely healed up. This rat was killed about five weeks after the first in- jection, about two to three weeks after the last, and its blood serum tested in corpore both on a guinea-pig and on a rat. In each case 250 cubic millimetres of living plague emulsion were mixed with 250 cubic millimetres of blood serum. Both animals died of plague, as did the control in each instance. It follows from these experiments that no conspicuous amount of germicidal substance' is produced in the blood of the rat when it has been efficiently protected, whether by Hafi'kine's prophylactic alone or by passing in addition through a mild form of the plague. Plague therefore difi"ers from some other infective diseases (cholera, diphtheria, etc.) in the circumstance that a previous immunisation of an animal against plague does not necessarily create in the blood of this animal an appreciable amount of germicidal substance which may be in turn used for conferring either passive immunity on a fresh animal or for neutralising a fatal dose of living plague culture. It is necessary, however, to remember that in all these experiments only relatively small amounts of blood serum was used, and it is quite possible that if huge doses of the serum, say several cubic centimetres, had been injected, the result might have been different. But for our purposes, viz. to see whether appreci- able amounts of germicidal (specific) substances were present in the blood, large doses of the serum were not to be recommended. Recent research has shown that large doses of blood serum of even normal blood contain substances which act deleteriously on microbes. The above negative 242 ORIENTAL PLAGUE chap. results do not touch the question of specific antitoxins, these being different from lysins or germicidal substances ; it is quite possible that such specific antitoxins may have been present in the blood of the prepared animals, anti- toxins, that is, which could be utilised for therapeutic purposes, such as recommended by Yersin, Calmette, and others. After collecting evidence on the subject, the Indian Plague Commission have expressed the view (Report, vol. V.) that the agglutination test for purposes of diagnosis is not of sufficiently reliable kind, and a similar view has been expressed by Dr. Simpson in his Treatise on Plague. Nevertheless, I am inchned to think, from the large number of observations which I have made, that under certain conditions of experimentation the agglutination test is of value, and a similar view has also been published in Dr. Chalmers' Report on Plague in Glasgow, in 1900. Recently Captain Holmes of the Indian Veterinary Service has made a number of experiments in my laboratory in the same direction. Guinea-pigs and rats, which had been previously protected by injection of my new organ prophylactic, were tested with virulent culture of B. pestis. They had been found immune against plague, and several weeks later their blood was subjected to the agglutination test on culture of B. pestis. The proportion of blood serum and emulsion of B. pestis was 1 : 1 and 1 : 2. "Whereas the blood serum of normal guinea-pigs and normal rats gave invariably a negative result, the blood serum of both the guinea-pigs and the rats which had survived the plague test gave striking and unmistakable positive results. Although the dilution vni AGGLUTINATION OF B. PESTIS 243 used was not great, yet a comparison witli normal blood proved conclusively that the test with plague blood is distinctly of value. I have recently had occasion to test the blood serum of two monkeys which had been previously protected by injection of my organ prophylactic (see later), and had then been tested for immunity by subcutaneous injection of virulent B. pestis. Fourteen days after the sub- cutaneous injection of a multiple fatal dose of virulent B. pestis into the previously protected monkeys, and which injection caused no abnormal symptom of any kind, the blood of these monkeys was tested on salt emulsion of B. pestis. To three drops of the emulsion a small loop of the blood serum of monkey 1 was added, the proportion of serum to emulsion was about 1 : 20. After twenty minutes there were distinct signs of agglutination ; after thirty minutes agglutination was striking and complete, all the bacilli of the emulsion having become massed together into smaller and larger clumps. The blood serum of monkey 2 used in the same way acted also distinctly but not quite so markedly as that of monkey 1, since here, even after one hour, agglutination was not complete, although numerous smaller and larger clumps could be met with. CHAPTER IX PROTECTIVE INOCULATION AGAINST PLAGUE^ Since the appearance of epidemic plague at Bombay in 1896 Dr. Haffkine has employed on a considerable scale as a protective inoculation the sterilised broth culture of virulent plague bacilli, which is now known as HafFkine's plague prophylactic fluid. From time to time since 1898 Eeports have been published from the Bombay Laboratory and from different localities in India giving an account and statistical tables of the results of the prophylactic injection of the fluid by Haffkine, his assistants, and different medical ofiicers. From these Reports it appears that as to the real prophylactic value of these injections there can be no manner of doubt. The Indian Plague Commission (Report, vol. v.) critically sifted the evidence brought before them by Haffkine and by many other medical ofl&cers, and although some of the statistics produced were not admitted by them to be satisfactorily collected and did not conclusively prove in the particular instances the value claimed for the injections, there nevertheless were available statistics from a number of places, such as jails and hospitals, which in the opinion of the Commissioners fully established ' Report of the Medical Officer of the Local Government Board for 1901-1902, p. 357 and passim. 244 CHAP. IX PEOTECTIVE. INOCULATION 245 the value of a prophylactic injection of the HafFkine fluid. Simpson (ia the Practitioner for December 1905) says : " The Indian Plague Commission, while accepting the facts which proved the general protective effect of the prophylactic, were indisposed to follow HafFkine in his conclusion as to protection in the incubation stage. They recorded their opinion that, ' in view of the short incuba- tion period of plague, and in view of the fact that our experience in the case of other diseases, both in animals and man, indicates that protection is not at all rapidly established, it seems to us unlikely that the anti-plague inoculation can exert any favourable influence on persons who are already incubating plague.' ^ Further facts laid before them appear, however, to have somewhat modified their view, for in the conclusion to their Report they state that ' inoculation does not appear to confer any great degree of protection within the first days after the inoculation has been performed.' ^ " Calmette and the Oporto International Commission went still further, for they demonstrated, by actual experiment on mice, that Hafi"kine's prophylactic rendered these animals immune only after an elapse of eight to ten days, and that the prophylactic, given simultaneously with a small and feeble dose of the plague virus, increased the virulence of the disease, rendering death certain even in cases in which there might otherwise be a percentage of recoveries. " Calmette and Salimbeni, in their Eeport, conclude that ' it is certain that after injection of the prophylactic, ' Report of the Indian Plague Commission, vol. v. p. 252. 2 Ibid. p. 262. 246 ORIENTAL PLAGUE chap. and until the immunity it confers is established — that is to say, during eight to ten days after the vaccinal injection (as always exists after active immunisation by living microbes or by their toxins) — the organism is, for the time being, sensitive to an infection even very slight." ^ Experiments which I have made on rats with my organ prophylactic (see later) show, however, that these animals do not show any increased susceptibility to plague when injected with my organ prophylactic, even when the testing with B. pestis is made as early as two to four days after the injection of the prophylactic. Eats tested six days after the injection of the prophylactic were fully protected against an otherwise fatal dose of B. pestis inoculated cutaneously. Haflfkine himself admitted that owing to the stress of circumstances (the demand for the fluid in India alone was, owing to the spread of the plague, enormous) a great many points concerning the precise nature and the best method of employment of the fluid remained still un- solved. For instance, the Plague Commissioners justly point out that, from the evidence brought before them, there does not seem to be any advantage in reinjection of the same individual, provided the dose in the first instance has produced the anticipated physiological action. Further, as the Commissioners justly observe, there is as yet a great deal of uncertainty as to the dosage for each injection. Haffkine states, provisionally, that the dose for a human being should be such as to cause, a few hours after subcutaneous injection, a rise of temperature of at least 2-3 degrees Fahrenheit. But the determination of the dose on these lines would on a priori grounds ^ Annales de Vlnstiiut Pasteur, No. 12, 1899. IX PROTECTIVE INOCULATION 247 meet with great difficulties, because it can hardly be supposed that all human beings injected with the same amount would react in the same manner. Another method — also provisional — adopted by Haffkine in judging the dose of the prophylactic is the amount of solid matter (bacterial growth) present in the culture. But this method is evidently beset with quite as great difficulties, for, even assuming that simple inspection could approximately determine the relative amount of growth in different brews, there must, owing to the bacterial growth being largely in the form of granules and flocculi, be great uncertainty in any attempt to distribute this solid matter in a uniform manner during the customary decantation of the fluid into the several small bottles or tubes ready for use. Of not less importance, and of equal uncertainty, is the action of the different constituents of the prophylactic, e.g. the bacterial bodies, and the fluid in which they are suspended. The Plague Commissioners, for instance, cannot satisfy themselves as to the presence in the fluid, per se, of any toxin or of any bacterial products necessary for the object of prophylaxis. A further point which unquestionably must be assumed to be of importance is the quality of the strain of the plague bacilli used in establishing a culture. On grounds of analogy — e.g. vibrio cholerse, bac. of typhoid — ^it is to be anticipated that the initial virulence of the microbe determines, cceteris paribus, the degree of protective potency of the ensuing culture. And as a last point worthy of consideration, there is the question of the nature of the change in the blood and tissues of a human being or of an animal injected with the prophylactic — 248 ORIENTAL PLAGUE chap. that is to say, the question of the degree of immunity conferred by inoculation against infection, and to what extent are agglutinating, antitoxic, and germicidal substances to be met with in the blood of the injected animal. All the points above enumerated require to be elucidated before claim can be made to a fair under- standing of the action of the prophylactic — ^before, that is, a rule-of-thumb practice can be superseded by a scientific- ally proved method of standardising and of using the prophylactic. I now proceed to describe the experiments and observations which have been undertaken towards the elucidation of some of these matters. The Preparation of Haffkine Plague Prophylactic. — The fluid which Haffkine {Proceedings, Royal Society, June 1900) prepares for distribution and transmission is a broth culture of B. pestis incubated for four to six weeks, and then sterilised at 65-70° C. for one hour. It is next decanted into and preserved in special bottles, each containing about 0"5 percent carbolic acid.-' The prophy- lactic employed in the experiments to be recorded was in most respects prepared like Haffkine's broth culture, with addition, that is, of a few drops of sterile clarified butter. It was decanted into test tubes, each capable of containing 32-36 cc, which were then sealed and finally sterilised at 70° C. for one hour. No preservative, however, was added. Haffkine has pointed out that different brews of the prophylactic started from the same plague culture — 1 At present (1906) the prophylactic is preserved iu Bombay without the addition of preserrative. IX PKOTECTIVE INOCULATION 249 notwitlistanding tliat tlie broth itself, the addition of clarified butter, the temperature, and all other conditions are as far as possible the same — show after a like period of incubation different amounts of bacterial growth in the form of floccular and granular sediment. My experience fully bears this out. Thus of a group of flasks (8-12) treated seemingly, and indeed intentionally, in exactly the same manner — i.e. same make of peptone broth, same amount of ghee added, same stock culture of plague used for infection, same platinum needle used in this process, same temperature of incubation, same duration of incuba- tion — not all show the same amount of sediment of solid growth. While some flasks of this brew contain a comparatively large amount of the floccular and granular sediment, others show this to a conspicuously less degree. I have found that, ccBteris paribus, the incubation of the flasks at 25° C. for the last fortnight or three weeks of preparation — the first fortnight having been passed by the flasks in an incubator at 37° C. — yields the greatest amount of sediment, certainly greater than if the flasks are kept for the whole five weeks at 37° C. Another point in which I fully confirm Haffkine's statement, and one which I think of importance, is this : The presence of a thin layer of droplets of ghee on the surface of the broth is an excellent and sure means of increasiug the amount of bacterial growth. This is particularly well shown after the inoculated flasks are transferred to a temperature of 25° C. The ghee drops at this temperature become solid flat platelets ; and in connection with them, and extending underneath them rapidly, the growth appears in the form of a whitish scum (with stalactites), which, on shaking, becomes 250 ORIENTAL PLAGUE chap. readily detached and falls to the bottom of the fluid, only to be in the course of a few days replaced by a similar fresh scum. In this way, viz. by keeping the flasks for the last two to three weeks at the temperature of 25° C. and shaking the flasks every three or four days, the greatest amount of sediment (granules and flocculi of growth) will be obtained. It is a fact, although it does not well agree with a general assumption, that not even after four weeks is the growth finished, i.e. is the nutritive material in broth exhausted. This may appear strange, since in the case of a rapidly growing microbe like the \B. pestis one would a priori expect that at a temperature of 37° C. the growth would have been completed and the broth "exhausted" in the space of ten days or a fortnight. But this is manifestly not the case ; after a fortnight's incubation at 37° C. the flasks, on transference to a temperature of 25° C, exhibit a conspicuous further growth, which continues even to the end of six weeks. In regard of all flasks so treated, subcultures were made on gelatine and agar with a platinum loop, a single loopful being transferred from the flask to the new culture medium. In every instance great numbers of colonies developed, particularly in the gelatine tubes. This proves that the bacilli in the flasks were still living and active ; that they had not, as was to be anticipated, died off in the course of a few weeks in large numbers. I think, with HafiTiine, that the addition of the clarified butter is the important means by which the bacillary growth is maintained and its amount increased. In the course of the last two years I have sealed and sterilised nearly 12,000 tubes (each containing IX PROTECTIVE INOCULATION 251 32 to 36 cc.) without a single failure. All of them showed, when kept in an upright position, a perfectly clear fluid with the granular and floccular sediment. Accidental and extraneous contamination did not occur. Constitutional Changes in Animals injected with Plague Pkophylactic In order to supply means of comparing the effects of injections of the plague prophylactic, I submit here a tabular account of the changes of the temperature and of body weight of rabbits sub- mitted to injection of, at first sterile, afterwards living (solid) culture of B. pestis. Babbit No. 1 First subcutaneous injection, May 6, with sterile culture : — Tempera- ture, 12 noon. Body Weight. Tempera- ture, 12 noon. Body Weight. Before injection •F. 102-6 Grammes. 1155 May 16 . 'P. 103-4 Grammes. 1160 May 7 . . Anim May 8 . Animal appears a 105-3 al off its feed. 104-4 1 right and fe 1105 1090 eds again. „ 17 . „ 18 . „ 20 . . 102-8 102-7 103 1122 1148 1097 May 9 104 1115 „ 21 . . 103-1 1074 „ 10 . 102-6 1087 „ 22 . . 102-5 1090 „ 11 104-8 1068 „ 23 . . 103-3 1090 „ 13 . 103 1065 „ 24 . . 103 1103 „ 14 . 103-2 1089 „ 25 . 103-2 1128 „ 15 . 102-4 1115 252 ORIENTAL PLAGUE chap. Second intravenous injection with sterilised culture on May 28:— Tempera- ture, 12 noon. Body Weight. Tempera- ture, 12 noon. Body Weight. Before injection May 29 „ 30 „ 31 June 1 „ 3 „ 4 „ 5 "P. 103-2 103-8 104-4 103-3 103-3 102-4 103 103 Grammes. 1102 1129 1108 1126 1144 1146 1180 1221 June 6 7 10 11 12 13 "F. 103-6 103-6 103-4 103-2 103-8 103 103-3 Grammes. 1257 1315 1302 1281 1283 1266 1313 Third injection of the rabbit per ear vein with sterilised culture : — Tempera- ture, 12 noon. Body Weight. Tempera- ture, 12 noon. Body Weight. °P. Grammes. "F. Grammes. June 14 . 103-7 1284 June 22 . 103-5 1319 „ 15 . 104-4 1303 „ 24 . 102 1319 „ 17 . 102-6 1269 „ 25 . . 102-8 1312 „ 18 . 102-6 1242 „ 26 . . 103 1335 „ 19 . 101-6 1277 „ 20 . 102-5 1343 July 9 . 103 1280 ,, 21 . 102-4 1281 IX PROTECTIVE INOCULATION 253 Fourth intravenous injection with small dose of emulsion of living culture : — Tempera- ture, 12 noon. Body Weight. Tempera- ture, 12 uoon. Body Weiglit. July 10 . „ 11 „ 12 . „ 13 „ 15 . "F. 102-6 105-1 106-1 106-4 106-8 Grammes. 1310 1355 1352 1324 1345 July 16 . „ 17 . . „ 18 . . „ 19 . . „ 20 . . °F. 106-5 104 105 103-6 103-4 Grammes. 1353 1278 1286 1245 1177 RabUt No. 2 First intravenous injection with sterilised culture on May 6 :- Tempera- ture, 12 noon. Body Weight. Tempera- ture, 12 noon. Body Weight. °F. Grammes. •P. Grammes. Before injection 102-5 1106 May 17 102-7 1061 May 7 . 104 1069 „ 18 . 102-8 1088 „ 8 . 104 1015 „ 20 103 1097 „ 9 . 104 1062 „ 21 . 102-8 1071 „ 10 . 103-7 1046 „ 22 . 102-8 1102 „ 11 . 105 1039 „ 23 102-7 1113 „ 13 . 103-7 1031 „ 24 . 103 1109 „ 14 . 103 1062 „ 25 102-7 1128 „ 15 . 103 1095 „ 28 102-8 1093 „ 16 . 103-4 1124 254 OEIENTAL PLAGUE chap. Second intravenous injection with sterilised culture : — Tempera- ture, 12 noon. Body Weight. Tempera- ture, 12 noon. Body Weight. May 29 . „ 80 . . „ 31 . . June 1 „ 3 . . „ 4 ■ . „ 5 'P. 103-8 103-8 103-1 103-4 103 103-4 103 Grammea. 1098 1080 1102 1121 1132 1154 1179 June 6 . „ 7 . „ 8 „ 10 . „ 11 . ,, 12 . „ 13 . •F. 103-2 104 103 102-6 103-6 102-8 103-2 Grammes. 1208 1266 1288 1250 1236 1236 1279 Third intravenous injection with sterilised culture : — Tempera- ture, 12 noon. Body Weight. Tempera- ture, 12 noon. Body Weight. June 14 . „ 15 „ 17 „ 18 „ 19 •F. 103-6 103-4 103 102-4 102-4 Grammes. 1256 1287 1261 1243 1275 June 20 „ 21 „ 22 „ 24 . „ 26 "F. 102-4 102-4 103-4 103-2 103 Grammes. 1322 1283 1310 1349 1409 From these records it appears that — (1) No definite conclusion can be drawn from the alteration of body weight as to whether or not the injection of sterile or even of living culture exerts any influence on the animal's metabolism. (2) The injection of sterile culture appears to cause a distinct and immediate (in twenty-four hours) rise of the body temperature, which lasts a few days. The second injection of the same culture causes a renewed rise of temperature, but this sets in not twenty-four but forty-eight hours after the injection, and is of shorter duration than that following the first injection. From the experiment on rabbit No. 1 it is further seen that intravenous injection of living IX PROTECTIVE INOCULATION 255 culture following on a third intravenous injection of sterile culture causes, on the second day, a very considerable rise of the body temperature, lasting for more than a week. It is curious, however, to find that the animal did not lose in weight till the temperature again commenced to fall. But, as mentioned above, the body weight is of very uncertain value. It has to be added in this connection that the animals were always kept as to food and all other conditions under precisely the same favourable conditions. Babbit No. 3 First subcutaneous injection with 10 cc. Hafikine prophylactic on June 17 :— Tempera- ture, 12 noon. Body Weight. Tempera- ture, 12 noon. Body Weight. •F. Grammes. 'F. Grammes. Before injection 102-3 1176 June 24 . 102-6 1161 June 18 . 105 '5 1129 „ 25 . 102-2 1167 „ 19 . 105-4 1262 „ 26 . 102-6 1185 „ 20 . 103-7 1138 „ 27 . . 102-1 1193 „ 21 . . 101-7 1110 „ 28 102 1186 „ 22 . . 102-5 1150 ,, 29 . 101-4 1138 As has been recorded in connection with various experiments here reported on, this animal was injected and reinjected sub- cutaneously a second, third, fourth, fifth, and sixth time, on each occasion with 1 cc, and a seventh and eighth time, on each occasion with 20 cc. of Haffkine's prophylactic. But there was no corre- sponding alteration observed in the body temperature. The body weight, however, was constantly varying upwards and downwards in an erratic fashion. It is, however, seen that the first injection caused a sudden and considerable rise of temperature, lasting for two or three days — that is to say, a change of the same kind as was noted in the case of rabbit No. 1 after the first intravenous injection of that animal with sterilised bacteria taken from solid medium. Subcutaneous injection, therefore, into a rabbit of under 1200 grammes 256 OEIENTAL PLAGUE CHAP. weight of 10 cc. of the plague prophylactic caused the same decisive constitutional disturbance, as manifested by a rise of body tempera- ture of over 3°r., as did intravenous injection of a mass of bacilli amounting to three-fourths of the growth uniformly covering the slanting surface (6 centimetres by 2 centimetres) of an agar culture. It is important to bear this in mind, since the fact will again be referred to when comparison is made of the relative merits of injection of sterilised (solid) culture and of Haffkine's (broth) prophylactic. In order to show that this constitutional disturbance, qua body temperature, is real, I mention here an experiment made on a companion rabbit, No. 4, which animal unfortunately succumbed immediately after the second injection, and on post-mortem examination was found to be affected with extensive psorospermosis. Babbit No. 4 First subcutaneous injection of 10 cc. plague prophylactic on June 17 : — Tempera- ture, 12 noon. Body Weiglit. Tempera- ture, 12 noon. Body Weight. Before injection June 18 . „ 19 „ 20 . „ 21 „ 22 . "F. 102-6 105-5 105-7 103-2 102-6 103 Grammes. 1367 1315 1333 1331 1292 1340 June 24 . „ 25 . . „ 26 . „ 27 . . „ 28 . „ 29 'V. 103-6 103-2 103 102-6 102-4 102-2 Grammes. 1365 1360 1364 1350 1321 1255 There is here decided rise of temperature (3° F.) the day after the injection, and this was maintained on the day following. Also there is observed a curious initial fall of body weight, with rise again as the temperature decreased after an initial rise. IX PROTECTIVE INOCULATION 257 Babbits Nos. 5 and 6. Both these animals were for the first time injected on July 1 with 5 cc. of Haflfkine's prophylactic :- — Temperature, 12 noon. Body Weight. No. 6. No. 6. No. 5. No. 6. Before injection •P. 102-1 "F. 102-4 Grammes. 1396 Grammes. 1605 July 2 103-9 104-8 1336 1514 „ 3 103-6 104-2 1325 1543 „ 4 . . . 103-8 103 1321 1526 „ 5 . . 103-2 103 1320 1590 „ 6 . . . 104 104-6 1363 1565 „ 8 . 102-6 102-8 1300 1506 „ 9 • 103-1 103 1288 1493 „ 10 . . . 102-6 102-4 1282 1490 „ 11 . . . 102-1 102-4 1275 1489 „ 12 . . . 103 103-1 1270 1497 „ 13 . . . 103 103-4 1233 1486 „ 15 ... 102-8 102-7 1253 1515 „ 16 102-5 102-4 1224 1504 „ 17 ... 102 103-3 1110 1480 „ 18 . . 102 103-6 1121 1483 „ 19 ... 103-2 103-8 1163 1432 From this it appears that intravenous injection of the prophy- lactic was followed by a little less decisive rise of temperature than was subcutaneous injection in the former cases. The body weight fluctuated considerably — fluctuation which was on the whole fairly parallel for the two animals ; that is to say, when it rose in one it rose also in the other rabbit, and vice versa. S 258 OEIENTAL PLAGUE CHAP. Babbits Nos. 7 and 8. These two animals, as mentioned on p. 227, were injected sub- cutaneously with 20 cc. of the filtrate of Haffkine's prophylactic on three separate occasions. First subcutaneous injection of 20 cc. of the filtrate on Septem- ber 10 :— Temperature, 12 noon. Body Weight. No. 7. No. 8. No. 7. No. 8. Before injection . •F. 103 •P. 103-4 Grammes. 1645 Grammes. 2120 September 11 104 103-7 1638 2155 12 . . . 103-2 102-4 1651 2169 „ 13 . . . 103 102-6 1688 2196 14 . . . 102-8 102-1 1697 2207 „ 16 . . 102-4 102-4 1640 2170 17 . . . 102-5 102-2 1604 2110 Second injection with 20 cc. of the filtrate .- — Temperature) 12 noon. Body Weight. No. 7. No. 8. No. 7. No. 8. September 18 . . . 19 „ 20 . . . 21 . . . 23 > . . •F. 104 103-2 103 102-6 102-4 • F. 103 102-3 102-1 102-4 102 Grammes. 1670 1626 1671 1653 1614 Grammes. 2169 2123 2138 2128 2072 It appears from this series that the first injection of 20 cc. of the filtrate did not cause any but an insignificant rise of the body temperature (1° F. in rabbit No. 7, 0-3° F. in rabbit No. 8), a rise so small as to be well within the limits of natural fluctuation. The second injection of 20 cc. of the filtrate appears to have been IX PROTECTIVE INOCULATION 259 a little more active in temporarily raising the body temperature (1-5° F. in rabbit No. 7, 0-8° F. in rabbit No. 8); but here also the rise is not sufficiently striking to warrant assumption of any specific action. It is possible that the effect of injecting sub- cutaneously 20 cc. of any fluid containing in solution chemical substances of various composition, such as naturally result from the long-continued (four to six weeks) growth of bacteria in broth, would be similar as regards temperature. However this may be, it is certain that the blood of these animals did not contain agglutinating substances even after the fourth injection of 20 cc. of the filtrate. Observations as to Protection against Plague Infection conferred on Animals by previous Injection of Haffkine Plague Prophylactic. A. — Guinea-pigs. From the experiments recorded in Chapter VIII. it will have been obvious that repeated injection of the dead [i.e. sterilised) bacilli taken from the surface of solid media confers on the guinea-pigs and rabbits a certain degree of immunity. The subsequent injection of living culture of B.pestis did not cause a fatal issue. But as in 1896-1897, so also now, the immunity thus conferred on the guinea- pig, viz. by this injection of sterilised bacilli, was not of a high order, since on each subsequent subcutaneous injection of living culture the animals reacted, as shown by the development of a bubo on the inoculated side, which bubo soon, however, suppurated and healed up. I have at present in the laboratory a guinea-pig which exactly a year ago, May 6, was injected the first time with the growth scraped from the whole surface (6 centimetres by 2 centimetres) of a gelatine culture of -B. pestis. The growth was sterilised as a salt emulsion 260 ORIENTAL PLAGUE chap. and then injected intraperitoneally ; and injection in this way was repeated in the same amount on May 22 and on June 5. The animal was then injected intra- peritoneally with small doses of living culture on eight separate occasions. Finally, on December 28, it Was injected subcutaneously with an ordinary lethal dose of living culture. The animal remaiued alive, but it developed a fair bubo, which suppurated and healed up in about a fortnight. On May 15, 1901 — a year, that is, after the first injection — it was injected, for the thirteenth time, sub- cutaneously with an ordinary lethal dose of plague material. The animal remained alive and fairly lively, and it fed well, but it again developed a bubo in the inguinal region which extended on to the thigh and became nearly as big as a pigeon's egg. This bubo suppurated by the end of a week, and had not quite healed by the end of a fortnight. This is by no means an isolated instance as regards the guinea-pig. I have had several such cases in 1896-1897 (see my Eeport to the Local Government Board), and I have quite a number of similar in- stances in the present investigation. All show that a high degree of immunity in the guinea-pig does not exist even after a good many previous injections of sterihsed and also living plague bacilli. The animals acquire no doubt a certain resistance against fatal in- fection, but this resistance does not prevent the develop- ment of a well-marked bubo with living bacilli in the early stages. In view of this experience, it was not to be expected that the injection of the Haffkine prophylactic could IX PROTECTIVE mOCULATION 261 produce results more favourable tlian the repeated in- jection of living plague bacilli. In 1899 - 1900, with. Professor Haflfkine, at the instance of the Local Govern- ment Board, I made a number of experiments with the Haffkine plague prophylactic. In these a series of guinea-pigs received by a single subcutaneous in- jection various amounts of the plague prophylactic — 5 cc, 10 cc, 30 cc, 40 cc, and even 60 cc. They were subsequently injected with lethal dose of living plague bacilli, as were, at the same time, a similar series of control guinea-pigs. The result was this: — Of the eight control guinea-pigs all died of plague. Of the eight prepared guinea-pigs seven died of plague ; in the eighth animal the bubo suppurated and ultimately healed. During later experiments several guinea-pigs were, as mentioned in a previous chapter, repeatedly (as often as eight times) injected (subcutaneously and intraperi- toneally) with Haffkine prophylactic, and afterwards with living culture. They developed typical bubo. I have at present a guinea-pig which had been injected eight times intraperitoneally with Haffkine prophylactic between June 17 and October 21, receiving altogether 51 cc. of the fluid. On December 28 it was injected subcutane- ously with small dose of living culture of B. pestis. It developed typical bubo. On May 5 of this year it was again injected with an ordinary lethal dose. It remained alive, but by the end of the week it had a bubo of the size of a pigeon's egg. The same negative results were obtained by injecting guinea-pigs with the clear filtrate of Haffkine's prophy- lactic ; and it is not necessary to detail them beyond noting that neither the subcutaneous nor the intraperi- 262 ORIENTAL PLAGUE chap. toneal injection of 10 cc. in each instance of this clear filtrate on three separate occasions (within six weeks) had any influence in inhibiting the ordinary results of subsequent injection of small and large doses of liviog B. pestis. B. — Rabbits. The experiments made in conjunction with Professor Hafi'kine on rabbits, although numerous, were on the whole of an unsatisfactory nature, mainly because of the difficulty and uncertainty in ascertaining what is a normal fatal dose of plague culture for the rabbit. A large series of rabbits were carefully noted as to body temperature and body weight, before and after injection, with varying amounts of the prophylactic (10 cc. to 34 cc). Control rabbits, equally carefully noted as to body weight, were kept separate, but corresponded as nearly as possible in body weight to the prepared rabbits. In due time each animal in both sets was injected with what ought to have been a fatal dose of living plague culture. The result was disappointing, because an equal proportion of prepared rabbits and control rabbits succumbed to plague.'' The percentage of deaths in each class of rabbit was, however; less than 50, whereas in the case of both guinea-pigs and rats (used as controls) a fatal issue can always be ensured. The experiments which I have made in the course of the present year on rabbits with sterilised solid plague culture, with Haffkine prophylactic, and with the filtrate of the prophylactic, were of an equally unsatisfactory nature, and for the same reason, viz. unless extra large ' I note with surprise the statement by Professor Balfoui' Stewart [Thompsm- Yates Laboratory, vol. ii. p. 19) that he found 2 co. of the Haffkine prophylactic sufficient to imnmniae a rabbit of 1400 grammes body weight. IX PEOTECTIVE INOCULATION 263 doses of living plague culture be injected (against wMch, of course, no prophylactic would be efficacious) the control animals did not die. A series of rabbits were prepared, some by repeated injection of sterilised solid culture, others by repeated injection of Haflfkine prophylactic, and still others by repeated injection of the filtrate of Haffkine prophylactic. At the proper phase of the experiment they, as also corresponding rabbits {i.e. corresponding in body weight), were injected with what in a preliminary experiment on a control rabbit acted as a fatal dose, i.e. half of a gelatine culture (6 centimetres by 2 centimetres surface) three days old. Unfortunately this crucial experiment failed to elucidate the point and to answer the question, viz. whether or no any, and if so which, of the prepared rabbits were protected. The control rabbits did not any of them die. I have not therefore repeated the experiments, because I think it proved that, owing to its varying and unstable susceptibility, the rabbit is not a suitable animal for this kind of experiment. C. — Bats. 1. Actionofthe complete Haffkine Plague Prophylactic. — ^Fortunately in the rat we possess a test animal which, in my experience, is thoroughly reliable. I have in the course of preparing the large amounts of the Haffkine plague prophylactic (about 60,000 doses) invariably used rats for testing this prophylactic, and my test has always been carried out in the following manner : — With each particular brew (comprisiag 6 to 12 flasks of the same broth, inoculated at the same time under the same con- 264 ORIENTAL PLAGUE chap. ditions, decanted, sealed, and sterilised at the same time) I have generally inoculated four rats, each being made to receive subcutaneously 10 cc. of the finished product. Except in the earliest experiments, white rats, half to full grown, have been employed, as I find these highly susceptible to plague, much easier to handle, and less liable to accidental and spontaneous death than the brown (wild) sewer or house rat. Eight to ten days (on occasion twelve days) after this injection with the prophylactic the prepared rats, together with two fresh or unprepared rats, are injected with living plague culture, in amount sufficient to cause death from typical plague in both controls, while permitting the prepared rats to remain (if protected) alive. As a result of my experience in the above sense of a considerable number of brews of the prophylactic on a considerable number of rats, I am prepared emphatically to maintain that 10 cc. of the Hafi'kine prophylactic is capable of fully protecting a rat (half-grown to adult) against a subsequent injection of a dose of living plague culture that acts lethally without fail on control rats. And a similar experience was obtained in association with M. Hafi'kine, when he and I tested on rats the prophylactic brought by him from Bombay, viz. those which received an injection of 10 cc. of the prophylactic withstood sub- sequent infection with living culture of B. pestis. It is not necessary to detail all the above experiments that were made on the rats with the prophylactic prepared by me here in London. I have already given their general purport, and I therefore proceed to describe the equally satisfactory results which I obtained with the sterilised bacillary bodies from the prophylactic, as also the results IX PROTECTIVE INOCULATION 265 of certain experiments with the clear filtrate after removal of the bacilli. 2. Action of Sterilised Bacillary Bodies. — The bodies of the sterilised bacilli were employed in the form in which they occur in the Haffkine prophylactic. The manner of obtaining them was very simple. As was mentioned on a former page of this chapter, the prophylactic was preserved by me in sealed tubes without the addition of any preservative, each tube containing 30, 32, and 36 cc. When left standing upright all the bacillary bodies settle at the bottom of the tube, whereas the fluid above becomes and remains quite limpid. From such a tube — after opening it by breaking the sealed end — the fluid is siphoned ofi", a process very easily achieved. The remaining sediment is then distributed in salt solution in amount equal to the quantity of broth siphoned off'. Of this emulsion 10 cc. are used subcutaneously per rat. As a matter of fact, the 30 to 36 cc. of the fluid in a given tube, salt solution plus bacillary sediment, were used for three rats. The result was complete protection in each instance by this preliminary injection against the subsequent injection of Uving culture. I have made two series of such experi- ments, each comprising three prepared rats and one control, and in both series the result was positive, viz. death of the control rat and survival of the prepared animals. 3. Action of the Filtrate per se of Haffkine's Pro- phylactic. — From what has just now been stated, viz. that practically the bacillary sediment and the complete Haffkine prophylactic are equally protective, it was to be inferred that the fluid itself — i.e. the broth in which the bacilli had been growing, but minus the bacilli — is of no 266 ORIENTAL PLAGUE chap. use in assisting or in sharing in the protective action of the Haffkine prophylactic. As a matter of fact, the Indian Plague Commission deny (vol. v.) any action, toxic or otherwise, of this fluid per se, and as far as can be gathered from the questions put by some of the members of the Commission to Professor Haffkine during his examination before the Commission in Bombay, it seems as if Professor Haffkine had been reproached for having used broth culture (of course, sterilised) as plague prophylactic, seeing that his cholera prophylactic was an emulsion made from the growth of the cholera vibrio on solid media. And, further, Calmette, in his Harben Lectures (1900), assumes that all the prophylactic action of a sterilised culture is and must necessarily be lodged in the bacillary bodies themselves. Moreover, Professor Haffkine himself has repeatedly pointed out (see his evidence before the Plague Commission) the importance of copious bacillary growth in his broth culture ; as a matter of fact, the prophylactic dose recommended per human individual has in practice been estimated according to the amount of bacillary growth in the flask, the amount of the dose being in inverse ratio to the turbidity, i.e. amount of bacillary growth. While all these are facts of common knowledge, I venture seriously to doubt the assumed inefl&cacy and superfluity of the fluid part of the prophylactic. And my doubts are based on good experimental grounds as follows : — (a) Four half-grown rats were injected with filtrate of the prophylactic, i.e. with the clear fluid siphoned off from a tube (see above) and passed through a Pasteur- Chamberland filter. Each rat received subcutaneously IX PEOTBCTIVE INOCULATION 267 10 cc. of this filtrate on two separate occasions, November 21 and December 31. On February 6, i.e. thirty-seven days later, they were injected with a dose each of living culture which killed a control rat on the fourth day. Of the four prepared rats, two died of plague on the fifth day, the nature of this fatal malady being confirmed on microscopic, macroscopic, and cultural evidence. The two others survived. (b) Four half-grown rats received each 10 cc. of this filtrate on March 11, and again 10 cc. on March 18. On May 5 they were injected with living plague culture at the same time that a control rat received an equal dose of this infection. The result was instructive. The con- trol rat died of typical plague on the third day ; one of the prepared rats died of plague on the fourth day ; another of the prepared rats died of plague on the sixth day ; a third of these prepared rats died of plague on the twelfth day. But the fourth survived. From these experiments I think it is justifiable to conclude that, although the efi'ect of the filtrate (20 cc. per animal) was small, it was nevertheless of a positive nature, since the prepared animals behaved somewhat difierently from the control rats. Some of the former were found distinctly protected, while those not protected died always later than the control rats. The^ principle underlying the preparation of plague prophylactics such as have hitherto been employed has its basis in the well-known fact that immunity of an animal to plague may be induced by injecting into it a certain ^ Preliminary Report to the Local Government Board on a New Plague Prophy- lactic, December 19, 1906. 268 ORIENTAL PLAGUE chap. dose of culture of dead plague bacilli or their extracts. Thus Haffkine uses a broth culture containing a large amount of bacillary growth, which culture has previously been subjected to heat (70° C.) suflficient to kill the bacilh. As Haffkine has shown, and as is generally the practice wherever this prophylactic is used, the amount of bacillary growth determines in a somewhat rough-and-ready manner the efficacy and therefore the dosage of the prophylactic. With Calmette, as also at the Pasteur Institute, the prophylactic is a sterilised emulsion of the bacillary growth taken from the surface of solid agar cultures. The German Plague Commission also recommended an emulsion of agar culture sterilised at 65° C. On the other hand, Lustig uses in preparation of his prophylactic, or rather his curative serum, the precipitate obtained from an alkaline emulsion of an agar culture of B. pestis. Similar processes are employed by others in preparation of their plague prophylactic. According to numerous results hitherto published in India, South Africa, and elsewhere, the first two prophylactics, viz. Haffkine's and prophylactic prepared in the manner adopted by Calmette and the Pasteur Institute, are those which are most reliable. Such disadvantages as are attached to them are the disadvantages generally inherent to all fluids prepared from artificial cultures, viz. the difficulty of preservation, and, above all, the difficulty of securing, when large amounts of material are prepared at one time, uniformity of strength, i.e. efficacy for every single dose. The above disadvantages have led me to investigate the matter in a new direction — to attempt, that is, to obtain a prophylactic free from the above defects. The IX PROTECTIVE INOCULATION 269 results so far obtained by me in a large number of experi- ments carried out witb this view justify, I think, the claim I am making of having succeeded in my object. The procedure which I adopt in preparing this new prophylactic is based on the following considerations and observations : — (1) Investigating the vitality of B. pestis in certain organs (bubo, spleen, lung) of animals dead of plague — organs which had been subjected to drying on various materials (wood, cloth, Hnen) at various temperatures over sulphuric acid — I found that, after all B. pestis originally contained in such plague organs had been killed in the process of drying, emulsion made of these dried organs, and injected in definite amount into mice and rats, was capable of causing death of these rodents within twenty hours or less — the animals exhibiting phenomena not differing from those observed in acute plague, except, of course, that their tissues did not after death contain any B. pestis. Also I found, when employ- ing for injection an amount of emulsion insufficient to cause speedy death, that the animals, though made ill — exhibiting, for instance, local tumour and more or less constitutional disturbance, — commonly recovered ; and, farther, that these recovered animals when tested later on by injection with virulent B. pestis were refractory to plague infection. From this it would seem that the dried plague organs, though not containing any living B. pestis, are nevertheless imbued with a powerful plague toxin which in appropriate dosage may serve as a prophylactic. (2) I have shown in my Reports to the Local Govern- ment Board for 1901-1902 and 1902-1903 that guinea- 270 ORIENTAL PLAGUE chap. pigs inoculated cutaneously with plague material (by an abrasion or a scratch of the cutis) develop, as a general rule (unless, indeed, the infective material be of extreme virulence), plague in what I have termed the " subacute form " ; a form marked by necrotic bubo, necrotic nodules in the spleen and liver, and particularly by necrotic nodules and necrotic patches in the lungs. In these cases death occurs generally in from four to seven or nine days (rarely earlier than four or later than nine days), provided the infecting material be of a moderate degree of virulence, such, for instance, as on subcutaneous injection causes death in three to four days, without the above necrotic changes.^ Examining sections of the organs containing the necrotic nodules and necrotic patches of guinea-pigs dead of subacute plague, it is seen that while the central parts of the necrotic nodules are crowded with B. pestis, the peripheral portions (except their vessels), although quite broken down into dead debris, contain few, if any, bacilli. From this it may be inferred that, as is the case in other bacterial diseases associated with necrotic changes of the tissues, such necrosis is not caused by the mere presence of the bacilli themselves, but by the toxin produced by them. As an illustration may be mentioned the necrotic action of the diphtheria toxin on a mucous membrane. In view of the above two considerations, I determined to inject into a series of animals the dried organs (contain- ing organ-toxin and dead bacilli) of various rodents dead of plague, with the purpose of ascertaining the ability ^ As I have on a former page pointed out, there exists in respect of cutaneous inoculation a. marked difference of reaction between the guinea-pig and the rat ; in the latter animal cutaneous inoculation is the most reliable way of causing acute plague with fatal issue in two to three days. IX PROTECTIVE INOCULATION 271 of these materials to protect similar rodents against subsequent infection with virulent B. pestis. A considerable number of experiments and observations were in the first instance made by me in order to ascertain the best mode of preparing and preserving prophylactic material of this nature, as weU as to determine which portions of the body of an animal dead of plague are the most efficacious for the purpose. It is not necessary to describe in detail here all the steps adopted ; they will be fully dealt with in a forthcoming Report of the Medical Officer of the Local Government Board. Suffice it to say that they comprised experiments with — (a) Dried material of all the organs of mice, of guinea- pigs, and of rats dead of acute virulent plague ; (fe) Dried material of the bubo and spleen alone of mice, guinea-pigs, and rats dead of acute plague ; (c) Dried material of all the organs of 'guinea-pigs dead of subacute plague, i.e. of guinea-pigs in which death occurred after four or five days with necrosis of the bubo, necrotic nodules of the spleen, liver, and lungs ; and {d) Dried material of those organs alone which showed necrotic changes — that is, bubo, spleen, lungs, and liver of guinea-pigs dead of subacute plague. These several materials were dried — (e) At the temperature of the laboratory over sulphuric acid; (/) At the temperature of 20° C. over sulphuric acid ; (g) At the temperature of 37° C. over sulphuric acid ; {h) At the temperature of 46° to 47° C. over sulphuric acid. The result of these experiments showed that a variety 272 OEIENTAL PLAGUE chap. of tissues — the bubo, the enlarged spleen, and tlie aflfected lung containing abundance of necrotic masses, as also the liver when it contains abundance of necrotic nodules — of guinea-pigs dead of subacute plague (i.e. dead after five to nine days), cut out and finely minced aseptically, spread out in thin layers in sterile glass plate dishes and dried over sulphuric acid at 46° to 47° C, yield a material which not only can be very easily and rapidly prepared, but which is of a uniform and reliable efficacy, and in every way, indeed, superior to any of the other prophy- lactics. The guinea-pig, as compared with the rat, being a " clean " animal, appears greatly preferable for the above purpose. There is no difficulty in preparing and pre- serving the above necrotic organs, which yield com- paratively the greatest amount of material, in a clean manner, and the exposure to 46° C. prevents growth and multiplication in them of any stray or accidental bacteria. A guinea-pig of about 300 to 400 grammes weight will yield 5 to 7 grammes of dry powder prepared from the bubo, spleen, lungs, and liver ; and as the reliably protec- tive dose for an adult rat (see below) is 10 to 15 milli- grammes, it follows, therefore, that one large guinea-pig can yield about 400 to 600 doses. Three days' drying in thin layers over sulphuric acid at 46° C. was found more than sufficient to devitalise all B. pestis contained in these organs. After three days' drying the dry scales of material are rubbed down to a fine powder in a sterile mortar ; this powder is then transferred to a sterile wide- mouthed bottle, plugged with sterile cotton-wool, which is placed for two to three days at 37° C. in order to thoroughly complete the process of drying. At the end IX PROTECTIVE INOCULATION 273 of these three additional days the cotton-wool plug is re- placed by a glass stopper, and the prophylactic is ready for use. It can be thus preserved indefinitely in a dry state by a layer of paraffin over the stopper. Such material tested by cultivation is found sterile ; it yields no growth of any kind. In preparing the prophylactic for use the desired amount of powder is weighed out, well rubbed down in a desired amount of sterile warm distilled water, and the turbid emulsion thus obtained is injected subcutaneously. The principal consideration is, of course, the amount of dry powder ; the amount of water used per dose is immaterial. I generally use ^ cc. of water per dose, but there is no reason why ^ cc. or 1 cc. should not be used. As I have indicated, the material contains not only the acutely active toxin, but also the dead bodies of all the B. pestis originally present in large numbers in the necrotic organs (bubo, spleen, liver, and lungs), with addition probably of other substances of an undetermined nature and action. That the prophylactic efficacy of the material is not solely due to the bacillary bodies (known to possess both toxic and prophylactic action), retained after drying, can be gathered from the fact that an amount of dead bacilli from culture considerably larger than the quantity contained, say, in 10 milligrammes of dry spleen material, possesses neither the same toxic nor equal immunising efficacy as the latter. Eor instance, 5 cc. of Haffkine prophylactic strongly turbid with flakes and masses of bacilli does not confer immunity on an adult rat ; 10 cc. is the required dose. On the other hand, 10 to 15 milligrammes of the dry 274 OEIENTAL PLAGUE chap. powder above referred to does confer immunity on the adult rat. I now summarise the results obtained by using the above - described dried material in a large number of experiments, comprising several dozen white mice, five to six dozen guinea-pigs, and considerably over 150 rats, chiefly white : — (1) The above prophylactic kills a large percentage of mice within bwenty to twenty-four hours in doses of 1 to 5 milligrammes. (2) It kills a percentage (12 to 25) of half-grown white rats in doses of 5 to 8 milligrammes, if the material is derived from acute virulent cases ; but if obtained from the necrotic organs of guinea - pigs dead of subacute plague (death five to nine days) as much as 10 to 12 milligrammes are required for fatal effect. The dead animals show local swelling, with oedema and punctiform haemorrhages ; the spleen is enlarged, the lungs congested. No B. pestis are, however, to be found in their bodies anywhere. (3) Even as much as 20 milligrammes fails to kill a guiuea-pig of 200 to 300 grammes weight. (4) An adult rat (weighing 120 to 200 grammes) injected with 10 to 15 milligrammes of the prophylactic of medium virulence such as I recommend, or with two doses of 1 milligrammes each at an interval of nine to ten days, is secured complete protection against even the most virulent B. pestis. I have a considerable number of rats which, after injection with the prophylactic, were tested by cutaneous inoculation (the most successful mode of infection of the rat) with virulent B. pestis at various periods from one to thirteen weeks. These were all found fully protected, whereas the control animals inoculated IX PROTECTIVE INOCULATION 275 cutaneously at the same time and with the same material died from typical acute plague in thirty -six to seventy-two hours. (5) As is well known, guinea-pigs are less susceptible to plague than white rats, the latter being, of all the rat races which I have experimented with, the most susceptible to plague. In the case of the guinea-pig a dose of 20 milligrammes of the prophylactic now in question twice injected at intervals of ten to fourteen days does not afford protection in more than 50 per cent of the animals ; the remainder die on subsequent injection with virulent material of plague, though their death is delayed several days (death in nine to twelve days or later), and they show in the great majority of instances suppurating bubo. The disease induced in these animals differs, how- ever, from the subacute plague in an unprotected (control) guinea-pig as follows : — (a) There is but slight enlarge- ment of the spleen, with few necrotic nodules ; (b) the liver contains either no necrotic nodules, or such nodules only very sparingly ; (c) there is scarcity of B. pestis in the bubo and in the spleen — in unprotected guinea-pigs dead of subacute plague these two tissues being crowded with B. pestis ; and (d) there is much greater amount of necrosis in the lungs, the necrotic parts being packed with B. pestis. It seems, therefore, that while in the un- protected guinea-pig the bubo, spleen, and liver are more involved and richer in B. pestis than in the protected guinea-pig, the reverse is the case as regards the lungs. In the experiments which in 1899 I along with Dr. Haffkine made with his prophylactic, and in the experi- ments which I have repeatedly made since with Haffkine prophylactic as prepared by myself, it was shown that for 276 ORIENTAL PLAGUE chap. an adult rat 10 cc. are required to ensure protection ; an amount which represents, according to the statistics in India and elsewhere, at least double that required for protection of an adult human being. I assume, therefore, that 5 to 7 milligrammes of the dry prophylactic might suffice as a dose for the human subject. On this estimate a single large guinea-pig dead of subacute plague would, by means of its necrotic bubo, spleen, liver, and lungs, yield something like 800 to 1000 human doses of the new prophylactic, an amount of protective material equal to 3 to 5 litres of Haffkine's fluid. When it is borne in mind — (1) that this dried pro- phylactic does not require more than about ten to twelve days for its preparation — Haffkine's requires four to six weeks ; (2) that a large amount can be prepared of uniform strength ; (3) that its efficacy is easily standardised by injection into the rat; (4) that, being dry and sterile, it can be preserved without any antiseptic and unaltered for any length of time ; and (5) that the protection afforded by its injection into the rat is of considerable duration, certainly many weeks ; and last, but not least, that the cost of preparation is incomparably smaller, the superiority of this organ-prophylactic to Haffkine's prophylactic must be obvious. As regards size of dose, it is true that the prophylactic prepared by Calmette and the Paris Pasteur Institute, which is an emulsion of dead bacilli derived from agar surface, is capable of protecting an adult white rat in doses so small as 1 to 2 cc. But here, again, different cultures cannot be relied upon as being of equal potency, and hence no uniformity can be ensured for different sets of cultures, or, for the matter of that, for two separate IX PROTECTIVE INOCULATION 277 cultures from the same source ; whereas greater uniformity is to be anticipated from material derived from the same breed of guinea-pigs, all animals being of about the same weight and inoculated with material of like activity. There remains to be determined the interesting and important question : Whence is derived the especial efficacy of the new prophylactic, which contains, be it remembered, not only the dead bodies of plague bacilli and associated tissue-toxin, but also, in all probability, other tissue constituents ? In this connection I have made experiments which prove that the clear filtrate from a watery emulsion of the prophylactic powder possesses undoubted prophylactic efficacy. Thus, injection of an amount of clear filtrate corresponding to, i.e. obtained from, 20 to 25 milligrammes of dry powder, confers immunity on the adult rat against a subsequent cutaneous infection with virulent B. pestis. This, of course, shows that the new prophylactic does not act solely by means of the bodies of the dead bacilli which it contains. These experiments also show, as might be expected, that the whole organs prophylactic — i.e. the entire powder — is more efficacious than the watery extract, since of a definite sample of the organ prophylactic, of which 15*6 milHgrammes of the entire material is sufficient to protect a rat, 20 to 25 milligrammes are required to yield an equally efficacious watery extract. Eoughly speaking, the pro- portion between a given entire prophylactic and its watery extract (filtrate) is as 15 to 25. A further important point ascertained was this, viz. that the filtrate of a watery emulsion (filtered simply through filter-paper) can be sterilised by heating it to 70° C. for fifteen minutes, and that even twice so heated, 278 OEIENTAL PLAGUE chap, ix i.e. on successive days, it loses none of its protective eflScacy. Tested by culture this so heated filtrate is found reliably sterile. It can in this form easily be preserved in sealed tubes. A large number of rats were tested with twice-heated filtrate of organ prophylactic, and it was ascertained that, supposing the dose of the mother-substance is 12 to 16 milligrammes, the dose per rat of the filtrate would amount to about one-third more, i.e. would correspond to 20 to 25 milligrammes of the entire prophylactic. CHAPTER X MODES OF DESTRTJCTIOIT OF BACILLI PBSTIS 1. By Drying. 2. Spontaneous. 3. By Chemical Disinfection. 1. Drying. — Already in Chapters VII. and IX. we have fully described experiments by which it was shown that plague materials exposed in the laboratory to various forms of drying on diflferent materials — cloth, linen, wood, grain, in earth, and in sand — lose their infective power, i.e. their efBcacy qua B. pestis ; that is to say, the B. pestis contained in these materials become sooner or later devitalised; and there is no reason to doubt that such would be the case also under natural conditions. Experi- ments of drying thin watery or salt emulsions or broth cultures, applied as thin films on cover-glasses — a method practised by some observers in determining the death point of B. pestis by drying — are not of much practical value, since this method of drying does not occur in nature. The experiments with plague organs and gelatine cultures which I have described in Chapter VII. were fully in harmony with and in imitation of what we might suppose to occur under natural conditions. The B. pestis, being a non-sporing microbe, comports itself like other non- sporing bacteria, inasmuch as when thin films of salt or 279 280 ORIENTAL PLAGUE chap. watery emulsions of cultures, or prepared direct from broth cultures, are exposed to drying such as can be eflfected at 45° to 46° C. in less than twenty-four hours, at 37° C. in twenty - four hours, over sulphuric acid at ordinary temperature in forty-eight hours, the microbes of such films become thereby quite devitalised; for if the cover films are, after drying, placed in nutrient broth and in- cubated, no growth of B. pestis takes place. It stands to reason, and direct experiment proves it, that the period of drying of B. pestis in a viscid material — e.g. blood, spleen tissue, gelatine culture (melted in warm water) — requires to be considerably extended. Take, for instance, the B. pestis in blood or spleen tissue exposed to 46° C. even over sulphuric acid. Under these con- ditions the B. pestis cannot with certainty be considered dead after twenty-four hours. I have had cases when even after thirty-six hours not all B. pestis were dead, though three days of such drying can be fully relied on. 2. Spontaneous. — It has been pointed out in a former chapter that transferring B. pestis from one culture to another its virulence gradually diminishes ; this is a fact also observed with other microbes. As regards B. pestis we have pointed out an important difference, viz. this, that while some strains lose in artificial cultures their virulence slowly, others do so very rapidly, even with complete extinction of virulence. We have shown that in this respect the rat type plague bacillus (type 2), at starting already endowed with lesser virulence than the human type (type 1), is apt to lose its virulence in a relatively very short time, and not only to become less and less virulent, but to become ultimately a quite harmless saprophyte. Might not this find its counterpart under X MODES OF DESTEUCTION OP B. PESTIS 281 natural conditions ? That is to say, provided a certain race of B. pestis is restricted to carrying on its existence in outside nature, and is prevented from finding entrance into an animal body, in which, like other non-sporing microbes, it might be able to again regain or enhance its virulence — in other words, provided the B. pestis is doomed to live as a saprophyte, and- is prevented from resuming its parasitic existence — might this not have the result that by and by it would altogether cease to be possessed of infective power for the animal body ? The experiments which we have mentioned of type 2 certainly seem to warrant such an assumption. Assuming that this is possible in nature, we could understand how B. pestis (in a concrete plague case), when introduced into a locality in which it is not endemic, if debarred by preventive sanitary measures from gaining access to a further human being, would, owing to the saprophytic conditions to which under these restrictions it would be doomed to live, soon become deprived of all further infective power. This would particularly apply to the rat type bacillus (type 2), which, rapidly losing its virulence altogether, would equally rapidly cease to be infective. The B. pestis is not particularly selective in its nutritive materials ; it, like, for instance, the Proteus vulgaris, can grow almost in any medium containing albuminous materials ; it can grow well in neutral, in alkaline, and even in slightly acid materials — that is to say, it can maintain its existence in most localities and in most ordinary materials of filth in which Proteus, Staphylococci, B. coli, B. typhosus, and Vibrio cholerce can exist and multiply, particularly when the medium is in a solid form. There is no reason to suppose that B. 282 ORIENTAL PLAGUE chap. pestis introduced into a locality cannot and does not carry on its existence, grow, and multiply in outside nature ; but the important point is that it should be prevented from gaining access to an animal body, for if restricted to a saprophytic life it would soon cease to be dangerous. The gradually diminishing capability of the attenuated or rat type B. pestis (type 2) — although capable of con- tinuous transference from rat to rat — to infect human beings, as has been exemplified in several instances (see previous chapters), would ultimately lead to cessation of infection of the human subject. 3. Chemical Disinfectants. — In respect of the great and constantly widening subject of the various dis- infectant agents commonly employed for destroying bacteria and infective microbes, it has to be remembered that laboratory experiments in which pure cultures of one or the other microbe are exposed for a stated time to the action of a given agent are not exactly analogous to what occurs in practice when infective materials in the form of secretions, excretions, and tissues of an infected animal body are subjected to disinfection. I have shown this by direct experiments both with regard to Staphylococcus aureus and coli-typhoid bacilli. I quote in illustration a paper which I published in the British Medical Journal, July 2, 1904 :— The usual method of testing and comparing disinfectants consists in exposing for a given time cultures or emulsions of a particular microbe to dilutions of the disinfectant. This, no doubt, is of value in comparing with one another various disinfectants or their dilutions, and although it affords a sufficiently reliable index of the efficacy and power of a given disinfectant in a definite dilution and for a definite time exposure, it cannot, for reasons to be mentioned X MODES OF DESTRUCTION OF B. PESTIS 283 presently, supply an absolute guide for the application of the dis- infectant in actual practice. In practical life a disinfectant is applied by a surgeon, by the sanitarian, or by the nurse, not to an artificial culture or to an emulsion of an artificial culture, but to materials, such as excretions, secretions, morbid products, and morbid tissues, derived directly or indirectly from the human or animal bodies. The microbes to be acted upon by the disinfectant are embedded in, surrounded by, and mixed with various materials. This condition cannot obviously be compared with that of a microbe in a broth culture, or with a watery or salt emulsion of the growth taken from an artificial culture. The surgeon who wishes to disinfect a wound and to keep it antiseptic has to apply the disinfectant to tissues and not to a watery emulsion ; the nurse who is supposed to disinfect a typhoid stool with a given disinfectant is not acting on a watery or saline emulsion of a culture of the typhoid bacillus, but on materials of a highly complex composition, and altogether of a different nature from the laboratory culture. An illustration is sufficient to prove the difference between the one kind of disinfectant and the other. Staphylococcus pyogenes aureus (of a recent and active culture) is justly considered one of the hardiest non-sporing microbes, at any rate as far as chemical disin- fectants are concerned, and for this reason bacteriologists are in the habit of using this microbe in their laboratory tests. Now, the Staphylococcus aureus, taken from a culture (broth or agar) and placed into a watery solution or distributed in a disinfectant, is by simple agitation in most cases readily emulsified ; the fluid viewed under the microscope shows the microbes almost uniformly distributed as single cocci or as diplococci or as very small groups. Compare with this a microscopic specimen of the contents of an abscess or of the secretion of a wound or ulcer. Here we find, besides crowds of various tissue elements, leucocytes, debris, tissue fibres, fatty granule-cells, etc., large and small clumps of cocci and diplococci not only in the fluid menstruum, but within the protoplasm of leucocytes, within debris, and within masses of fibres. The disinfectant which is to act on the microbe so surrounded and lodged has a task to fulfil quite diff'erent from what it has when it is added to a broth culture or other uniform emulsion of the microbe. The same, mutatis mutandis, applies to diphtherial membrane, to sputum, to the typhoid stool, and other animal excretions. In the following experiments I wish to show by direct observation that in a 284 OEIENTAL PLAGUE chap. number of tests which I have made in this direction, marked differ- ences exist in the action of a certain disinfectant, with which I have been well acquainted for some years, to wit, izal, as applied to microbes, such as Staphylococcus aureus, B. coli, B. typhosus, in different surroundings ; in one case the microbes were taken from artificial cultures, and in the other were in their natural habitat. The izal used was the fluid sold as ordinary izal in the ordinary pharmacy. Method 1. In the case of pus of acute abscess, the pus and blood, immediately after collecting them from the abscess in sterile test tube, were diluted with sterile distilled water, 1 part of pus being added to 49 parts of water. From this dilution a control culture was made on agar, one platinum loopful of the mixture for one agar surface culture. The result of this control culture indicated the amount of staphylococcus present, and allowed the number of colonies in the control tube to be compared with those that appeared in the culture tubes after medication. To the above dilution of the pus was added a definite amount of izal direct as sold, and then well shaken up. The proportion of izal to the volume of diluted pus represented the strength of izal actually used in the experiment. 2. In the case of urine a definite amount of izal was added, well shaken ; then, after being kept for the required time, the necessary cultures were made on agar and in broth. 3. In the case of the typhoid stool only typical fluid (pea-soup) stools were used ; of these a definite quantity was added to a definite quantity of sterile water. This was well shaken up ; to it was added a definite amount of izal as in the other cases. Also in the last two instances control cultures on agar with one platinum loop were made from the diluted materials previous to the addition of the izal, so as to be able to compare the actual number of microbes of the coli-typhoid type before and after exposure to the disinfectant. After the addition of izal, cultures were made at the desired periods from the medicated fluids on agar surface and in broth, each culture tube receiving three platinum loops of the medicated material; these tubes were then incubated at 37° C. Inspection and notification were made after the tubes had been incubated for three or four days, for by this time all growth, if any, had become complete. X MODES OF DESTRUCTION OF B. PESTIS 285 Experiments First Series. — Pus of Acute Abscess. Experiment 1. — Of pus and blood of an acute abscess of the female breast, 1 ccm. was added to 49 ccm. of sterile distilled water (1 in 50). One platinum loop yielded about 100 colonies oi ■ Staphylococcus aureus. Added to diluted pus 0-1 ccm. of izal well shaken up. This made, therefore, 1 izal in 500. Cultures were made with 3 platinum loops for each tube after 5, 15, and 30 minutes with this result: — a. After 5 minutes; agar tube has 12 colonies of Staphylococcus aureus ; broth-tube uniformly turbid. This broth-tube was subcultured, with the result that it proved a pure culture of Staphylococcus aureus. h. After 15 minutes : on agar 2 colonies of Staphylococcus aureus; broth-tube uniformly turbid. Subculture proved this broth-tube to be a pure culture of Staphylo- coccus aureus. c. After 30 minutes : on agar 2 colonies of Staphylococcus av/reus; broth -tube greatly retarded growth, only faintly turbid after 3 days' incubation. Considering that a single loop of the diluted pus yielded before the addition of the izal about 100 colonies of Staphylococcus aureus, whereas 3 loops (same loop as used in control) yielded after 5 minutes' exposure to the izal only 12 colonies, the process of disinfec- tion must be considered already after this short space of time of a fair degree ; this is well shown in experiment c, after 30 minutes' exposure, when 3 loops yielded only 2 colonies; that is to say, of 300 microbes only 2 had survived. The broth - tube bears witness to this, since the broth showed greatly retarded and scanty growth. The result of this experiment 1 is, then, that izal 1 in 500 may for practical purposes be considered a fair, though not complete disinfectant for pus of acute abscess (Staphylococcus aureus) after 30 minutes' exposure. Experiment 2. — The same pus as above was used ; 1 ccm. of the 286 ORIENTAL PLAGUE chap. pus was added to 39 ccm. of sterile distilled water (1 in 40), then O'l ccm. of the izal was added (1 in 400), well shaken, and cultures were made as above after 5, 15, and 30 minutes on agar and in broth, using 3 platinum loops for each tube. The result was this : — a. After 5 minutes' exposure : on agar 1 5 colonies of Staphylo- coccus aureus ; broth uniformly turbid. Subculture of this proved pure culture of Staphylococcus aureus. b. After 15 minutes : both tubes free of growth. c. After 30 minutes : both tubes free of growth. From this it follows that izal 1 in 400 completely disinfects in 1 5 minutes ; in 5 minutes already the number of living microbes being greatly reduced (300 to 15). Experiment 3. — Pus of an acute submental abscess (mixed with blood) was obtained ; 1 ccm. of the pus was diluted with 39 ccm. of sterile distilled water (1 in 40). With 1 loop of this dilution made control agar culture. In this about 1 2 dozen colonies came up ; these were partly colonies of streptococci, partly colonies of Staphylococcus aureus and albus. O'l ccm. of izal was added to the diluted pus (1 in 400); after well shaking it and keeping it for 5, 15, and 30 minutes, cultures were made on agar and in broth, using for each tube 3 loops. Incubated at 37° C. for 4 days. The result was this : — a. After 5 minutes : on agar 1 5 colonies of mixture of Staphylo- coccus aureus and albus ; no colonies of streptococci ; broth slightly turbid. Subculture of the broth showed mixture of Staphylococcus aureus and albus, but the great majority were those of Staphylococcus aureus ; no colonies of streptococci. b. After 1 5 minutes : both tubes were free of growth. c. After 30 minutes : both tubes were free of growth. From this experiment it follows that izal 1 in 400 disinfects completely streptococcus in 5 minutes ; that it reduces living Staphylo- coccus aweus and albus in 5 minutes to a considerable degree (from 432 to 15), and that it completely disinfects them in 15 minutes. The following table summarises the preceding results as regards the capability or incapability of izal to disinfect the microbes of pus of acute abscess : — X MODES OF DESTRUCTION OF B. PESTIS 287 Table I Sample. Nature of Dilution. Time of Exposure. 5 minutes. 15 minutes. 30 minutes. Pus No. 1 . „ „ 1 • • „ „ 2 1 izal in 500 1 izal in 400 1 izal in 400 + reduced + reduced + reduced + reduced + greatly reduced Positive sign means growth, negative sign means absence of growth, after medication. Experiment 4. — This experiment is a control to the preceding experiments with Staphylococcus aureus, and serves to compare the effect of the disinfectant when used on a culture of the microbe in watery emulsion. Of a 48 hours' agar active culture of Staphylococcus aureus added to sterile distilled water, sufficient to form slight but distinct turbidity. One loop of emulsion brought forth on agar an almost confluent mass of Staphylococcus aureus. a. To 50 ccm. of the staphylococcus emulsion added O'l ccm. izal, 1 in 500. b. To 60 ccm. of the staphylococcus emulsion added O'l ccm. izal, 1 in 600. c. To 75 ccm. of the staphylococcus emulsion added O'l ccm. izal, 1 in 750. After 5 minutes' exposure, made with 3 loops 1 agar and 1 broth culture, incubation at 37° C, with result as follows : — a. 1 in 500, 5 minutes' exposure : no growth in either tube. b. 1 in 600, 5 minutes' exposure : no growth in either tube. c. 1 in 750, 5 minutes' exposure: agar shows 18 colonies. Broth uniformly turbid with Staphylococcus aureus. Table II. summarises the preceding results : — Table 288 ORIENTAL PLAGUE CHA?. Table II Sample. Nature of Dilution. Time of Exposure 6 minutes. "Watery emulsion of culture of Staphylococcus aureus )j J) j> )) I' )j 1 in 500 1 in 600 1 in 760 + greatly reduced From this it follows that for Staphylococcus aureus of culture izal 1 in 600 is a complete disinfectant in 5 minutes. This result is in so far interesting as it shows that Staphylococcus aureus of culture is disinfected quicker and with greater dilutions of izal than when it is acted upon in its natural habitat, that is pus. It will be remembered that for pus izal 1 in 400, 15 minutes' exposure, was the limit for completely disinfecting Staphylococcus aureus, whereas for disinfection of this microbe in watery emulsion 1 in 600 izal for 5 minutes' exposure was sufficient. This result emphasises the importance of testing the disinfecting power of any given substance on the pus microbes while in their natural media, for only thus is an absolute index for practical guidance acquired. Second Series. — Typhoid Stools. . Experiment 5. — Typical (pea-soup) typhoid stool (1) of a case of typhoid fever, 22nd day of illness. This stool was tested in high dilutions by means of Drigalski Conradi plates, and was found to contain about 14 millions of B. coli, about the same number or a little more of streptococci, and 3 millions of the B. typhosus per 1 ccm. of original stool. The disinfection experiment was made in the following manner : — 1 ccm. of the stool was added to 49 ccm. of sterile distilled water (1 in 50) ; this was well shaken up till a fair and uniform emulsion was obtained. Control agar culture with 1 loop showed innumerable colonies of above microbes. To it was then added O'l ccm. of the izal and well shaken up; this made, then, a dilution of 1 izal in 500. Cultures were made after 15 minutes', after 30 minutes', and X MODES OF DESTRUCTION OF B. PESTIS 289 after 1 hour's exposure, 3 loops of the medicated fluid being added to each agar and broth tube. The result was this : — a. After 1 5 minutes : on agar 1 colony of streptococci ; broth slightly turbid. Subculture of this broth showed colonies of streptococci only. h. After 30 minutes : on agar no colonies; broth very slightly turbid. Subculture of this broth showed colonies of streptococci only. c. After 1 hour : on agar no growth ; broth very slightly turbid (streptococci). From this experiment it follows that the microbes of the coli- typhoid type were completely disinfected in 15 minutes by izal 1 in 500 ; but the streptococci, although disinfected for agar in 30 minutes, were not quite disinfected for broth though very largely reduced in number in 1 hour. Experiment 6. — The same stool (2) as in experiment 5 was treated with izal 1 in 600, after exactly the same manner as described above. Eesult : — a. After 1 5 minutes : agar free of growth ; broth slightly turbid {B. coli). b. After 30 minutes : both tubes free of growth. c. After 1 hour : both tubes free of growth. Experiment 7. — The same stool (3) treated with izal 1 in 750. Result : — a. After 15 minutes: agar showed 5 colonies (5. eoli) ; broth uniformly turbid (B. coli). b. After 30 minutes : agar shows 3 colonies (B. coli) ; broth very slightly turbid {B. coli). c. After 1 hour : agar no growth ; broth no growth. The result of these two experiments, 6 and 7. is then : — Izal 1 in 600 completely disinfected the microbes of the coli- typhoid group in 30 minutes, but not in 15 minutes. Izal 1 in 750 completely disinfected these microbes in 1 hour, but not in 30 minutes. Experiment 8. — Typical (pea-soup) typhoid stool (4) of a case, 19th day of illness, was treated in exactly the same manner as the stool in experiment 5 — namely, 1 in 500 — with this result : — a. After 15 minutes : no growth on agar or in broth. b. After 30 minutes : no growth on agar or in broth. c. After 1 hour : no growth on agar or in broth. In this case, then, izal 1 in 500 caused in 15 minutes complete U 290 ORIENTAL PLAGUE chap. disinfection of the microbes of the coli-typhoid type as well as of the streptococci. (Control experiments made of this stool in high dilution by means of Drigalski and Conradi plates showed: 16 millions B. coli, 2 millions B. typhosus, and about 10 millions streptococci per 1 ccm.) Experiment 9. — The same stool (5) as used in experiment 8 was treated with izal 1 in 600. Result : — a. After 15 minutes : agar, no growth; broth, no growth. J. After 30 minutes : agar, no growth ; broth, no growth. c. After 1 hour : agar, no growth ; broth, no growth. From this it follows that izal as 1 in 600 completely disinfected in 15 minutes. Experiment 10. — The same stool (6) as in experiments 8 and 9, izal 1 in 750. Eesult : — a. After 1 5 minutes : agar shows 2 colonies (B. coli) ; broth uniformly turbid (B. coli). b. After 30 minutes : agar, no growth ; broth uniformly turbid {B. coli). c. After 1 hour : both cultures free of any growth. From this it follows that izal as 1 in 750 completely disinfected in 1 hour, but not in 30 minutes. Experiment 11. — Semi-solid stool (7) of a case of typhoid, 10th day of illness. Added 1 gramme to 50 ccm. of sterile distilled water. (From this dilution, 1 in 50, made with one loop an agar culture, with the result that after incubation the agar surface was covered with innumerable colonies, in many cases confluent.) To the above dilution, 1 in 50, added O'l ccm. izal, that is 1 in 500. Cultures from the medicated fluid were made after 15 and 30 minutes and after 1 hour, using for each culture tube 3 loops. Result : — a. After 1 5 minutes : agar shows 1 colony of sporing B. mesen- tericus ; broth-tube turbid, due to cocci and streptococci (no bacilli). 6. After 30 minutes : both tubes free of growth. c. After an hour : both tubes free of growth. In this experiment, then, izal 1 in 500 disinfected the microbes of the coli-typhoid group in 15 minutes, though not those of cocci. Experiment 12. — The same stool (8) was used as above, izal 1 in 600. X MODES OF DESTEUCTION OF B. PESTIS 291 Eesult : — a. After 1 5 minutes : agar free of growth ; broth free of growth. I. After 30 minutes : agar has 1 colony {B. coli 1) ; broth free of growth. c. After 1 hour : both tubes free of growth. From this it follows that izal 1 in 600 completely disinfected the microbes of the coli-typhoid group in 1 hour ; but already in 30 minutes the reduction of all microbes was enormous, since only the agar tubes showed one single colony, but it was not quite clear whether B. coli or not. For practical purposes 30 minutes would therefore suffice. Experiment 13. — The same stool (9) was used as above, izal 1 in 750. Eesult : — a. After 15 minutes : agar shows large number of coli-like colonies ; broth clear. 6. After 30 minutes : both tubes without growth. c. After 1 hour: agar shows 1 colony of sporing £. mesenierkus. The following Table III. summarises the results of all experiments made with typhoid stools in respect of the microbes of the coli- typhoid group : — Table III Sample. Nature of Dilution. Time of Exposure. 15 minutes. 30 minutes. 1 hour. Typhoid stool (1) „ (2) „ (3) „ (4) „ „ (5) „ „ (6) „ (7) ., (8) ,, (9) 1 in 500 1 in 600 1 in 750 1 in 500 1 in 600 1 in 750 1 in 500 1 in 600 1 in 750 + reduced + reduced + reduced + + reduced + reduced ? - 292 ORIENTAL PLAGUE chap. Third Series. — Urine. Experiment 14. — Turbid urine of a case of typhoid (end of second week). An agar control culture was made with 1 loop of the urine ; it showed after incubation 36 colonies of various kinds of microbes, chiefly belonging to the coli-typhoid group. To 70 ccm. of the urine (practically the whole of the urine obtainable) O'l ccm. izal was added ; this represents, therefore, 1 in 700. Cultures were made, using 3 loops for each culture tube, after 5, 15, and 30 minutes, with this result.: — a. After 5 minutes : agar, no growth ; broth turbid. i. After 15 minutes : agar, no growth; broth, no growth. c. After 30 minutes : agar, no growth ; broth, no growth. From this experiment it appears that 15 minutes was sufficient for izal 1 in 700 to cause complete disinfection of this urine. Experiment 15. — Normal urine was filtered and then sterilised by heating it for 10 minutes at 70° C. To the sterile clear urine added of a recent culture of B. typhosus sufficient to produce slight turbidity. One platinum loop of this was transferred to the surface of gelatine. It brought forth a very large number of colonies of the B. typhosus. a. To 50 ccm. of the typhoid urine was added 0"1 ccm. of izal, this being equal to izal 1 in 500. b. To 60 ccm. of the typhoid urine was added 0*1 ccm. of izal, this being equal to izal 1 in 600. c. To 75 ccm. of the typhoid urine was added O'l ccm. of izal, this being equal to izal 1 in 750. After 5 minutes' exposure, cultures were made on agar and broth, each tube receiving 3 platinum loops. Incubation 37° C. The result was as follows : — a. 1 in 500, 5 minutes' exposure : no growth in either tube. b. 1 in 600, 5 minutes' exposure : no growth in either tube. c. 1 in 750, 5 minutes' exposure : good growth in both tubes, proved to be pure B. typhosus. It follows from this that 1 in 600 for 5 minutes is the limit of izal disinfection for B. typhosus distributed in urine. Experiment 16. — For control and comparison of the above experiments sterile distilled water was substituted for the stools and urine. In other respects all conditions remained the same ; namely, of a recent culture of B. typhosus (same as used above) sufficient X MODES OF DESTRUCTION OF B. FESTIS 293 growth was added to the water so as to produce slight, though distinct, turbidity. A single platinum loop of the watery emulsion yielded a very large number of colonies of B. typhosus. a. To 50 ccm. of the typhoid water added O'l ccm. izal, 1 in 500. b. To 60 ccm. of the typhoid water added 0-1 ccm. izal, 1 in 600. c. To 75 ccm. of the typhoid water added O'l ccm. izal, 1 in 750. After 5 minutes' exposure made cultures on agar and in broth with 3 loops. Incubation at 37° C. with the following result : — a. 1 in 500, 5 minutes' exposure : no growth in either tube. b. 1 in 600, 5 minutes' exposure : no growth in either tube. c. 1 in 750, 5 minutes' exposure : no growth on agar ; slight turbidity of broth due to B. typhosus. This, then, agrees with experiment 15 as to complete disinfection of B. typhosus by izal 1 in 600 in 5 minutes ; but as regards izal 1 in 750, the typhoid watery emulsion appears to be more amenable to disinfection than the typhoid urine, for while in the latter good growth appeared in the broth-tube, in the former the broth only showed retarded and diminished growth of the B. typhosus. That the slight turbidity of this broth was really due to B. typhosus was proved not only by subcultures but by the positive agglutination test, the bacilli becoming completely agglutinated by typhoid serum (of a typhoid protected rabbit) 1 in 200 in 5 minutes. Comparing these experiments of watery emulsion of B. typhosus with those of the typhoid stool the difference becomes obvious ; for while izal 1 in 600 completely disinfected the watery emulsion in 5 minutes, and even as 1 in 750 greatly reduced the number of bacilli in 5 minutes (no growth on agar, slight turbidity in broth), in the typhoid stool (2) izal 1 in 600 did not disinfect in 15 minutes, though it succeeded in doing so in 30 minutes ; in another case (stool 9) izal 1 in 750 had no effect in 15 minutes, though it caused complete disinfection in 30 minutes. Coming now to experiments of disinfection of culture of B. pestis with cyllin, phenol, and formalin, I quote a paper which I published in Public Health, June 1904 : — " The following experiments were undertaken to test and compare the relative actions of ' cyllin,' ' phenol,' and ' formalin ' on B. pestis of a virulent strain. This 294 OEIENTAL PLAGUE chap. Had been originally derived from the bubo of a fatal case of bubonic plague in a man in Cardiff in 1901. The strain had been kept up in the laboratory by continued subcultures till the commencement of this year, when it was used for infecting rats. A trace of an agar culture of recent date (forty-eight hours at 37" C.) inoculated into a superficial incision of the skin of a rat caused typical fatal plague within three days. The culture actually used in the experiments to be described here was derived from the spleen of a rat dead on March 23, 1904, which rat had been cutaneously inoculated on March 20, 1904. In all our tests, of a forty -eight hours old agar culture — copious growth over the whole of the sloped surface (6 centimetres by 2 centimetres) — an emulsion was made with sterile distilled water. The emulsion was a strongly turbid fluid. A single platinum loop of this emulsion spread over a sloped agar surface brought forth innumer- able colonies of the B. pestis. In all instances to 5 cc. of the disinfectant contained in a sterile test tube, 5 drops (from a definite drop bottle) of the plague emulsion were added and well shaken, and after the required time of exposure cultures were made ; in all instances three loops of the medicated fluid being spread out over a sloped surface of gelatine or agar, or added to nutrient broth, as the case might be. The culture tubes were then incubated at 21° C. (gelatine), or at 37° C. (agar or broth), and inspected from time to time until for some days no further change was noticeable. Amongst the several dozen cultures thus made, in no single instance was there any accidental or stray microbe observed ; the tubes contained either no growth at all, or they contained colonies of the B. pestis in pure culture only, in varying X MODES OF DESTRUCTION OF B. PESTIS 295 numbers, as will presently be described. In this con- nection it will be necessary to bear in mind that three platinum loops of the mixture (5 cc. of the disinfectant and 5 drops of the emulsion of B. pestis) yielded in the positive instances innumerable colonies of B. pestis in the culture tubes. This disposes at once of an objection that might possibly be raised, viz. that the amount of dis- infectant carried over from the mixture to the culture tubes might inhibit the subsequent growth of the microbe, although the latter might still be alive. It also disposes of a further criticism, viz. that the number of microbes carried over by three platinum loops might not be large enough. As just mentioned, in the fully positive in- stances the whole culture surface was covered with crowds of colonies. Series I. — March 25, 1904. A. — Watery solution of pure phenol . . 1 in 200 B. — Watery solution of pure phenol . . 1 in 100 C. — Watery solution of formalin (40 per cent) 1 in 100 D. — Watery solution of formalin (40 per cent) 1 in 50 Time of exposure of -B. pestis, 5, 10, and 15 minutes. Cultures after exposure were made on sloped gelatine (21° C), and inspected on April 5, with the following result : — 1. — Phenol 1 in 200, 5 minutes' exposure. Innumerable colonies — confluent mass. ■^^ jj )i )j J) At* jj jj )) J, 2. — Phenol 1 in 100, 5 minutes' exposure. Innumerable colonies. 10 „ ,, About 7 doz. colonies. 15 „ „ 6 colonies. 296 OEIENTAL PLAGUE CHAP. 3. — Formalin 1 in 100, 5 minutes' exposure. Innumerable colonies. 10 ), „ » jj 4. — Formalin 1 in 50, 5 minutes' exposure. Innumerable colonies. 10 j> » )i )> 15 „ „ ,, ), Series //.— March 28, 1904. A. — Watery distribution of cyllin . . 1 in 1500 B.— „ „ „ . . 1 in 1000 G- „ „ „ . . lin 500 Time of exposure, 5, 10, and 15 minutes. Cultures after exposure were made on sloped gelatine (21° C.) and inspected on April 10, when all tubes were found to be free of any growth. Series 777.— April 8, 1904. A. — Watery distribution of cyllin . . 1 in 1500 B.— „ „ „ . . lin 1000 Time of exposure, 5, 10, and 15 minutes. Cultures after exposure were made on sloped agar and in broth, and incubated at 37° C, inspection being made on April 16, 1904. Result : All tubes free of any growth. Series IV. — April 7, 1904. A. — Watery solution of phenol B. — „ „ formalin C. — Distribution of cyllin D.— E. — ,, ,, 1 in 80 1 in 30 1 in 2000 1 in 1800 1 in 1600 Time of exposure, 5, 10, and 15 minutes X MODES OF DESTEUCTION OF B. PESTIS 297 Cultures were made on gelatine (21° C.) and agar (37° C), and inspected on April 16, with the following result : — 1. — Phenol 1 in 80, 5 minutes' exposure. On gelatine 3 doz. colonies. On agar 10 „ „ In both tubes no growth. 1 fi ■*■" )» J) )? J) >j 2. — Formalin 1 in 30, 5 minutes' exposure. Crowds of colonies in both tubes. 10 „ „ Numerous colonies. 15 „ „ About 5 dozen colonies. 3. — Cyllin 1 in 2000, 5, 10, and 15 minutes' exposure. All tubes free of growth. 1 in 1800 1 in 1600 Series F!— April 11, 1904. A. — Watery distribution of cyllin . . 1 in 2400 B.— „ „ „ . . 1 in 2200 Time of exposure, 5, 10, and 15 minutes. Cultures were made on agar (37° C.) and gelatine (21° C), and inspected on April 18, with this result : — 1.— Cyllin 1 in 2400, 5 minutes' exposure. Gelatine tube had one colony of B. pedis. The agar tube had a small amount of growth in the con- densation water ; this was allowed to spread over the sloped surface of the agar, with the result that copious growth of B. pestis covered the surface next day. 10 „ „ No growth in any tube. Ay J, » )) j> )) 298 OEIENTAL PLAGUE CHAP. 2. — Cyllin 1 in 2200, 5 minutes' exposure. All tubes free of any growth. From these experiments it follows: (1) that formalin even 1 in 30 failed to disinfect B. pestis in fifteen minutes ; (2) that phenol 1 in 80 failed to disinfect B. pestis in five minutes, but did disinfect in ten minutes; and (3) that cyllin 1 in 2400 failed in five minutes, but succeeded in ten minutes. From the following tables it will be seen that — (1) Phenol 1 in 80 is a stronger disinfectant for B. pestis than formalin 1 in 30 ; and (2) Phenol 1 in 80 stands in about the same position as cyllin 1 in 2400, inasmuch as both failed to completely devitalise the B. pestis in five minutes, though they both succeeded in doing so in ten minutes. Expressed in a different form, cyllin possesses for watery emulsion of B. pestis a disinfecting power which is more than 27 "5 (in fact about 30) times as great as that of absolute phenol. TEST No. 1 (April 22, 1904). B. Pestis, 48 houes' Agar Cttlture at 37° C. Koom Tbmperatuee IS'-IS" C. Sample. Dilution. Time Culture ex- posed to Action of Disinfectant. Subculture. Bemarks. M 5 inute 10 3. 15 Period of Incubation. Temperature. Formalin (40%) 1:100 + + + 7 days 37° C. Copious growth. 1:50 + + + j> )} 1:30 + + + >> )) Slight re- duction in 15 minutes. Pure Phenol . 1:80 + " ~' J) )» Reduction in 5 minutes. Carbolic acid coeificient of formalin is under '37. X MODES OF DESTRUCTION OF B. PESTIS 299 TEST No. 2 (April 22, 1904). B. Pbstis, 48 Houas' Agar Ctjltuke at 37° C. Room Tbmpeeattjke 15°-1l8° C Sample. Dilution. Time Culture ex- posed to Action of Disinfectant. Subculture. Remarks. 1 5 linute 10 s. 15 Period of Incubation. Temperature. CylUn . Pure Phenol . 1 : 2400 1 : 2200 1 : 2000 1 : 1800 1:80 + + - - 7 days 37° C. Great reduc- tion in 5 minutes. Reduction in 5 minutes. Carbolic acid coefficient of cyllin is 30 '0. I conclude here with the description of the result of experiments on disinfection with izal on culture of B. pestis directly derived from a bubo : — Time of Exposure. Sample. Dilution. Temperature. 5 min. 10 min. 15 min. Izal ordinary 1 : 2200 + + - 37° C. )j )> 1 : 2000 + - - )) jj 1 : 1800 + - fj » 1:1600 - - - Phenol 1 : 100 + + - )» 1:80 + - - »» 1 :60 - - - )J Carbolic coefficient between 22-5 and 26-6. 300 OKIENTAL PLAGUE chap. Taking a certain dilution of carbolic acid as being capable of completely disinfecting in five minutes B. pestis of culture, the figures of carbolic coefficient for cyllin and izal work out something like 24 to 30 for cyllin, 22 "5 to 26*6 for izal. It will be seen from this that cyllin and izal leave phenol, and still more formalin (when used in fluid form) far behind, and, with the exception of bichloride of mercury, are more powerful disinfectants than certain disinfectants which, when tested under similar conditions on non-sporing microbes, have a co- efficient inferior to phenol. Although I have made no special experiments on JB. pestis with chloros, kerol, or other agents, either belonging to the group of strong oxidisers or to the group of tar products, judged by what these substances are capable of eflfecting when tested on B. typhosus I have no doubt that they will be found powerful disinfectants also for B. pestis. Be it added here that although the figures given here of phenol, formalin, cyllin, and izal apply to experiments on watery emulsions of pure culture of B. pestis, it does not follow that they apply in exactly the same degree if disinfection is performed on plague organs direct, such as would have to be dealt with in actual practice. For under the latter conditions the relations of disinfectant to infective material, i.e. open and free contact of the disinfecting fluid with the B. pestis contained within the viscid and gelatinous albuminous materials — blood, intes- tinal contents, sputum, viscera, — may be, and probably are, difi'erent from what they are when watery emulsions of pure cultures are used. Moreover, the degree of efficacy of one as compared with the other disinfectant may be altered. Not that cyllin and izal, chloros and kerol, and some X MODES OF DESTRUCTION OF B. PESTIS 301 others would be found to be less powerful than phenol or formalin, but that their actual phenol coefl&cient need not be the same as when working with pure culture. This is shown by the experiments of Kenwood and Hewlett {Public Health, February 1906, p. 269), by which it was ascertained that, using cyllin and izal for disinfection of B. typhosus in faeces or urine, the coefl&cient is lower than when using pure culture of the B. typhosus — as I myself had already previously demonstrated, — and further, that the relative position of these two substances qud phenol coefficient may be equal or even reversed. THE END Printed by R. & R. Clark, Limited, Edinburgh NEW AND RECENT WORKS ON MEDICINE AND SURGERY Prof. ALLBUTT— Dr. H. D. ROLLESTON A SYSTEM OF MEDICINE. By many Writers. Second Edition. Edited by T. Clifford Allbutt, M.D., and Humphry Davy Rolleston, M.D. Vol.1. Prolegomena and Infectious Diseases. 8vo. 25s.net. Vol. II. Part I. Infectious Diseases (coniinued). Intoxications. 8vo. 25 s. net. Vol. II. Part II. (/« /^e Press.) Prof. ALLBUTT— Dr. W. S. PLAYFAIR— Dr. T. W. EDEN A SYSTEM OF GYNAECOLOGY. By many Writers. Edited by T. 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