Hostname: page-component-848d4c4894-p2v8j Total loading time: 0 Render date: 2024-06-07T23:27:56.089Z Has data issue: false hasContentIssue false

Virulence, Immunity and Bacteriological Variation in Relation to Plague

Published online by Cambridge University Press:  15 May 2009

A. S. Burgess
Affiliation:
(From the Medical Research Institute, Accra.)
Rights & Permissions [Opens in a new window]

Extract

Core share and HTML view are not available for this content. However, as you have access to this content, a full PDF is available via the ‘Save PDF’ action button.

1. African pouched rats (Cricetomys gambianus) are very suitable animals for plague experiments on account of their tolerance of captivity and their extreme susceptibility. After inoculation with small doses of plague culture of ordinary virulence they always die.

2. Broth-grown vaccine was much more efficient as a prophylactic than agar-grown vaccine. When two doses were given a survival rate of 56 per cent, was obtained with the former and 25 per cent, with the latter.

3. A vaccine composed of carbolised spleen pulp from animals, which had died of acute plague, was rather more efficient than broth vaccine, giving a survival rate of 75 per cent. But it is not likely to be of practical value, as preparation is difficult, there are undesirable local effects and its superiority over broth vaccine is not very great. Its efficiency is attributed to the fact that the organisms which it contains are a true “body strain.” The method of preparation is similar to that of Hindle's yellow fever prophylactic.

4. A number of experiments are described in which virulence was abolished or reduced by passage through immune or partially immune rats. This occurred only when the passage animal showed a considerable degree of immunity, as indicated by the length of the survival period after the test infection. Cultures made from the abscess at the site of infection were less often attenuated than those from the liver of an immunised animal, but this was observed only in the case of large well-defined abscesses. It is suggested that a firm abscess wall protects organisms inside it against the action of antibodies appearing in the general circulation.

A culture attenuated by passage through an immunised rat was restored to normal virulence by successive passages through normal rats, but the process was slower than in the case of cultures attenuated by long cultivation, five passages being required in the former case and only one in the latter.

5. Cultures used in the later work, unlike those used in the earlier work, lost virulence rapidly when kept at room temperature. Experiments and observations are described which suggest that old strains, even when subjected to rat passage, are less stable as regards virulence than those recently isolated from human epidemic cases, and that the high temperature of the Gold Coast has an adverse effect upon virulence.

6. Attempts to isolate stable variants of B. pestis were not successful. Colonies vary much in form. Three types of colony are mentioned, but all intermediate grades were observed. Certain old avirulent strains had a greater tendency to produce large irregular colonies than recent strains, but the relation was so loose that the form of colony gave little indication of the degree of virulence. In old avirulent strains the bacilli tend to become longer and filaments of great length may be present. Salt stability tends to become less as a strain grows old and avirulent, but the change is not very marked and is apt to be masked by individual fluctuations.

Type
Research Article
Copyright
Copyright © Cambridge University Press 1930

References

REFERENCES

Bezsonova, A., Semekoz, T. and Kotelnikov, G. (1927). Atypic forms of the colonies of B. Pestis. (In Russian with English summary.) Rev. de Microbiol. et Epidemiol. 6, 472.Google Scholar
Burgess, A. S. (1927). The selection of a strain of Bacillus pestis for the preparation of vaccine, with special reference to the effect of animal passage on virulence. J. Hygiene, 26, 152.CrossRefGoogle Scholar
Dieudonné, and Otto, (1928), in Kolle and Wassermann: Handbuch der Pathogenen Mikroorganismen, 3rd Ed., 4, p. 190 and PI. I, figs. 1, 3 opposite p. 412.Google Scholar
Drennan, G. J. and Teague, O. (1917). A selective medium for the isolation of B. Pestis from contaminated plague lesions and observations on the growth of B. pestis. J. Med. Res. 26, 519.Google Scholar
Hindle, E. (1929). An experimental study of yellow fever. Trans. Roy. Soc. of Trop. Med. and Hyg. 22, 405.CrossRefGoogle Scholar
Markl, J. G. (1914). Zur Frage der Mutation bei Pestbacillen. Centralbl. f. Bakt., etc., Abt. 1, Orig. 74, 529.Google Scholar
Rowland, S. (1915). Further experiments on vaccination against a body strain of plague. J. Hygiene, Plague Supplement IV, 752.Google ScholarPubMed
Young, W. A. (1926–1927). Annual Report of the Medical Research Institute, Gold Coast, in the Annual Report of the Medical and Sanitation Department of the Gold Coast, p. 64.Google Scholar