Hostname: page-component-8448b6f56d-mp689 Total loading time: 0 Render date: 2024-04-19T07:19:55.846Z Has data issue: false hasContentIssue false

Bacteriophage, virulence and agglutination tests with a strain of Salmonella typhi of low virulence

Published online by Cambridge University Press:  15 May 2009

A. Felix
Affiliation:
From the Central Enteric Reference Laboratory and Bureau, Public Health Laboratory Service (Medical Research Council), London
E. S. Anderson
Affiliation:
From the Central Enteric Reference Laboratory and Bureau, Public Health Laboratory Service (Medical Research Council), London
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. The low Vi-antigen content and low mouse virulence of freshly isolated cultures of the Oswestry strain of Salm. typhi reflected its low virulence for man. This is additional evidence of the association between the degree of virulence of Salm. typhi and its Vi-antigen content.

2. The prediction that the epidemic caused by this typhoid strain of low mouse virulence would resemble a paratyphoid-B outbreak more closely than an average typhoid outbreak proved to be correct.

3. Sera from convalescent patients in this typhoid outbreak showed significant Vi-agglutinin titres in spite of the low Vi-antigen content of freshly isolated cultures.

4. The nutritional requirements of the Oswestry strain were unusual, and its sensitivity to the specific Vi-typing phages was variable. This caused considerable difficulty in the typing of the cultures.

5. Additional tests of identity had to be employed in order to distinguish the epidemic strain from other strains of the same Vi-phage type isolated in the vicinity. Colony size, colonial morphology, biochemical reactions and sensitivity to anti-O bacteriophage served as useful ancillary criteria.

Type
Research Article
Copyright
Copyright © Cambridge University Press 1951

References

REFERENCES

Bradley, W. H., Evans, W. & Taylor, I. (1951). J. Hyg., Camb., 49, 324.Google Scholar
Craigie, J. & Brandon, K. F. (1936). J. Path. Bact. 43, 233.CrossRefGoogle Scholar
Craigie, J. & Felix, A. (1947). Lancet, 1, 823.CrossRefGoogle Scholar
Craigie, J. & Yen, C. H. (1938). Canad. publ. Hlth J. 29, 448, 484.Google Scholar
Felix, A. (1938). J. Hyg., Camb., 38, 750.Google Scholar
Felix, A. (1943). Brit. med. J. 1, 435.CrossRefGoogle Scholar
Felix, A. (1944). Brit. med. Bidl. 2, 269.CrossRefGoogle Scholar
Felix, A.. (1948). Proc. 4th Int. Congr. trop. Med. & Malaria, p. 283. Washington.Google Scholar
Felix, A. (1951). Brit. med. Bull. 7, 153.CrossRefGoogle Scholar
Felix, A. & Callow, B. R. (1943). Brit. med. J. 2, 127.CrossRefGoogle Scholar
Felix, A. & Pitt, R. M. (1951). J. Hyg., Camb., 49, 92.CrossRefGoogle Scholar
Findlay, H. T. (1951). J. Hyg., Camb., 49, 111.CrossRefGoogle Scholar
Giovanardi, A. (1938). Zbl. Bakt. Abt. I, Orig., 141, 341.Google Scholar
International Committee For Enteric Phage Typing (1949). Proc. 4th Int. Congr. Microbiol. (1947), p. 621. Copenhagen.Google Scholar
International Committee For Enteric Phage Typing (1951). Proc. 5th Int. Congr. Microbiol. (1950) (in the Press). Rio de Janeiro.Google Scholar
Jones, A. C. (1951). J. Hyg., Camb., 49, 335.Google Scholar
Jude, A. & Nicolle, P. (1949). Ann. Inst. Pasteur, 77, 550.Google Scholar
Kristensen, M. (1938). J. Hyg., Camb., 38, 688.Google Scholar
Kristensen, M. & Henriksen, H. C. D. (1926). Acta path, microbiol. scand. 3, 551.CrossRefGoogle Scholar
Marmion, B. P. & Martin, A. E. (1946). Mon. Bull. Minist. Hlth & Emerg. Publ. Hlth Lab. Serv., Lond., 5, 205.Google Scholar
MINISTRY OF HEALTH (1945). Mon. Bull. Minist. Hlth & Emerg. Publ. Hlth Lab. Serv., Lond., 4, 224.Google Scholar