Hostname: page-component-78c5997874-v9fdk Total loading time: 0 Render date: 2024-11-04T19:47:49.212Z Has data issue: false hasContentIssue false

An environmental survey of bakehouses and abattoirs for salmonellae

Published online by Cambridge University Press:  15 May 2009

R. W. S. Harvey
Affiliation:
Public Health Laboratory, Cardiff
W. Powell Phillips
Affiliation:
Medical Officer of Health, Cardiff
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. Moore's gauze swabs have, in our hands, been shown to be a reliable instrument for the survey of salmonella infection in the environment of two food premises.

2. A large bakery was demonstrated to be regularly contaminated with salmonellae. Thirty-one floor gully swabs out of 111 (27·9%) were positive for salmonellae. Little spread of infection to the general public was experienced.

3. Staff infection with salmonellae was shown to occur in this bakery. Fifteen positive specimens of staff sewage out of 93 were obtained (16·1%). There was little evidence of prolonged contamination of the sewers with salmonellae. Staff infections were probably, therefore, of short duration. The staff probably became infected from contaminated goods in the bakehouse. Rat contamination of sewers was excluded by water trapping.

4. It is not thought that regular examination of staff excreta would be a profitable means of discovering carriers or of preventing contamination of the products. The frequency with which such examinations would have to be performed to discover short-term excreters would be administratively impossible.

5. Of 274 swabs from gullies in abattoirs, 111 were positive for salmonellac (40·5%). Twenty-one different serotypes were isolated. Seventeen of these serotypes are known to occur in animal feedingstuffs.

6. Parallel examination of abattoir swabs and excreta from human infections for S. typhimurium, coupled with phage-typing of the strains, provided information of the geographically local nature of much sporadic illness due to this serotype. Of a total of 30 typable strains, 23 belonged to phage-types found in the abattoirs, or on local farms. Sporadic incidents were represented by 25 of these cultures, 18 of which corresponded in phage-type to those found in the abattoirs or in local farm animals. The phage-types of S. typhimurium isolated from the slaughter houses not infrequently corresponded in timing with the strains isolated from human infections.

Type
Research Article
Copyright
Copyright © Cambridge University Press 1961

References

REFERENCES

Anderson, E. S. (1960). Roy. Soc. Hlth J. 80, 260.Google Scholar
Bernstein, A. (1958). Mon. Bull. Minist. Hlth Lab. Serv. 18, 92.Google Scholar
Callow, , the late Bessie R. (1959). J. Hyg., Camb., 57, 346.CrossRefGoogle Scholar
Culley, A. R. (1953). Med. Offr, 89, 243, 257.Google Scholar
Editorial Note (1951). Med. Offr, 86, 166.Google Scholar
Felix, A. (1956). J. gen. Microbiol. 14, 208.CrossRefGoogle Scholar
Felix, A. & Callow, B. R. (1943). Brit. med. J. ii, 127.CrossRefGoogle Scholar
Felix, A. & Callow, B. R. (1951). Lancet, ii, 10.CrossRefGoogle Scholar
Galton, M. G., Lowery, W. D. & Hardy, A. V. (1954). J. infect. Dis. 95, 232.CrossRefGoogle Scholar
Harvey, R. W. S. (1956). Mon. Bull. Minist. Hlth Lab. Serv. 15, 118.Google Scholar
Harvey, R. W. S. (1957). Brit. J. clin. Pract. 11, 751.CrossRefGoogle Scholar
Harvey, R. W. S. & Phillips, W. P. (1955). Lancet, ii, 137.CrossRefGoogle Scholar
Harvey, R. W. S., Price, T. H., Davis, A. R. & Morley-Davies, R. B. (1961). J. Hyg., Camb., 59, 105.CrossRefGoogle Scholar
Harvey, R. W. S. & Thomson, S. (1953). Mon. Bull. Minist. Hlth Lab. Serv. 12, 149.Google Scholar
Hobbs, B. C. & Greenwood Wilson, J. G. (1959). Mon. Bull. Minist. Hlth Lab. Serv. 18, 198.Google Scholar
Leading Article (1958). Lancet, ii, 1216.Google Scholar
Loureiro, J. A. de (1942). J. Hyg., Camb., 42, 224.CrossRefGoogle Scholar
McCann, M. B. & Cross, C. (1956). Med. Offr, 96, 241.Google Scholar
McCullough, N. B. & Eisele, C. W. (1951 a). J. infect. Dis. 88, 278.CrossRefGoogle Scholar
McCullough, N. B. & Eisele, C. W. (1951 b). J. infect. Dis. 89, 209.CrossRefGoogle Scholar
McDonagh, V. P. & Smith, H. G. (1958). J. Hyg., Camb., 56, 271.CrossRefGoogle Scholar
Moore, B. (1948). Mon. Bull. Minist. Hlth Lab. Serv. 7, 241.Google Scholar
Newell, K. W. (1955). Mon. Bull. Minist. Hlth Lab. Serv. 14, 146.Google Scholar
Newell, K. W., Hobbs, B. C. & Wallace, E. J. G. (1955). Brit. med. J. ii, 1296.CrossRefGoogle Scholar
Newell, K. W., McClarin, R., Murdock, C. R., MacDonald, W. N. & Hutchinson, H. L. (1959). J. Hyg., Camb., 57, 92.CrossRefGoogle Scholar
Nicol, C. G. M. (1956). Mon. Bull. Minist. Hlth Lab. Serv. 15, 240.Google Scholar
Smith, M. E. & Hobbs, B. C. (1955). Mon. Bull. Minist. Hlth Lab. Ser. 14, 154.Google Scholar
Thomson, S. (1953). Mon. Bull. Minist. Hlth Lab. Serv. 12, 187.Google Scholar
Wilosn, W. J. & Darling, G. (1918). Lancet, ii, 105.Google Scholar