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Mercury resistance of Staphylococcus aureus

Published online by Cambridge University Press:  15 May 2009

Barbara M. Hall
Affiliation:
Department of Clinical Pathology, University College Hospital, London, W.C.1
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Reasons for the accumulation of mercury-resistant strains of Staphylococcus aureus in hospital have been studied. A collection of paired strains, that is staphylococci similar in every respect except sensitivity to mercury salts, was made. Tests were made in an attempt to demonstrate a link between mercury resistance and some other factor which might aid survival, viz. resistance to drying and heat, production of bound coagulase, growth in the presence of sublethal amounts of tetracycline, survival in human blood at 37°C. and uptake by polymorphs at 30°0. and 37°C., development of resistance to antibiotics and competition in mixed cultures. It was not possible to demonstrate any consistent link between mercury resistance and any of these properties. Paper strips impregnated with the mercurial diuretic, Mersalyl, were shown to differentiate between mercury-resistant and -sensitive strains in vitro. Furthermore, development of resistance to mercury by passage in mercuric chloride-broth was demonstrated.

It is proposed that mercury resistance has developed as a result of exposure to the mercury ion. Mercurial diuretics have been frequently used in medical and geriatric patients and it is among these that the higher carrier rates of mercury-resistant strains are found even when the local endemic strain is disregarded. In obstetric patients, where mercurials are seldom used, mercury-resistant strains are rare.

Nasal carriage of factory workers exposed to mercury products showed that this group is likely to carry resistant or partially resistant strains.

Type
Research Article
Copyright
Copyright © Cambridge University Press 1970

References

Akinlade, N. D. (1962). A trial of mercuric chloride for the rapid identification of epidemic strains of Staphylococcus pyogenes. West African Medical Journal 11, 35.Google ScholarPubMed
Duthie, E. S. (1955). The action of fibrinogen on certain pathogenic cocci. Journal of General Microbiology 13, 383.CrossRefGoogle ScholarPubMed
Gould, J. C. (1958). Environmental penicillin and penicillin-resistant Staphylococcus aureus. Lancet i, 489.CrossRefGoogle ScholarPubMed
Hall, B. M. (1966). A study of antibiotic-resistant Staphylococcus pyogenes in a hospital community with particular reference to Moore's mercury sensitivity test as a guide to strains of epidemic importance. Ph.D. Thesis, University of London.Google Scholar
Hall, B. M. (1970). Distribution of mercury resistance among Staphylococcus aureus isolated from a hospital community. Journal of Hygiene 68, 111.CrossRefGoogle ScholarPubMed
Jessen, O., Rosendal, K., Faber, V., Hove, K. & Erikson, K. R. (1963). Some properties of Staphylococcus aureus possibly related to pathogenicity. Acta Pathologica et Microbiologica Scandinavica 58, 85.CrossRefGoogle ScholarPubMed
Li, I. W., Mudd, S. & Kapral, F. A. (1963). Dissociation of phagocytosis and intracellular killing of Staphylococcus aureus by human blood leukocytes. Journal of Immunology 90, 804.CrossRefGoogle ScholarPubMed
Meyer, W. (1966). Ergebnisse der Sublimatresistenzbestimmung bei Staphylococcus-aureus-Stämmen humaner und animaler Herkunft. Zeitschrift fär die gesamte Hygiene und ihre Grenzgebiete 12, 974.Google Scholar
Moore, B. (1960). A new screen test and selective medium for the rapid detection of epidemic strains of Staph. aureus. Lancet ii, 453.CrossRefGoogle ScholarPubMed
Richmond, M. H. & John, M. (1964). Co-transduction by a staphylococcal phage of the genes responsible for penicillinase synthesis and resistance to mercury salts. Nature 202, 1360.CrossRefGoogle ScholarPubMed
Richmond, M. H., Parker, M. T., Jevons, M. P. & John, M. (1964). High penicillinase production correlated with multiple antibiotic resistance in Staphylococcus aureus. Lancet i, 293.CrossRefGoogle ScholarPubMed
Stokes, E. J., Hall, B. M., Richards, J. D. M. & Riley, D. J. (1965). Control of hospital staphylococci. Lancet ii, 197.CrossRefGoogle ScholarPubMed
Turner, G. C. & Willis, A. T. (1962). Staphylococcal invasion of a new surgical ward. Journal of Pathology and Bacteriology 84, 349.CrossRefGoogle ScholarPubMed