Hostname: page-component-84b7d79bbc-tsvsl Total loading time: 0 Render date: 2024-07-25T10:28:42.506Z Has data issue: false hasContentIssue false

Change of drug resistance patterns and genetic properties of R plasmids in Salmonella typhimurium of bovine origin isolated from 1970 to 1979 in northern Japan

Published online by Cambridge University Press:  25 March 2010

S. Makino
Affiliation:
Department of Veterinary Public Health, Obihiro University of Agriculture and Veterinary Medicine, Obihiro 080, Japan
N. Ishiguro
Affiliation:
Department of Veterinary Public Health, Obihiro University of Agriculture and Veterinary Medicine, Obihiro 080, Japan
G. Sato
Affiliation:
Department of Veterinary Public Health, Obihiro University of Agriculture and Veterinary Medicine, Obihiro 080, Japan
N. Seno
Affiliation:
Tokachi Livestock Hygiene Service Centre, Obihiro 080, Japan
Rights & Permissions [Opens in a new window]

Summary

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.

A total of 321 Salmonella typhimurium strains of bovine origin obtained in northern Japan during the period 1970–1979 were tested for drug resistance and detection of conjugative R plasmids. Three hundred and eighteen (99·1 %) of these strains were resistant to one or more drugs. The isolation frequency of multiply drug-resistant strains tended to increase year by year. Two hundred and thirty-seven (74·5%) of these resistant strains carried conjugative R plasmids. A total of 308 R plasmids including 174 (56·5 %) thermosensitive (ts) R plasmids were derived from the 237 drug-resistant strains, indicating that 71 (30·0%) strains have two different conjugative R plasmids in a single host cell. Of the 308 R plasmids examined for fertility inhibition (fi), 167 ts and 131 non-ts R plasmids were fi. Of the 60 ts R plasmids examined for incompatibility, 50 were classified into H1 group and 10 into H2 group. Of the 52 non-ts R plasmids examined, 35 were classified into the Iα group and the remaining plasmids were untypable in our tests. Mercury resistance marker was found in about 20% of H1 R plasmids coding for multiresistance, and all of H2 R plasmids coded for resistance to tellurite. The clonal distribution of an S. typhimurium strain which carried an H1 R plasmid coding for resistance to six drugs and mercury was recognized in 1978 and 1979.

Type
Research Article
Copyright
Copyright © Cambridge University Press 1981

References

Anderson, E. S. (1968). Drug resistance in Salmonella typhimurium and its implications. British Medical Journal 3, 333339.CrossRefGoogle ScholarPubMed
Anderson, E. S., Threlfall, E. J., Carr, J. M., McConnel, M. M. & Smith, H. R. (1977). Clonal distribution of resistance plasmid-carrying Salmonella typhimurium. mainly in the Middle East. Journal of Hygiene 79, 425448.CrossRefGoogle ScholarPubMed
Datta, N., Hughes, V. M., Nugent, M. E. & Richards, H. (1979). Plasmids and transposons and their stability and mutability in bacteria isolated during an outbreak of hospital infection. Plasmid 2, 182196.CrossRefGoogle ScholarPubMed
Davies, M. & Stewart, P. R. (1978). Transferable drug resistance in man and animals: Genetic relationship between R-plasmids in enteric bacteria from man and domestic pets. Australian Veterinary Journal 54, 507512.CrossRefGoogle ScholarPubMed
Hirsh, D. C. & Wigner, N. (1977). Effect of tetracycline upon transfer of R plasmids from calves to human being. American Journal of Veterinary Research 38, 11371139.Google Scholar
Ishiguro, N., Goto, J. & Sato, G. (1980 A). Genetical relationship between R plasmids derived from Salmonella and Escherichia coli obtained from a pig farm, and its epidemiological significance. Journal of Hygiene 84, 365379.CrossRefGoogle ScholarPubMed
Ishiguro, N., Makino, S., Sato, G. & Hashimoto, K. (1980b). Antiobiotic resistance and genetic properties of R plasmids in Salmonella isolates of swine origin in Japan. American Journal of Veterinary Research 41, 4650.Google Scholar
Ishiguro, N., Oka, C., Hanzawa, Y. & Sato, G. (1979). Plasmids in Escherichia coli controlling citrate-utilizing ability. Applied and Environmental Microbiology 38, 956964.CrossRefGoogle ScholarPubMed
Ishiguro, N., Sato, G., Ichijo, S. & Konishi, T. (1980 c). Incompatibility of R plasmids derived from Salmonella and Escherichia coli isolated simultaneously from a bovine fecal sample. American Journal of Veterinary Research 41, 1982–1986.Google ScholarPubMed
Jacob, A. E., Shapiro, J. A., Yamamoto, L., Smith, D. I., Cohen, S. N. & Berg, D. (1977). Plasmids studies in Escherichia coli and other enteric bacteria. In DNA Insertion Elements, Plasmids, and Episomes (ed. Bukhari, A. I., Shapiro, J. A. and Adhya, S. L.). Cold Spring Harbor Laboratory, USA., p. 607.Google Scholar
Kashiwazaki, M., Namioka, S., Hechelmann, H. & Leistner, L. (1974). Incidence of R factors among Salmonella strains isolated from animals in Japan. National Institute of Animal Health Quarterly 14, 2930.Google ScholarPubMed
Lennox, E. S. (1955). Transduction of linked genetic characters of the host by bacteriophage P1. Virology 1, 190206.CrossRefGoogle ScholarPubMed
Levy, S. B., Fitzgerald, G. B. & Macone, A. B. (1976). Spread of antibiotic resistance plasmids from chicken to chicken and from chicken to man. Nature, London 260, 40–24.CrossRefGoogle ScholarPubMed
McConnell, M. M., Smith, H. R., Lronardopoulos, J. & Anderson, E. S. (1979). The value of plasmid studies in the epidemiology of infections due to drug-resistant Salmonella wien. Journal of Infectious Diseases 139, 178190.CrossRefGoogle ScholarPubMed
Nakahara, H., Ishikawa, Y., Sarai, Y., Kondo, I. & Kozukue, H. (1977). Mercury resistance and R plasmids in clinical isolates of Klebsiella pneumoniae. Zentralblatt für Bakteriologie, Parasitenkunde, Infektionskrankheiten und Hygiene, Abteilung I: Orig. A 238, 5158.Google Scholar
Rowe, B., Threlfall, E. J., Ward, L. R. & Ashely, A. S. (1979). International spread of multiresistant strains of Salmonella typhimurium phage types 204 and 193 from Britain to Europe. Veterinary Record 105, 468469.CrossRefGoogle ScholarPubMed
Sato, G. & Terakado, N. (1977). R factor types found in Salmonella typhimurium and Escherichia coli isolated from calves in a confined environment. American Journal of Veterinary Research 38, 743747.Google Scholar
Smith, H. R., Grindley, N. D. F., Humphrey, G. O. & Anderson, E. S. (1973). Interactions of group H resistance factors with the F factor. Journal of Bacteriology 115, 623628.CrossRefGoogle Scholar
Sojka, W., Wray, D. & Hudson, E. B. (1977). A survey of drug resistance in salmonellae isolated from animals in England and Wales during 1973 and 1974. British Veterinary Journal 133, 292311.CrossRefGoogle ScholarPubMed
Stephan, R., Bulling, E. & Steinbeck, A. (1977). Die entwicklung der Antibiotikaresistanz von der Bundesrepublik Deutschland einschließlich Berlin (West). Zentralblatt für Bakteriologie, Parasitenkunde, Infektionskrankheiten und Hygiene, Abteilung I: Orig. A 237, 264273.Google Scholar
Summers, A. O. & Jacoby, G. A. (1977). Plasmid-determined resistance to tellurium compounds. Journal of Bacteriology 129, 276281.CrossRefGoogle ScholarPubMed
Takahashi, I. (1976). Drug resistance of Salmonella isolated from domestic animal and fowl in Japan (in Japanese). Modern Media, Tokyo 22, 248259.Google Scholar
Taylor, D. E. & Grant, R. B. (1976). Inhibition of bacteriophage Lambda, T1 and T7 development by R plasmids of the H incompatibility group. Antimicrobial Agents and Chemotherapy 10, 762764.CrossRefGoogle Scholar
Terakado, N., Ohya, T., Ueda, H. & Isayama, Y. (1980). A survey of drug resistance and R plasmids in Salmonella isolated from domestic animals in Japan. Japanese Journal of Veterinary Science 42, 543550.Google Scholar
Terakado, N. & Sato, G. (1978). Detection of an R plasmid of incompatibility group H in Salmonella typhimurium of bovine origin. National Institute of Animal Health Quarterly 18, 180181.Google Scholar
Threlfall, E. J., Ward, L. R. & Rowe, B. (1978 a). Spread of multiresistant strains of Salmonella typhimurium phage types 204 and 193 in Britain. British Medical Journal 2, 997.CrossRefGoogle ScholarPubMed
Threlfall, E. J., Ward, L. R. & Rowe, B. (1978 b). Epidemic spread of a chloramphenicolresistant strain of Salmonella typhimurium phage type 204 in bovine animals in Britain. Veterinary Record 103, 438440.CrossRefGoogle ScholarPubMed
Timony, J. F. (1978). The epidemiology and genetics of antibiotic resistance of Salmonella typhimurium isolated from diseased animals in New York. Journal of Infectious Diseases 137, 6773.CrossRefGoogle Scholar