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Molecular epidemiology of shigella infection in Central Australia

Published online by Cambridge University Press:  15 May 2009

M. John Albert ,
K. V. Singh ,
B. E. Murray  and
J. Erlich
M. John Albert
Affiliation:
Alice Springs Hospital, Alice Springs, Northern Territory, Australia Menzies School of Health Research, Casuarina, Northern Territory, Australia
K. V. Singh
Affiliation:
Programme in Infectious Diseases and Clinical Microbiology, University of Texas Health Science Centre, Houston, Texas, USA
B. E. Murray
Affiliation:
Programme in Infectious Diseases and Clinical Microbiology, University of Texas Health Science Centre, Houston, Texas, USA
J. Erlich
Affiliation:
Alice Springs Hospital, Alice Springs, Northern Territory, Australia
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Summary

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Shigellosis is endemic in Central Australia and the infections are predominantly due to Shigella flexneri 6, Shigella flexneri 2a and Shigella sonnei. Plasmid profiles of isolates collected from 1985–9, suggested that infections caused by Shigella flexneri 6 were predominantly due to a single clone, whereas those caused by Shigella flexneri 2a and Shigella sonnei were due to several genetically diverse strains, although strains with identical plasmid profiles were found in widely separated geographical areas and in different years.

Type
Special Article
Information
Epidemiology & Infection , Volume 105 , Issue 1 , August 1990 , pp. 51 - 57
Copyright
Copyright © Cambridge University Press 1990

References

REFERENCES

1.Palchauduri, S, Kumar, R, Sen, D et al. , Molecular epidemiology of plasmid patterns in Shigella dysenteriae type 1 obtained from an outbreak in West Bengal (India). FEMS Lett 1985; 30: 187–91.CrossRefGoogle Scholar
2.Prado, D, Murray, BE, Cleary, TG, Pickering, LK. Limitations of using the plasmid pattern as an epidemiological tool for clinical isolates of Shigella sonnei. J Infect Dis 1987; 155: 314–16.CrossRefGoogle ScholarPubMed
3.Kado, CI, Liu, ST. Rapid procedure for detection and isolation of large and small plasmids. J Bacteriol 1981: 145: 1365–73.CrossRefGoogle ScholarPubMed
4.Birnboim, HC, Doly, J. A rapid alkaline extraction procedure for screening recombinant plasmid DNA. Nucleic Acids Res 1979; 7: 1513–23.CrossRefGoogle ScholarPubMed
5.Currier, TC, Nester, EW. Isolation of co-valently closed circular DNA of high molecular weight from bacteria. Analyst Biochem 1976; 76: 431–41.CrossRefGoogle Scholar
6.Meyers, JA, Sanchez, D, Elwell, LP, Falkow, S. Simple agarose gel electrophoretic method for the identification and characterisation of plasmid deoxyribonucleic acid. J Bacteriol 1976; 127: 1529–37.CrossRefGoogle ScholarPubMed
7.Bauer, AW, Kirby, WMM, Sherris, JC, Turck, M. Antibiotic susceptibility by a standardized single disk method. Am J Clin Pathol 1966; 45: 493–6.CrossRefGoogle ScholarPubMed
8.Sansonnetti, PJ, Kopeko, DJ, Formal, SB. Shigella sonnei plasmids: evidence that a large plasmid is necessary for virulence. Infect Immun 1981; 34: 75–83.CrossRefGoogle Scholar
9.Silva, RM, Toledo, MRF, Trabulsi, LR. Plasmid-mediated virulence in Shigella species. J Infect Dis 1982; 146: 99.CrossRefGoogle Scholar
10.Haider, K, Huq, MI, Talukder, KA, Ahmad, QS. Electropherotyping of plasmid DNA of different serotypes of Shigella flexneri isolated in Bangladesh. Epidemiol Infect 1989; 102: 421–8.CrossRefGoogle ScholarPubMed
11.Haider, K, Kay, BA, Talukder, KA, Huq, MI. Plasmid analysis of Shigella dysenteriae type 1 isolates obtained from widely scattered geographical locations. J Clin Microbiol 1988; 26: 2083–6.CrossRefGoogle ScholarPubMed