Rapid pulsed-field gel electrophoresis protocol for typing of Escherichia coli O157:H7 and other gram-negative organisms in 1 day

Author:

Gautom R K1

Affiliation:

1. Washington State Department of Health, Public Health Laboratories, Seattle 98155, USA.

Abstract

Genomic DNA patterns generated by pulsed-field gel electrophoresis are highly specific for different strains of an organism and have significant value in epidemiologic investigations of infectious-disease outbreaks. Unfortunately, time-consuming and tedious specimen processing is an inherent problem which limits the use of this powerful technology as a real-time epidemic investigational tool. Here, I describe a rapid method to improve the response time and provide specific bacterial strain identification for the typing of Escherichia coli O157:H7 and other gram-negative organisms in a single day.

Publisher

American Society for Microbiology

Subject

Microbiology (medical)

Reference28 articles.

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2. Pulsed-field gel electrophoresis as a replacement for bacteriophage typing of Staphylococcus aureus;Bannerman T. L.;J. Clin. Microbiol.,1995

3. Laboratory investigation of a multistate food-borne outbreak of Escherichia coli O157:H7 by using pulsedfield gel electrophoresis and phage typing;Barrett T. J.;J. Clin. Microbiol.,1994

4. Birren B. and E. Lai. 1993. Pulsed field gel electrophoresis: a practical guide. Academic Press Inc. San Diego Calif.

5. DNA fingerprinting of Escherichia coli O157:H7 strains by pulsed-field gel electrophoresis;Böhm H.;J. Clin. Microbiol.,1992

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