Detection of coliform bacteria and Escherichia coli by multiplex polymerase chain reaction: comparison with defined substrate and plating methods for water quality monitoring

Author:

Bej A K1,McCarty S C1,Atlas R M1

Affiliation:

1. Department of Biology, University of Louisville, Kentucky 40292.

Abstract

Multiplex polymerase chain reaction (PCR) and gene probe detection of target lacZ and uidA genes were used to detect total coliform bacteria and Escherichia coli, respectively, for determining water quality. In tests of environmental water samples, the lacZ PCR method gave results statistically equivalent to those of the plate count and defined substrate methods accepted by the U.S. Environmental Protection Agency for water quality monitoring and the uidA PCR method was more sensitive than 4-methylumbelliferyl-beta-D-glucuronide-based defined substrate tests for specific detection of E. coli.

Publisher

American Society for Microbiology

Subject

Ecology,Applied Microbiology and Biotechnology,Food Science,Biotechnology

Reference19 articles.

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3. Ausubel F. M. R. Brent R. E. Kingston D. D. Moore J. A. Smith J. G. Sideman and K. Struhl (ed.). 1987. Current protocols in molecular biology. John Wiley & Sons Inc. New York.

4. Detection of Escherichia coli and Shigella spp. in water by using the polymerase chain reaction and gene probes for uid;Bej A. K.;Appl. Environ. Microbiol.,1991

5. Multiplex PCR amplification and immobilized capture probes for detection of bacterial pathogens and indicators in water;Bej A. K.;Mol. Cell. Probes,1990

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