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Applied and Environmental Microbiology, November 1998, p. 4210-4216, Vol. 64, No. 11
Guelph Molecular Supercentre, Laboratory
Services Division, University of Guelph, Guelph, Ontario, Canada
N1H 8J71;
Biotronics Technologies Corp.,
Lowell, Massachusetts 018512;
Health
of Animals Laboratory, Health Canada, Guelph, Ontario, Canada N1G
3W43; and
Office of Research,
University of Guelph, Guelph, Ontario, Canada N1G
2W14
Received 23 April 1998/Accepted 12 August 1998
An automated fluorescence-based PCR system (a model AG-9600
AmpliSensor analyzer) was investigated to determine whether it could
detect Shiga toxin-producing Escherichia coli (STEC). The AmpliSensor PCR assay involves amplification-mediated disruption of a
fluorogenic DNA signal duplex (AmpliSensor) that is homologous to
conserved target sequences in a 323-bp amplified fragment of Shiga
toxin genes stx1, stx2,
and stxe. Using the Amplisensor assay, we
detected 113 strains of STEC belonging to 50 different serotypes, while
18 strains of non-Shiga-toxin-producing E. coli and 68 strains of other bacteria were not detected. The detection limits of
the assay were less than 1 to 5 CFU per PCR mixture when pure cultures
of five reference strains were used and 3 CFU per 25 g of food
when spiked ground beef samples that were preenriched overnight were
used. The performance of the assay was also evaluated by using 53 naturally contaminated meat samples and 48 raw milk samples. Thirty-two
STEC-positive samples that were confirmed to be positive by the culture
assay were found to be positive when the AmpliSensor assay was used.
Nine samples that were found to be positive when the PCR assay was used
were culture negative. The system described here is an automated
PCR-based system that can be used for detection of all serotypes of
STEC in food or clinical samples.
0099-2240/98/$04.00+0
Copyright © 1998, American Society for Microbiology. All rights reserved.
An Automated Fluorescent PCR Method for Detection
of Shiga Toxin-Producing Escherichia coli in
Foods

*
Corresponding author. Mailing address: Office of
Research, University of Guelph, Reynolds Building, Guelph, Ontario,
Canada N1G 2W1. Phone: (519) 824-4120, ext. 3523. Fax: (519) 821-5236. E-mail: steph{at}ornet.or.uoguelph.ca.
Present address: Affymetrix, Santa Clara, CA 95051.
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