Rapid procedure for detecting enterohemorrhagic Escherichia coli O157:H7 in food

Author:

Padhye N V1,Doyle M P1

Affiliation:

1. Department of Food Microbiology and Toxicology, University of Wisconsin-Madison 53706.

Abstract

A sensitive, specific procedure was developed for detecting Escherichia coli O157:H7 in food in less than 20 h. The procedure involves enrichment of 25 g of food in 225 ml of a selective enrichment medium for 16 to 18 h at 37 degrees C with agitation (150 rpm). The enrichment culture is applied to a sandwich enzyme-linked immunosorbent assay (ELISA) with a polyclonal antibody specific for E. coli O157 antigen as the capture antibody and a monoclonal antibody specific for enterohemorrhagic E. coli of serotypes O157:H7 and O26:H11 as the detection antibody. The ELISA can be completed within 3 h. The sensitivity of the procedure, determined by using E. coli O157:H7-inoculated ground beef and dairy products, including different varieties of cheese, was 0.2 to 0.9 cell per g of food. A survey of retail fresh ground beef and farm raw milk samples with this procedure revealed that 3 (2.8%) of 107 ground beef samples and 11 (10%) of 115 raw milk samples were positive for E. coli O157:H7. Most-probable-number determinations revealed E. coli O157:H7 populations of 0.4 to 1.5 cells per g in the three ground beef samples. In addition to being highly specific, sensitive, and rapid, this procedure is easy to perform and is amenable to use by laboratories performing routine microbiological testing.

Publisher

American Society for Microbiology

Subject

Ecology,Applied Microbiology and Biotechnology,Food Science,Biotechnology

Reference20 articles.

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3. Doyle M. P. and J. L. Schoeni. 1987. Isolation of Escherichia coli 0157:H7 from retail fresh meats and poultry. Appl. Envi ron. Microbiol. 53:2394-2396.

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5. The use of sorbitol-MacConkey agar in conjunction with a specific antiserum for the detection of verocytotoxinproducing strains of Escherichia coli 0157:H7;Kleanthous H.;Epidemiol. Infect.,1988

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