P2-142 Performance of a Molecular Detection System for the Detection of Salmonella and Escherichia coli O157 in Food and Carcass Samples

Tuesday, July 24, 2012
Exhibit Hall (Rhode Island Convention Center)
Julie Yang, 3M, Saint Paul, MN
Micki Rosauer, 3M, St Paul, MN
Cynthia Zook, 3M, St. Paul, MN
John David, 3M, St. Paul, MN
John david, 3M, St. Paul, MN
John David, 3M, St. Paul, MN
Introduction: Testing for Salmonella and E. coli O157:H7 is a critical component of food safety programs as contamination by these pathogens can result in significant adverse health conditions and economic loss. The 3M™ Molecular Detection Assay Salmonella and the 3M™ Molecular Detection Assay E. coli O157 (including H7) were developed for the rapid and specific detection of these organisms after enrichment. The assay uses a combination of isothermal amplification of unique DNA target sequences and bioluminescence to detect the amplified sequences.

Purpose: To evaluate the performance of detection methods using a variety of foods and poultry and beef carcasses.

Methods: Salmonella and E. coli O157 were used to artificially contaminate > 95 food samples with 5-13 CFU of target pathogen per sample size. Additional > 140 samples beef and poultry carcasses were also tested. Two test periods were conducted: 1) one sample was enriched blank and one was artificially contaminated with ~10 CFU of the target organism and 2) samples were enriched blank to evaluate for native contamination. Enrichments were tested using detection molecular assays and selective and differential agar &/or quantitative PCR.

Results: Compared to agar or qPCR, accuracy, specificity and sensitivity were: 97.6%, 100%, and 93.9% for the molecular detection assay Salmonella, and 95%, 100%, and 92% for the 3M Molecular Detection Assay E. coli O157 (including H7).

Significance: The methods demonstrated comparable results to the other methods for the rapid, automated detection of these organisms.