4.7 Article

Studies on Simultaneous Enrichment and Detection of Escherichia coli O157:H7 during Sample Shipment

Journal

FOODS
Volume 11, Issue 22, Pages -

Publisher

MDPI
DOI: 10.3390/foods11223653

Keywords

E. coli O157:H7; Shiga toxin-producing E. coli; bacteriophage; culture enrichment; foodborne pathogen; pathogen detection

Funding

  1. U.S. Department of Agriculture, Agricultural Research Service, Food Safety program [8072-42000-093-00D, 8072-42000-09400D, 59-8072-1-002]
  2. USDA National Institute of Food and Agriculture, Hatch project [1004830]

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The USDA-FSIS has zero tolerance for E. coli O157:H7 in raw ground beef and currently collects samples from beef processing facilities for testing. This study assessed the potential of using a phage-based luminescence detection assay during sample transportation, and the results suggest that this approach is feasible.
The USDA-FSIS has zero tolerance for E. coli O157:H7 in raw ground beef. Currently, FSIS collects samples from beef processing facilities and ships them overnight to regional testing laboratories. Pathogen detection requires robust methods that employ an initial 15-24 h culture enrichment. This study assessed the potential of using the Phi V10nluc phage-based luminescence detection assay during enrichment while the sample is in transit. Parameters including phage concentrations, temperature, and media-to-sample ratios were evaluated. Results in liquid media showed that 1.73 x 10(3) pfu/mL of Phi V10nluc was able to detect 2 CFU in 10 h. The detection of E. coli O157:H7 was further evaluated in kinetic studies using ratios of 1:3, 1:2, and 1:1 ground beef sample to enrichment media, yielding positive results for as little as 2-3 CFU in 325 g ground beef in about 15 h at 37 degrees C. These results suggest that this approach is feasible, allowing the detection of a presumptive positive upon arrival of the sample to the testing lab. As the current cargo hold controlled temperature is required to be 15-25 degrees C, the need for elevated temperature should be easily addressed. If successful, this approach could be expanded to other pathogens and foods.

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