Development, Evaluation, and Peer Verification of a Rapid Real-Time PCR Method for the Detection of Animal Material

Authors: Yancy, Haile F.1; Washington, Jewell D.2; Callahan, Lauren3; Mason, Jacquline A.4; Deaver, Christine M.2; Farrell, Dorothy E.2; Ha, Tai5; Sespico, Eric6; Falmlen, Daniel6; Myers, Michael J.2

Source: Journal of Food Protection®, Volume 72, Number 11, November 2009 , pp. 2368-2374(7)

Publisher: International Association for Food Protection

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Abstract:

Four real-time PCR assays that can be used with U.S.- and European Union-rendered materials to detect three ruminant species (bovine, caprine, and ovine) and a select set of avians (chicken, goose, and turkey) were developed. This method was evaluated against stringent acceptance criteria previously developed by the U.S. Food and Drug Administration, Center for Veterinary Medicine's Office of Research. Acceptance criteria for determining success used a statistical approach requiring a 90% probability of achieving the correct response, within a 95% confidence interval. A minimum detection level of 0.1% meat and bone meal (MBM) was required, consistent with the sensitivity of the validated PCR-based method currently used by the U.S. Food and Drug Administration as an aid in enforcement of the Agency's feed ban. PCR primer specificity was determined by using a panel of DNA samples derived from 16 different animal species. The method is able to detect 0.1% rendered material in complete feed in less than 1.5 h of total assay time, a significant improvement over the current method, which requires 7 to 8 h for completion. The real-time assay for the detection of animal material passed stringent acceptance criteria for sensitivity, selectivity, and specificity. The method also passed ruggedness, real-time platform, and second analyst trials. Two external laboratories participating in a peer-verification trial demonstrated 100% specificity in identifying bovine MBM, ovine MBM, or caprine meat meal, while exhibiting a 0.6% rate of false positives. These results demonstrated that this method was capable of being used by other laboratories.

Document Type: Research article

Affiliations: 1: U.S. Food and Drug Administration, Center for Veterinary Medicine, Office of Research, 8401 Muirkirk Road, Laurel, Maryland 20708, USA. Hyancy@cvm.fda.gov 2: U.S. Food and Drug Administration, Center for Veterinary Medicine, Office of Research, 8401 Muirkirk Road, Laurel, Maryland 20708, USA 3: St. Mary's College of Maryland, 18952 East Fisher Road, St. Mary's City, Maryland 20686, USA 4: Howard University, Washington, D.C. 20059, USA 5: Nebraska Department of Agriculture, 301 Centennial Mall, South, Lincoln, Nebraska 68508, USA 6: Florida Department of Agriculture, P.O. Box 147100, Gainesville, Florida 32614, USA

Publication date: 2009-11-01

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    First published in 1937, the Journal of Food Protection®, is a refereed monthly publication. Each issue contains scientific research and authoritative review articles reporting on a variety of topics in food science pertaining to food safety and quality. The Journal is internationally recognized as the leading publication in the field of food microbiology with a readership exceeding 11,000 scientists from 70 countries. The Journal of Food Protection® is indexed in Index Medicus, Current Contents, BIOSIS, PubMed, Medline, and many others.

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