Gilbert Carl, Winters Debra, O'Leary Awilda, Slavik Michael
Department of Poultry Science, Center of Excellence for Poultry Science, University of Arkansas, POSC O-310, Fayetteville, AR 72701, USA.
Mol Cell Probes. 2003 Aug;17(4):135-8. doi: 10.1016/s0890-8508(03)00043-4.
A triplex PCR assay was developed and evaluated for efficacy in detecting Campylobacter jejuni, Salmonella spp., and Escherichia coli O157:H7 in a variety of raw and ready-to-eat food products. Following a short enrichment period, artificially contaminated food samples were subjected to a triplex PCR assay, which incorporated published primers for each food pathogen, a protocol for sample collection, and a PCR procedure designed specifically for the assay. The selected primers amplified fragment sizes of 159 bp, 252 bp, and 360 bp for C. jejuni, E. coli O157:H7, and Salmonella spp., respectively. This assay provides specific and reliable results and allows for the cost-effective detection of all three bacterial pathogens in one reaction tube.
开发并评估了一种三重PCR检测方法,以检测各种生的和即食食品中的空肠弯曲菌、沙门氏菌属和大肠杆菌O157:H7。经过短暂的富集期后,将人工污染的食品样本进行三重PCR检测,该检测方法采用了针对每种食品病原体已发表的引物、样本采集方案以及专门为此检测设计的PCR程序。所选引物分别扩增出空肠弯曲菌、大肠杆菌O157:H7和沙门氏菌属的片段大小为159 bp、252 bp和360 bp的片段。该检测方法提供了特异且可靠的结果,并能够在一个反应管中经济高效地检测出所有三种细菌病原体。