Food Hygiene Laboratory, National Food Research Institute, Tsukuba, Japan.
Foodborne Pathog Dis. 2010 May;7(5):549-54. doi: 10.1089/fpd.2009.0465.
Salmonella sp., Listeria monocytogenes, and Escherichia coli O157:H7 are foodborne pathogens capable of causing serious gastrointestinal illness. We previously described simultaneous detection of these pathogens by multiplex polymerase chain reaction (PCR) in 44 types of spiked food samples, including meat, produce, fish, and dairy products, targeting genes specific for each pathogen. Based on the previous work, a multiplex real-time PCR assay using fluorescent probes was developed to detect and accurately quantify Salmonella sp., L. monocytogenes, and E. coli O157:H7 in ground pork samples. The detection sensitivity for this method was 2.0 x 10(2) CFU/mL for each pathogen, and the quantification range was 10(2)-10(7) CFU/mL with a high correlation coefficient (R(2) > 0.99) and high PCR efficiency (84.2% to 99.2%). When this protocol was used for the detection of each of the pathogens in spiked pork samples, one cell per 25 g of inoculated sample after enrichment for 20 h could be detected within 24 h. As a result, this multiplex real-time PCR assay will be valuable as a screening method for foods contaminated with these pathogens.
沙门氏菌、单增李斯特菌和大肠杆菌 O157:H7 是食源性致病菌,能够导致严重的胃肠道疾病。我们之前曾描述过,通过针对每种病原体的特定基因的多重聚合酶链反应(PCR),可以同时检测 44 种添加食品样本中的这些病原体,包括肉类、农产品、鱼类和乳制品。基于之前的工作,我们开发了一种使用荧光探针的多重实时 PCR 检测方法,用于检测和准确定量猪肉样品中的沙门氏菌、单增李斯特菌和大肠杆菌 O157:H7。该方法的检测灵敏度为每种病原体 2.0 x 10(2) CFU/mL,定量范围为 10(2)-10(7) CFU/mL,具有高相关性系数(R(2) > 0.99)和高 PCR 效率(84.2%至 99.2%)。当使用该方案检测添加猪肉样本中的每种病原体时,在富集 20 小时后,每 25 g 接种样本中可检测到一个细胞,24 小时内即可检测到。因此,这种多重实时 PCR 检测方法将成为检测受这些病原体污染的食品的一种有价值的筛选方法。