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食品中肠出血性大肠杆菌O157:H7的快速检测方法

Rapid procedure for detecting enterohemorrhagic Escherichia coli O157:H7 in food.

作者信息

Padhye N V, Doyle M P

机构信息

Department of Food Microbiology and Toxicology, University of Wisconsin-Madison 53706.

出版信息

Appl Environ Microbiol. 1991 Sep;57(9):2693-8. doi: 10.1128/aem.57.9.2693-2698.1991.

Abstract

A sensitive, specific procedure was developed for detecting Escherichia coli O157:H7 in food in less than 20 h. The procedure involves enrichment of 25 g of food in 225 ml of a selective enrichment medium for 16 to 18 h at 37 degrees C with agitation (150 rpm). The enrichment culture is applied to a sandwich enzyme-linked immunosorbent assay (ELISA) with a polyclonal antibody specific for E. coli O157 antigen as the capture antibody and a monoclonal antibody specific for enterohemorrhagic E. coli of serotypes O157:H7 and O26:H11 as the detection antibody. The ELISA can be completed within 3 h. The sensitivity of the procedure, determined by using E. coli O157:H7-inoculated ground beef and dairy products, including different varieties of cheese, was 0.2 to 0.9 cell per g of food. A survey of retail fresh ground beef and farm raw milk samples with this procedure revealed that 3 (2.8%) of 107 ground beef samples and 11 (10%) of 115 raw milk samples were positive for E. coli O157:H7. Most-probable-number determinations revealed E. coli O157:H7 populations of 0.4 to 1.5 cells per g in the three ground beef samples. In addition to being highly specific, sensitive, and rapid, this procedure is easy to perform and is amenable to use by laboratories performing routine microbiological testing.

摘要

已开发出一种灵敏、特异的方法,可在不到20小时内检测食品中的大肠杆菌O157:H7。该方法包括将25克食品在225毫升选择性富集培养基中于37℃搅拌(150转/分钟)培养16至18小时。将富集培养物应用于夹心酶联免疫吸附测定(ELISA),以针对大肠杆菌O157抗原的多克隆抗体作为捕获抗体,以针对血清型O157:H7和O26:H11的肠出血性大肠杆菌的单克隆抗体作为检测抗体。ELISA可在3小时内完成。通过使用接种了大肠杆菌O157:H7的绞碎牛肉和乳制品(包括不同品种的奶酪)确定该方法的灵敏度为每克食品0.2至0.9个细胞。用该方法对零售新鲜绞碎牛肉和农场原料奶样品进行的一项调查显示,107份绞碎牛肉样品中有3份(2.8%)、115份原料奶样品中有11份(10%)大肠杆菌O157:H7呈阳性。最大可能数测定显示,三份绞碎牛肉样品中大肠杆菌O157:H7的数量为每克0.4至1.5个细胞。除了具有高度特异性、灵敏性和快速性外,该方法易于操作,适合进行常规微生物检测的实验室使用。

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