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应用多重 PCR 技术检测人工污染牛肉拭子、牛肉切块和绞碎牛肉中属于血清型 O157、O103、O91、O113、O145、O111 和 O26 的产志贺毒素大肠杆菌。

Multiplex PCR detection of Shiga toxin-producing Escherichia coli strains belonging to serogroups O157, O103, O91, O113, O145, O111, and O26 experimentally inoculated in beef carcass swabs, beef trim, and ground beef.

机构信息

Department of Food Science, The Pennsylvania State University, University Park, Pennsylvania 16802, USA.

出版信息

J Food Prot. 2011 Feb;74(2):228-39. doi: 10.4315/0362-028X.JFP-10-386.

DOI:10.4315/0362-028X.JFP-10-386
PMID:21333142
Abstract

Numerous foodborne outbreaks are attributed to Shiga toxin-producing Escherichia coli (STEC) and have been recognized for causing gastrointestinal disease in humans. Beef products have been considered the principal source of STEC. A multiplex PCR assay enabling simultaneous detection of STEC O103, O91, O113, O145, O111, O157, and O26 was developed and evaluated in artificially contaminated beef carcass swabs, beef trim, and ground beef after overnight enrichment. Individual serogroups were experimentally inoculated at low (1 to 10 CFU/ml) and high (11 to 100 CFU/ml) levels, and with a cocktail of strains belonging to two, four, and six serogroups. There was no significant difference in detecting single STEC strains under the different conditions. Only when strains were combined were there significant differences in detection of all cocktail isolates in some of the beef products. To address this issue, four serogroups were experimentally inoculated together at three different estimated levels (10, 10(2), and 10(3) CFU/ml) in all three beef products. Results yielded no significant difference in detecting STEC at the three inoculation levels (10, 10(2), and 10(3) CFU/ml) in trim and carcass swabs, but there was a significant difference in detecting STEC at the lowest levels (10 and 10(2) CFU/ml) in the 80:20 nonirradiated ground beef, and in the detection of STEC in irradiated ground beef. The findings from this study could provide industry and government agencies with a tool to evaluate the prevalence and incidence of STEC in beef products and their processing environments.

摘要

许多食源性疾病爆发归因于产志贺毒素大肠杆菌(STEC),并已被确认可导致人类胃肠道疾病。牛肉产品被认为是 STEC 的主要来源。开发了一种多重 PCR 检测方法,可同时检测 STEC O103、O91、O113、O145、O111、O157 和 O26,并在人工污染的牛肉胴体拭子、牛肉切块和绞肉中进行了 overnight enrichment 后进行了评估。将各个血清群在低水平(1 至 10 CFU/ml)和高水平(11 至 100 CFU/ml)以及属于两个、四个和六个血清群的菌株混合物下进行了实验接种。在不同条件下,检测单个 STEC 菌株时没有显着差异。只有当菌株混合时,在某些牛肉产品中,所有鸡尾酒分离株的检测才会存在显着差异。为了解决这个问题,在所有三种牛肉产品中,将四个血清群一起以三个不同的估计水平(10、10(2)和 10(3) CFU/ml)进行了实验接种。结果在修剪和胴体拭子中,在三个接种水平(10、10(2)和 10(3) CFU/ml)检测 STEC 时没有显着差异,但在 80:20 非辐照绞肉中检测 STEC 的最低水平(10 和 10(2) CFU/ml)以及辐照绞肉中检测 STEC 时存在显着差异。本研究的结果可以为行业和政府机构提供一种工具,用于评估牛肉产品及其加工环境中 STEC 的流行率和发生率。

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