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用于检测致病性大肠杆菌的多重聚合酶链反应-脱氧核糖核酸探针检测法

Multiplex PCR-DNA probe assay for the detection of pathogenic Escherichia coli.

作者信息

Watterworth Leigh, Topp Edward, Schraft Heidi, Leung Kam Tin

机构信息

Department of Biology, Lakehead University, 955 Oliver Road, Thunder Bay, Ontario, Canada P7B 5E1.

出版信息

J Microbiol Methods. 2005 Jan;60(1):93-105. doi: 10.1016/j.mimet.2004.08.016.

Abstract

A multiplex PCR-DNA probing assay was developed to detect four major Escherichia coli virotypes. Six highly specific polymerase chain reaction (PCR) primer sets and DIG-labeled chemiluminescent probes were designed to target the Shiga-like toxin I and II genes (stxI and stxII) of verotoxigenic E. coli (VTEC), heat-stable and heat-labile toxin genes of enterotoxigenic E. coli (ETEC), adherence factor (EAF) of enteropathogenic E. coli (EPEC) and a fragment of the invasiveness plasmid (IAL) of enteroinvasive E. coli (EIEC). The primer pairs generate products of 350, 262, 170, 322, 293 and 390 bp in length, respectively. The multiplex primers and probes were tested for specificity against 31 pathogenic E. coli strains, nine nonpathogenic E. coli and non-E.coli enteric and environmental bacterial strains. The results showed a high degree of specificity of the primers and probes for strains from corresponding virotypes and no reaction with the nontarget bacterial strains. The proposed multiplex PCR-DNA probing assay provides rapid and specific detection of four major virotypes of E. coli.

摘要

开发了一种多重PCR-DNA探针检测方法来检测四种主要的大肠杆菌毒型。设计了六组高度特异性的聚合酶链反应(PCR)引物和地高辛标记的化学发光探针,以靶向产志贺毒素大肠杆菌(VTEC)的志贺样毒素I和II基因(stxI和stxII)、肠产毒素大肠杆菌(ETEC)的耐热和不耐热毒素基因、肠致病性大肠杆菌(EPEC)的黏附因子(EAF)以及肠侵袭性大肠杆菌(EIEC)的侵袭性质粒片段(IAL)。这些引物对分别产生长度为350、262、170、322、293和390 bp的产物。对多重引物和探针针对31种致病性大肠杆菌菌株、9种非致病性大肠杆菌以及非大肠杆菌的肠道和环境细菌菌株进行了特异性测试。结果表明,引物和探针对相应毒型的菌株具有高度特异性,与非靶标细菌菌株无反应。所提出的多重PCR-DNA探针检测方法可快速、特异性地检测四种主要的大肠杆菌毒型。

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