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用于鉴定人致腹泻性大肠杆菌的多重聚合酶链反应检测法

Multiplex PCR assay for identification of human diarrheagenic Escherichia coli.

作者信息

Toma Claudia, Lu Yan, Higa Naomi, Nakasone Noboru, Chinen Isabel, Baschkier Ariela, Rivas Marta, Iwanaga Masaaki

机构信息

Department of Bacteriology, Faculty of Medicine, University of the Ryukyus, Nishihara, Okinawa 903-0215, Japan.

出版信息

J Clin Microbiol. 2003 Jun;41(6):2669-71. doi: 10.1128/JCM.41.6.2669-2671.2003.

DOI:10.1128/JCM.41.6.2669-2671.2003
PMID:12791900
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC156568/
Abstract

A multiplex PCR assay for the identification of human diarrheagenic Escherichia coli was developed. The targets selected for each category were eae for enteropathogenic E. coli, stx for Shiga toxin-producing E. coli, elt and est for enterotoxigenic E. coli, ipaH for enteroinvasive E. coli, and aggR for enteroaggregative E. coli. This assay allowed the categorization of a diarrheagenic E. coli strain in a single reaction tube.

摘要

开发了一种用于鉴定人致泻性大肠杆菌的多重聚合酶链反应(PCR)检测方法。为每一类选定的靶标分别是:肠致病性大肠杆菌的eae、产志贺毒素大肠杆菌的stx、肠产毒素大肠杆菌的elt和est、肠侵袭性大肠杆菌的ipaH以及肠聚集性大肠杆菌的aggR。该检测方法可在单个反应管中对致泻性大肠杆菌菌株进行分类。

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本文引用的文献

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Diagn Microbiol Infect Dis. 2002 May;43(1):7-12. doi: 10.1016/s0732-8893(02)00363-2.
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Comparison of DNA hybridization and PCR assays for detection of putative pathogenic enteroadherent Escherichia coli.用于检测假定致病性肠道黏附性大肠杆菌的DNA杂交和聚合酶链反应检测方法的比较
J Clin Microbiol. 2002 Apr;40(4):1254-8. doi: 10.1128/JCM.40.4.1254-1258.2002.
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Direct detection and characterization of Shiga toxigenic Escherichia coli by multiplex PCR for stx1, stx2, eae, ehxA, and saa.通过针对stx1、stx2、eae、ehxA和saa的多重PCR直接检测和鉴定产志贺毒素大肠杆菌
J Clin Microbiol. 2002 Jan;40(1):271-4. doi: 10.1128/JCM.40.1.271-274.2002.
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