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大肠杆菌O3和O21 O抗原基因簇的特征分析及血清群特异性PCR检测方法的建立。

Characterization of Escherichia coli O3 and O21 O antigen gene clusters and development of serogroup-specific PCR assays.

作者信息

Ren Yi, Liu Bin, Cheng Jiansong, Liu Fenxia, Feng Lu, Wang Lei

机构信息

TEDA School of Biological Sciences and Biotechnology, Nankai University, 23 Hongda Street, TEDA, Tianjin 300457, China.

出版信息

J Microbiol Methods. 2008 Oct;75(2):329-34. doi: 10.1016/j.mimet.2008.07.010. Epub 2008 Jul 20.

Abstract

Escherichia coli O3 and O21 are associated with enteroaggregative E. coli (EAEC). EAEC strains are often non-typable using the routine agglutination method due to their aggregative phenotype. Typing of E. coli O3 and O21 may also be impeded by cross-reactions with O152 or O83. In this study, the O antigen gene clusters of E. coli O3 and O21 were characterized, and PCR assays based on O antigen specific genes wzx (encoding O unit flippase) and wzy (encoding O unit polymerase) from each strain were developed. By screening against all 186 known E. coli O serotypes, the PCR assays were shown to be highly specific to O3 and O21 respectively. The sensitivity of the assays was determined to be 1 pg per microl of chromosomal DNA and 2 CFU per 10 g of water samples. The PCR assays were also applied to 658 clinical E. coli isolates, and 100% of detection accuracy was obtained. The PCR assays developed here are suitable for the detection and identification of E. coli O3 and O21 strains in environmental and clinical samples.

摘要

大肠杆菌O3和O21与肠集聚性大肠杆菌(EAEC)有关。由于其集聚性表型,EAEC菌株通常无法使用常规凝集方法进行分型。大肠杆菌O3和O21的分型也可能因与O152或O83的交叉反应而受到阻碍。在本研究中,对大肠杆菌O3和O21的O抗原基因簇进行了表征,并基于每个菌株的O抗原特异性基因wzx(编码O单位翻转酶)和wzy(编码O单位聚合酶)开发了PCR检测方法。通过对所有186种已知大肠杆菌O血清型进行筛选,结果表明这些PCR检测方法分别对O3和O21具有高度特异性。检测方法的灵敏度确定为每微升染色体DNA 1 pg以及每10克水样2 CFU。这些PCR检测方法还应用于658株临床大肠杆菌分离株,获得了100%的检测准确率。此处开发的PCR检测方法适用于环境和临床样本中大肠杆菌O3和O21菌株的检测和鉴定。

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