Ren Yi, Liu Bin, Cheng Jiansong, Liu Fenxia, Feng Lu, Wang Lei
TEDA School of Biological Sciences and Biotechnology, Nankai University, 23 Hongda Street, TEDA, Tianjin 300457, China.
J Microbiol Methods. 2008 Oct;75(2):329-34. doi: 10.1016/j.mimet.2008.07.010. Epub 2008 Jul 20.
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.
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。