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通过自动化5'核酸酶聚合酶链反应检测和鉴定产志贺毒素大肠杆菌

Detection and characterization of verocytotoxin-producing Escherichia coli by automated 5' nuclease PCR assay.

作者信息

Nielsen Eva Møller, Andersen Marianne Thorup

机构信息

Danish Veterinary Institute, Copenhagen, Denmark.

出版信息

J Clin Microbiol. 2003 Jul;41(7):2884-93. doi: 10.1128/JCM.41.7.2884-2893.2003.

Abstract

In recent years increased attention has been focused on infections caused by isolates of verocytotoxin-producing Escherichia coli (VTEC) serotypes other than O157. These non-O157 VTEC isolates are commonly present in food and food production animals. Easy detection, isolation, and characterization of non-O157 VTEC isolates are essential for improving our knowledge of these organisms. In the present study, we detected VTEC isolates in bovine fecal samples by a duplex 5' nuclease PCR assay (real-time PCR) that targets vtx1 and vtx2. VTEC isolates were obtained by colony replication by use of hydrophobic-grid membrane filters and DNA probe hybridization. Furthermore, we have developed 5' nuclease PCR assays for the detection of virulence factors typically present in VTEC isolates, including subtypes of three genes of the locus of enterocyte effacement (LEE) pathogenicity island. The 22 assays included assays for the detection of verocytotoxin genes (vtx1, vtx2), pO157-associated genes (ehxA, katP, espP, and etpD), a recently identified adhesin (saa), intimin (eae, all variants), seven subtypes of eae, four subtypes of tir, and three subtypes of espD. A number of reference strains (VTEC and enteropathogenic E. coli strains) and VTEC strains isolated from calves were tested to validate the PCR assays. The expected virulence profiles were detected for all reference strains. In addition, new information on the subtypes of LEE genes was obtained. For reference strains as well as bovine isolates, a consistent relationship between subtypes of the LEE genes was found, so that a total of seven different combinations of these were recognized (corresponding to the seven subtypes of eae). Isolates with 15 different serogroup-virulence profiles were isolated from 16 calves. Among these, 53% harbored LEE and 73% harbored factors carried by the large virulence plasmid. One LEE-negative isolate had the gene for the adhesin Saa. The most common virulence profile among the bovine isolates was vtx1, eae-zeta, tir-alpha, ehxA, and espP. This panel of assays offers an easy method for the extensive characterization of VTEC isolates.

摘要

近年来,人们越来越关注由产志贺毒素大肠杆菌(VTEC)O157以外血清型的分离株引起的感染。这些非O157 VTEC分离株常见于食品和食用动物中。对非O157 VTEC分离株进行简便的检测、分离和鉴定对于增进我们对这些微生物的了解至关重要。在本研究中,我们通过针对vtx1和vtx2的双重5'核酸酶PCR检测法(实时PCR)检测牛粪便样本中的VTEC分离株。利用疏水网格膜过滤器通过菌落复制和DNA探针杂交获得VTEC分离株。此外,我们还开发了5'核酸酶PCR检测法,用于检测VTEC分离株中通常存在的毒力因子,包括肠细胞脱落位点(LEE)致病岛三个基因的亚型。这22种检测方法包括检测志贺毒素基因(vtx1、vtx2)、pO157相关基因(ehxA、katP、espP和etpD)、一种最近鉴定的黏附素(saa)、紧密黏附素(eae,所有变体)、eae的七个亚型、tir的四个亚型以及espD的三个亚型。对许多参考菌株(VTEC和肠致病性大肠杆菌菌株)以及从犊牛分离的VTEC菌株进行检测以验证PCR检测方法。所有参考菌株均检测到预期的毒力谱。此外,还获得了关于LEE基因亚型的新信息。对于参考菌株和牛分离株,发现LEE基因亚型之间存在一致的关系,因此总共识别出七种不同的组合(对应于eae的七个亚型)。从16头犊牛中分离出具有15种不同血清群 - 毒力谱的分离株。其中,53%携带LEE,73%携带大毒力质粒携带的因子。一株LEE阴性分离株具有黏附素Saa基因。牛分离株中最常见的毒力谱是vtx1、eae - ζ、tir - α、ehxA和espP。这组检测方法为广泛鉴定VTEC分离株提供了一种简便方法。

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