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从动物、食品和人类中分离出的大肠杆菌中2型志贺毒素变体的鉴定与特性分析。

Identification and characterization of Shiga toxin type 2 variants in Escherichia coli isolates from animals, food, and humans.

作者信息

Zheng Jie, Cui Shenghui, Teel Louise D, Zhao Shaohua, Singh Ruby, O'Brien Alison D, Meng Jianghong

机构信息

Department of Nutrition and Food Science, 0112 Skinner Building, University of Maryland, College Park, MD 20742, USA.

出版信息

Appl Environ Microbiol. 2008 Sep;74(18):5645-52. doi: 10.1128/AEM.00503-08. Epub 2008 Jul 25.

Abstract

There is considerable heterogeneity among the Shiga toxin type 2 (Stx2) toxins elaborated by Shiga toxin-producing Escherichia coli (STEC). One such Stx2 variant, the Stx2d mucus-activatable toxin (Stx2dact), is rendered more toxic by the action of elastase present in intestinal mucus, which cleaves the last two amino acids of the A2 portion of the toxin A subunit. We screened 153 STEC isolates from food, animals, and humans for the gene encoding Stx2dact by using a novel one-step PCR procedure. This method targeted the region of stx(2dact) that encodes the elastase recognition site. The presence of stx(2dact) was confirmed by DNA sequencing of the complete toxin genes. Seven STEC isolates from cows (four isolates), meat (two isolates), and a human (one isolate) that carried the putative stx(2dact) gene were identified; all were eae negative, and none was the O157:H7 serotype. Three of the isolates (CVM9322, CVM9557, and CVM9584) also carried stx(1), two (P1332 and P1334) carried stx(1) and stx(2c), and one (CL-15) carried stx(2c). One isolate, P1130, harbored only stx(2dact). The Vero cell cytotoxicities of supernatants from P1130 and stx(1) deletion mutants of CVM9322, CVM9557, and CVM9584 were increased 13- to 30-fold after treatment with porcine elastase. Thus, Stx2dact-producing strains, as detected by our one-step PCR method, can be isolated not only from humans, as previously documented, but also from food and animals. The latter finding has important public health implications based on a recent report from Europe of a link between disease severity and infection with STEC isolates that produce Stx2dact.

摘要

产志贺毒素大肠杆菌(STEC)产生的2型志贺毒素(Stx2)毒素之间存在相当大的异质性。其中一种Stx2变体,即Stx2d黏液激活毒素(Stx2dact),在肠道黏液中存在的弹性蛋白酶作用下毒性增强,该酶可切割毒素A亚基A2部分的最后两个氨基酸。我们使用一种新颖的一步PCR程序,从食品、动物和人类中筛选了153株STEC分离株,以检测编码Stx2dact的基因。该方法针对stx(2dact)中编码弹性蛋白酶识别位点的区域。通过对完整毒素基因进行DNA测序,确认了stx(2dact)的存在。鉴定出7株携带假定stx(2dact)基因的STEC分离株,分别来自奶牛(4株)、肉类(2株)和一名人类(1株);所有分离株eae均为阴性,且均非O157:H7血清型。其中3株分离株(CVM9322、CVM9557和CVM9584)还携带stx(1),2株(P1332和P1334)携带stx(1)和stx(2c),1株(CL-15)携带stx(2c)。1株分离株P1130仅携带stx(2dact)。用猪弹性蛋白酶处理后,P1130以及CVM9322、CVM9557和CVM9584的stx(1)缺失突变体的上清液对Vero细胞的细胞毒性增加了13至30倍。因此,通过我们的一步PCR方法检测到的产Stx2dact菌株,不仅如先前文献记载的那样可从人类中分离得到,也可从食品和动物中分离得到。基于欧洲最近一份关于疾病严重程度与产Stx2dact的STEC分离株感染之间联系的报告,后一发现具有重要的公共卫生意义。

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