Association between the effacing (eae) gene and the Shiga-like toxin-encoding genes in Escherichia coli isolates from cattle.

Association between the effacing (eae) gene and the Shiga-like toxin-encoding genes in Escherichia coli isolates from cattle.
复制标题

牛大肠杆菌中的擦除 (eae) 基因与志贺样毒素编码基因之间的关联。

DOI:
10.2460/ajvr.1993.54.07.1064
复制
发表时间:
1993
影响因子:
1
通讯作者:
P. Pohl
P. Pohl
中科院分区:
农林科学4区
文献类型:
--
作者:
J. Mainil;E. Jacquemin;A. Kaeckenbeeck;P. Pohl

文献摘要

被引文献

相似文献

用7种基因探针对296株从腹泻犊牛粪便或肠道中分离的大肠杆菌进行杂交。一个探针(eae探针)来自eae基因,该基因编码一种蛋白质,该蛋白质参与由称为附着和消除大肠杆菌(AEEC)的细菌群消除肠上皮细胞微绒毛,2个探针来自编码由verocytotoxic大肠杆菌(VTEC)产生的志贺样毒素(shiga-like toxins,SHG)1和2的基因。其他4个探针来自与肠粘附性大肠杆菌(EAEC)对培养细胞的粘附特性相关的DNA序列(EAF探针用于局部粘附模式,探针F1845和AIDA-1用于扩散粘附模式,以及Agg探针用于聚集粘附模式)。eae探针的杂交结果与先前发表的微绒毛消失的表型结果一致,除了8个分离株中的1个。后者以前被报道为隐去小牛肠上皮细胞的微绒毛,但eae探针阴性。两类分离物与eae探针杂交。第一类的成员(60个分离株)另外用1个或两个探针产生阳性信号(VTEC-AEEC分离株)。与eae和SLT 1探针杂交的分离株是最常见的:56株分离株(即所有VTEC-AEEC的93%)。第二类(10个分离株)的成员未能与任何一种荧光探针(非VTEC-AEEC分离株)杂交。(250字处删节)
Two hundred ninety-six Escherichia coli isolates from feces or intestines of calves with diarrhea were hybridized with 7 gene probes. One probe (the eae probe) was derived from the eae gene coding for a protein involved in the effacement of the enterocyte microvilli by the group of bacteria called attaching and effacing E coli (AEEC), and 2 probes were derived from genes coding for the Shiga-like toxins (SLT) 1 and 2 produced by the verocytotoxic E coli (VTEC). The other 4 probes were derived from DNA sequences associated with the adhesive properties of enteroadherent E coli (EAEC) to cultured cells (the EAF probe for the localized adherence pattern, probes F1845 and AIDA-1 for the diffuse adherence pattern, and the Agg probe for the aggregative adherence pattern). Hybridization results for the eae probe were in agreement, for all but 1 of the 8 isolates, with previously published phenotypic results of microvilli effacement. The latter was previously reported as effacing the microvilli of calf enterocytes, but was eae probe-negative. Two classes of isolates hybridized with the eae probe. Members of a first class (60 isolates) additionally produced a positive signal with 1 or both of the SLT probes (VTEC-AEEC isolates). Isolates hybridizing with the eae and the SLT1 probes were the most frequent: 56 isolates (ie, 93% of all VTEC-AEEC). Members of the second class (10 isolates) failed to hybridize with either SLT probe (non-VTEC-AEEC isolates).(ABSTRACT TRUNCATED AT 250 WORDS)