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首页> 外文期刊>Journal of Clinical Microbiology >Identification, Characterization, and Distribution of a Shiga Toxin 1 Gene Variant (stx1c) in Escherichia coli Strains Isolated from Humans
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Identification, Characterization, and Distribution of a Shiga Toxin 1 Gene Variant (stx1c) in Escherichia coli Strains Isolated from Humans

机译:志贺毒素1基因变异(stx1c)的分离,鉴定和分布在人类分离的大肠杆菌菌株中。

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By using sequence analysis of Shiga toxin 1 (Stx 1) genes from human and ovine Stx-producing Escherichia coli (STEC) strains, we identified an Stx1 variant in STEC of human origin that was identical to the Stx1 variant from ovine STEC, but demonstrated only 97.1 and 96.6% amino acid sequence identity in its A and B subunits, respectively, to the Stx1 encoded by bacteriophage 933J. We designated this variant “Stx1c” and developed stxB1 restriction fragment length polymorphism and stx1c-specific PCR strategies to determine the frequency and distribution of stx1c among 212 STEC strains isolated from humans. stx1c was identified in 36 (17.0%) of 212 STEC strains, 19 of which originated from asymptomatic subjects and 16 of which were from patients with uncomplicated diarrhea. stx1c was most frequently (in 23 STEC strains [63.9%]) associated with stx2d, but 12 (33.3%) of the 36 STEC strains possessed stx1c only. A single STEC strain possessed stx1c together with stx2 and was isolated from a patient with hemolytic-uremic syndrome. All 36 stx1c-positive STEC strains were eae negative and belonged to 10 different serogroups, none of which was O157, O26, O103, O111, or O145. Stx1c was produced by all stx1c-containing STEC strains, but reacted weakly with a commercial immunoassay. We conclude that STEC strains harboring the stx1c variant account for a significant proportion of human STEC isolates. The procedures developed in this study now allow the determination of the frequency of STEC strains harboring stx1c among clinical STEC isolates and their association with human disease in prospective studies.
机译:通过使用人类和绵羊产Stx的大肠杆菌(STEC)菌株的志贺毒素1(Stx 1)基因的序列分析,我们在人源STEC中鉴定出与Stx1相同的Stx1变体变体来自绵羊STEC,但在其A和B亚基中分别仅表现出与噬菌体933J编码的Stx1相同的97.1和96.6%氨基酸序列同一性。我们将此变体命名为“ Stx1c”,并开发了 stxB 1 限制性片段长度多态性和 stx 1c 特异性PCR策略确定 stx 1c 在从人类分离的212株STEC菌株中的频率和分布。在212株STEC菌株中,有36株(17.0%)被鉴定为 stx 1c ,其中19株来自无症状受试者,其中16株来自无并发症腹泻患者。 stx 1c stx 2d 相关的频率最高(在23个STEC菌株[63.9%]中),但12 36个STEC菌株中(33.3%)仅具有 stx 1c 。单个STEC菌株具有 stx 1c stx 2 ,并从溶血性尿毒症综合征患者中分离出来。所有36株 stx 1c 阳性STEC菌株均为 eae 阴性,并且属于10个不同的血清群,其中一个都不是O157,O26,O103,O111或O145。 Stx1c由所有包含 stx 1c 的STEC菌株产生,但与市售免疫测定反应较弱。我们得出的结论是,带有 stx 1c 变体的STEC菌株占人类STEC分离株的很大比例。本研究开发的程序现在可以确定前瞻性研究中临床STEC分离株中带有 stx 1c 的STEC菌株的频率及其与人类疾病的关系。

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