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对具有编码一种尿路致病性特异性蛋白基因的尿路致病性大肠杆菌染色体中一个假定毒力岛的特征分析。

Characterization of a putative virulence island in the chromosome of uropathogenic Escherichia coli possessing a gene encoding a uropathogenic-specific protein.

作者信息

Kurazono H, Yamamoto S, Nakano M, Nair G B, Terai A, Chaicumpa W, Hayashi H

机构信息

Department of Medical Technology, School of Health Sciences, Okayama University, 2-5-1 Shikata-cho, Okayama, 700-8558, Japan.

出版信息

Microb Pathog. 2000 Mar;28(3):183-9. doi: 10.1006/mpat.1999.0331.

Abstract

This study was initiated to search for a homologue of the Vibrio cholerae zot gene in uropathogenic Escherichia coli (UPEC) using a specific DNA probe. The faint signal obtained at low stringency with some UPEC strains associated with prostatitis cases prompted us to examine UPEC strains by PCR using primers designed from the conserved regions of the proteins of the Zot group of putative NTPases containing the classical NTP binding motif. This led to the discovery of a DNA fragment in UPEC strains which hybridized with a probe designed from the PCR. Further analysis of this DNA fragment revealed an ORF which was designated as uropathogenic specific protein (Usp). The gene encoding Usp was 1038 bp long and codes for 346 amino acids with an appropriate SD sequence. Upstream and downstream analysis of usp revealed motifs of prokaryotic consensus promoters and three small ORFs with SDs and ribosome binding sites transcribed in the same direction of usp. The proximity of these set of genes in a specific area of the bacterial chromosome resembling a block of genes preferentially associated with UPEC coupled with the presence of a motif matching that of a Tn3 transposon family lead us to believe that this could be an hitherto unknown pathogenicity island.

摘要

本研究旨在使用特异性DNA探针在尿路致病性大肠杆菌(UPEC)中寻找霍乱弧菌zot基因的同源物。在低严谨度条件下,一些与前列腺炎病例相关的UPEC菌株获得了微弱信号,这促使我们使用根据含有经典NTP结合基序的假定NTP酶Zot组蛋白保守区域设计的引物,通过PCR检测UPEC菌株。这导致在UPEC菌株中发现了一个与根据PCR设计的探针杂交的DNA片段。对该DNA片段的进一步分析揭示了一个开放阅读框,被命名为尿路致病性特异性蛋白(Usp)。编码Usp的基因长1038 bp,编码346个氨基酸,并带有合适的SD序列。对usp的上下游分析揭示了原核共有启动子的基序以及三个带有SD序列和核糖体结合位点的小开放阅读框,它们与usp转录方向相同。这组基因在细菌染色体的特定区域紧密相邻,类似于一组优先与UPEC相关的基因,再加上存在与Tn3转座子家族基序匹配的基序,使我们相信这可能是一个迄今未知的致病岛。

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