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产肠毒素脆弱拟杆菌脆弱溶素致病性岛的分子特征

Molecular characterization of the fragilysin pathogenicity islet of enterotoxigenic Bacteroides fragilis.

作者信息

Moncrief J S, Duncan A J, Wright R L, Barroso L A, Wilkins T D

机构信息

Department of Biochemistry, Fralin Center for Biotechnology, Virginia Polytechnic Institute and State University, Blacksburg 24061-0346, USA.

出版信息

Infect Immun. 1998 Apr;66(4):1735-9. doi: 10.1128/IAI.66.4.1735-1739.1998.

Abstract

Enterotoxigenic strains of Bacteroides fragilis produce an extracellular metalloprotease toxin (termed fragilysin) which is cytopathic to intestinal epithelial cells and induces fluid secretion and tissue damage in ligated intestinal loops. We report here that the fragilysin gene is contained within a small genetic element termed the fragilysin pathogenicity islet. The pathogenicity islet of B. fragilis VPI 13784 was defined as 6,033 bp in length and contained nearly perfect 12-bp direct repeats near its ends. Sequencing across the ends of the pathogenicity islet from two additional enterotoxigenic strains, along with PCR analysis of 20 additional enterotoxigenic strains, revealed that the islet is inserted at a specific site on the B. fragilis chromosome. The site of integration in three nontoxigenic strains contained a 17-bp GC-rich sequence which was not present in toxigenic strains and may represent a target sequence for chromosomal integration. In addition to the fragilysin gene, we identified an open reading frame encoding a predicted protein with a size and structural features similar to those of fragilysin. The deduced amino acid sequence was 28.5% identical and 56.3% similar to fragilysin and contained a nearly identical zinc-binding motif and methionine-turn region.

摘要

脆弱拟杆菌的产肠毒素菌株可产生一种细胞外金属蛋白酶毒素(称为脆弱溶素),该毒素对肠上皮细胞具有细胞病变作用,并可在结扎的肠袢中诱导液体分泌和组织损伤。我们在此报告,脆弱溶素基因包含在一个称为脆弱溶素致病岛的小遗传元件中。脆弱拟杆菌VPI 13784的致病岛长度为6033 bp,在其末端附近含有近乎完美的12 bp直接重复序列。对另外两个产肠毒素菌株的致病岛末端进行测序,并对另外20个产肠毒素菌株进行PCR分析,结果表明该致病岛插入在脆弱拟杆菌染色体的一个特定位点上。三个非产毒素菌株中的整合位点含有一个17 bp的富含GC的序列,该序列在产毒素菌株中不存在,可能代表染色体整合的靶序列。除了脆弱溶素基因外,我们还鉴定了一个开放阅读框,其编码的预测蛋白在大小和结构特征上与脆弱溶素相似。推导的氨基酸序列与脆弱溶素的同一性为28.5%,相似性为56.3%,并含有一个几乎相同的锌结合基序和甲硫氨酸转折区。

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