首页> 外文期刊>Microbial Pathogenesis >Vibrio cholerae cytolysin is essential for high enterotoxicity and apoptosis induction produced by a cholera toxin gene-negative V. cholerae non-O1, non-O139 strain
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Vibrio cholerae cytolysin is essential for high enterotoxicity and apoptosis induction produced by a cholera toxin gene-negative V. cholerae non-O1, non-O139 strain

机译:霍乱弧菌溶血素对霍乱毒素基因阴性霍乱弧菌非O1,非O139菌株产生的高肠毒性和诱导细胞凋亡至关重要

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Cholera toxin (CT) gene-negative Vibrio cholerae non-O1, non-O139 strains may cause severe diarrhea though their pathogenic mechanism remains unclear. V. cholerae cytolysin (VCC) is a pore-forming exotoxin encoded in the hlyA gene of V. cholerae whose contribution to the pathogenesis is not fully understood. In this work, the virulence properties of a CT gene-negative V. cholerae non-O1, non-O139 strain causing a cholera-like syndrome were analyzed. Inoculation of rabbit ileal loops with the wild type strain induced extensive fluid accumulation, accompanied by severe histopathological damage characterized by villus shortening, lymphangiectasia and focal areas of necrosis. These pathogenic effects were abrogated by mutation of the hlyA gene thus pointing out the main role of VCC in the virulence of the strain. Interestingly, this toxin was capable of triggering apoptosis in human intestinal cell lines due to its anion channel activity. Moreover, the wild type strain also induced increased apoptosis of the intestinal epithelium cells which was not observed upon inoculation of the VCC null mutant strain, indicating that VCC may trigger apoptotic cell death during infection in vivo. Altogether, these results support a main role of VCC in the pathogenesis of the CT gene-negative V. cholerae non-O1, non-O139 strain and identify apoptosis as a previously unrecognized cell death pathway triggered by VCC.
机译:霍乱毒素(CT)基因阴性的霍乱弧菌非O1,非O139菌株可能引起严重腹泻,尽管其致病机理尚不清楚。霍乱弧菌溶细胞素(VCC)是霍乱弧菌hlyA基因中编码的成孔外毒素,其对发病机理的作用尚不完全清楚。在这项工作中,分析了导致霍乱样综合征的CT基因阴性霍乱弧菌非O1,非O139毒株的毒力特性。用野生型菌株接种兔回肠loop会引起大量积液,并伴有以绒毛缩短,淋巴管扩张和坏死灶性区域为特征的严重组织病理学损害。 hlyA基因的突变消除了这些致病作用,从而指出了VCC在菌株毒力中的主要作用。有趣的是,这种毒素由于其阴离子通道活性而能够触发人肠道细胞凋亡。此外,野生型菌株还诱导了肠上皮细胞凋亡的增加,这在接种VCC无效突变菌株后未观察到,表明VCC可能在体内感染期间触发凋亡性细胞死亡。总之,这些结果支持了VCC在CT基因阴性霍乱弧菌非O1,非O139菌株的发病机理中的主要作用,并将细胞凋亡鉴定为由VCC触发的先前无法识别的细胞死亡途径。

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