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霍乱弧菌细胞毒素对于霍乱毒素基因阴性的霍乱弧菌非O1、非O139菌株产生的高肠毒性和诱导细胞凋亡至关重要。

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.

作者信息

Saka Hector Alex, Bidinost Carla, Sola Claudia, Carranza Pablo, Collino Cesar, Ortiz Susana, Echenique Jose Ricardo, Bocco José Luis

机构信息

Departamento de Bioquímica Clínica, Facultad de Ciencias Químicas, Universidad Nacional de Córdoba, Centro de Investigaciones en Bioquímica e Inmunología ClBICI-CONICET, Córdoba, Argentina.

出版信息

Microb Pathog. 2008 Feb;44(2):118-28. doi: 10.1016/j.micpath.2007.08.013. Epub 2007 Aug 31.

Abstract

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.

摘要

霍乱毒素(CT)基因阴性的霍乱弧菌非O1、非O139菌株可能会导致严重腹泻,但其致病机制尚不清楚。霍乱弧菌溶细胞素(VCC)是一种由霍乱弧菌hlyA基因编码的成孔外毒素,其对发病机制的作用尚未完全明确。在本研究中,对一株引起霍乱样综合征的CT基因阴性霍乱弧菌非O1、非O139菌株的毒力特性进行了分析。用野生型菌株接种兔回肠袢可诱导大量液体蓄积,并伴有严重的组织病理学损伤,其特征为绒毛缩短、淋巴管扩张和局灶性坏死区域。hlyA基因突变消除了这些致病作用,从而指出VCC在该菌株毒力中的主要作用。有趣的是,由于其阴离子通道活性,这种毒素能够在人肠道细胞系中引发细胞凋亡。此外,野生型菌株还诱导肠上皮细胞凋亡增加,而接种VCC缺失突变株时未观察到这种现象,这表明VCC可能在体内感染过程中触发凋亡性细胞死亡。总之,这些结果支持VCC在CT基因阴性霍乱弧菌非O1、非O139菌株发病机制中的主要作用,并确定细胞凋亡是由VCC触发的一种先前未被认识的细胞死亡途径。

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