Bhattacharyya Shalmoli, Shant Jasleen, Ganguly Nirmal K, Majumdar Siddhartha, Ghosh Sujata
Department of Biophysics, Panjab University, Chandigarh, India.
Curr Microbiol. 2008 Jan;56(1):98-103. doi: 10.1007/s00284-007-9048-x. Epub 2007 Nov 8.
Certain species of Vibrio cholerae have evolved mechanisms to become pathogenic to humans, with the potential to cause a severe life-threatening diarrheal disease, cholera. Cholera can emerge as explosive outbreaks in the human population. V. cholerae illness is produced primarily through the expression of a potent toxin (cholera toxin) within the human intestine. The present study has been carried out on a novel toxin purified from V. cholerae W07, an epidemic cholera strain devoid of cholera toxin gene (ctx). A modified method of purification improved purification fold as well as yield of this toxin. Heating was found to be the essential and sufficient condition for dissociation of the two subunits (58 kDa and 40 kDa) of this toxin (pI 5.2). The 40-kDa subunit of the purified toxin was identified as the carbohydrate binding subunit. This toxin was found to induce apoptosis in HEp-2 cells. Thus, the WO7 toxin seems to have potential importance in the pathogenesis of disease associated with Vibrio cholerae WO7.
某些霍乱弧菌菌株已经进化出对人类致病的机制,有可能引发一种严重的、危及生命的腹泻疾病——霍乱。霍乱可能会在人群中爆发。霍乱弧菌疾病主要是通过在人体肠道内表达一种强效毒素(霍乱毒素)而产生的。本研究针对从霍乱弧菌W07(一种不含霍乱毒素基因(ctx)的霍乱流行菌株)中纯化出的一种新型毒素展开。一种改良的纯化方法提高了这种毒素的纯化倍数和产量。研究发现加热是使该毒素(pI 5.2)的两个亚基(58 kDa和40 kDa)解离的必要且充分条件。纯化毒素的40 kDa亚基被鉴定为碳水化合物结合亚基。该毒素被发现可诱导HEp - 2细胞凋亡。因此,W07毒素似乎在与霍乱弧菌W07相关疾病的发病机制中具有潜在重要性。