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Glucose-Dependent Activation of Bacillus anthracis Toxin Gene Expression and Virulence Requires the Carbon Catabolite Protein CcpA

机译:炭疽芽孢杆菌毒素基因表达和毒力的葡萄糖依赖性激活需要碳分解代谢蛋白CcpA。

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摘要

Sensing environmental conditions is an essential aspect of bacterial physiology and virulence. In Bacillus anthracis, the causative agent of anthrax, transcription of the two major virulence factors, toxin and capsule, is triggered by bicarbonate, a major compound in the mammalian body. Here it is shown that glucose is an additional signaling molecule recognized by B. anthracis for toxin synthesis. The presence of glucose increased the expression of the protective antigen toxin component-encoding gene (pagA) by stimulating induction of transcription of the AtxA virulence transcription factor. Induction of atxA transcription by glucose required the carbon catabolite protein CcpA via an indirect mechanism. CcpA did not bind specifically to any region of the extended atxA promoter. The virulence of a B. anthracis strain from which the ccpA gene was deleted was significantly attenuated in a mouse model of infection. The data demonstrated that glucose is an important host environment-derived signaling molecule and that CcpA is a molecular link between environmental sensing and B. anthracis pathogenesis.
机译:感知环境条件是细菌生理和毒力的重要方面。在炭疽杆菌中,炭疽是哺乳动物体内的一种主要化合物,它是炭疽的病原体,是两个主要毒力因子(毒素和荚膜)的转录。此处显示葡萄糖是炭疽芽孢杆菌识别的用于毒素合成的另一种信号分子。葡萄糖的存在通过刺激AtxA毒力转录因子的转录诱导而增加了保护性抗原毒素成分编码基因(pagA)的表达。葡萄糖诱导的atxA转录需要通过间接机制的碳分解代谢蛋白CcpA。 CcpA没有特异性结合扩展atxA启动子的任何区域。在感染的小鼠模型中,删除了ccpA基因的炭疽芽孢杆菌菌株的毒力显着减弱。数据表明,葡萄糖是宿主环境中重要的信号分子,CcpA是环境感知与炭疽芽孢杆菌发病机理之间的分子联系。

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