细菌中碳代谢与毒力的关系。

Contributions to microbiology Pub Date : 2009-01-01 Epub Date: 2009-06-02 DOI:10.1159/000219374
Sandrine Poncet, Eliane Milohanic, Alain Mazé, Jamila Nait Abdallah, Francine Aké, Mireille Larribe, Ala-Eddine Deghmane, Muhamed-Kheir Taha, Marie Dozot, Xavier De Bolle, Jean Jacques Letesson, Josef Deutscher
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引用次数: 129

摘要

细菌已经发展出几种机制,当这些有机体暴露于混合碳源时,它们可以优先利用最有效代谢的碳水化合物。有趣的是,一些病原体使用相同或类似的机制来控制其感染过程的各个步骤。碳源的有效代谢可能是适当适应的信号。或者,特定碳源的存在可能向细菌细胞表明,它们在与感染相关的器官、组织或细胞中茁壮成长,并且应该打开或关闭特定的毒力基因。通常,毒力基因调控因子受到碳源可用性变化的影响。例如,编码化脓性链球菌毒力调节因子Mga的基因表达受厚壁菌中经典的碳分解代谢抑制(CCR)机制控制。PrfA是单核增生李斯特菌的主要毒力调节因子,其活性似乎受磷酸转移酶系统(PTS)组分的磷酸化状态控制。在霍乱弧菌中,调节运动所需基因表达的HapR的合成通过Crp/cAMP CCR机制来控制,而在致病性岛中抑制基因的肠沙门氏菌HilE的合成则由糖反应性的pts控制的Mlc来调节。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Correlations between carbon metabolism and virulence in bacteria.

Bacteria have developed several mechanisms which allow the preferred utilization of the most efficiently metabolizable carbohydrates when these organisms are exposed to a mixture of carbon sources. Interestingly, the same or similar mechanisms are used by some pathogens to control various steps of their infection process. The efficient metabolism of a carbon source might serve as signal for proper fitness. Alternatively, the presence of a specific carbon source might indicate to bacterial cells that they thrive in infection-related organs, tissues or cells and that specific virulence genes should be turned on or switched off. Frequently, virulence gene regulators are affected by changes in carbon source availability. For example, expression of the gene encoding the Streptococcus pyogenes virulence regulator Mga is controlled by the classical carbon catabolite repression (CCR) mechanism operative in Firmicutes. The activity of PrfA, the major virulence regulator in Listeria monocytogenes, seems to be controlled by the phosphorylation state of phosphotransferase system(PTS) components. In Vibrio cholerae synthesis of HapR, which regulates the expression of genes required for motility, is controlled via the Crp/cAMP CCR mechanism, whereas synthesis of Salmonella enterica HilE, which represses genes in a pathogenicity island, is regulated by the carbohydrate-responsive, PTS-controlled Mlc.

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