Churchward Gordon
Department of Microbiology and Immunology, Emory University, Atlanta, GA 30322, USA.
Mol Microbiol. 2007 Apr;64(1):34-41. doi: 10.1111/j.1365-2958.2007.05649.x.
The group A streptococcus (GAS) causes a variety of human diseases, including toxic shock syndrome and necrotizing fasciitis, which are both associated with significant mortality. Even the superficial self-limiting diseases caused by GAS, such as pharyngitis, impose a significant economic burden on society. GAS can cause a wide spectrum of diseases because it elaborates virulence factors that enable it to spread and survive in different environmental niches within the human host. The production of many of these virulence factors is directly controlled by the activity of the CovR/S two-component regulatory system. CovS acts in one direction as a kinase primarily to activate the response regulator CovR and repress the expression of major virulence factors and in the other direction as a phosphatase to permit gene expression in response to environmental changes that mimic conditions found during human infection. This Janus-like behaviour of the CovR/S system is recapitulated in the binding of CovR to the promoters that it directly regulates. Interactions between different faces of the CovR DNA binding domain appear to depend upon DNA sequence, leading to the potential for differential regulation of virulence gene expression.
A群链球菌(GAS)可引发多种人类疾病,包括中毒性休克综合征和坏死性筋膜炎,这两种疾病均与高死亡率相关。即便由GAS引起的如咽炎这类表面上自限性的疾病,也给社会带来了巨大的经济负担。GAS能够引发广泛的疾病,因为它能产生毒力因子,使其能够在人类宿主内的不同生态位中传播和存活。许多这些毒力因子的产生直接受CovR/S双组分调节系统活性的控制。CovS一方面作为激酶主要激活应答调节因子CovR并抑制主要毒力因子的表达,另一方面作为磷酸酶允许基因表达以响应模拟人类感染期间发现的条件的环境变化。CovR/S系统这种两面神似的行为在CovR与其直接调控的启动子的结合中得以体现。CovR DNA结合结构域不同面之间的相互作用似乎取决于DNA序列,从而导致毒力基因表达存在差异调节的可能性。