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粘质沙雷氏菌中 RssAB-FlhDC-ShlBA 作为主要的发病机制途径。

RssAB-FlhDC-ShlBA as a major pathogenesis pathway in Serratia marcescens.

机构信息

Department of Medical Biotechnology and Laboratory Science, Chang-Gung University, Kweishan, Taoyuan, Taiwan, Republic of China.

出版信息

Infect Immun. 2010 Nov;78(11):4870-81. doi: 10.1128/IAI.00661-10. Epub 2010 Aug 16.

Abstract

Serratia marcescens has long been recognized as an important opportunistic pathogen, but the underlying pathogenesis mechanism is not completely clear. Here, we report a key pathogenesis pathway in S. marcescens comprising the RssAB two-component system and its downstream elements, FlhDC and the dominant virulence factor hemolysin ShlBA. Expression of shlBA is under the positive control of FlhDC, which is repressed by RssAB signaling. At 37°C, functional RssAB inhibits swarming, represses hemolysin production, and promotes S. marcescens biofilm formation. In comparison, when rssBA is deleted, S. marcescens displays aberrant multicellularity favoring motile swarming with unbridled hemolysin production. Cellular and animal infection models further demonstrate that loss of rssBA transforms this opportunistic pathogen into hypervirulent phenotypes, leading to extensive inflammatory responses coupled with destructive and systemic infection. Hemolysin production is essential in this context. Collectively, a major virulence regulatory pathway is identified in S. marcescens.

摘要

粘质沙雷氏菌长期以来被认为是一种重要的机会致病菌,但潜在的发病机制尚不完全清楚。在这里,我们报告了粘质沙雷氏菌中的一个关键发病机制途径,该途径包括 RssAB 双组分系统及其下游元件 FlhDC 和主要毒力因子溶血素 ShlBA。shlBA 的表达受 FlhDC 的正调控,而受 RssAB 信号的抑制。在 37°C 下,功能正常的 RssAB 抑制群集运动,抑制溶血素的产生,并促进粘质沙雷氏菌生物膜的形成。相比之下,当 rssBA 缺失时,粘质沙雷氏菌表现出异常的多细胞性,有利于运动性的群集运动,且溶血素的产生不受控制。细胞和动物感染模型进一步表明,rssBA 的缺失使这种机会致病菌转变为高毒力表型,导致广泛的炎症反应,并伴有破坏性和全身性感染。在此情况下,溶血素的产生是必不可少的。总的来说,在粘质沙雷氏菌中确定了一条主要的毒力调控途径。

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