Standish Alistair J, Stroeher Uwe H, Paton James C
Australian Bacterial Pathogenesis Program, School of Molecular and Biomedical Science, University of Adelaide, Adelaide SA 5005, Australia.
Proc Natl Acad Sci U S A. 2005 May 24;102(21):7701-6. doi: 10.1073/pnas.0409377102. Epub 2005 May 16.
Streptococcus pneumoniae encounters a number of environmental niches in the body, including the nasopharynx, lungs, blood, middle ear, and brain. Recent studies have identified 13 putative two-component signal-transduction systems in S. pneumoniae, which are likely to be important for gene regulation in response to external stimuli. Here, we present conclusive evidence for the regulation of choline binding protein A (CbpA), a major pneumococcal virulence factor and protective antigen, by one of these two-component signal-transduction systems. We have demonstrated divergent expression of cbpA in unmarked hk06 and rr06 deletion mutants relative to wild-type S. pneumoniae D39 by using Western immunoblotting and real-time RT-PCR. Electrophoretic mobility-shift and solid-phase binding assays have demonstrated the binding of RR06 to the promoter region of cbpA, suggesting that RR06/HK06 directly regulates cbpA transcription. We have also shown that this system is important for the ability of the pneumococcus to adhere to epithelial cells in vitro and to survive and proliferate in an in vivo mouse model. Thus, the RR06/HK06 system has a significant role in pathogenesis, both in colonization and invasive disease.
肺炎链球菌在体内会遇到多种环境微生态位,包括鼻咽部、肺部、血液、中耳和大脑。最近的研究在肺炎链球菌中鉴定出13个假定的双组分信号转导系统,这些系统可能对响应外部刺激的基因调控很重要。在此,我们提供了确凿证据,证明其中一个双组分信号转导系统对胆碱结合蛋白A(CbpA)具有调控作用,CbpA是一种主要的肺炎球菌毒力因子和保护性抗原。通过蛋白质免疫印迹法和实时逆转录-聚合酶链反应,我们已证明在无标记的hk06和rr06缺失突变体中,相对于野生型肺炎链球菌D39,cbpA呈现出不同的表达。电泳迁移率变动分析和固相结合试验已证明RR06与cbpA的启动子区域结合,这表明RR06/HK06直接调控cbpA转录。我们还表明,该系统对于肺炎球菌在体外黏附上皮细胞以及在体内小鼠模型中存活和增殖的能力很重要。因此,RR06/HK06系统在定植和侵袭性疾病的发病机制中均具有重要作用。