Wu Youcong, Wu Yang, Zhu Tao, Han Haiyan, Liu Huayong, Xu Tao, Francois Patrice, Fischer Adrien, Bai Li, Götz Friedrich, Qu Di
Key Laboratory of Medical Molecular Virology of Ministries of Education and Health, Institute of Medical Microbiology and Institutes of Biomedical Sciences, Shanghai Medical College of Fudan University, Shanghai, China Integrated Laboratory of Pathogenic Biology, College of Preclinical Medicine, Dali University, Dali, China.
Key Laboratory of Medical Molecular Virology of Ministries of Education and Health, Institute of Medical Microbiology and Institutes of Biomedical Sciences, Shanghai Medical College of Fudan University, Shanghai, China.
J Bacteriol. 2015 Feb;197(3):459-76. doi: 10.1128/JB.02231-14. Epub 2014 Nov 17.
SrrAB expression in Staphylococcus epidermidis strain 1457 (SE1457) was upregulated during a shift from oxic to microaerobic conditions. An srrA deletion (ΔsrrA) mutant was constructed for studying the regulatory function of SrrAB. The deletion resulted in retarded growth and abolished biofilm formation both in vitro and in vivo and under both oxic and microaerobic conditions. Associated with the reduced biofilm formation, the ΔsrrA mutant produced much less polysaccharide intercellular adhesion (PIA) and showed decreased initial adherence capacity. Microarray analysis showed that the srrA mutation affected transcription of 230 genes under microaerobic conditions, and 51 genes under oxic conditions. Quantitative real-time PCR confirmed this observation and showed downregulation of genes involved in maintaining the electron transport chain by supporting cytochrome and quinol-oxidase assembly (e.g., qoxB and ctaA) and in anaerobic metabolism (e.g., pflBA and nrdD). In the ΔsrrA mutant, the expression of the biofilm formation-related gene icaR was upregulated under oxic conditions and downregulated under microaerobic conditions, whereas icaA was downregulated under both conditions. An electrophoretic mobility shift assay further revealed that phosphorylated SrrA bound to the promoter regions of icaR, icaA, qoxB, and pflBA, as well as its own promoter region. These findings demonstrate that in S. epidermidis SrrAB is an autoregulator and regulates biofilm formation in an ica-dependent manner. Under oxic conditions, SrrAB modulates electron transport chain activity by positively regulating qoxBACD transcription. Under microaerobic conditions, it regulates fermentation processes and DNA synthesis by modulating the expression of both the pfl operon and nrdDG.
在表皮葡萄球菌1457菌株(SE1457)中,从有氧条件转变为微需氧条件时,SrrAB的表达上调。构建了一个srrA缺失(ΔsrrA)突变体用于研究SrrAB的调控功能。该缺失导致体外和体内以及有氧和微需氧条件下的生长迟缓以及生物膜形成被消除。与生物膜形成减少相关,ΔsrrA突变体产生的胞间多糖黏附素(PIA)少得多,并且初始黏附能力降低。微阵列分析表明,srrA突变在微需氧条件下影响230个基因的转录,在有氧条件下影响51个基因的转录。定量实时PCR证实了这一观察结果,并显示参与通过支持细胞色素和喹啉氧化酶组装来维持电子传递链的基因(例如qoxB和ctaA)以及参与厌氧代谢的基因(例如pflBA和nrdD)下调。在ΔsrrA突变体中,生物膜形成相关基因icaR的表达在有氧条件下上调,在微需氧条件下下调,而icaA在两种条件下均下调。电泳迁移率变动分析进一步表明,磷酸化的SrrA与icaR、icaA、qoxB和pflBA的启动子区域以及其自身的启动子区域结合。这些发现表明,在表皮葡萄球菌中,SrrAB是一种自调节因子,并以ica依赖性方式调节生物膜形成。在有氧条件下,SrrAB通过正向调节qoxBACD转录来调节电子传递链活性。在微需氧条件下,它通过调节pfl操纵子和nrdDG的表达来调节发酵过程和DNA合成。