Vriesema A J, Dankert J, Zaat S A
Department of Medical Microbiology, Academic Medical Center, 1105 AZ Amsterdam, The Netherlands.
Infect Immun. 2000 Mar;68(3):1061-8. doi: 10.1128/IAI.68.3.1061-1068.2000.
Viridans group streptococci (VS) from the oral cavity entering the bloodstream may initiate infective endocarditis (IE). We aimed to identify genes expressed in response to a pH increase from slightly acidic (pH 6.2) to neutral (pH 7.3) as encountered by VS entering the bloodstream from the oral cavity. Using a recently developed promoter-screening vector, we isolated five promoter fragments from the genomic DNA of Streptococcus gordonii CH1 responding to this stimulus. No common regulatory sequences were identified in these promoter fragments that could account for the coordinate expression of the corresponding genes. One of the isolated fragments contained the promoter region and 5' end of a gene highly homologous to the methionine sulfoxide reductase gene (msrA) of various bacterial and eukaryotic species. This gene has been found to be activated in S. gordonii strain V288 in a rabbit model of IE (A. O. Kiliç, M. C. Herzberg, M. W. Meyer, X. Zhao, and L. Tao, Plasmid 42:67-72, 1999). We isolated and characterized the msrA gene of S. gordonii CH1 and constructed a chromosomal insertion mutant. This mutant was more sensitive to hydrogen peroxide, suggesting a role for the streptococcal MsrA in protecting against oxidative stress. Moreover, MsrA appeared to be important for the growth of S. gordonii CH1 under aerobic and anaerobic conditions. Both these properties of MsrA may contribute to the ability of S. gordonii to cause IE.
来自口腔的草绿色链球菌(VS)进入血液循环可能引发感染性心内膜炎(IE)。我们旨在鉴定VS从口腔进入血液循环时,因pH值从微酸性(pH 6.2)升高到中性(pH 7.3)而表达的基因。使用最近开发的启动子筛选载体,我们从戈登链球菌CH1的基因组DNA中分离出五个响应此刺激的启动子片段。在这些启动子片段中未鉴定出可解释相应基因协同表达的共同调控序列。其中一个分离片段包含一个与各种细菌和真核生物的甲硫氨酸亚砜还原酶基因(msrA)高度同源的基因的启动子区域和5'端。已发现该基因在IE兔模型中的戈登链球菌V288菌株中被激活(A. O. Kiliç、M. C. Herzberg、M. W. Meyer、X. Zhao和L. Tao,《质粒》42:67 - 72,1999)。我们分离并鉴定了戈登链球菌CH1的msrA基因,并构建了一个染色体插入突变体。该突变体对过氧化氢更敏感,表明链球菌MsrA在抵抗氧化应激中起作用。此外,MsrA似乎对戈登链球菌CH1在有氧和无氧条件下的生长很重要。MsrA的这两个特性可能都有助于戈登链球菌引起IE的能力。