Perry J A, Lévesque C M, Suntharaligam P, Mair R W, Bu M, Cline R T, Peterson S N, Cvitkovitch D G
Dental Research Institute, Faculty of Dentistry, University of Toronto, Toronto, Ontario, Canada.
Lett Appl Microbiol. 2008 Nov;47(5):439-44. doi: 10.1111/j.1472-765X.2008.02455.x.
To identify the genes regulated by RR11, the regulator of the Streptococcus mutans HK/RR11 two-component system.
The S. mutans RR11-encoding gene was inactivated, and the effects of gene disruption on the cell's ability to form biofilms under stresses and acquire extracellular DNA were tested. Biofilm was reduced in cells lacking RR11 following exposure to oxidative stress. RR11-defective cells showed approx. 20-fold reduction in transformation efficiency. Microarray used to decipher the RR11-regulated genes in biofilm showed that approx. 5% of the UA159 genome underwent a significant change in expression. RR11 was found to regulate 174 genes, including genes involved in competence, stress-response and cell division.
Target genes controlled by RR11during biofilm growth have been identified by a comparison of transcriptional profiles between an RR11 defective mutant and the parental strain. The results demonstrated that RR11 is involved in the control of diverse cellular processes, including the formation of biofilm under oxidative stress and development of genetic competence.
The regulator of HK/RR11 system controls a large regulon and is an important regulator involved in stress response during S. mutans biofilm growth enabling the survival and persistence of its progeny in the microbial community.
鉴定变形链球菌HK/RR11双组分系统的调控因子RR11所调控的基因。
使变形链球菌RR11编码基因失活,并测试基因破坏对细胞在应激条件下形成生物膜以及获取细胞外DNA能力的影响。暴露于氧化应激后,缺乏RR11的细胞中生物膜减少。RR11缺陷型细胞的转化效率降低了约20倍。用于解读生物膜中RR11调控基因的微阵列显示,约5%的UA159基因组表达发生了显著变化。发现RR11调控174个基因,包括参与感受态、应激反应和细胞分裂的基因。
通过比较RR11缺陷型突变体和亲本菌株之间的转录谱,确定了RR11在生物膜生长过程中控制的靶基因。结果表明,RR11参与多种细胞过程的调控,包括氧化应激下生物膜的形成和遗传感受态的发展。
HK/RR11系统的调控因子控制着一个大的调控子,是变形链球菌生物膜生长过程中参与应激反应的重要调控因子,使其后代能够在微生物群落中存活和持续存在。