Blehert David S, Palmer Robert J, Xavier Joao B, Almeida Jonas S, Kolenbrander Paul E
Oral Infection and Immunity Branch, National Institute of Dental and Craniofacial Research, National Institutes of Health, Bethesda, Maryland 20892, USA.
J Bacteriol. 2003 Aug;185(16):4851-60. doi: 10.1128/JB.185.16.4851-4860.2003.
The luxS gene, present in many bacterial genera, encodes the autoinducer 2 (AI-2) synthase. AI-2 has been implicated in bacterial signaling, and this study investigated its role in biofilm formation by Streptococcus gordonii, an organism that colonizes human tooth enamel within the first few hours after professional cleaning. Northern blotting and primer extension analyses revealed that S. gordonii luxS is monocistronic. AI-2 production was dependent on nutritional conditions, and maximum AI-2 induction was detected when S. gordonii was grown in the presence of serum and carbonate. In planktonic cultures, AI-2 production rose sharply during the transition from exponential to stationary phase, and the AI-2 concentration peaked approximately 4 h into stationary phase. An S. gordonii luxS mutant that did not produce AI-2 was constructed by homologous recombination. Complementation of the mutant by insertion of an intact luxS gene into the chromosome in tandem with the disrupted gene restored AI-2 production to a level similar to that of the wild-type strain. In planktonic culture, no growth differences were observed between the mutant and wild-type strains when five different media were used. However, when grown for 4 h as biofilms in 25% human saliva under flow, the luxS mutant formed tall microcolonies that differed from those formed by the wild-type and complemented mutant strains. Biofilms of the luxS mutant exhibited finger-like projections of cells that extended into the flow cell lumen. Thus, the inability to produce AI-2 is associated with altered microcolony architecture within S. gordonii biofilms formed in saliva during a time frame consistent with initial colonization of freshly cleaned enamel surfaces.
许多细菌属中都存在的luxS基因编码自诱导物2(AI-2)合酶。AI-2与细菌信号传导有关,本研究调查了其在戈登链球菌生物膜形成中的作用,戈登链球菌是一种在专业清洁后的最初几个小时内定植于人类牙釉质的微生物。Northern印迹和引物延伸分析表明,戈登链球菌luxS是单顺反子。AI-2的产生取决于营养条件,当戈登链球菌在血清和碳酸盐存在的情况下生长时,检测到最大的AI-2诱导。在浮游培养中,AI-2的产生在从指数生长期到稳定期的转变过程中急剧上升,并且AI-2浓度在稳定期约4小时达到峰值。通过同源重组构建了不产生AI-2的戈登链球菌luxS突变体。通过将完整的luxS基因与 disrupted 基因串联插入染色体来补充突变体,可将AI-2的产生恢复到与野生型菌株相似的水平。在浮游培养中,当使用五种不同培养基时,未观察到突变体和野生型菌株之间的生长差异。然而,当在流动条件下于25%的人唾液中作为生物膜生长4小时时,luxS突变体形成了高大的微菌落,这与野生型和互补突变体菌株形成的微菌落不同。luxS突变体的生物膜表现出延伸到流动池腔中的指状细胞突起。因此,在与新清洁的牙釉质表面初始定植一致的时间范围内,无法产生AI-2与在唾液中形成的戈登链球菌生物膜内微菌落结构的改变有关。