Sztajer Helena, Lemme André, Vilchez Ramiro, Schulz Stefan, Geffers Robert, Yip Cindy Ying Yin, Levesque Celine M, Cvitkovitch Dennis G, Wagner-Döbler Irene
Helmholtz-Center for Infection Research, Division of Cell Biology, Inhoffenstr. 7, D-38124 Braunschweig, Germany.
J Bacteriol. 2008 Jan;190(1):401-15. doi: 10.1128/JB.01086-07. Epub 2007 Nov 2.
Autoinducer 2 (AI-2) is the only species-nonspecific autoinducer known in bacteria and is produced by both gram-negative and gram-positive organisms. Consequently, it is proposed to function as a universal quorum-sensing signal for interaction between bacterial species. AI-2 is produced as the by-product of a metabolic transformation carried out by the LuxS enzyme. To separate the metabolic function of the LuxS enzyme from the signaling role of AI-2, we carried out a global transcriptome analysis of a luxS null mutant culture of Streptococcus mutans UA159, an important cariogenic bacterium and a crucial component of the dental plaque biofilm community, in comparison to a luxS null mutant culture supplemented with chemically pure 4,5-dihydroxy-2,3-pentanedione, the precursor of AI-2. The data revealed fundamental changes in gene expression affecting 585 genes (30% of the genome) which could not be restored by the signal molecule AI-2 and are therefore not caused by quorum sensing but by lack of the transformation carried out by the LuxS enzyme in the activated methyl cycle. All functional classes of enzymes were affected, including genes known to be important for biofilm formation, bacteriocin synthesis, competence, and acid tolerance. At the same time, 59 genes were identified whose transcription clearly responded to the addition of AI-2. Some of them were related to protein synthesis, stress, and cell division. Three membrane transport proteins were upregulated which are not related to any of the known AI-2 transporters. Three transcription factors were identified whose transcription was stimulated repeatedly by AI-2 addition during growth. Finally, a global regulatory protein, the delta subunit of the RNA polymerase (rpoE), was induced 147-fold by AI-2, representing the largest differential gene expression observed. The data show that many phenotypes related to the luxS mutation cannot be ascribed to quorum sensing and have identified for the first time regulatory proteins potentially mediating AI-2-based signaling in gram-positive bacteria.
自诱导物2(AI-2)是细菌中已知的唯一一种不依赖物种的自诱导物,革兰氏阴性菌和革兰氏阳性菌均可产生。因此,有人提出它作为一种通用的群体感应信号,用于细菌物种间的相互作用。AI-2是LuxS酶进行代谢转化的副产物。为了将LuxS酶的代谢功能与AI-2的信号传导作用区分开来,我们对变形链球菌UA159(一种重要的致龋菌,也是牙菌斑生物膜群落的关键组成部分)的luxS基因缺失突变体培养物进行了全转录组分析,并与添加了化学纯的4,5-二羟基-2,3-戊二酮(AI-2的前体)的luxS基因缺失突变体培养物进行比较。数据显示,基因表达发生了根本性变化,影响了585个基因(占基因组的30%),这些变化无法被信号分子AI-2恢复,因此不是由群体感应引起的,而是由LuxS酶在活化甲基循环中进行的转化缺失导致的。所有功能类别的酶都受到了影响,包括已知对生物膜形成、细菌素合成、感受态和耐酸性很重要的基因。同时,鉴定出59个基因,其转录明显对AI-2的添加有反应。其中一些与蛋白质合成、应激和细胞分裂有关。三种膜转运蛋白被上调,它们与任何已知的AI-2转运蛋白均无关。鉴定出三种转录因子,其转录在生长过程中因添加AI-2而反复受到刺激。最后,一种全局调节蛋白,RNA聚合酶的δ亚基(rpoE),被AI-2诱导了147倍,这是观察到的最大差异基因表达。数据表明,许多与luxS突变相关的表型不能归因于群体感应,并且首次鉴定出了可能介导革兰氏阳性菌中基于AI-2的信号传导的调节蛋白。