McKessar Stuart J, Hakenbeck Regine
Department of Microbiology, University of Kaiserslautern, Paul Ehrlich Strasse 23, D-67663 Kaiserslautern, Germany.
J Bacteriol. 2007 Feb;189(4):1342-50. doi: 10.1128/JB.01170-06. Epub 2006 Oct 6.
The two-component system TCS08 is one of the regulatory systems that is important for virulence of Streptococcus pneumoniae. In order to investigate the TCS08 regulon, we have analyzed transcription profiles of mutants derived from S. pneumoniae R6 by microarray analysis. Since deletion mutants are often without a significant phenotype, we constructed a mutation in the histidine kinase HK08, T133P, in analogy to the phosphatase mutation T230P in the H box of the S. pneumoniae CiaH kinase described recently (D. Zähner, K. Kaminski, M. van der Linden, T. Mascher, M. Merai, and R. Hakenbeck, J. Mol. Microbiol. Biotechnol. 4:211-216, 2002). In addition, a deletion mutation was constructed in rr08, encoding the cognate response regulator. The most heavily suppressed genes in the hk08 mutant were spr0276 to spr0282, encoding a putative cellobiose phosphoenolpyruvate sugar phosphotransferase system (PTS). Whereas the R6 Sm(r) parent strain and the Deltarr08 mutant readily grew on cellobiose, the hk08 mutant and selected mutants with deletions in the PTS cluster did not, strongly suggesting that TCS08 is involved in the catabolism of cellobiose. Homologues of the TCS08 system were found in closely related streptococci and other gram-positive cocci. However, the genes spr0276 to spr0282, encoding the putative cellobiose PTS, represent a genomic island in S. pneumoniae and homologues were found in Streptococcus gordonii only, suggesting that this system might contribute to the pathogenicity potential of the pneumococcus.
双组分系统TCS08是对肺炎链球菌毒力至关重要的调控系统之一。为了研究TCS08调控子,我们通过微阵列分析对源自肺炎链球菌R6的突变体的转录谱进行了分析。由于缺失突变体通常没有明显的表型,我们构建了组氨酸激酶HK08中的T133P突变,类似于最近描述的肺炎链球菌CiaH激酶H框中的磷酸酶突变T230P(D. 察纳、K. 卡明斯基、M. 范德林登、T. 马舍尔、M. 梅拉伊和R. 哈肯贝克,《分子微生物学与生物技术杂志》4:211 - 216,2002年)。此外,在编码同源应答调节因子的rr08中构建了缺失突变。hk08突变体中抑制最严重的基因是spr0276至spr0282,它们编码一种假定的纤维二糖磷酸烯醇丙酮酸糖磷酸转移酶系统(PTS)。虽然R6 Sm(r)亲本菌株和Deltarr08突变体能够在纤维二糖上轻松生长,但hk08突变体和PTS簇中具有缺失的选定突变体则不能,这强烈表明TCS08参与纤维二糖的分解代谢。在密切相关的链球菌和其他革兰氏阳性球菌中发现了TCS08系统的同源物。然而,编码假定的纤维二糖PTS的基因spr0276至spr0282是肺炎链球菌中的一个基因组岛,仅在戈登链球菌中发现了同源物,这表明该系统可能有助于肺炎球菌的致病潜力。