Hendriksen Wouter T, Silva Nuno, Bootsma Hester J, Blue Clare E, Paterson Gavin K, Kerr Alison R, de Jong Anne, Kuipers Oscar P, Hermans Peter W M, Mitchell Tim J
Department of Pediatrics, Erasmus MC-Sophia Children's Hospital, Rotterdam, The Netherlands.
J Bacteriol. 2007 Feb;189(4):1382-9. doi: 10.1128/JB.01144-06. Epub 2006 Nov 3.
Recent murine studies have demonstrated that the role of response regulator 09 (RR09) of Streptococcus pneumoniae in virulence is different in different strains. In the present study, we used a murine pneumonia model of infection to assess the virulence of a TIGR4 rr09 mutant, and we found that TIGR4Deltarr09 was attenuated after intranasal infection. Furthermore, we investigated the in vitro transcriptional changes in pneumococcal rr09 mutants of two strains, D39 and TIGR4, by microarray analysis. The transcriptional profiles of the rr09 mutants of both strains had clear differences compared to the profiles of the parental wild-type strains. In D39Deltarr09, but not in TIGR4Deltarr09, genes involved in competence (e.g., comAB) were upregulated. In TIGR4, genes located on the rlrA pathogenicity islet, which are not present in the D39 genome, appeared to be regulated by RR09. Furthermore, several phosphotransferase systems (PTSs) believed to be involved in sugar uptake (e.g., the PTS encoded by sp0060 to sp0066) were strongly downregulated in D39Deltarr09, while they were not regulated by RR09 in TIGR4. To examine the role of one of these PTSs in virulence, D39Deltasp0063 was constructed and tested in a murine infection model. No difference between the virulence of this strain and the virulence of the wild type was found, indicating that downregulation of the sp0063 gene alone is not the cause of the avirulent phenotype of D39Deltarr09. Finally, expression of rr09 and expression of three of our identified RR09 targets during infection in mice were assessed. This in vivo experiment confirmed that there were differences between expression in wild-type strain TIGR4 and expression in the rr09 mutant, as well as differences between expression in wild-type strain D39 and expression in wild-type strain TIGR4. In conclusion, our results indicate that there is strain-specific regulation of pneumococcal gene expression by RR09.
近期的小鼠研究表明,肺炎链球菌应答调节因子09(RR09)在不同菌株中的毒力作用有所不同。在本研究中,我们使用小鼠肺炎感染模型来评估TIGR4 rr09突变体的毒力,发现鼻内感染后TIGR4Deltarr09的毒力减弱。此外,我们通过微阵列分析研究了两株菌株D39和TIGR4的肺炎链球菌rr09突变体的体外转录变化。与亲本野生型菌株的转录谱相比,两株rr09突变体的转录谱有明显差异。在D39Deltarr09中,但不在TIGR4Deltarr09中,参与感受态的基因(如comAB)上调。在TIGR4中,位于rlrA致病岛的基因(D39基因组中不存在)似乎受RR09调控。此外,几个被认为参与糖摄取的磷酸转移酶系统(PTSs)(如由sp0060至sp0066编码的PTS)在D39Deltarr09中强烈下调,而在TIGR4中不受RR09调控。为了研究其中一个PTS在毒力中的作用,构建了D39Deltasp0063并在小鼠感染模型中进行测试。未发现该菌株的毒力与野生型毒力之间存在差异,这表明单独下调sp0063基因不是D39Deltarr09无毒表型的原因。最后,评估了rr09的表达以及我们鉴定的RR09的三个靶标在小鼠感染过程中的表达。这项体内实验证实,野生型菌株TIGR4与rr09突变体中的表达之间存在差异,以及野生型菌株D39与野生型菌株TIGR4中的表达之间存在差异。总之,我们的结果表明RR09对肺炎链球菌基因表达存在菌株特异性调控。