Kowalko J E, Sebert M E
Department of Pediatrics, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania 19104, USA.
Infect Immun. 2008 Jul;76(7):3131-40. doi: 10.1128/IAI.01696-07. Epub 2008 Apr 28.
The Streptococcus pneumoniae ComDE two-component signaling system controls the development of genetic competence in the bacterium and affects virulence in models of pneumonia and bacteremia. We have investigated the impact of the competence pathway during colonization of the nasopharynx, the principal ecological niche of the pneumococcus. Previous work showed that deletion of the pneumococcal CiaRH signaling system inhibited colonization and increased expression of genes required for competence. We anticipated that signaling by the competence pathway might similarly reduce carriage. Consistent with this expectation, a comE deletion that blocked transformation increased colonization fitness such that the mutant outcompeted the wild type in an infant rat model of asymptomatic carriage. Deletion of comD-immediately upstream of comE and likewise required for competence-similarly increased colonization fitness if the orientation of the antibiotic resistance cassette inserted into the comD locus was such that it reduced transcription of comE. However, an alternative comD deletion mutation that caused an increase in comE transcription impaired colonization instead. Activation of the competence system through a comE(D143Y) mutation did not affect colonization, but an inability to secrete the competence-stimulating peptide due to deletion of comAB produced a density-dependent reduction in colonization fitness. These results suggest a model in which signaling by the unactivated form of ComE reduces colonization fitness compared to that of bacteria in which it is either activated or absent entirely, with the most substantial fitness gain accompanying deletion of comE. This observation demonstrates that the pneumococcus incurs a substantial fitness cost in order to retain a functional competence regulatory system.
肺炎链球菌的ComDE双组分信号系统控制着该细菌遗传感受态的发展,并影响肺炎和菌血症模型中的毒力。我们研究了感受态途径在肺炎链球菌主要生态位——鼻咽部定殖过程中的影响。先前的研究表明,肺炎链球菌CiaRH信号系统的缺失会抑制定殖,并增加感受态所需基因的表达。我们预计感受态途径的信号传导可能同样会减少携带。与这一预期一致的是,阻断转化的comE缺失增加了定殖适应性,使得该突变体在无症状携带的幼鼠模型中比野生型更具竞争力。如果插入comD基因座的抗生素抗性盒的方向使得其减少comE的转录,那么紧接在comE上游且同样是感受态所必需的comD缺失同样会增加定殖适应性。然而,另一种导致comE转录增加的comD缺失突变反而损害了定殖。通过comE(D143Y)突变激活感受态系统并不影响定殖,但由于comAB缺失而无法分泌感受态刺激肽会导致定殖适应性呈密度依赖性降低。这些结果提示了一种模型,即与ComE未激活形式进行信号传导的细菌相比,ComE激活形式或完全缺失ComE的细菌定殖适应性降低,其中comE缺失带来的适应性增加最为显著。这一观察结果表明,肺炎链球菌为了保留功能性的感受态调节系统会付出巨大的适应性代价。