Song Xin-Ming, Connor Wayne, Hokamp Karsten, Babiuk Lorne A, Potter Andrew A
Vaccine and Infectious Disease Organization (VIDO), University of Saskatchewan, 120 Veterinary Road, Saskatoon, Saskatchewan, S7N 5E3 Canada.
Microb Pathog. 2009 Jan;46(1):28-35. doi: 10.1016/j.micpath.2008.10.006. Epub 2008 Oct 17.
The two-component system TCS08 of Streptococcus pneumoniae contributes to the virulence in vivo and regulates phosphotransferase system (PTS) genes in an avirulent strain. However, its role in pathogenic strains and virulence mechanism are largely unknown. In this study, we constructed TCS08 knockout mutants in a serotype 4 encapsulated pathogenic strain TIGR4, and investigated target genes regulated by TCS08 through transcriptional profile analysis. Compared to TIGR4, expression of the rlrA islet genes (SP0461-SP0468) encoding pneumococcal pili was found to be up-regulated in the rr08 mutant (Deltarr08). Further quantitative real-time PCR (qRT-PCR) analysis revealed that such induction was more significant when the strains were grown to late-logarithmic phase. In phenotype analyses, disruption of both hk08 and rr08 genes (DeltaTCS08) resulted in increased adherence to human lung epithelial cells (A549) at 3 h at late-logarithmic and stationary phases. However, the invasion level of DeltaTCS08 was reduced at different growth phases. Similar phenotype changes, though less significant, were also observed when the assays were performed on human nasopharyngeal epithelial cells (Detroit 562). These data suggest that TCS08 is involved in adhesion and invasion of host epithelial cells, which is likely mediated via regulation of the pilus locus genes in a growth phase-dependent manner.
肺炎链球菌的双组分系统TCS08有助于体内毒力,并在无毒力菌株中调节磷酸转移酶系统(PTS)基因。然而,其在致病菌株中的作用和毒力机制在很大程度上尚不清楚。在本研究中,我们在4型荚膜致病菌株TIGR4中构建了TCS08基因敲除突变体,并通过转录谱分析研究了TCS08调控的靶基因。与TIGR4相比,发现编码肺炎球菌菌毛的rlrA胰岛基因(SP0461-SP0468)在rr08突变体(Deltarr08)中的表达上调。进一步的定量实时PCR(qRT-PCR)分析表明,当菌株生长到对数后期时,这种诱导作用更为显著。在表型分析中,hk08和rr08基因(DeltaTCS08)的破坏导致在对数后期和稳定期3小时时对人肺上皮细胞(A549)的粘附增加。然而,DeltaTCS08在不同生长阶段的侵袭水平降低。当在人鼻咽上皮细胞(Detroit 562)上进行检测时,也观察到了类似的表型变化,尽管不太明显。这些数据表明,TCS08参与宿主上皮细胞的粘附和侵袭,这可能是通过以生长阶段依赖的方式调节菌毛基因座基因介导的。