Rosch Jason W, Mann Beth, Thornton Justin, Sublett Jack, Tuomanen Elaine
Department of Infectious Diseases, St. Jude Children's Research Hospital, 332 N. Lauderdale, Memphis, TN 38105, USA.
Infect Immun. 2008 Jul;76(7):3187-96. doi: 10.1128/IAI.00054-08. Epub 2008 Apr 28.
The rlrA pilus locus of Streptococcus pneumoniae is an example of a pathogenicity island acquired through genetic recombination. Many acquired genetic elements commandeer preexisting networks of the new organism for transcriptional regulation. We hypothesized that the rlrA locus has integrated into transcriptional regulatory networks controlling expression of virulence factors important in adhesion and invasion. To test this hypothesis, we determined the impact on pilus expression of known regulators controlling adherence, including the two-component systems CbpR/S and HK/RR03 and the transcriptional regulators of divalent cation transporters MerR and PsaR in vitro and in vivo. It was determined that the pilus locus is down-regulated by preexisting networks designed for adhesion and cation transport/response and that its regulation occurs through RlrA. The pilus locus was found to participate in invasion specifically restricted to lung epithelial cells in vitro. While expression of pili had only a small effect on virulence with an intranasal infection model, pili were critically important with an intratracheal infection model. Thus, expression of pili appears to have become integrated into the regulatory circuits for lung-specific invasion by pneumococci.
肺炎链球菌的rlrA菌毛基因座是通过基因重组获得的致病岛的一个例子。许多获得的遗传元件会征用新生物体中预先存在的网络进行转录调控。我们假设rlrA基因座已整合到控制对黏附和侵袭很重要的毒力因子表达的转录调控网络中。为了验证这一假设,我们在体外和体内确定了已知的控制黏附的调节因子对菌毛表达的影响,这些调节因子包括双组分系统CbpR/S和HK/RR03以及二价阳离子转运体的转录调节因子MerR和PsaR。结果确定,菌毛基因座被为黏附和阳离子转运/反应设计的预先存在的网络下调,并且其调节通过RlrA发生。发现菌毛基因座在体外参与了专门局限于肺上皮细胞的侵袭。虽然在鼻内感染模型中菌毛的表达对毒力只有很小的影响,但在气管内感染模型中菌毛至关重要。因此,菌毛的表达似乎已整合到肺炎链球菌肺特异性侵袭的调节回路中。