Department of Microbiology, University of Texas Southwestern Medical Center, Dallas, TX 75390-9048, USA.
J Infect Dis. 2011 Jun 15;203(12):1859-65. doi: 10.1093/infdis/jir190.
Haemophilus ducreyi 35000HP contains a homolog of the CpxRA 2-component signal transduction system, which controls the cell envelope stress response system in other gram-negative bacteria and regulates some important H. ducreyi virulence factors. A H. ducreyi cpxR mutant was compared with its parent for virulence in the human challenge model of experimental chancroid. The pustule formation rate in 5 volunteers was 33% (95% confidence interval [CI], 1.3%-65.3%) at 15 parent sites and 40% (95% CI, 18.1%-61.9%) at 15 mutant sites (P = .35). Thus, the cpxR mutant was not attenuated for virulence. Inactivation of the H. ducreyi cpxR gene did not reduce the ability of this mutant to express certain proven virulence factors, including the DsrA serum resistance protein and the LspA2 protein, which inhibits phagocytosis. These results expand our understanding of the involvement of the CpxRA system in regulating virulence expression in H. ducreyi.
杜克雷嗜血杆菌 35000HP 含有与 CpxRA 双组分信号转导系统的同源物,该系统控制其他革兰氏阴性菌的细胞包膜应激反应系统,并调节一些重要的杜克雷嗜血杆菌毒力因子。将杜克雷嗜血杆菌 cpxR 突变体与其亲本在实验性软下疳的人体挑战模型中进行了毒力比较。在 5 名志愿者的 15 个亲本部位,脓疱形成率为 33%(95%置信区间[CI],1.3%-65.3%),在 15 个突变部位为 40%(95%CI,18.1%-61.9%)(P =.35)。因此,cpxR 突变体的毒力没有减弱。CpxRA 基因的失活并未降低该突变体表达某些已证实的毒力因子的能力,包括 DsrA 血清抵抗蛋白和抑制吞噬作用的 LspA2 蛋白。这些结果扩展了我们对 CpxRA 系统在调节杜克雷嗜血杆菌毒力表达中的参与的理解。