Qin Aiping, Scott David W, Mann Barbara J
Department of Medicine, University of Virginia, Charlottesville, VA 22908, USA.
Infect Immun. 2008 Jul;76(7):3086-92. doi: 10.1128/IAI.00363-08. Epub 2008 May 5.
Francisella tularensis subsp. tularensis is a highly virulent bacterium that is a CDC select agent. Despite advancements in the understanding of its biology, details pertaining to virulence are poorly understood. In previous work, we identified a transposon insertion mutant in the FTT0107c locus that was defective in intracellular survival in HepG2 and J77A.1 cells. Here, we report that this mutant was also highly attenuated in vivo. The FTT0107c locus is predicted to encode an ortholog of the disulfide bond formation B protein (DsbB). This designation was confirmed by complementation of an Escherichia coli dsbB mutant. This dsbB mutant of Schu S4 was highly attenuated in mice, but unlike what has been reported for Francisella novicida, intranasal immunization with a sublethal dose did not induce protection against wild-type challenge. dsbB was found to be transcribed in an operon with acrA and acrB, which encode an RND-type efflux pump. However, this pump did not make a significant contribution to virulence because strains with nonpolar deletions in acrA and acrB behaved like wild-type strain Schu S4 with respect to intracellular growth and in vivo virulence. This result is in contrast to a report that an acrB mutant of a live vaccine strain of F. tularensis has decreased virulence in mice. Overall, these results demonstrate key differences between the virulence requirements of Schu S4 and less virulent subspecies of Francisella. We have shown that DsbB is a key participant in intracellular growth and virulence, and our results suggest that there are critical virulence factors that contain disulfide bonds.
土拉热弗朗西斯菌土拉热亚种是一种剧毒细菌,属于美国疾病控制与预防中心的特定病原体。尽管对其生物学特性的认识有所进展,但关于其毒力的细节仍知之甚少。在之前的研究中,我们在FTT0107c位点鉴定出一个转座子插入突变体,该突变体在HepG2和J77A.1细胞内的存活存在缺陷。在此,我们报告该突变体在体内也高度减毒。FTT0107c位点预计编码二硫键形成B蛋白(DsbB)的直系同源物。通过对大肠杆菌dsbB突变体的互补作用证实了这一命名。Schu S4的这个dsbB突变体在小鼠中高度减毒,但与新凶手弗朗西斯菌的报道不同,用亚致死剂量进行鼻内免疫并未诱导对野生型攻击的保护作用。发现dsbB与acrA和acrB在一个操纵子中转录,acrA和acrB编码一种RND型外排泵。然而,该泵对毒力没有显著贡献,因为在acrA和acrB中存在非极性缺失的菌株在细胞内生长和体内毒力方面表现得与野生型菌株Schu S4相似。这一结果与一份关于土拉热弗朗西斯菌活疫苗株的acrB突变体在小鼠中毒力降低的报告形成对比。总体而言,这些结果表明Schu S4与弗朗西斯菌毒力较低的亚种在毒力需求上存在关键差异。我们已经表明DsbB是细胞内生长和毒力的关键参与者,我们的结果表明存在含有二硫键的关键毒力因子。