Institute of Microbiology and Infection, University of Birmingham, Birmingham, United Kingdom.
Institute of Microbiology and Infection, University of Birmingham, Birmingham, United Kingdom
Infect Immun. 2018 Oct 25;86(11). doi: 10.1128/IAI.00829-17. Print 2018 Nov.
Mutations in σ-regulated lipoproteins have previously been shown to impact bacterial viability under conditions of stress and during infection. YraP is conserved across a number of Gram-negative pathogens, including , where the homolog is a component of the Bexsero meningococcal group B vaccine. Investigations using laboratory-adapted K-12 have shown that mutants have elevated sensitivity to a range of compounds, including detergents and normally ineffective antibiotics. In this study, we investigate the role of the outer membrane lipoprotein YraP in the pathogenesis of serovar Typhimurium. We show that mutations in Typhimurium result in a defective outer membrane barrier with elevated sensitivity to a range of compounds. This defect is associated with attenuated virulence in an oral infection model and during the early stages of systemic infection. We show that this attenuation is not a result of defects in lipopolysaccharide and O-antigen synthesis, changes in outer membrane protein levels, or the ability to adhere to and invade eukaryotic cell lines .
先前的研究表明,σ 调控脂蛋白中的突变会影响细菌在应激条件下和感染期间的生存能力。YraP 在许多革兰氏阴性病原体中都保守存在,包括 ,其同源物是 Bexsero 脑膜炎球菌 B 型疫苗的一个组成部分。使用实验室适应的 K-12 进行的研究表明, 突变体对一系列化合物(包括清洁剂和通常无效的抗生素)的敏感性升高。在这项研究中,我们研究了外膜脂蛋白 YraP 在 鼠伤寒血清型发病机制中的作用。我们表明, Typhimurium 中的突变导致外膜屏障缺陷,对一系列化合物的敏感性增加。这种缺陷与口服感染模型和全身感染早期阶段的毒力减弱有关。我们表明,这种衰减不是由于脂多糖和 O-抗原合成的缺陷、外膜蛋白水平的变化或粘附和侵袭真核细胞系的能力造成的。