Nickerson C A, Curtiss R
Department of Biology, Washington University, St. Louis, Missouri 63130, USA.
Infect Immun. 1997 May;65(5):1814-23. doi: 10.1128/iai.65.5.1814-1823.1997.
The sigma factor RpoS mediates the stationary-phase expression of a large group of genes, including those involved in resistance to a variety of environmental stresses, such as starvation, oxidation, and low pH. In addition, RpoS has been shown to regulate Salmonella virulence. In Salmonella typhimurium, RpoS controls the expression of the Salmonella plasmid virulence (spv) genes, which are required for systemic infection. However, the mechanism by which RpoS affects the pathogenicity of Salmonella remains incompletely defined. In this study, we focused on the ability of rpoS to affect the early stages of the infection process of S. typhimurium. An rpoS mutant of S. typhimurium exhibited wild-type abilities to attach to and invade Int-407 cells and J774 macrophage-like cells. In addition, rpoS did not affect the intracellular survival of S. typhimurium in either J774 macrophage-like cells or rat bone marrow-derived macrophages. However, the rpoS mutant demonstrated a decreased ability to colonize murine Peyer's patches after oral inoculation than its wild-type virulent parent strain showed. In addition, virulence plasmid-cured derivatives of the rpoS mutant were recovered in lower numbers from murine Peyer's patches than were plasmid-cured derivatives of the isogenic wild-type S. typhimurium. This indicates that RpoS regulation of chromosomally encoded genes is important for colonization of the gut-associated lymphoid tissue (GALT) by S. typhimurium. Microscopic analysis of histological sections taken from Peyer's patches after peroral infection of mice showed that, unlike its wild-type virulent parent strain, the isogenic rpoS mutant did not destroy the follicle-associated epithelium of the GALT. Furthermore, the rpoS mutant demonstrated a decreased ability to adhere to histological sections of murine Peyer's patches than its wild-type parent showed. Our data provide evidence for a role of RpoS in the interaction of Salmonella with cells of the GALT, specifically the Peyer's patches. This implicates the involvement of rpoS in the initial stages of systemic infection by Salmonella as opposed to infection leading to gastroenteritis.
σ因子RpoS介导一大组基因的稳定期表达,这些基因包括那些参与抵抗多种环境压力的基因,如饥饿、氧化和低pH值。此外,RpoS已被证明可调节沙门氏菌的毒力。在鼠伤寒沙门氏菌中,RpoS控制沙门氏菌质粒毒力(spv)基因的表达,这些基因是全身感染所必需的。然而,RpoS影响沙门氏菌致病性的机制仍未完全明确。在本研究中,我们重点关注rpoS影响鼠伤寒沙门氏菌感染过程早期阶段的能力。鼠伤寒沙门氏菌的rpoS突变体在附着和侵入Int-407细胞及J774巨噬细胞样细胞方面表现出野生型能力。此外,rpoS对鼠伤寒沙门氏菌在J774巨噬细胞样细胞或大鼠骨髓来源巨噬细胞中的细胞内存活没有影响。然而,与野生型有毒亲本菌株相比,rpoS突变体经口服接种后在小鼠派伊尔结中定殖的能力下降。此外,从鼠派伊尔结中回收的rpoS突变体的毒力质粒治愈衍生物数量比同基因野生型鼠伤寒沙门氏菌的质粒治愈衍生物少。这表明RpoS对染色体编码基因的调控对于鼠伤寒沙门氏菌在肠道相关淋巴组织(GALT)中的定殖很重要。对经口感染小鼠后取自派伊尔结的组织切片进行显微镜分析表明,与其野生型有毒亲本菌株不同,同基因rpoS突变体不会破坏GALT的滤泡相关上皮。此外,与野生型亲本相比,rpoS突变体附着于小鼠派伊尔结组织切片的能力下降。我们的数据为RpoS在沙门氏菌与GALT细胞(特别是派伊尔结)相互作用中的作用提供了证据。这意味着rpoS参与沙门氏菌全身感染的初始阶段,而不是导致肠胃炎的感染。