Robbe-Saule Véronique, Algorta Gabriela, Rouilhac Isabelle, Norel Françoise
Unité de Génétique des Bactéries Intracellulaires, Institut Pasteur, 75724 Paris Cedex 15, France.
Appl Environ Microbiol. 2003 Aug;69(8):4352-8. doi: 10.1128/AEM.69.8.4352-4358.2003.
The stationary-phase-inducible sigma factor, sigma(S) (RpoS), is the master regulator of the general stress response in Salmonella and is required for virulence in mice. rpoS mutants can frequently be isolated from highly passaged laboratory strains of Salmonella: We examined the rpoS status of 116 human clinical isolates of Salmonella, including 41 Salmonella enterica serotype Typhi strains isolated from blood, 38 S. enterica serotype Typhimurium strains isolated from blood, and 37 Salmonella serotype Typhimurium strains isolated from feces. We examined the abilities of these strains to produce the sigma(S) protein, to express RpoS-dependent catalase activity, and to resist to oxidative stress in the stationary phase of growth. We also carried out complementation experiments with a cloned wild-type rpoS gene. Our results showed that 15 of the 41 Salmonella serotype Typhi isolates were defective in RpoS. We sequenced the rpoS allele of 12 strains. This led to identification of small insertions, deletions, and point mutations resulting in premature stop codons or affecting regions 1 and 2 of sigma(S), showing that the rpoS mutations are not clonal. Thus, mutant rpoS alleles can be found in freshly isolated clinical strains of Salmonella serotype Typhi, and they may affect virulence properties. Interestingly however, no rpoS mutants were found among the 75 Salmonella serotype Typhimurium isolates. Strains that differed in catalase activity and resistance to hydrogen peroxide were found, but the differences were not linked to the rpoS status. This suggests that Salmonella serotype Typhimurium rpoS mutants are counterselected because rpoS plays a role in the pathogenesis of Salmonella serotype Typhimurium in humans or in the transmission cycle of the disease.
静止期诱导型σ因子σ(S)(RpoS)是沙门氏菌一般应激反应的主要调节因子,也是小鼠致病力所必需的。rpoS突变体常常可从高度传代的沙门氏菌实验室菌株中分离得到:我们检测了116株人类临床分离的沙门氏菌的rpoS状态,包括从血液中分离的41株肠炎沙门氏菌伤寒血清型菌株、从血液中分离的38株肠炎沙门氏菌鼠伤寒血清型菌株以及从粪便中分离的37株沙门氏菌鼠伤寒血清型菌株。我们检测了这些菌株产生σ(S)蛋白的能力、表达RpoS依赖性过氧化氢酶活性的能力以及在生长静止期抵抗氧化应激的能力。我们还进行了用克隆的野生型rpoS基因的互补实验。我们的结果表明,41株沙门氏菌伤寒血清型分离株中有15株RpoS存在缺陷。我们对12株菌株的rpoS等位基因进行了测序。这导致鉴定出小的插入、缺失和点突变,这些突变导致过早的终止密码子或影响σ(S)的区域1和区域2,表明rpoS突变不是克隆性的。因此,在新分离的临床肠炎沙门氏菌伤寒血清型菌株中可发现突变的rpoS等位基因,它们可能影响毒力特性。然而,有趣的是,在75株沙门氏菌鼠伤寒血清型分离株中未发现rpoS突变体。发现了过氧化氢酶活性和对过氧化氢抗性不同的菌株,但这些差异与rpoS状态无关。这表明沙门氏菌鼠伤寒血清型rpoS突变体被反向选择,因为rpoS在人类沙门氏菌鼠伤寒血清型的发病机制或疾病传播周期中起作用。