Pizarro-Cerdá Javier, Tedin Karsten
Institut Pasteur, Unité Interactions Bactéries-Cellules, 28 Rue du Docteur Roux, F-75724 Cedex 15 Paris, France.
Mol Microbiol. 2004 Jun;52(6):1827-44. doi: 10.1111/j.1365-2958.2004.04122.x.
Numerous, overlapping global regulatory systems mediate the environmental signalling controlling the virulence of Salmonella typhimurium. With both extra- and intracellular lifestyles, unravelling the mechanisms involved in regulating Salmonella pathogenesis has been complex. Here, we report a factor co-ordinating environmental signals with global regulators involved in pathogenesis. An S. typhimuriumDeltarelADeltaspoT strain deficient in guanosine tetraphosphate (ppGpp) synthesis was found to be highly attenuated in vivo and non-invasive in vitro. The DeltarelADeltaspoT strain exhibited severely reduced expression of hilA and invF, encoding major transcriptional activators required for Salmonella pathogenicity island 1 (SPI-1) gene expression and at least two other pathogenicity islands. None of the growth conditions intended to mimic the intestinal milieu was capable of inducing hilA expression in the absence of ppGpp. However, the expression of global regulators of Salmonella virulence, RpoS and PhoP/Q, and RpoS- and PhoP/Q-dependent, non-virulence-related genes was not significantly different from the wild-type strain. The results indicate that ppGpp plays a central role as a regulator of virulence gene expression in S. typhimurium and implicates ppGpp as a major factor in the environmental and host-dependent regulation of Salmonella pathogenesis.
众多相互重叠的全局调控系统介导了控制鼠伤寒沙门氏菌毒力的环境信号传导。由于沙门氏菌具有胞外和胞内两种生活方式,阐明其致病机制一直很复杂。在此,我们报告了一个将环境信号与参与致病过程的全局调控因子相协调的因子。发现一株缺乏四磷酸鸟苷(ppGpp)合成能力的鼠伤寒沙门氏菌ΔrelAΔspoT菌株在体内高度减毒且在体外无侵袭性。ΔrelAΔspoT菌株中编码鼠伤寒沙门氏菌致病岛1(SPI-1)基因表达所需的主要转录激活因子以及至少其他两个致病岛的hilA和invF的表达严重降低。在没有ppGpp的情况下,旨在模拟肠道环境的任何生长条件都无法诱导hilA表达。然而,沙门氏菌毒力的全局调控因子RpoS和PhoP/Q以及RpoS和PhoP/Q依赖性非毒力相关基因的表达与野生型菌株没有显著差异。结果表明,ppGpp在鼠伤寒沙门氏菌毒力基因表达调控中起核心作用,并表明ppGpp是沙门氏菌致病过程中环境和宿主依赖性调控的主要因素。