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Role of the dosR-dosS Two-Component Regulatory System in Mycobacterium tuberculosis Virulence in Three Animal Models

机译:在三种动物模型中dosR-dosS两组分调节系统在结核分枝杆菌毒力中的作用

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摘要

The Mycobacterium tuberculosis dosR gene (Rv3133c) is part of an operon, Rv3134c-Rv3132c, and encodes a response regulator that has been shown to be upregulated by hypoxia and other in vitro stress conditions and may be important for bacterial survival within granulomatous lesions found in tuberculosis. DosR is activated in response to hypoxia and nitric oxide by DosS (Rv3132c) or DosT (Rv2027c). We compared the virulence levels of an M. tuberculosis dosR-dosS deletion mutant (ΔdosR-dosS [ΔdosR-S]), a dosR-complemented strain, and wild-type H37Rv in rabbits, guinea pigs, and mice infected by the aerosol route and in a mouse hollow-fiber model that may mimic in vivo granulomatous conditions. In the mouse and the guinea pig models, the ΔdosR-S mutant exhibited a growth defect. In the rabbit, the ΔdosR-S mutant did not replicate more than the wild type. In the hollow-fiber model, the mutant phenotype was not different from that of the wild-type strain. Our analyses reveal that the dosR and dosS genes are required for full virulence and that there may be differences in the patterns of attenuation of this mutant between the animal models studied.
机译:结核分枝杆菌dosR基因(Rv3133c)是操纵子Rv3134c-Rv3132c的一部分,其编码的反应调节因子已被低氧和其他体外应激条件上调,并且可能对发现于肉芽肿性病变中的细菌存活很重要结核。 DosR响应DosS(Rv3132c)或DosT(Rv2027c)的缺氧和一氧化氮而被激活。我们比较了兔子,豚鼠和通过气溶胶途径感染的小鼠中结核分枝杆菌dosR-dosS缺失突变体(ΔdosR-dosS[ΔdosR-S]),dosR互补菌株和野生型H37Rv的毒力水平。在可能模仿体内肉芽肿病的小鼠中空纤维模型中。在小鼠和豚鼠模型中,ΔdosR-S突变体表现出生长缺陷。在兔子中,ΔdosR-S突变体的复制不超过野生型。在中空纤维模型中,突变型与野生型无差异。我们的分析表明,dosR和dosS基因是完整毒力所必需的,在研究的动物模型之间,此突变体的减毒模式可能有所不同。

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