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RelA 和 SpoT 在伯克霍尔德氏菌毒力和免疫中的作用。

Role of RelA and SpoT in Burkholderia pseudomallei virulence and immunity.

机构信息

College of Life and Environmental Sciences, Biosciences, University of Exeter, Exeter, Devon, United Kingdom.

出版信息

Infect Immun. 2012 Sep;80(9):3247-55. doi: 10.1128/IAI.00178-12. Epub 2012 Jul 9.

Abstract

Burkholderia pseudomallei is a Gram-negative soil bacterium and the causative agent of melioidosis, a disease of humans and animals. It is also listed as a category B bioterrorism threat agent by the U.S. Centers for Disease Control and Prevention, and there is currently no melioidosis vaccine available. Small modified nucleotides such as the hyperphosphorylated guanosine molecules ppGpp and pppGpp play an important role as signaling molecules in prokaryotes. They mediate a global stress response under starvation conditions and have been implicated in the regulation of virulence and survival factors in many bacterial species. In this study, we created a relA spoT double mutant in B. pseudomallei strain K96243, which lacks (p)ppGpp-synthesizing enzymes, and investigated its phenotype in vitro and in vivo. The B. pseudomallei ΔrelA ΔspoT mutant displayed a defect in stationary-phase survival and intracellular replication in murine macrophages. Moreover, the mutant was attenuated in the Galleria mellonella insect model and in both acute and chronic mouse models of melioidosis. Vaccination of mice with the ΔrelA ΔspoT mutant resulted in partial protection against infection with wild-type B. pseudomallei. In summary, (p)ppGpp signaling appears to represent an essential component of the regulatory network governing virulence gene expression and stress adaptation in B. pseudomallei, and the ΔrelA ΔspoT mutant may be a promising live-attenuated vaccine candidate.

摘要

类鼻疽伯克霍尔德菌是一种革兰氏阴性土壤细菌,也是人类和动物类鼻疽病的病原体。它也被美国疾病控制与预防中心列为 B 类生物恐怖威胁剂,目前尚无类鼻疽疫苗。像高磷酸化鸟苷分子 ppGpp 和 pppGpp 这样的小修饰核苷酸在原核生物中作为信号分子发挥着重要作用。它们在饥饿条件下介导全局应激反应,并与许多细菌物种的毒力和生存因子的调节有关。在这项研究中,我们在类鼻疽伯克霍尔德菌 K96243 菌株中创建了一个 relA spoT 双突变体,该突变体缺乏 (p)ppGpp 合成酶,并研究了其在体外和体内的表型。类鼻疽伯克霍尔德菌 ΔrelA ΔspoT 突变体在静止期存活和在鼠巨噬细胞内的复制方面存在缺陷。此外,该突变体在大蜡螟昆虫模型以及急性和慢性类鼻疽小鼠模型中均呈减毒状态。用 ΔrelA ΔspoT 突变体对小鼠进行疫苗接种可导致对野生型类鼻疽伯克霍尔德菌感染的部分保护。总之,(p)ppGpp 信号似乎代表了调节网络的一个重要组成部分,该网络控制着类鼻疽伯克霍尔德菌毒力基因表达和应激适应,ΔrelA ΔspoT 突变体可能是一种有前途的活减毒疫苗候选物。

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