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代谢物转运蛋白PEG344是高毒力肺炎克雷伯菌菌株hvKP1肺部感染而非皮下感染后实现完全毒力所必需的。

Metabolite Transporter PEG344 Is Required for Full Virulence of Hypervirulent Klebsiella pneumoniae Strain hvKP1 after Pulmonary but Not Subcutaneous Challenge.

作者信息

Bulger Jeffrey, MacDonald Ulrike, Olson Ruth, Beanan Janet, Russo Thomas A

机构信息

School of Medicine, University at Buffalo-State University of New York, Buffalo, New York, USA.

Department of Medicine, University at Buffalo-State University of New York, Buffalo, New York, USA.

出版信息

Infect Immun. 2017 Sep 20;85(10). doi: 10.1128/IAI.00093-17. Print 2017 Oct.

Abstract

Hypervirulent (hvKP) is an emerging pathotype that is capable of causing tissue-invasive and organ- and life-threatening infections in healthy individuals from the community. Knowledge on the virulence factors specific to hvKP is limited. In this report, we describe a new factor (PEG344) that increases the virulence of hvKP strain hvKP1. is present on the hvKP1 virulence plasmid, is broadly prevalent among hvKP strains, and has increased RNA abundance when grown in human ascites. An isogenic derivative of hvKP1 (hvKP1Δ) was constructed and compared with its wild-type parent strain in , , and infection model studies. Both survival and competition experiments with outbred CD1 mice demonstrated that PEG344 was required for full virulence after pulmonary challenge but, interestingly, not after subcutaneous challenge. analysis suggested that PEG344 serves as an inner membrane transporter. Compared to hvKP1, a small but significant decrease in the growth/survival of hvKP1Δ was observed in human ascites, but resistance to the bactericidal activity of complement was similar. These data suggested that PEG344 may transport an unidentified growth factor present in ascites. The data presented are important since they expand our limited knowledge base on virulence factors unique to hvKP, which is needed to lay the groundwork for translational approaches to prevent or treat these devastating infections.

摘要

高毒力肺炎克雷伯菌(hvKP)是一种新出现的致病型,能够在社区健康个体中引起组织侵袭性、器官威胁性和生命威胁性感染。关于hvKP特有的毒力因子的知识有限。在本报告中,我们描述了一种新的因子(PEG344),它可增加hvKP菌株hvKP1的毒力。PEG344存在于hvKP1毒力质粒上,在hvKP菌株中广泛流行,并且在人腹水中生长时RNA丰度增加。构建了hvKP1的同基因衍生物(hvKP1Δ),并在体外、体内和感染模型研究中与野生型亲本菌株进行比较。与远交系CD1小鼠进行的生存和竞争实验均表明,肺部攻击后PEG344是完全毒力所必需的,但有趣的是,皮下攻击后并非如此。基因分析表明PEG344作为一种内膜转运蛋白。与hvKP1相比,在人腹水中观察到hvKP1Δ的生长/存活有小幅但显著的下降,但对补体杀菌活性的抗性相似。这些数据表明PEG344可能转运腹水中存在的一种未鉴定的生长因子。所呈现的数据很重要,因为它们扩展了我们关于hvKP特有的毒力因子的有限知识库,这是为预防或治疗这些毁灭性感染的转化方法奠定基础所必需的。

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