质粒调控的沙眼衣原体CT084的TargeTron失活导致非裂解表型。

IF 2.7 4区 医学 Q3 IMMUNOLOGY
Una Karanovic, Lei Lei, Craig A Martens, Kent Barbian, Grant McClarty, Harlan D Caldwell, Chunfu Yang
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引用次数: 0

摘要

沙眼衣原体是一种专性细胞内细菌,可引起致盲性沙眼和性传播疾病。衣原体质粒是这些疾病发病机制中的关键毒力因子。质粒基因蛋白4(Pgp4)通过调节染色体基因和Pgp3的表达在衣原体毒力中起主要作用。尽管Pgp4在介导宿主细胞裂解性退出中具有重要作用,但其作用的致病机制尚不清楚。CT084是一个高度保守的染色体基因,与磷脂酶D同源。我们发现CT084的表达受Pgp4的调节,并在衣原体发育周期后期表达。为了研究CT084在感染细胞的衣原体裂解出口中的作用,我们使用Targetron制备了CT084无效菌株(CT084::bla)。与野生型菌株相比,ct084::bla菌株在体外生长正常,然而,该菌株没有裂解感染的细胞,产生的斑块明显更少、更小。总之,我们的发现表明,Pgp4调节CT084介导的衣原体从受感染的宿主细胞中溶出。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
TargeTron inactivation of plasmid-regulated Chlamydia trachomatis CT084 results in a nonlytic phenotype.

Chlamydia trachomatis is an obligate intracellular bacterium that causes blinding trachoma and sexually transmitted disease. The chlamydial plasmid is a critical virulence factor in the pathogenesis of these diseases. Plasmid gene protein 4 (Pgp4) plays a major role in chlamydial virulence by regulating the expression of both chromosomal genes and Pgp3. Despite the importance of Pgp4 in mediating lytic exit from host cells the pathogenic mechanism by which it functions is unknown. CT084 is a highly conserved chromosomal gene with homology to phospholipase D. We showed CT084 expression is regulated by Pgp4 and expressed late in the chlamydial developmental cycle. To investigate the function of CT084 in chlamydial lytic exit from infected cells, we made a CT084 null strain (ct084::bla) by using Targetron. The ct084::bla strain grew normally in vitro compared to wild-type strain; however, the strain did not lyse infected cells and produced significantly less and smaller plaques. Collectively, our finding shows Pgp4-regulated CT084-mediated chlamydia lytic exit from infected host cells.

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来源期刊
Pathogens and disease
Pathogens and disease IMMUNOLOGY-INFECTIOUS DISEASES
CiteScore
7.40
自引率
3.00%
发文量
44
期刊介绍: Pathogens and Disease publishes outstanding primary research on hypothesis- and discovery-driven studies on pathogens, host-pathogen interactions, host response to infection and their molecular and cellular correlates. It covers all pathogens – eukaryotes, prokaryotes, and viruses – and includes zoonotic pathogens and experimental translational applications.
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