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分枝杆菌来源蛋白 Rv0674 定位于线粒体,与 D 环相互作用,并调节 OXPHOS,以促进结核分枝杆菌在细胞内的持续存在。

Mycobacterial origin protein Rv0674 localizes into mitochondria, interacts with D-loop and regulates OXPHOS for intracellular persistence of Mycobacterium tuberculosis.

机构信息

Division of Microbiology, CSIR-Central Drug Research Institute, Lucknow 226031, India.

Division of Microbiology and Academy of Scientific and Innovative Research, India; Division of Microbiology, CSIR-Central Drug Research Institute, Lucknow 226031, India.

出版信息

Mitochondrion. 2021 Mar;57:241-256. doi: 10.1016/j.mito.2020.11.014. Epub 2020 Dec 3.

DOI:10.1016/j.mito.2020.11.014
PMID:33279599
Abstract

Mycobacterium tuberculosis (Mtb) employs diverse strategies to survive inside the host macrophages. In this study, we have identified a conserved hypothetical protein of Mtb; Rv0674, which is present in the mitochondria of the host cell. The genetic knock-out of rv0674 (Mtb-KO) showed increased growth of Mtb. The intracellular infection with recombinant Mycobacterium smegmatis (MSMEG) expressing Rv0674 (MS_Rv0674), established that the protein is involved in promoting the apoptotic cell death of the macrophage. To investigate the mechanism incurred in mitochondria, we observed that the protein physically interacts with the control region (D-loop) of the mitochondrial DNA (LSP and HSP promoters of the loop) of the macrophages and facilitates the increased expression of mRNA in all the complexes of mitochondrial encoded OXPHOS subunits. The changes in OXPHOS levels corroborated with the ATP synthesis, mitochondrial membrane potential and superoxide production. The infection with MS_Rv0674 confirmed the role of this protein in effecting the intracellular infection. The fluorescent and confocal microscopy confirmed that the protein is localized in the mitochondria of infected macrophages and in the cells of BAL of TB patients. Together these findings indicate towards the novel function of the protein which is unlike to the earlier established mechanisms of mycobacterial physiology.

摘要

结核分枝杆菌(Mtb)采用多种策略在宿主巨噬细胞内存活。在这项研究中,我们鉴定了 Mtb 中一种保守的假定蛋白 Rv0674,它存在于宿主细胞的线粒体中。rv0674 的基因敲除(Mtb-KO)显示 Mtb 的生长增加。用表达 Rv0674 的重组耻垢分枝杆菌(MSMEG)进行细胞内感染(MS_Rv0674),表明该蛋白参与促进巨噬细胞的凋亡细胞死亡。为了研究线粒体中涉及的机制,我们观察到该蛋白与巨噬细胞中线粒体 DNA 的控制区(D-环)(环中的 LSP 和 HSP 启动子)发生物理相互作用,并促进所有线粒体编码 OXPHOS 亚基复合物中的 mRNA 表达增加。OXPHOS 水平的变化与 ATP 合成、线粒体膜电位和超氧化物产生相符。用 MS_Rv0674 感染证实了该蛋白在影响细胞内感染中的作用。荧光和共聚焦显微镜证实该蛋白定位于感染巨噬细胞的线粒体中和 TB 患者 BAL 中的细胞中。这些发现共同表明该蛋白具有不同于先前确立的分枝杆菌生理学机制的新功能。

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