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结核分枝杆菌H37Rv的染色体parDE2毒素-抗毒素系统:遗传与功能特性分析

The Chromosomal parDE2 Toxin-Antitoxin System of Mycobacterium tuberculosis H37Rv: Genetic and Functional Characterization.

作者信息

Gupta Manish, Nayyar Nishtha, Chawla Meenakshi, Sitaraman Ramakrishnan, Bhatnagar Rakesh, Banerjee Nirupama

机构信息

Department of Biotechnology, TERI University, NewDelhi, India; Molecular and Cell Biology Laboratory, School of Biotechnology, Jawaharlal Nehru UniversityNew Delhi, India.

Institute of Stem Cell Biology and Regenerative Medicine, National Centre for Biological Sciences Bangalore, India.

出版信息

Front Microbiol. 2016 Jun 14;7:886. doi: 10.3389/fmicb.2016.00886. eCollection 2016.

Abstract

Mycobacterium tuberculosis H37Rv escapes host-generated stresses by entering a dormant persistent state. Activation of toxin-antitoxin modules is one of the mechanisms known to trigger such a state with low metabolic activity. M. tuberculosis harbors a large number of TA systems mostly located within discernible genomic islands. We have investigated the parDE2 operon of M. tuberculosis H37Rv encoding MParE2 toxin and MParD2 antitoxin proteins. The parDE2 locus was transcriptionally active from growth phase till late stationary phase in M. tuberculosis. A functional promoter located upstream of parD2 GTG start-site was identified by 5'-RACE and lacZ reporter assay. The MParD2 protein transcriptionally regulated the P parDE2 promoter by interacting through Arg16 and Ser15 residues located in the N-terminus. In Escherichia coli, ectopic expression of MParE2 inhibited growth in early stages, with a drastic reduction in colony forming units. Live-dead analysis revealed that the reduction was not due to cell death alone but due to formation of viable but non-culturable cells (VBNCs) also. The toxic activity of the protein, identified in the C-terminal residues Glu98 and Arg102, was neutralized by the antitoxin MParD2, both in vivo and in vitro. MParE2 inhibited mycobacterial DNA gyrase and interacted with the GyrB subunit without affecting its ATPase activity. Introduction of parE2 gene in the heterologous M. smegmatis host prevented growth and colony formation by the transformed cells. An M. smegmatis strain containing the parDE2 operon also switched to a non-culturable phenotype in response to oxidative stress. Loss in colony-forming ability of a major part of the MParE2 expressing cells suggests its potential role in dormancy, a cellular strategy for adaptation to environmental stresses. Our study has laid the foundation for future investigations to explore the physiological significance of parDE2 operon in mycobacterial pathogenesis.

摘要

结核分枝杆菌H37Rv通过进入休眠持续状态来逃避宿主产生的应激。毒素-抗毒素模块的激活是已知触发这种低代谢活性状态的机制之一。结核分枝杆菌含有大量主要位于可识别基因组岛中的TA系统。我们研究了结核分枝杆菌H37Rv编码MParE2毒素和MParD2抗毒素蛋白的parDE2操纵子。parDE2基因座在结核分枝杆菌的生长阶段直至稳定期末期均具有转录活性。通过5'-RACE和lacZ报告基因测定法鉴定了位于parD2 GTG起始位点上游的功能性启动子。MParD2蛋白通过位于N端的Arg16和Ser15残基相互作用,对P parDE2启动子进行转录调控。在大肠杆菌中,MParE2的异位表达在早期抑制生长,菌落形成单位急剧减少。活死分析表明,减少不仅是由于细胞死亡,还由于形成了活的但不可培养的细胞(VBNCs)。在C端残基Glu98和Arg102中鉴定出的该蛋白的毒性活性在体内和体外均被抗毒素MParD2中和。MParE2抑制分枝杆菌DNA促旋酶并与GyrB亚基相互作用,而不影响其ATPase活性。在异源耻垢分枝杆菌宿主中引入parE2基因可阻止转化细胞的生长和菌落形成。含有parDE2操纵子的耻垢分枝杆菌菌株在氧化应激下也转变为不可培养表型。表达MParE2的细胞的大部分丧失菌落形成能力表明其在休眠中的潜在作用,这是一种适应环境应激的细胞策略。我们的研究为未来探索parDE2操纵子在分枝杆菌致病机制中的生理意义奠定了基础。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/282c/4906023/0652779be93b/fmicb-07-00886-g001.jpg

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