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1
Cyclic di-AMP-mediated interaction between Mycobacterium tuberculosis ΔcnpB and macrophages implicates a novel strategy for improving BCG vaccination.分枝杆菌环二鸟苷酸介导的Δ cnpB 与巨噬细胞的相互作用提示了一种改进卡介苗接种的新策略。
Pathog Dis. 2018 Mar 1;76(2). doi: 10.1093/femspd/fty008.
2
Novel structural features drive DNA binding properties of Cmr, a CRP family protein in TB complex mycobacteria.新型结构特征驱动 CRP 家族蛋白 Cmr 在结核分枝杆菌中的 DNA 结合特性。
Nucleic Acids Res. 2018 Jan 9;46(1):403-420. doi: 10.1093/nar/gkx1148.
3
Cyclic di-GMP regulates Mycobacterium tuberculosis resistance to ethionamide.环二鸟苷酸调控结核分枝杆菌对乙硫异烟胺的耐药性。
Sci Rep. 2017 Jul 19;7(1):5860. doi: 10.1038/s41598-017-06289-7.
4
Cmr is a redox-responsive regulator of DosR that contributes to M. tuberculosis virulence.Cmr是DosR的一种氧化还原反应调节因子,它有助于结核分枝杆菌的毒力。
Nucleic Acids Res. 2017 Jun 20;45(11):6600-6612. doi: 10.1093/nar/gkx406.
5
Chemical activation of adenylyl cyclase Rv1625c inhibits growth of Mycobacterium tuberculosis on cholesterol and modulates intramacrophage signaling.腺苷酸环化酶Rv1625c的化学激活抑制结核分枝杆菌在胆固醇上的生长并调节巨噬细胞内信号传导。
Mol Microbiol. 2017 Jul;105(2):294-308. doi: 10.1111/mmi.13701. Epub 2017 May 23.
6
Cyclic di-GMP: second messenger extraordinaire.环二鸟苷酸:非凡的第二信使。
Nat Rev Microbiol. 2017 May;15(5):271-284. doi: 10.1038/nrmicro.2016.190. Epub 2017 Feb 6.
7
Inhibition of innate immune cytosolic surveillance by an M. tuberculosis phosphodiesterase.结核分枝杆菌磷酸二酯酶抑制固有免疫胞质监视。
Nat Chem Biol. 2017 Feb;13(2):210-217. doi: 10.1038/nchembio.2254. Epub 2016 Dec 12.
8
Interaction of Erp Protein of Mycobacterium tuberculosis with Rv2212 Enhances Intracellular Survival of Mycobacterium smegmatis.结核分枝杆菌的Erp蛋白与Rv2212的相互作用增强耻垢分枝杆菌的细胞内存活能力。
J Bacteriol. 2016 Sep 22;198(20):2841-52. doi: 10.1128/JB.00120-16. Print 2016 Oct 15.
9
Structural and biochemical insight into the mechanism of Rv2837c from Mycobacterium tuberculosis as a c-di-NMP phosphodiesterase.结核分枝杆菌Rv2837c作为环二核苷酸磷酸二酯酶作用机制的结构与生化见解。
J Biol Chem. 2016 Jul 1;291(27):14386-14387. doi: 10.1074/jbc.A115.699801.
10
Too much of a good thing: regulated depletion of c-di-AMP in the bacterial cytoplasm.过犹不及:细菌细胞质中环状二腺苷单磷酸(c-di-AMP)的调控性消耗
Curr Opin Microbiol. 2016 Apr;30:22-29. doi: 10.1016/j.mib.2015.12.007. Epub 2016 Jan 7.

分枝杆菌中环核苷酸信号:不断扩展的 repertoire。

Cyclic nucleotide signaling in Mycobacterium tuberculosis: an expanding repertoire.

机构信息

Department of Biomedical Sciences, School of Public Health, University at Albany, SUNY, Albany, NY 12201-2002, USA.

Wadsworth Center, New York State Department of Health, Albany, NY 12201-2002, USA.

出版信息

Pathog Dis. 2018 Jul 1;76(5). doi: 10.1093/femspd/fty048.

DOI:10.1093/femspd/fty048
PMID:29905867
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6693379/
Abstract

Mycobacterium tuberculosis (Mtb) is one of the most successful microbial pathogens, and currently infects over a quarter of the world's population. Mtb's success depends on the ability of the bacterium to sense and respond to dynamic and hostile environments within the host, including the ability to regulate bacterial metabolism and interactions with the host immune system. One of the ways Mtb senses and responds to conditions it faces during infection is through the concerted action of multiple cyclic nucleotide signaling pathways. This review will describe how Mtb uses cyclic AMP, cyclic di-AMP and cyclic di-GMP to regulate important physiological processes, and how these signaling pathways can be exploited for the development of novel thereapeutics and vaccines.

摘要

结核分枝杆菌(Mtb)是最成功的微生物病原体之一,目前感染了世界上超过四分之一的人口。Mtb 的成功取决于其感知和响应宿主内动态和恶劣环境的能力,包括调节细菌代谢和与宿主免疫系统相互作用的能力。Mtb 感知和响应感染过程中面临的条件的一种方式是通过多种环核苷酸信号通路的协同作用。这篇综述将描述 Mtb 如何使用环 AMP、环二 AMP 和环二 GMP 来调节重要的生理过程,以及这些信号通路如何被用于开发新的治疗方法和疫苗。