Biochemistry of Reactivation of Dormant Mycobacteria

IF 2.3 4区 生物学 Q3 BIOCHEMISTRY & MOLECULAR BIOLOGY
Margarita O. Shleeva, Galina R. Demina, Arseny S. Kaprelyants
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Abstract

An important aspect of medical microbiology is identification of the causes and mechanisms of reactivation (resuscitation) of dormant non-sporulating bacteria. In particular, dormant Mycobacterium tuberculosis (Mtb) can cause latent tuberculosis (TB), which could be reactivated in the human organism to the active form of the disease. Analysis of experimental data suggested that reactivation of mycobacteria and reversion of the growth processes include several stages. The initial stage is associated with breakdown of the storage substances like trehalose upon the action of trehalase and with peptidoglycan hydrolysis. Demethylation of tetramethyl porphyrins accumulated in hydrophobic sites (membranes) of the dormant cell also occur in this stage. Metabolic reactivation, starting with cAMP synthesis and subsequent activation of metabolic reactions and biosynthetic processes take place at the stage two as has been shown in the omics studies. Mechanisms of cell reactivation by exogenous free fatty acids via activation of adenylate cyclase and cAMP production have been also suggested. Onset of the cell division is a key benchmark of the third and final stage. Hydrolysis of peptidoglycan as a result of enzymatic action of peptidoglycan hydrolases of the Rpf family is an important process in reactivation of the dormant mycobacteria. Two possible mechanisms for participation of Rpf proteins in reactivation of the dormant bacteria are discussed. On the one hand, muropeptides could be formed as products of peptidoglycan hydrolysis, which could interact with appropriate receptors in bacterial cells transducing activating signal via the PknB phosphotransferase. On the other hand, Rpf protein could presumably change structure of the cell wall, making it more permeable to nutrients and substrates. Both hypotheses were examined in this review. Upon reactivation, independent enzymatic reactions resume their functioning from the beginning of reactivation. Such activation of the entire metabolism occurs rather stochastically, which concludes in combining all biochemical processes in one. This review presents current knowledge regarding biochemical mechanisms of the dormant mycobacteria reactivation, which is important for both fundamental and medical microbiology.

休眠分枝杆菌再活化的生物化学研究
医学微生物学的一个重要方面是鉴定休眠的非孢子菌的重新激活(复苏)的原因和机制。特别是,休眠结核分枝杆菌(Mtb)可引起潜伏性结核病(TB),潜伏性结核病可在人体机体中重新激活为活动性结核病。实验数据分析表明,分枝杆菌的再活化和生长过程的逆转包括几个阶段。初始阶段与海藻糖酶作用下海藻糖等储存物质的分解和肽聚糖水解有关。四甲基卟啉在休眠细胞疏水部位(膜)的去甲基化也发生在这一阶段。代谢再激活,从cAMP合成开始,随后的代谢反应和生物合成过程的激活发生在第二阶段,正如组学研究所显示的那样。外源性游离脂肪酸通过激活腺苷酸环化酶和cAMP生成来激活细胞的机制也被提出。细胞分裂的开始是第三阶段和最后阶段的关键指标。肽聚糖水解是Rpf家族肽聚糖水解酶的酶促作用的结果,是休眠分枝杆菌再激活的重要过程。讨论了Rpf蛋白参与休眠细菌再激活的两种可能机制。一方面,多肽可以作为肽聚糖水解的产物形成,它可以与细菌细胞中合适的受体相互作用,通过PknB磷酸转移酶转导激活信号。另一方面,Rpf蛋白可能会改变细胞壁的结构,使其对营养物质和底物更具渗透性。本综述对这两种假设都进行了检验。在再激活后,独立的酶反应从再激活开始恢复其功能。整个代谢过程的激活是随机发生的,其结果是所有生化过程合而为一。本文综述了目前关于休眠分枝杆菌再激活的生化机制的知识,这对基础和医学微生物学都很重要。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Biochemistry (Moscow)
Biochemistry (Moscow) 生物-生化与分子生物学
CiteScore
4.70
自引率
3.60%
发文量
139
审稿时长
2 months
期刊介绍: Biochemistry (Moscow) is the journal that includes research papers in all fields of biochemistry as well as biochemical aspects of molecular biology, bioorganic chemistry, microbiology, immunology, physiology, and biomedical sciences. Coverage also extends to new experimental methods in biochemistry, theoretical contributions of biochemical importance, reviews of contemporary biochemical topics, and mini-reviews (News in Biochemistry).
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