摘要
背景:分枝杆菌属导致结核病和麻风病等致命疾病。属于此属的细菌细胞壁在许多方面是独特的。它在宿主内的发病机制和细胞内存活中起主要作用。在细胞内病原体中,其细胞壁作为分子屏障并与宿主细胞环境相互作用以调节宿主防御反应。 目的:在这篇综述中,我们总结了参与独特分枝杆菌细胞壁生物合成的因素,了解它们作为药物靶点的潜力以及最近被评估为可能的药物靶点的发展。 结果:在细胞壁成分如抗原85复合物,糖基转移酶(GTs),LM(脂甘露聚糖)和LAM(脂阿拉伯甘露聚糖),mAGP复合物,脂肪分解酶的合成中发挥关键作用的几种细胞壁相关因子已被明确记录。大多数目前使用的抗TB方案中断了细胞壁合成,但是耐药菌株的出现使其必须识别新的药物靶标。已经在全世界范围内对抑制细胞壁成分合成的新型候选药物进行了深入的研究。 结论:研究表明细胞壁成分在其在分枝杆菌发病机制中的贡献是独特的。针对这些可以妨碍结核分枝杆菌的生长。在这项研究中,我们仔细审查了试验中的药物,并通过计算机发现筛选出潜在的候选药物。
关键词: 细胞壁,发病机理,抗TB方案,结核分枝杆菌,药物设计,药物发现。
图形摘要
Current Drug Targets
Title:Cell Wall Associated Factors of Mycobacterium tuberculosis as Major Virulence Determinants: Current Perspectives in Drugs Discovery and Design
Volume: 18 Issue: 16
关键词: 细胞壁,发病机理,抗TB方案,结核分枝杆菌,药物设计,药物发现。
摘要: Background: Mycobacteria genus is responsible for deadly diseases like tuberculosis and leprosy. Cell wall of bacteria belonging to this genus is unique in many ways. It plays a major role in the pathogenesis and intracellular survival inside the host. In intracellular pathogens, their cell wall acts as molecular shield and interacts with host cell milieu to modulate host defense responses.
Objectives: In this review, we summarize the factors that participate in the biosynthesis of unique mycobacterial cell wall, understand their potential as drug targets and the recent developments where they have been evaluated as possible drug targets.
Results: Several cell wall associated factors that play crucial roles in the synthesis of cell wall components like Antigen 85 complex, Glycosyltransferases (GTs), LM (lipomannan) and LAM (lipoarabinomannan), mAGP Complex, lipolytic enzyme have been categorically documented. Most of the presently used anti TB regimens interrupted cell wall synthesis, but the emergence of drug resistant strains made it mandatory to identify new drug targets. Novel drug candidates which could inhibit the synthesis of cell wall components have been thoroughly studied worldwide.
Conclusion: Studies demonstrated that the cell wall components are unique in terms of their contribution in mycobacterium pathogenesis. Targeting these can hamper the growth of M. tuberculosis. In this study, we scrutinize the drugs under trials and the potential candidates screened through in silico findings.
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Cite this article as:
Cell Wall Associated Factors of Mycobacterium tuberculosis as Major Virulence Determinants: Current Perspectives in Drugs Discovery and Design, Current Drug Targets 2017; 18 (16) . https://dx.doi.org/10.2174/1389450118666170711150034
DOI https://dx.doi.org/10.2174/1389450118666170711150034 |
Print ISSN 1389-4501 |
Publisher Name Bentham Science Publisher |
Online ISSN 1873-5592 |
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