ESX分泌系统:分枝杆菌生存能力和发病机制的守门人。

Sadhana Roy, Debika Ghatak, Payel Das, Somdeb BoseDasgupta
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引用次数: 8

摘要

结核病的病原体结核分枝杆菌多年来一直困扰着人类,随着耐药性的出现,它比以往任何时候都更加强大。分枝杆菌擅长逃避宿主免疫系统,通过参与宿主因子和分泌多种毒力因子来建立感染。因此,这些分泌系统在分枝杆菌的发病机制中起关键作用。VII型分泌系统或ESX(早期分泌抗原靶(ESAT6)分泌)系统就是这样一个至关重要的系统,它包括五种不同的途径,在分枝杆菌增殖、发病机制、巨噬细胞内胞质逃逸、巨噬细胞凋亡调节、金属离子稳态等方面发挥着不同的作用。ESX 1-5系统涉及大量蛋白质的分泌,其中只有少数具有功能特征。在这里,我们总结了目前对分枝杆菌ESX分泌系统的了解,特别关注ESX-1和ESX-5系统,它们破坏巨噬细胞防御并帮助分枝杆菌在巨噬细胞内建立其生态位。
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ESX secretion system: The gatekeepers of mycobacterial survivability and pathogenesis.

Mycobacterium tuberculosis, the causative agent of Tuberculosis has plagued humankind for ages and has surfaced stronger than ever with the advent of drug resistance. Mycobacteria are adept at evading the host immune system and establishing infection by engaging host factors and secreting several virulence factors. Hence these secretion systems play a key role in mycobacterial pathogenesis. The type VII secretion system or ESX (early secretory antigenic target (ESAT6) secretion) system is one such crucial system that comprises five different pathways having distinct roles in mycobacterial proliferation, pathogenesis, cytosolic escape within macrophages, regulation of macrophage apoptosis, metal ion homeostasis, etc. ESX 1-5 systems are implicated in the secretion of a plethora of proteins, of which only a few are functionally characterized. Here we summarize the current knowledge of ESX secretion systems of mycobacteria with a special focus on ESX-1 and ESX-5 systems that subvert macrophage defenses and help mycobacteria to establish their niche within the macrophage.

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