挥舞双刃剑:病毒利用宿主 DNA 修复系统促进复制,同时绕过免疫激活

IF 2 Q4 VIROLOGY Frontiers in virology Pub Date : 2024-04-22 DOI:10.3389/fviro.2024.1410258
Nicholas Saladino, Daniel J. Salamango
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引用次数: 0

摘要

病毒是一种强制性细胞内病原体,它劫持宿主细胞的无数过程,以促进复制和抑制宿主的抗病毒防御。从本质上讲,病毒是一段外来核酸,它与宿主细胞机制结合,驱动病毒基因组复制、基因转录和蛋白质合成,从而产生后代病毒。正因为如此,宿主生物已经开发出复杂的检测系统,在识别到异常核酸后启动抗病毒防御系统。例如,宿主 DNA 修复蛋白对病毒核酸的识别会导致病毒基因组完整性受损、诱发抗病毒炎症程序、细胞周期停滞和细胞凋亡。毫不奇怪,各种病毒家族已经进化出多种策略,对宿主 DNA 修复反应进行微调,以抑制抗病毒防御系统的激活,同时劫持 DNA 修复蛋白以促进病毒复制。本综述总结了病毒利用宿主 DNA 修复机制的常见分子策略。
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Wielding a double-edged sword: viruses exploit host DNA repair systems to facilitate replication while bypassing immune activation
Viruses are obligate intracellular pathogens that hijack a myriad of host cell processes to facilitate replication and suppress host antiviral defenses. In its essence, a virus is a segment of foreign nucleic acid that engages host cell machinery to drive viral genome replication, gene transcription, and protein synthesis to generate progeny virions. Because of this, host organisms have developed sophisticated detection systems that activate antiviral defenses following recognition of aberrant nucleic acids. For example, recognition of viral nucleic acids by host DNA repair proteins results in compromised viral genome integrity, induction of antiviral inflammatory programs, cell cycle arrest, and apoptosis. Unsurprisingly, diverse viral families have evolved multiple strategies that fine-tune host DNA repair responses to suppress activation of antiviral defenses while simultaneously hijacking DNA repair proteins to facilitate virus replication. This review summarizes common molecular strategies viruses deploy to exploit host DNA repair mechanisms.
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