Wielding a double-edged sword: viruses exploit host DNA repair systems to facilitate replication while bypassing immune activation

IF 2 Q4 VIROLOGY Frontiers in virology Pub Date : 2024-04-22 DOI:10.3389/fviro.2024.1410258
Nicholas Saladino, Daniel J. Salamango
{"title":"Wielding a double-edged sword: viruses exploit host DNA repair systems to facilitate replication while bypassing immune activation","authors":"Nicholas Saladino, Daniel J. Salamango","doi":"10.3389/fviro.2024.1410258","DOIUrl":null,"url":null,"abstract":"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.","PeriodicalId":73114,"journal":{"name":"Frontiers in virology","volume":"3 1","pages":""},"PeriodicalIF":2.0000,"publicationDate":"2024-04-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Frontiers in virology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.3389/fviro.2024.1410258","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"VIROLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

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.
查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
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
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。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
自引率
0.00%
发文量
0
期刊最新文献
Frontiers | Phylogenetic-based methods for fine-scale classification of PRRSV-2 ORF5 sequences: a comparison of their robustness and reproducibility Frontiers | A proposed new Tombusviridae genus featuring extremely long 5' untranslated regions and a luteo/polerovirus-like gene block Frontiers | Severe Acute Respiratory Syndrome Coronavirus-2 seroprevalence in non-vaccinated People Living with HIV in Uganda during the year 2022 Frontiers | Predicting Antibody and ACE2 Affinity for SARS-CoV-2 BA.2.86 and JN.1 with In Silico Protein Modeling and Docking Frontiers | HIV latency potential may beis influenced by intra-subtype genetic differences in the viral long-terminal repeat
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1