Autophagy machinery as exploited by viruses.

Autophagy reports Pub Date : 2025-03-18 eCollection Date: 2025-12-31 DOI:10.1080/27694127.2025.2464986
Christian Münz, Grant R Campbell, Audrey Esclatine, Mathias Faure, Patrick Labonte, Marion Lussignol, Anthony Orvedahl, Nihal Altan-Bonnet, Ralf Bartenschlager, Rupert Beale, Mara Cirone, Lucile Espert, Jae Jung, David Leib, Fulvio Reggiori, Sumana Sanyal, Stephen A Spector, Volker Thiel, Christophe Viret, Yu Wei, Thomas Wileman, Harald Wodrich
{"title":"Autophagy machinery as exploited by viruses.","authors":"Christian Münz, Grant R Campbell, Audrey Esclatine, Mathias Faure, Patrick Labonte, Marion Lussignol, Anthony Orvedahl, Nihal Altan-Bonnet, Ralf Bartenschlager, Rupert Beale, Mara Cirone, Lucile Espert, Jae Jung, David Leib, Fulvio Reggiori, Sumana Sanyal, Stephen A Spector, Volker Thiel, Christophe Viret, Yu Wei, Thomas Wileman, Harald Wodrich","doi":"10.1080/27694127.2025.2464986","DOIUrl":null,"url":null,"abstract":"<p><p>Viruses adapt and modulate cellular pathways to allow their replication in host cells. The catabolic pathway of macroautophagy, for simplicity referred to as autophagy, is no exception. In this review, we discuss anti-viral functions of both autophagy and select components of the autophagy machinery, and how viruses have evaded them. Some viruses use the membrane remodeling ability of the autophagy machinery to build their replication compartments in the cytosol or efficiently egress from cells in a non-lytic fashion. Some of the autophagy machinery components and their remodeled membranes can even be found in viral particles as envelopes or single membranes around virus packages that protect them during spreading and transmission. Therefore, studies on autophagy regulation by viral infections can reveal functions of the autophagy machinery beyond lysosomal degradation of cytosolic constituents. Furthermore, they can also pinpoint molecular interactions with which the autophagy machinery can most efficiently be manipulated, and this may be relevant to develop effective disease treatments based on autophagy modulation.</p>","PeriodicalId":72341,"journal":{"name":"Autophagy reports","volume":"4 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2025-03-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11921968/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Autophagy reports","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1080/27694127.2025.2464986","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/12/31 0:00:00","PubModel":"eCollection","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

Viruses adapt and modulate cellular pathways to allow their replication in host cells. The catabolic pathway of macroautophagy, for simplicity referred to as autophagy, is no exception. In this review, we discuss anti-viral functions of both autophagy and select components of the autophagy machinery, and how viruses have evaded them. Some viruses use the membrane remodeling ability of the autophagy machinery to build their replication compartments in the cytosol or efficiently egress from cells in a non-lytic fashion. Some of the autophagy machinery components and their remodeled membranes can even be found in viral particles as envelopes or single membranes around virus packages that protect them during spreading and transmission. Therefore, studies on autophagy regulation by viral infections can reveal functions of the autophagy machinery beyond lysosomal degradation of cytosolic constituents. Furthermore, they can also pinpoint molecular interactions with which the autophagy machinery can most efficiently be manipulated, and this may be relevant to develop effective disease treatments based on autophagy modulation.

Abstract Image

Abstract Image

Abstract Image

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
病毒利用的自噬机制。
病毒适应并调节细胞途径,使其能够在宿主细胞中复制。大自噬的分解代谢途径也不例外,为简单起见,我们称之为自噬。在这篇综述中,我们将讨论自噬和自噬机制某些组成部分的抗病毒功能,以及病毒是如何规避这些功能的。一些病毒利用自噬机制的膜重塑能力在细胞质中构建复制区,或以非溶解方式从细胞中有效排出。自噬机制的某些成分及其重塑的膜甚至可以作为病毒包膜或病毒包周围的单层膜存在于病毒颗粒中,在传播和传染过程中保护病毒。因此,研究病毒感染对自噬的调控可以揭示自噬机制的功能,而不仅仅是溶酶体降解细胞膜成分。此外,这些研究还能确定可最有效操纵自噬机制的分子相互作用,这可能与开发基于自噬调节的有效疾病治疗方法有关。
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
RETREG1/FAM134B-mediated micro-ER-phagy in the retrovirus-SERINC5 arms race. TFEB-mediated autophagy stimulation as an anabolic strategy for bone: insights from TFEB activation in the osteoblast lineage. Involvement of ACSL3 in the formation of autophagosomes and lipid droplets during starvation conditions. Autophagy cargo profiles in skeletal muscle during starvation and exercise. Illuminating the regulatory link between blue light and autophagy in photomorphogenesis.
×
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:604180095
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