Münz Christian, Campbell Grant R, Esclatine Audrey, Faure Mathias, Labonte Patrick, Lussignol Marion, Orvedahl Anthony, Altan-Bonnet Nihal, Bartenschlager Ralf, Beale Rupert, Cirone Mara, Espert Lucile, Jung Jae, Leib David, Reggiori Fulvio, Sanyal Sumana, Spector Stephen A, Thiel Volker, Viret Christophe, Wei Yu, Wileman Thomas, Wodrich Harald
Viral Immunobiology, Institute of Experimental Immunology, University of Zürich, Zürich Switzerland.
Division of Basic Biomedical Sciences, Sanford School of Medicine, University of SD, Vermillion, SD, USA.
Autophagy Rep. 2025 Mar 18;4(1). doi: 10.1080/27694127.2025.2464986. eCollection 2025 Dec 31.
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.
病毒会适应并调节细胞通路以使其能够在宿主细胞中复制。宏观自噬的分解代谢途径,简称为自噬,也不例外。在本综述中,我们讨论了自噬及其部分机制组分的抗病毒功能,以及病毒是如何逃避这些功能的。一些病毒利用自噬机制的膜重塑能力在细胞质中构建其复制区室,或以非裂解方式有效地从细胞中释放出来。甚至可以在病毒颗粒中发现一些自噬机制组分及其重塑的膜,它们作为包膜或围绕病毒包裹的单层膜,在病毒传播和传递过程中保护病毒。因此,关于病毒感染对自噬调节的研究可以揭示自噬机制除了对细胞质成分进行溶酶体降解之外的功能。此外,这些研究还可以确定能够最有效地操纵自噬机制的分子相互作用,这可能与基于自噬调节开发有效的疾病治疗方法相关。