HKU-Pasteur Research Pole, School of Public Health, University of Hong Kong, Hong Kong.
HKU-Pasteur Research Pole, School of Public Health, University of Hong Kong, Hong Kong; School of Biomedical Sciences, LKS Faculty of Medicine, University of Hong Kong, Hong Kong.
Semin Cell Dev Biol. 2020 May;101:3-11. doi: 10.1016/j.semcdb.2019.07.013. Epub 2019 Aug 8.
Autophagy is an evolutionarily conserved process central to host metabolism. Among its major functions are conservation of energy during starvation, recycling organelles, and turnover of long-lived proteins. Besides, autophagy plays a critical role in removing intracellular pathogens and very likely represents a primordial intrinsic cellular defence mechanism. More recent findings indicate that it has not only retained its ability to degrade intracellular pathogens, but also functions to augment and fine tune antiviral immune responses. Interestingly, viruses have also co-evolved strategies to manipulate this pathway and use it to their advantage. Particularly intriguing is infection-dependent activation of autophagy with positive stranded (+)RNA virus infections, which benefit from the pathway without succumbing to lysosomal degradation. In this review we summarise recent data on viral manipulation of autophagy, with a particular emphasis on +RNA viruses and highlight key unanswered questions in the field that we believe merit further attention.
自噬是一种进化上保守的过程,对宿主代谢至关重要。其主要功能包括在饥饿时节约能量、回收细胞器和长寿命蛋白质的更新。此外,自噬在清除细胞内病原体方面起着关键作用,很可能代表了一种原始的内在细胞防御机制。最近的研究结果表明,它不仅保留了降解细胞内病原体的能力,而且还能够增强和微调抗病毒免疫反应。有趣的是,病毒也进化出了操纵这一途径的策略,并利用它为自己服务。特别引人注目的是,依赖于感染的自噬激活与正链(+)RNA 病毒感染有关,这些病毒受益于该途径而不被溶酶体降解。在这篇综述中,我们总结了最近关于病毒对自噬的操纵的研究数据,特别强调了+RNA 病毒,并强调了该领域中我们认为值得进一步关注的关键未解决问题。