Department of Oncology, Sidney Kimmel Comprehensive Cancer Center, Johns Hopkins University School of Medicine, Baltimore, MD, 21287, USA.
Department of Cell Biology, Institute for Basic Biomedical Sciences, Johns Hopkins University School of Medicine, Baltimore, MD, 21205, USA.
Nat Commun. 2019 Jul 19;10(1):3203. doi: 10.1038/s41467-019-11164-2.
Viral control of mitochondrial quality and content has emerged as an important mechanism for counteracting the host response to virus infection. Despite the knowledge of this crucial function of some viruses, little is known about how herpesviruses regulate mitochondrial homeostasis during infection. Human herpesvirus 8 (HHV-8) is an oncogenic virus causally related to AIDS-associated malignancies. Here, we show that HHV-8-encoded viral interferon regulatory factor 1 (vIRF-1) promotes mitochondrial clearance by activating mitophagy to support virus replication. Genetic interference with vIRF-1 expression or targeting to the mitochondria inhibits HHV-8 replication-induced mitophagy and leads to an accumulation of mitochondria. Moreover, vIRF-1 binds directly to a mitophagy receptor, NIX, on the mitochondria and activates NIX-mediated mitophagy to promote mitochondrial clearance. Genetic and pharmacological interruption of vIRF-1/NIX-activated mitophagy inhibits HHV-8 productive replication. Our findings uncover an essential role of vIRF-1 in mitophagy activation and promotion of HHV-8 lytic replication via this mechanism.
病毒对线粒体质量和含量的控制已成为抵抗宿主对病毒感染反应的重要机制。尽管人们已经了解到某些病毒具有这一关键功能,但对于疱疹病毒在感染过程中如何调节线粒体动态平衡知之甚少。人类疱疹病毒 8 型(HHV-8)是一种致癌病毒,与艾滋病相关恶性肿瘤有因果关系。在这里,我们发现 HHV-8 编码的病毒干扰素调节因子 1(vIRF-1)通过激活线粒体自噬来促进线粒体清除,从而支持病毒复制。干扰 vIRF-1 的表达或靶向线粒体的基因抑制 HHV-8 复制诱导的线粒体自噬,导致线粒体积累。此外,vIRF-1 直接与线粒体上的线粒体自噬受体 NIX 结合,并激活 NIX 介导的线粒体自噬,促进线粒体清除。vIRF-1/NIX 激活的线粒体自噬的遗传和药理学中断抑制了 HHV-8 的有效复制。我们的研究结果揭示了 vIRF-1 在通过这种机制激活线粒体自噬和促进 HHV-8 裂解复制中的重要作用。