Department of Microbiology and Immunology, University of Texas Medical Branch, Galveston, TX 77555, USA.
Institute for Human Infections and Immunity, University of Texas Medical Branch, Galveston, TX 77555, USA.
Viruses. 2021 Feb 26;13(3):369. doi: 10.3390/v13030369.
Ubiquitination of proteins is a post-translational modification process with many different cellular functions, including protein stability, immune signaling, antiviral functions and virus replication. While ubiquitination of viral proteins can be used by the host as a defense mechanism by destroying the incoming pathogen, viruses have adapted to take advantage of this cellular process. The ubiquitin system can be hijacked by viruses to enhance various steps of the replication cycle and increase pathogenesis. Emerging viruses, including severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), flaviviruses like Zika and dengue, as well as highly pathogenic viruses like Ebola and Nipah, have the ability to directly use the ubiquitination process to enhance their viral-replication cycle, and evade immune responses. Some of these mechanisms are conserved among different virus families, especially early during virus entry, providing an opportunity to develop broad-spectrum antivirals. Here, we discuss the mechanisms used by emergent viruses to exploit the host ubiquitin system, with the main focus on the role of ubiquitin in enhancing virus replication.
蛋白质泛素化是一种具有许多不同细胞功能的翻译后修饰过程,包括蛋白质稳定性、免疫信号、抗病毒功能和病毒复制。虽然病毒蛋白的泛素化可以被宿主用作防御机制,通过破坏进入的病原体,但病毒已经适应了利用这一细胞过程。泛素系统可以被病毒劫持,以增强复制周期的各个步骤,并增加发病机制。新兴病毒,包括严重急性呼吸综合征冠状病毒 2 (SARS-CoV-2)、寨卡病毒和登革热等黄病毒,以及埃博拉病毒和尼帕病毒等高致病性病毒,具有直接利用泛素化过程来增强其病毒复制周期的能力,并逃避免疫反应。其中一些机制在不同的病毒家族中是保守的,特别是在病毒进入的早期,这为开发广谱抗病毒药物提供了机会。在这里,我们讨论新兴病毒利用宿主泛素系统的机制,主要关注泛素在增强病毒复制中的作用。