Laboratory of Fish Molecular Immunology, College of Fisheries and Life Science, Shanghai Ocean University, Shanghai, China.
Laboratory for Marine Biology and Biotechnology, Qingdao Marine Science and Technology Center, Qingdao, China.
Elife. 2024 Sep 30;13:RP94898. doi: 10.7554/eLife.94898.
The incessant arms race between viruses and hosts has led to numerous evolutionary innovations that shape life's evolution. During this process, the interactions between viral receptors and viruses have garnered significant interest since viral receptors are cell surface proteins exploited by viruses to initiate infection. Our study sheds light on the arms race between the MDA5 receptor and 5'ppp-RNA virus in a lower vertebrate fish, . Firstly, the frequent and independent loss events of RIG-I in vertebrates prompted us to search for alternative immune substitutes, with homology-dependent genetic compensation response (HDGCR) being the main pathway. Our further analysis suggested that MDA5 of , the homolog of RIG-I, can replace RIG-I in recognizing 5'ppp-RNA virus, which may lead to redundancy of RIG-I and loss from the species genome during evolution. Secondly, as an adversarial strategy, 5'ppp-RNA SCRV can utilize the mA methylation mechanism to degrade MDA5 and weaken its antiviral immune ability, thus promoting its own replication and immune evasion. In summary, our study provides a snapshot into the interaction and coevolution between vertebrate and virus, offering valuable perspectives on the ecological and evolutionary factors that contribute to the diversity of the immune system.
病毒和宿主之间无休止的军备竞赛导致了许多进化创新,塑造了生命的进化。在这个过程中,病毒受体与病毒之间的相互作用引起了极大的关注,因为病毒受体是病毒用来启动感染的细胞表面蛋白。我们的研究揭示了在一种较低等的脊椎动物鱼类中 MDA5 受体与 5'ppp-RNA 病毒之间的军备竞赛。首先,脊椎动物中 RIG-I 的频繁和独立缺失事件促使我们寻找替代的免疫替代物,同源依赖性遗传补偿反应(HDGCR)是主要途径。我们的进一步分析表明,RIG-I 的同源物 MDA5 可以替代 RIG-I 识别 5'ppp-RNA 病毒,这可能导致 RIG-I 的冗余和在进化过程中从物种基因组中丢失。其次,作为一种对抗策略,5'ppp-RNA SCRV 可以利用 mA 甲基化机制降解 MDA5,削弱其抗病毒免疫能力,从而促进自身复制和免疫逃避。总之,我们的研究提供了一个脊椎动物和病毒相互作用和共同进化的快照,为免疫系统多样性的生态和进化因素提供了有价值的视角。