Wang Zixuan, Zhu Chunchun, Sun Xueyi, Deng Hongyan, Liu Wen, Jia Shuke, Bai Yao, Xiao Wuhan, Liu Xing
Key Laboratory of Breeding Biotechnology and Sustainable Aquaculture, Institute of Hydrobiology, Chinese Academy of Sciences, Wuhan, China.
University of the Chinese Academy of Sciences, Beijing, China.
J Virol. 2025 Jan 31;99(1):e0149124. doi: 10.1128/jvi.01491-24. Epub 2024 Nov 27.
The hypoxia signaling pathway controls hypoxia adaptation and tolerance of organisms, which is regulated by multiple mechanisms. Viral infection elicits various pathophysiological responses in the host. However, whether viral infection can affect the hypoxia response is not yet fully understood. In this study, we found that Spring viremia of carp virus (SVCV) infection in zebrafish caused symptoms similar to those in zebrafish under hypoxic conditions. Further assays indicated that SVCV infection activated the hypoxia signaling pathway in zebrafish. In addition, SVCV infection caused increased glycolysis and reactive oxygen species (ROS) levels in cells. Mechanistically, SVCV-G protein interacted with hif1α-a/b and attenuated their K48-linked polyubiquitination, leading to their stabilization and subsequent enhancement of target gene expression. Moreover, treatment with the HIF1α-specific inhibitor PX478 enhanced the antiviral ability against SVCV infection in zebrafish and zebrafish cells. This study reveals a relationship between SVCV infection and the hypoxia signaling pathway in fish and provides a strategy for reducing the damage of viral disease in the aquaculture industry.
Viral infection triggers various pathophysiological responses in the host. The hypoxia signaling pathway controls hypoxia adaptation and tolerance of organisms. However, whether viral infection can affect the hypoxia response is not yet fully understood. This study showed that Spring viremia of carp virus (SVCV) infection activated the hypoxia signaling pathway and induced a hypoxia response. The SVCV-G protein interacted with hif1α-a/b and reduced their K48-linked polyubiquitination, leading to their stabilization and subsequent enhancement of target gene expression. Additionally, treatment with the HIF1α-specific inhibitor PX478 enhanced the antiviral ability against SVCV infection in zebrafish and zebrafish cells. Our findings not only reveal a relationship between SVCV infection and the hypoxia signaling pathway in fish but also provide a strategy for reducing the damage of viral disease in the aquaculture industry.
缺氧信号通路控制着生物体的缺氧适应和耐受性,其受多种机制调节。病毒感染会在宿主体内引发各种病理生理反应。然而,病毒感染是否会影响缺氧反应尚未完全明了。在本研究中,我们发现斑马鱼感染鲤春病毒血症病毒(SVCV)会引发与缺氧条件下斑马鱼相似的症状。进一步检测表明,SVCV感染激活了斑马鱼体内的缺氧信号通路。此外,SVCV感染导致细胞内糖酵解增加和活性氧(ROS)水平升高。机制上,SVCV - G蛋白与hif1α - a/b相互作用并减弱其K48连接的多聚泛素化,导致它们的稳定以及随后靶基因表达的增强。此外,用HIF1α特异性抑制剂PX478处理可增强斑马鱼和斑马鱼细胞对SVCV感染的抗病毒能力。本研究揭示了鱼类中SVCV感染与缺氧信号通路之间的关系,并为减少水产养殖业中病毒性疾病的损害提供了一种策略。
病毒感染会在宿主体内引发各种病理生理反应。缺氧信号通路控制着生物体的缺氧适应和耐受性。然而,病毒感染是否会影响缺氧反应尚未完全明了。本研究表明,鲤春病毒血症病毒(SVCV)感染激活了缺氧信号通路并诱导了缺氧反应。SVCV - G蛋白与hif1α - a/b相互作用并减少其K48连接的多聚泛素化,导致它们的稳定以及随后靶基因表达的增强。此外,用HIF1α特异性抑制剂PX478处理可增强斑马鱼和斑马鱼细胞对SVCV感染的抗病毒能力。我们的研究结果不仅揭示了鱼类中SVCV感染与缺氧信号通路之间的关系,还为减少水产养殖业中病毒性疾病的损害提供了一种策略。