Spring viremia of carp virus infection induces hypoxia response in zebrafish by stabilizing hif1α.

IF 4 2区 医学 Q2 VIROLOGY Journal of Virology Pub Date : 2024-11-27 DOI:10.1128/jvi.01491-24
Zixuan Wang, Chunchun Zhu, Xueyi Sun, Hongyan Deng, Wen Liu, Shuke Jia, Yao Bai, Wuhan Xiao, Xing Liu
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Abstract

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.

Importance: 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.

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鲤鱼病毒感染的春季病毒血症通过稳定 hif1α 诱导斑马鱼的缺氧反应。
低氧信号通路控制着生物的低氧适应性和耐受性,它受到多种机制的调控。病毒感染会引起宿主的各种病理生理反应。然而,病毒感染是否会影响缺氧反应尚未完全明了。在这项研究中,我们发现斑马鱼感染鲤春病毒(SVCV)后会出现与缺氧条件下斑马鱼类似的症状。进一步的实验表明,SVCV 感染激活了斑马鱼体内的缺氧信号通路。此外,SVCV 感染还导致细胞中糖酵解和活性氧(ROS)水平升高。从机理上讲,SVCV-G 蛋白与 hif1α-a/b 相互作用,减弱了它们与 K48 链接的多泛素化,导致它们的稳定,进而增强了靶基因的表达。此外,用 HIF1α 特异性抑制剂 PX478 处理斑马鱼和斑马鱼细胞,可增强其抗 SVCV 感染的能力。这项研究揭示了鱼类 SVCV 感染与缺氧信号通路之间的关系,为减少水产养殖业中病毒性疾病的危害提供了一种策略:病毒感染会引发宿主的各种病理生理反应。缺氧信号通路控制着生物的缺氧适应性和耐受性。然而,病毒感染是否会影响缺氧反应尚不完全清楚。本研究表明,鲤春病毒(SVCV)感染激活了缺氧信号通路,诱导了缺氧反应。SVCV-G蛋白与hif1α-a/b相互作用,减少了它们与K48连接的多泛素化,导致它们的稳定,进而增强了靶基因的表达。此外,用HIF1α特异性抑制剂PX478处理斑马鱼和斑马鱼细胞可增强抗SVCV感染的能力。我们的研究结果不仅揭示了鱼类 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危害提供了一种策略。
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来源期刊
Journal of Virology
Journal of Virology 医学-病毒学
CiteScore
10.10
自引率
7.40%
发文量
906
审稿时长
1 months
期刊介绍: Journal of Virology (JVI) explores the nature of the viruses of animals, archaea, bacteria, fungi, plants, and protozoa. We welcome papers on virion structure and assembly, viral genome replication and regulation of gene expression, genetic diversity and evolution, virus-cell interactions, cellular responses to infection, transformation and oncogenesis, gene delivery, viral pathogenesis and immunity, and vaccines and antiviral agents.
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