Chaudhari Jayeshbhai, Lai Danh C, Vu Hiep L X
Nebraska Center for Virology, University of Nebraska-Lincoln, 68583, Lincoln, NE, USA.
Nebraska Center for Virology, University of Nebraska-Lincoln, 68583, Lincoln, NE, USA; Department of Animal Science, University of Nebraska-Lincoln, 68583, Lincoln, NE, USA.
Virology. 2025 Jan;602:110317. doi: 10.1016/j.virol.2024.110317. Epub 2024 Nov 26.
African swine fever virus (ASFV) is the causative agent of a lethal disease in pigs. Highly virulent strains of ASFV are known to suppress the induction of type I interferons (IFNs), while naturally attenuated strains do not exhibit this capability. Thus, the ability to suppress IFN is assumed to be associated with viral virulence. ASFV genome encodes many proteins capable of disrupting crucial components of host immune response pathways. Notably, these viral proteins interfere with the induction of type I IFNs by targeting various steps of the cGAS-STING signaling pathway. Additionally, certain viral proteins impede the expression of interferon-stimulated genes by interfering with the JAK-STAT pathway. Consequently, ASFV proteins hamper both IFN production and the induction of antiviral responses by IFNs. This review article summarizes the viral proteins responsible for suppressing various steps of the cGAS-STING and JAK-STAT signaling pathways and discusses the potential application of this knowledge to the rational design of a live-attenuated ASFV vaccine.
非洲猪瘟病毒(ASFV)是猪致命疾病的病原体。已知高毒力的ASFV毒株会抑制I型干扰素(IFN)的诱导,而自然减毒的毒株则不具备这种能力。因此,抑制IFN的能力被认为与病毒毒力有关。ASFV基因组编码许多能够破坏宿主免疫反应途径关键成分的蛋白质。值得注意的是,这些病毒蛋白通过靶向cGAS-STING信号通路的各个步骤来干扰I型IFN的诱导。此外,某些病毒蛋白通过干扰JAK-STAT途径来阻碍干扰素刺激基因的表达。因此,ASFV蛋白既阻碍IFN的产生,也阻碍IFN诱导的抗病毒反应。这篇综述文章总结了负责抑制cGAS-STING和JAK-STAT信号通路各个步骤的病毒蛋白,并讨论了这些知识在合理设计减毒活ASFV疫苗方面的潜在应用。