Journal of Virology · 2022 · 86 citations · 24 references
Life SciencesInfectious DiseasesMolecular BiologyInnate ImmunityMolecular VirologyVirologyAntiviral ImmunityHost-virus InteractionsInnate Immune ResponseInnate Immune Signaling PathwaysInterferon ResponsesViral PathogenesisAntiviral Innate SignalingAntiviral Signaling PathwaysAssayCell Signaling During Viral InfectionInnate Immune Recognition Of VirusesSars-cov-2 InfectionStress Granule AntagonismViral Immune Modulation
In this study, by in vitro assay and live SARS-CoV-2 virus infection, we provide solid evidence that the SARS-CoV-2 NP associates with G3BP1 and G3BP2 in vitro and in vivo . NP SARS-CoV-2 could efficiently suppress G3BP-mediated SG formation and potentiate viral infection by overcoming antiviral innate immunity mediated by G3BP1 in A549 cell lines and G3BP1 conditional knockout mice ( g3bp1 -cKO) mice, which provide in-depth evidence showing the mechanism underlying NP-related SARS-CoV-2 pathogenesis through G3BPs.
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