Journal of Virology · 2021 · 30 citations · 27 references
Life SciencesInfectious DiseasesMolecular BiologyInnate ImmunityMolecular VirologyVirologyAntiviral ImmunityInnate Immune ActivationInnate Immune ResponseInnate Immune Signaling PathwaysInterferon ResponsesViral PathogenesisAntiviral Innate SignalingInnate Immunity PathwaysInterferon ProductionInterferon Response To Viral InfectionInterferon-stimulated GenesLuciferase Reporter AssaysNf-κb SignalingType I Interferon Pathways
Previous studies investigated the interaction between SARS-CoV-2 viral proteins and interferon signaling and proposed that several SARS-CoV-2 viral proteins, including NSP12, could suppress IFN-β activation. However, most of these results were generated from IFN-β promoter luciferase reporter assay and have not been validated functionally. In our study, we found that, although NSP12 could suppress IFN-β promoter luciferase activity, it showed no inhibitory effect on IFN-β production or its downstream signaling. Further study revealed that contradictory results could be generated from different experiment systems. On one hand, we demonstrated that SARS-CoV-2 NSP12 could not suppress IFN-β signaling. On the other hand, our study suggests that caution needs to be taken with the interpretation of SARS-CoV-2-related luciferase assays.
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