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- W2943702971 abstract "Flaviviruses such as yellow fever virus (YFV), Zika virus (ZIKV), and dengue virus (DENV) are important human pathogens. A common flavivirus trait is the antagonism of interferon (IFN) signaling to enhance viral replication and spread. We report that like ZIKV NS5 and DENV NS5, YFV NS5 binds human STAT2 (hSTAT2) but not mouse STAT2 (mSTAT2), a type I IFN (IFN-α/β) pathway component. Additionally, we show that contrary to what has been demonstrated with ZIKV NS5 and DENV NS5, YFV NS5 is unable to interact with hSTAT2 in murine cells. We demonstrate that mSTAT2 restricts YFV replication in mice and that this correlates with a lack of IFN-α/β-induced YFV NS5 ubiquitination in murine cells. The lack of suitable animal models limits flavivirus pathogenesis, vaccine, and drug research. These data serve as further impetus for the development of an immunocompetent mouse model that can serve as a disease model for multiple flaviviruses." @default.
- W2943702971 created "2019-05-09" @default.
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- W2943702971 date "2019-07-15" @default.
- W2943702971 modified "2023-10-18" @default.
- W2943702971 title "Host-Specific NS5 Ubiquitination Determines Yellow Fever Virus Tropism" @default.
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- W2943702971 doi "https://doi.org/10.1128/jvi.00151-19" @default.
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