Peste des petits ruminants virus non-structural C protein inhibits the induction of interferon-β by potentially interacting with MAVS and RIG-I
Autor: | Ma Xiaoxia, Li Linjie, Cao Xin, Amjad Ali, Bai Jialin, Shi Xiaoling |
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Jazyk: | angličtina |
Rok vydání: | 2021 |
Předmět: |
Chemokine
Pest des petits ruminants virus Interferon-β (IFN-β) Viral Nonstructural Proteins Peste-des-petits-ruminants virus 03 medical and health sciences Interferon Virology Chlorocebus aethiops Peste-des-Petits-Ruminants Genetics medicine CXCL10 Animals Humans STAT1 Antiviral state Receptors Immunologic Molecular Biology Vero Cells 030304 developmental biology Adaptor Proteins Signal Transducing 0303 health sciences Original Paper Innate immune system biology RIG-I 030302 biochemistry & molecular biology Luciferase reporter assay General Medicine Interferon-beta ISG15 HEK293 Cells biology.protein DEAD Box Protein 58 Signal transduction medicine.drug Protein C Signal Transduction |
Zdroj: | Virus Genes |
ISSN: | 1572-994X 0920-8569 |
Popis: | Peste des petits ruminants virus (PPRV) causes an acute and highly contagious disease in domestic and wild small ruminants throughout the world, mainly by invoking immunosuppression in its natural hosts. It has been suggested that the non-structural C protein of PPRV helps in evading host responses but the molecular mechanisms by which it antagonizes the host responses have not been fully characterized. Here, we report the antagonistic effect of PPRV C protein on the expression of interferon-β (IFN-β) through both MAVS and RIG-I mediated pathways in vitro. Dual luciferase reporter assay and direct expression of IFN-β mRNA analysis indicated that PPRV C significantly down regulates IFN-β via its potential interaction with MAVS and RIG-I signaling molecules. Results further indicated that PPRV C protein significantly suppresses endogenous and exogenous IFN-β-induced anti-viral effects in PPRV, EMCV and SVS infections in vitro. Moreover, PPRV C protein not only down regulates IFN-β but also the downstream cytokines of interferon stimulated genes 56 (ISG56), ISG15, C-X-C motif chemokine (CXCL10) and RIG-I mediated activation of IFN promoter elements of ISRE and NF-κB. Further, this study deciphers that PPRV C protein could significantly inhibit the phosphorylation of STAT1 and interferes with the signal transmission in JAK-STAT signaling pathway. Collectively, this study indicates that PPRV C protein is important for innate immune evasion and disease progression. |
Databáze: | OpenAIRE |
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