4.7 Article

African Swine Fever Virus MGF360-14L Negatively Regulates Type I Interferon Signaling by Targeting IRF3

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Publisher

FRONTIERS MEDIA SA
DOI: 10.3389/fcimb.2021.818969

Keywords

African swine fever virus; interferon; IRF3; ubiquitination; immune evasion

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This study discovered that the non-structural protein MGF360-14L of African swine fever virus inhibits interferon production by interfering with the host immune system. The study also revealed that MGF360-14L interacts with and degrades the IRF3 protein, further suppressing immune response.
African swine fever (ASF) is a devastating infectious disease caused by African swine fever virus (ASFV). The ASFV genome encodes multiple structural and non-structural proteins that contribute to evasion of host immunity. In this study, we determined that the viral non-structural protein MGF360-14L inhibits interferon-beta (IFN-beta) promoter activity induced by cGAS-STING signaling. MGF360-14L was also found to downregulate expression of the IRF3 protein and promote its degradation through ubiquitin-meditated proteolysis. Moreover, MGF360-14L was shown to interact with and destabilize IRF3 by facilitating E3 ligase TRIM21-mediated K63-linked ubiquitination of IRF3. Overall, our study revealed that MGF360-14L promotes degradation of IRF3 through TRIM21, thereby inhibiting type I interferon production. These findings provide new insights into the mechanisms underlying ASFV immune evasion.

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