The African Swine Fever Virus Virulence Determinant DP96R Suppresses Type I IFN Production Targeting IRF3

• Published in: International journal of molecular sciences Vol. 25; no. 4; p. 2099
• Main Authors: Dodantenna, Niranjan, Cha, Ji-Won, Chathuranga, Kiramage, Chathuranga, W A Gayan, Weerawardhana, Asela, Ranathunga, Lakmal, Kim, Yongkwan, Jheong, Weonhwa, Lee, Jong-Soo
• Format: Journal Article
• Language: English
• Published: Switzerland MDPI AG 01.02.2024
• Subjects: African swine fever; African swine fever virus; African Swine Fever Virus - genetics; African Swine Fever Virus - pathogenicity; Animal experimentation; Animals; Biological response modifiers; Cytokines; Cytoplasm; DP96R (UK gene); Genes; Genetic transcription; Genomes; Hog cholera; Hogs; Humans; Immune response; Interferon; Interferon Regulatory Factor-3 - metabolism; Interferon Type I - metabolism; Interferons - metabolism; IRF3; Kinases; KPNA; Medical research; Medicine, Experimental; Phosphorylation; Plasmids; Proteins; RNA; Swine; Vaccines; Viral Proteins - metabolism; Virulence; Virulence (Microbiology); Virulence Factors - genetics; Viruses; United Kingdom; South Korea; Africa; DP96R (UK gene); African swine fever virus; KPNA; IRF3
• ISSN: 1422-0067; 1661-6596; 1422-0067
• DOI: 10.3390/ijms25042099

DP96R of African swine fever virus (ASFV), also known as uridine kinase ( ), encodes a virulence-associated protein. Previous studies have examined along with other genes in an effort to create live attenuated vaccines. While experiments in pigs have explored the impact of DP96R on the pathogenicity of ASFV, the precise molecular mechanism underlying this phenomenon remains unknown. Here, we describe a novel molecular mechanism by which DP96R suppresses interferon regulator factor-3 (IRF3)-mediated antiviral immune responses. DP96R interacts with a crucial karyopherin (KPNA) binding site within IRF3, disrupting the KPNA-IRF3 interaction and consequently impeding the translocation of IRF3 to the nucleus. Under this mechanistic basis, the ectopic expression of DP96R enhances the replication of DNA and RNA viruses by inhibiting the production of IFNs, whereas DP96R knock-down resulted in higher IFNs and IFN-stimulated gene (ISG) transcription during ASFV infection. Collectively, these findings underscore the pivotal role of DP96R in inhibiting IFN responses and increase our understanding of the relationship between DP96R and the virulence of ASFV.