ARIH1 inhibits influenza A virus replication and facilitates RIG-I dependent immune signaling by interacting with SQSTM1/p62

• Published in: Virology journal 2023-04, Vol.20 (1), p.58-58, Article 58
• Main Authors: Wang, Shengyu, Li, Zhenrong, Chen, Yaping, Gao, Sanli, Qiao, Junhua, Liu, Haoru, Song, Hong, Ao, Dishu, Sun, Xin
• Format: Article
• Language: English
• Subjects: Analysis; Antibodies; Antiviral Agents; ARIH1; Biotechnology; Cell culture; computer software; CXCL10 protein; DEAD Box Protein 58 - metabolism; Gene expression; Humans; Immune response; Immunity, Innate; Immunoprecipitation; Infections; Influenza; Influenza A; Influenza A virus; Influenza, Human; Innate immunity; Interferon; interferons; Laboratories; luciferase; p62; Pathogens; Plasmids; precipitin tests; Prevention; Proteins; RIG-I; Risk factors; Sequestosome-1 Protein - metabolism; Signal Transduction; SQSTM1; standard deviation; Statistical analysis; Swine flu; Tissue culture; Ubiquitin; Ubiquitin-proteasome system; Ubiquitin-protein ligase; Ubiquitin-Protein Ligases; Ubiquitination; Virus Replication; Viruses; Western blotting; β-Interferon
• ISSN: 1743-422X; 1743-422X
• DOI: 10.1186/s12985-023-02022-1

Multiple host factors are involved in modulating type I interferon expression induced by viruses; however, the mechanism is not fully elucidated. Influenza A virus infection causes severe respiratory symptoms and triggers a series of signaling cascades and host innate immune responses, including interferon production. The co-IP/MS technology was used to screen several antiviral factors in the early stage. Among these factors, ariadne-1 homolog (ARIH1) caught our attention. Western blot assay was performed to detect the level of proteins and software ImageJ was used to analyze the band intensities. Polymerase activity assay was conducted to evaluate the polymerase activity of influenza A virus. Tissue culture infective dose (TCID ) assay was performed to measure influenza A virus titers, and quantitative RT-PCR assay was applied to test the mRNA level of IFN-β, ISG56, and CXCL10. Luciferase reporter assay was used to confirm the target of ARIH1 in RIG-I signaling. Immunoprecipitation assay was performed to detect the interaction and the ubiquitination of the proteins. All data were analyzed by biostatistical methods and presented as means ± standard deviation from three independent experiments. Statistical significance was determined using two-tailed student's t test. A P value of less than 0.05 was considered statistically significant, and a P value of less than 0.01 was considered highly significant (ns, P ≥ 0.05; *, P