tetano
Editor, Senior Moderator
Npj Viruses
. 2024 Nov 21;2(1):57.
doi: 10.1038/s44298-024-00065-x. NEIL1 block IFN-β production and enhance vRNP function to facilitate influenza A virus proliferation
Huixia Zhang[SUP] #[/SUP][SUP] 1 [/SUP], Changyan Li[SUP] #[/SUP][SUP] 1 [/SUP], Ruiqi Sun[SUP] 1 [/SUP], Xinyi Zhang[SUP] 1 [/SUP], Zexing Li[SUP] 1 [/SUP], Deping Hua[SUP] 1 [/SUP], Boxuan Yin[SUP] 1 [/SUP], Liu Yang[SUP] 1 [/SUP], Lilin Zhang[SUP] 2 [/SUP], Jinhai Huang[SUP] 3 [/SUP]
Affiliations
Influenza A virus (IAV) has developed multiple tactics to hinder the innate immune response including the epigenetic regulation during IAV infection, but the novel epigenetic factors and their mechanism in innate immunity remain well studied. Here, through a non-biased high-throughput sgRNA screening of 1041 known epigenetic modifiers in a cellular model of IAV-induced interferon-beta (IFN-β) production, we identified nei endonuclease VIII-like 1 (NEIL1) as a critical regulator of IFN-β in response to viral infection. Further studies showed that NEIL1 promoted the replication of the influenza virus by regulating the methylation of cytonuclear IFN-β promoter (mainly CpG-345), inhibiting the expression of IFN-β and IFN-stimulating genes. The structural domains of NEIL1, especially the catalytic domain, were critical for the suppression of IFN-β production, but the enzymatic activity of NEIL1 was dispensable. Furthermore, our results revealed that NEIL1 relied on interactions with the N- and C-terminus of the nucleoprotein (NP) of IAV, and NEIL1 expression facilitated the entry of the NP into the nucleus, which further enhanced the stability of the viral ribonucleoprotein (vRNP) complex and thus contributed to IAV replication and transcription. These findings reveal an enzyme-independent mechanism of host NEIL1 that negatively regulates IFN-β expression, thereby facilitating IAV propagation. Our study provides new insights into the roles of NEIL1, both in directly promoting virus replication and in evading innate immunity in IAV infection
. 2024 Nov 21;2(1):57.
doi: 10.1038/s44298-024-00065-x. NEIL1 block IFN-β production and enhance vRNP function to facilitate influenza A virus proliferation
Huixia Zhang[SUP] #[/SUP][SUP] 1 [/SUP], Changyan Li[SUP] #[/SUP][SUP] 1 [/SUP], Ruiqi Sun[SUP] 1 [/SUP], Xinyi Zhang[SUP] 1 [/SUP], Zexing Li[SUP] 1 [/SUP], Deping Hua[SUP] 1 [/SUP], Boxuan Yin[SUP] 1 [/SUP], Liu Yang[SUP] 1 [/SUP], Lilin Zhang[SUP] 2 [/SUP], Jinhai Huang[SUP] 3 [/SUP]
Affiliations
- PMID: 40295715
- PMCID: PMC11721407
- DOI: 10.1038/s44298-024-00065-x
Influenza A virus (IAV) has developed multiple tactics to hinder the innate immune response including the epigenetic regulation during IAV infection, but the novel epigenetic factors and their mechanism in innate immunity remain well studied. Here, through a non-biased high-throughput sgRNA screening of 1041 known epigenetic modifiers in a cellular model of IAV-induced interferon-beta (IFN-β) production, we identified nei endonuclease VIII-like 1 (NEIL1) as a critical regulator of IFN-β in response to viral infection. Further studies showed that NEIL1 promoted the replication of the influenza virus by regulating the methylation of cytonuclear IFN-β promoter (mainly CpG-345), inhibiting the expression of IFN-β and IFN-stimulating genes. The structural domains of NEIL1, especially the catalytic domain, were critical for the suppression of IFN-β production, but the enzymatic activity of NEIL1 was dispensable. Furthermore, our results revealed that NEIL1 relied on interactions with the N- and C-terminus of the nucleoprotein (NP) of IAV, and NEIL1 expression facilitated the entry of the NP into the nucleus, which further enhanced the stability of the viral ribonucleoprotein (vRNP) complex and thus contributed to IAV replication and transcription. These findings reveal an enzyme-independent mechanism of host NEIL1 that negatively regulates IFN-β expression, thereby facilitating IAV propagation. Our study provides new insights into the roles of NEIL1, both in directly promoting virus replication and in evading innate immunity in IAV infection