IFIT3 RNA-binding activity promotes influenza A virus infection and translation efficiency

Host cells produce a vast network of antiviral factors in response to viral infection. The interferon-induced proteins with tetratricopeptide repeats (IFITs) are important effectors of a broad-spectrum antiviral response. In contrast to their canonical roles, we previously identified IFIT2 and IFIT3 as pro-viral host factors during influenza A virus (IAV) infection. During IAV infection, IFIT2 binds and enhances translation of AU-rich cellular mRNAs, including many IFN-stimulated gene products, establishing a model for its broad antiviral activity. However, IFIT2 also binds viral mRNAs and enhances their translation, resulting in increased viral replication. The ability of IFIT3 to bind RNA and whether this is important for its function was not known. Here, we validate direct interactions between IFIT3 and RNA using electrophoretic mobility shift assays. RNA-binding site identification experiments then identified an RNA-binding surface composed of residues conserved in IFIT3 orthologs and IFIT2 paralogs. Mutation of the RNA-binding site reduced the ability of IFIT3 to promote IAV gene expression and translation efficiency compared to wild-type IFIT3. The functional units of IFIT2 and IFIT3 are homo- and heterodimers; however, the RNA-binding surfaces are located near the dimerization interface. Using co-immunoprecipitation, we showed that mutations to these sites do not affect dimerization. Together, these data establish the link between IFIT3 RNA binding and its ability to modulate translation of viral mRNAs during IAV infection.IMPORTANCEInfluenza A viruses (IAVs) cause considerable morbidity and mortality through sporadic pandemics as well as annual epidemics. Zoonotic IAV strains pose an additional risk of spillover into a naive human population where prior immunity may have minimal effect. In this case, the first line of defense in the host is the innate immune response. Interferon-stimulated genes (ISGs) produce a suite of proteins that are front-line effectors of innate immune responses. While ISGs are typically considered antiviral, new research has revealed an emerging trend where viruses co-opt ISGs for pro-viral function. Here, we determine how the ISG IFIT3 is used by IAV as a pro-viral factor, advancing our understanding of IFIT3 function generally and specifically in the context of IAV infection.

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Publication Details

Journal
Journal of Virology
Published
2025-06-11
DOI
https://doi.org/10.1128/jvi.00286-25
Citations
3
Primary Topic
interferon and immune responses
Type
article
Field-Weighted Citation Impact
2.39

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article

IFIT3 RNA-binding activity promotes influenza A virus infection and translation efficiency

Andrew Mehle, Thomas Nipper, Daniel J. Nesbitt, Owen M. Sullivan et al.
3 citations
Journal of Virology
interferon and immune responses
2.39
article

IFIT3 RNA-binding activity promotes influenza A virus infection and translation efficiency

Andrew Mehle, Thomas Nipper, Daniel J. Nesbitt, Owen M. Sullivan, Cason R. King, Evgenia Shishkova, Steven G. Reed, Supasek Kongsomros, Joshua J. Coon, Grace A. Schaack, Elizabeth M. Feltman, Sarah L. Nelson
article en
3 citations

Abstract

Host cells produce a vast network of antiviral factors in response to viral infection. The interferon-induced proteins with tetratricopeptide repeats (IFITs) are important effectors of a broad-spectrum antiviral response. In contrast to their canonical roles, we previously identified IFIT2 and IFIT3 as pro-viral host factors during influenza A virus (IAV) infection. During IAV infection, IFIT2 binds and enhances translation of AU-rich cellular mRNAs, including many IFN-stimulated gene products, establishing a model for its broad antiviral activity. However, IFIT2 also binds viral mRNAs and enhances their translation, resulting in increased viral replication. The ability of IFIT3 to bind RNA and whether this is important for its function was not known. Here, we validate direct interactions between IFIT3 and RNA using electrophoretic mobility shift assays. RNA-binding site identification experiments then identified an RNA-binding surface composed of residues conserved in IFIT3 orthologs and IFIT2 paralogs. Mutation of the RNA-binding site reduced the ability of IFIT3 to promote IAV gene expression and translation efficiency compared to wild-type IFIT3. The functional units of IFIT2 and IFIT3 are homo- and heterodimers; however, the RNA-binding surfaces are located near the dimerization interface. Using co-immunoprecipitation, we showed that mutations to these sites do not affect dimerization. Together, these data establish the link between IFIT3 RNA binding and its ability to modulate translation of viral mRNAs during IAV infection.IMPORTANCEInfluenza A viruses (IAVs) cause considerable morbidity and mortality through sporadic pandemics as well as annual epidemics. Zoonotic IAV strains pose an additional risk of spillover into a naive human population where prior immunity may have minimal effect. In this case, the first line of defense in the host is the innate immune response. Interferon-stimulated genes (ISGs) produce a suite of proteins that are front-line effectors of innate immune responses. While ISGs are typically considered antiviral, new research has revealed an emerging trend where viruses co-opt ISGs for pro-viral function. Here, we determine how the ISG IFIT3 is used by IAV as a pro-viral factor, advancing our understanding of IFIT3 function generally and specifically in the context of IAV infection.

Journal of VirologyVol. 99(7)
University of Wisconsin–Madison (US), Mahidol University (TH), Morgridge Institute for Research (US), Quantitative BioSciences (US)
Burroughs Wellcome Fund, Wisconsin Alumni Research Foundation, Life Sciences Research Foundation, National Human Genome Research Institute, National Institute of General Medical Sciences, National Institute of Allergy and Infectious Diseases
Openalex Percentile: Top 11%
interferon and immune responses
2.39
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