TY - JOUR
T1 - Integrative multi-omics analysis in vivo identifies influenza virus host factors
AU - Shriver, Leah P.
AU - Polacco, Benjamin J.
AU - Eckhardt, Manon
AU - Chang, Max W.
AU - Martínez-Romero, Carles
AU - Adkins-Travis, Kayla
AU - Cahalane, Celina
AU - Haas, Kelsey
AU - Stein, David A.
AU - Fourati, Slim
AU - Martin-Sancho, Laura
AU - Metreveli, Giorgi
AU - Johnson, Jeffrey R.
AU - Muñoz-Moreno, Raquel
AU - Newton, Billy W.
AU - Kaake, Robyn M.
AU - Zhou, Yuan
AU - Jimenez-Morales, David
AU - VonDollen, John
AU - Verschueren, Erik
AU - Swaney, Danielle L.
AU - Nguyen, Thong T.
AU - Stevenson, Erica J.
AU - Stancliffe, Ethan
AU - Patti, Gary J.
AU - Albrecht, Randy
AU - Moulton, Hong M.
AU - Pache, Lars
AU - Sekaly, Rafick P.
AU - Benner, Christopher
AU - Hultquist, Judd F.
AU - Chanda, Sumit K.
AU - Garcia-Sastre, Adolfo
AU - Krogan, Nevan J.
N1 - Publisher Copyright:
© 2025
PY - 2025/11/21
Y1 - 2025/11/21
N2 - Influenza A virus (IAV) infection remodels cellular processes to support viral replication. The modulation of host factors by the virus drives pathogenesis during infection, and these factors may serve as therapeutic targets. Here, we infect mice with two IAV strains, H1N1 and H5N1, and analyze lung tissue with multi-omics. Using network propagation analysis, we identify twenty-four distinct host modules altered by infection, encompassing 2920 genes/proteins. Independently, we develop a computational pipeline, MidTOD, which integrates metabolomic data with other OMICs data-types, linking metabolites to gene/protein alterations. Combining datasets from both approaches reveals alterations in mitochondrial and peroxisomal metabolism in IAV-infected cells and identifies arginine:glycine amidinotransferase (GATM) as a host dependency factor in both human cells and mice. Knockdown of this enzyme reduces IAV-mediated pathology and host inflammatory responses after infection. Collectively, this work provides an integrated systems-level view of host changes during infection and identifies an abundance of IAV-host factors.
AB - Influenza A virus (IAV) infection remodels cellular processes to support viral replication. The modulation of host factors by the virus drives pathogenesis during infection, and these factors may serve as therapeutic targets. Here, we infect mice with two IAV strains, H1N1 and H5N1, and analyze lung tissue with multi-omics. Using network propagation analysis, we identify twenty-four distinct host modules altered by infection, encompassing 2920 genes/proteins. Independently, we develop a computational pipeline, MidTOD, which integrates metabolomic data with other OMICs data-types, linking metabolites to gene/protein alterations. Combining datasets from both approaches reveals alterations in mitochondrial and peroxisomal metabolism in IAV-infected cells and identifies arginine:glycine amidinotransferase (GATM) as a host dependency factor in both human cells and mice. Knockdown of this enzyme reduces IAV-mediated pathology and host inflammatory responses after infection. Collectively, this work provides an integrated systems-level view of host changes during infection and identifies an abundance of IAV-host factors.
KW - Biocomputational method
KW - Metabolomics
KW - Model organism
KW - Proteomics
KW - Transcriptomics
KW - Virology
UR - https://www.scopus.com/pages/publications/105018609134
U2 - 10.1016/j.isci.2025.113644
DO - 10.1016/j.isci.2025.113644
M3 - Article
C2 - 41142120
AN - SCOPUS:105018609134
SN - 2589-0042
VL - 28
JO - iScience
JF - iScience
IS - 11
M1 - 113644
ER -