Proteomic and genetic analyses of influenza A viruses identify pan-viral host targets

Kelsey M. Haas; Michael J. McGregor; Mehdi Bouhaddou; Benjamin J. Polacco; Eun Young Kim; Thong T. Nguyen; Billy W. Newton; Matthew Urbanowski; Heejin Kim; Michael A.P. Williams; Veronica V. Rezelj; Alexandra Hardy; Andrea Fossati; Erica J. Stevenson; Ellie Sukerman; Tiffany Kim; Sudhir Penugonda; Elena Moreno; Hannes Braberg; Yuan Zhou; Giorgi Metreveli; Bhavya Harjai; Tia A. Tummino; James E. Melnyk; Margaret Soucheray; Jyoti Batra; Lars Pache; Laura Martin-Sancho; Jared Carlson-Stevermer; Alexander S. Jureka; Christopher F. Basler; Kevan M. Shokat; Brian K. Shoichet; Leah P. Shriver; Jeffrey R. Johnson; Megan L. Shaw; Sumit K. Chanda; Dan M. Roden; Tonia C. Carter; Leah C. Kottyan; Rex L. Chisholm; Jennifer A. Pacheco; Maureen E. Smith; Steven J. Schrodi; Randy A. Albrecht; Marco Vignuzzi; Lorena Zuliani-Alvarez; Danielle L. Swaney; Manon Eckhardt; Steven M. Wolinsky; Kris M. White; Judd F. Hultquist; Robyn M. Kaake; Adolfo García-Sastre; Nevan J. Krogan

doi:10.1038/s41467-023-41442-z

Proteomic and genetic analyses of influenza A viruses identify pan-viral host targets

Kelsey M. Haas, Michael J. McGregor, Mehdi Bouhaddou, Benjamin J. Polacco, Eun Young Kim, Thong T. Nguyen, Billy W. Newton, Matthew Urbanowski, Heejin Kim, Michael A.P. Williams, Veronica V. Rezelj, Alexandra Hardy, Andrea Fossati, Erica J. Stevenson, Ellie Sukerman, Tiffany Kim, Sudhir Penugonda, Elena Moreno, Hannes Braberg, Yuan ZhouGiorgi Metreveli, Bhavya Harjai, Tia A. Tummino, James E. Melnyk, Margaret Soucheray, Jyoti Batra, Lars Pache, Laura Martin-Sancho, Jared Carlson-Stevermer, Alexander S. Jureka, Christopher F. Basler, Kevan M. Shokat, Brian K. Shoichet, Leah P. Shriver, Jeffrey R. Johnson, Megan L. Shaw, Sumit K. Chanda, Dan M. Roden, Tonia C. Carter, Leah C. Kottyan, Rex L. Chisholm, Jennifer A. Pacheco, Maureen E. Smith, Steven J. Schrodi, Randy A. Albrecht, Marco Vignuzzi, Lorena Zuliani-Alvarez, Danielle L. Swaney, Manon Eckhardt, Steven M. Wolinsky, Kris M. White, Judd F. Hultquist, Robyn M. Kaake, Adolfo García-Sastre, Nevan J. Krogan

Infectious Diseases

Research output: Contribution to journal › Article › peer-review

3 Scopus citations

Abstract

Influenza A Virus (IAV) is a recurring respiratory virus with limited availability of antiviral therapies. Understanding host proteins essential for IAV infection can identify targets for alternative host-directed therapies (HDTs). Using affinity purification-mass spectrometry and global phosphoproteomic and protein abundance analyses using three IAV strains (pH1N1, H3N2, H5N1) in three human cell types (A549, NHBE, THP-1), we map 332 IAV-human protein-protein interactions and identify 13 IAV-modulated kinases. Whole exome sequencing of patients who experienced severe influenza reveals several genes, including scaffold protein AHNAK, with predicted loss-of-function variants that are also identified in our proteomic analyses. Of our identified host factors, 54 significantly alter IAV infection upon siRNA knockdown, and two factors, AHNAK and coatomer subunit COPB1, are also essential for productive infection by SARS-CoV-2. Finally, 16 compounds targeting our identified host factors suppress IAV replication, with two targeting CDK2 and FLT3 showing pan-antiviral activity across influenza and coronavirus families. This study provides a comprehensive network model of IAV infection in human cells, identifying functional host targets for pan-viral HDT.

Original language	English (US)
Article number	6030
Journal	Nature communications
Volume	14
Issue number	1
DOIs	https://doi.org/10.1038/s41467-023-41442-z
State	Published - Dec 2023

ASJC Scopus subject areas

General Chemistry
General Biochemistry, Genetics and Molecular Biology
General Physics and Astronomy

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10.1038/s41467-023-41442-z

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Haas, K. M., McGregor, M. J., Bouhaddou, M., Polacco, B. J., Kim, E. Y., Nguyen, T. T., Newton, B. W., Urbanowski, M., Kim, H., Williams, M. A. P., Rezelj, V. V., Hardy, A., Fossati, A., Stevenson, E. J., Sukerman, E., Kim, T., Penugonda, S., Moreno, E., Braberg, H., ... Krogan, N. J. (2023). Proteomic and genetic analyses of influenza A viruses identify pan-viral host targets. Nature communications, 14(1), Article 6030. https://doi.org/10.1038/s41467-023-41442-z

Haas, KM, McGregor, MJ, Bouhaddou, M, Polacco, BJ, Kim, EY, Nguyen, TT, Newton, BW, Urbanowski, M, Kim, H, Williams, MAP, Rezelj, VV, Hardy, A, Fossati, A, Stevenson, EJ, Sukerman, E, Kim, T, Penugonda, S, Moreno, E, Braberg, H, Zhou, Y, Metreveli, G, Harjai, B, Tummino, TA, Melnyk, JE, Soucheray, M, Batra, J, Pache, L, Martin-Sancho, L, Carlson-Stevermer, J, Jureka, AS, Basler, CF, Shokat, KM, Shoichet, BK, Shriver, LP, Johnson, JR, Shaw, ML, Chanda, SK, Roden, DM, Carter, TC, Kottyan, LC, Chisholm, RL, Pacheco, JA, Smith, ME, Schrodi, SJ, Albrecht, RA, Vignuzzi, M, Zuliani-Alvarez, L, Swaney, DL, Eckhardt, M, Wolinsky, SM, White, KM, Hultquist, JF, Kaake, RM, García-Sastre, A & Krogan, NJ 2023, 'Proteomic and genetic analyses of influenza A viruses identify pan-viral host targets', Nature communications, vol. 14, no. 1, 6030. https://doi.org/10.1038/s41467-023-41442-z

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title = "Proteomic and genetic analyses of influenza A viruses identify pan-viral host targets",

abstract = "Influenza A Virus (IAV) is a recurring respiratory virus with limited availability of antiviral therapies. Understanding host proteins essential for IAV infection can identify targets for alternative host-directed therapies (HDTs). Using affinity purification-mass spectrometry and global phosphoproteomic and protein abundance analyses using three IAV strains (pH1N1, H3N2, H5N1) in three human cell types (A549, NHBE, THP-1), we map 332 IAV-human protein-protein interactions and identify 13 IAV-modulated kinases. Whole exome sequencing of patients who experienced severe influenza reveals several genes, including scaffold protein AHNAK, with predicted loss-of-function variants that are also identified in our proteomic analyses. Of our identified host factors, 54 significantly alter IAV infection upon siRNA knockdown, and two factors, AHNAK and coatomer subunit COPB1, are also essential for productive infection by SARS-CoV-2. Finally, 16 compounds targeting our identified host factors suppress IAV replication, with two targeting CDK2 and FLT3 showing pan-antiviral activity across influenza and coronavirus families. This study provides a comprehensive network model of IAV infection in human cells, identifying functional host targets for pan-viral HDT.",

author = "Haas, {Kelsey M.} and McGregor, {Michael J.} and Mehdi Bouhaddou and Polacco, {Benjamin J.} and Kim, {Eun Young} and Nguyen, {Thong T.} and Newton, {Billy W.} and Matthew Urbanowski and Heejin Kim and Williams, {Michael A.P.} and Rezelj, {Veronica V.} and Alexandra Hardy and Andrea Fossati and Stevenson, {Erica J.} and Ellie Sukerman and Tiffany Kim and Sudhir Penugonda and Elena Moreno and Hannes Braberg and Yuan Zhou and Giorgi Metreveli and Bhavya Harjai and Tummino, {Tia A.} and Melnyk, {James E.} and Margaret Soucheray and Jyoti Batra and Lars Pache and Laura Martin-Sancho and Jared Carlson-Stevermer and Jureka, {Alexander S.} and Basler, {Christopher F.} and Shokat, {Kevan M.} and Shoichet, {Brian K.} and Shriver, {Leah P.} and Johnson, {Jeffrey R.} and Shaw, {Megan L.} and Chanda, {Sumit K.} and Roden, {Dan M.} and Carter, {Tonia C.} and Kottyan, {Leah C.} and Chisholm, {Rex L.} and Pacheco, {Jennifer A.} and Smith, {Maureen E.} and Schrodi, {Steven J.} and Albrecht, {Randy A.} and Marco Vignuzzi and Lorena Zuliani-Alvarez and Swaney, {Danielle L.} and Manon Eckhardt and Wolinsky, {Steven M.} and White, {Kris M.} and Hultquist, {Judd F.} and Kaake, {Robyn M.} and Adolfo Garc{\'i}a-Sastre and Krogan, {Nevan J.}",

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year = "2023",

month = dec,

doi = "10.1038/s41467-023-41442-z",

language = "English (US)",

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T1 - Proteomic and genetic analyses of influenza A viruses identify pan-viral host targets

AU - Haas, Kelsey M.

AU - McGregor, Michael J.

AU - Bouhaddou, Mehdi

AU - Polacco, Benjamin J.

AU - Kim, Eun Young

AU - Nguyen, Thong T.

AU - Newton, Billy W.

AU - Urbanowski, Matthew

AU - Kim, Heejin

AU - Williams, Michael A.P.

AU - Rezelj, Veronica V.

AU - Hardy, Alexandra

AU - Fossati, Andrea

AU - Stevenson, Erica J.

AU - Sukerman, Ellie

AU - Kim, Tiffany

AU - Penugonda, Sudhir

AU - Moreno, Elena

AU - Braberg, Hannes

AU - Zhou, Yuan

AU - Metreveli, Giorgi

AU - Harjai, Bhavya

AU - Tummino, Tia A.

AU - Melnyk, James E.

AU - Soucheray, Margaret

AU - Batra, Jyoti

AU - Pache, Lars

AU - Martin-Sancho, Laura

AU - Carlson-Stevermer, Jared

AU - Jureka, Alexander S.

AU - Basler, Christopher F.

AU - Shokat, Kevan M.

AU - Shoichet, Brian K.

AU - Shriver, Leah P.

AU - Johnson, Jeffrey R.

AU - Shaw, Megan L.

AU - Chanda, Sumit K.

AU - Roden, Dan M.

AU - Carter, Tonia C.

AU - Kottyan, Leah C.

AU - Chisholm, Rex L.

AU - Pacheco, Jennifer A.

AU - Smith, Maureen E.

AU - Schrodi, Steven J.

AU - Albrecht, Randy A.

AU - Vignuzzi, Marco

AU - Zuliani-Alvarez, Lorena

AU - Swaney, Danielle L.

AU - Eckhardt, Manon

AU - Wolinsky, Steven M.

AU - White, Kris M.

AU - Hultquist, Judd F.

AU - Kaake, Robyn M.

AU - García-Sastre, Adolfo

AU - Krogan, Nevan J.

PY - 2023/12

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N2 - Influenza A Virus (IAV) is a recurring respiratory virus with limited availability of antiviral therapies. Understanding host proteins essential for IAV infection can identify targets for alternative host-directed therapies (HDTs). Using affinity purification-mass spectrometry and global phosphoproteomic and protein abundance analyses using three IAV strains (pH1N1, H3N2, H5N1) in three human cell types (A549, NHBE, THP-1), we map 332 IAV-human protein-protein interactions and identify 13 IAV-modulated kinases. Whole exome sequencing of patients who experienced severe influenza reveals several genes, including scaffold protein AHNAK, with predicted loss-of-function variants that are also identified in our proteomic analyses. Of our identified host factors, 54 significantly alter IAV infection upon siRNA knockdown, and two factors, AHNAK and coatomer subunit COPB1, are also essential for productive infection by SARS-CoV-2. Finally, 16 compounds targeting our identified host factors suppress IAV replication, with two targeting CDK2 and FLT3 showing pan-antiviral activity across influenza and coronavirus families. This study provides a comprehensive network model of IAV infection in human cells, identifying functional host targets for pan-viral HDT.

AB - Influenza A Virus (IAV) is a recurring respiratory virus with limited availability of antiviral therapies. Understanding host proteins essential for IAV infection can identify targets for alternative host-directed therapies (HDTs). Using affinity purification-mass spectrometry and global phosphoproteomic and protein abundance analyses using three IAV strains (pH1N1, H3N2, H5N1) in three human cell types (A549, NHBE, THP-1), we map 332 IAV-human protein-protein interactions and identify 13 IAV-modulated kinases. Whole exome sequencing of patients who experienced severe influenza reveals several genes, including scaffold protein AHNAK, with predicted loss-of-function variants that are also identified in our proteomic analyses. Of our identified host factors, 54 significantly alter IAV infection upon siRNA knockdown, and two factors, AHNAK and coatomer subunit COPB1, are also essential for productive infection by SARS-CoV-2. Finally, 16 compounds targeting our identified host factors suppress IAV replication, with two targeting CDK2 and FLT3 showing pan-antiviral activity across influenza and coronavirus families. This study provides a comprehensive network model of IAV infection in human cells, identifying functional host targets for pan-viral HDT.

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Proteomic and genetic analyses of influenza A viruses identify pan-viral host targets

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