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TMEM106A inhibits enveloped virus release from cell surface

Enveloped viruses pose constant threat to hosts from ocean to land. Virion particle release from cell surface is a critical step in the viral life cycle for most enveloped viruses, making it a common antiviral target for the host defense system. Here we report that host factor TMEM106A inhibits the...

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Detalles Bibliográficos
Autores principales: Mao, Dexin, Yan, Feixiang, Zhang, Xiaolin, Gao, Guangxia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8844723/
https://www.ncbi.nlm.nih.gov/pubmed/35198896
http://dx.doi.org/10.1016/j.isci.2022.103843
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author Mao, Dexin
Yan, Feixiang
Zhang, Xiaolin
Gao, Guangxia
author_facet Mao, Dexin
Yan, Feixiang
Zhang, Xiaolin
Gao, Guangxia
author_sort Mao, Dexin
collection PubMed
description Enveloped viruses pose constant threat to hosts from ocean to land. Virion particle release from cell surface is a critical step in the viral life cycle for most enveloped viruses, making it a common antiviral target for the host defense system. Here we report that host factor TMEM106A inhibits the release of enveloped viruses from the cell surface. TMEM106A is a type II transmembrane protein localized on the plasma membrane and can be incorporated into HIV-1 virion particles. Through intermolecular interactions of its C-terminal domains on virion particle and plasma membrane, TMEM106A traps virion particles to the cell surface. HIV-1 Env interacts with TMEM106A to interfere with the intermolecular interactions and partially suppresses its antiviral activity. TMEM106A orthologs from various species displayed potent antiviral activity against multiple enveloped viruses. These results suggest that TMEM106A is an evolutionarily conserved antiviral factor that inhibits the release of enveloped viruses from the cell surface.
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spelling pubmed-88447232022-02-22 TMEM106A inhibits enveloped virus release from cell surface Mao, Dexin Yan, Feixiang Zhang, Xiaolin Gao, Guangxia iScience Article Enveloped viruses pose constant threat to hosts from ocean to land. Virion particle release from cell surface is a critical step in the viral life cycle for most enveloped viruses, making it a common antiviral target for the host defense system. Here we report that host factor TMEM106A inhibits the release of enveloped viruses from the cell surface. TMEM106A is a type II transmembrane protein localized on the plasma membrane and can be incorporated into HIV-1 virion particles. Through intermolecular interactions of its C-terminal domains on virion particle and plasma membrane, TMEM106A traps virion particles to the cell surface. HIV-1 Env interacts with TMEM106A to interfere with the intermolecular interactions and partially suppresses its antiviral activity. TMEM106A orthologs from various species displayed potent antiviral activity against multiple enveloped viruses. These results suggest that TMEM106A is an evolutionarily conserved antiviral factor that inhibits the release of enveloped viruses from the cell surface. Elsevier 2022-02-01 /pmc/articles/PMC8844723/ /pubmed/35198896 http://dx.doi.org/10.1016/j.isci.2022.103843 Text en © 2022 The Authors https://creativecommons.org/licenses/by/4.0/This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Mao, Dexin
Yan, Feixiang
Zhang, Xiaolin
Gao, Guangxia
TMEM106A inhibits enveloped virus release from cell surface
title TMEM106A inhibits enveloped virus release from cell surface
title_full TMEM106A inhibits enveloped virus release from cell surface
title_fullStr TMEM106A inhibits enveloped virus release from cell surface
title_full_unstemmed TMEM106A inhibits enveloped virus release from cell surface
title_short TMEM106A inhibits enveloped virus release from cell surface
title_sort tmem106a inhibits enveloped virus release from cell surface
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8844723/
https://www.ncbi.nlm.nih.gov/pubmed/35198896
http://dx.doi.org/10.1016/j.isci.2022.103843
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