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Type I Interferon-Induced TMEM106A Blocks Attachment of EV-A71 Virus by Interacting With the Membrane Protein SCARB2

Enterovirus A71 (EV-A71) and Coxsackievirus A16 (CV-A16) are the main causative agents of hand, foot and mouth disease (HFMD) worldwide. Studies showed that EV-A71 and CV-A16 antagonize the interferon (IFN) signaling pathway; however, how IFN controls this viral infection is largely unknown. Here, w...

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Autores principales: Guo, Xuemin, Zeng, Shinuan, Ji, Xiaoxin, Meng, Xiaobin, Lei, Nanfeng, Yang, Hai, Mu, Xin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8963425/
https://www.ncbi.nlm.nih.gov/pubmed/35359978
http://dx.doi.org/10.3389/fimmu.2022.817835
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author Guo, Xuemin
Zeng, Shinuan
Ji, Xiaoxin
Meng, Xiaobin
Lei, Nanfeng
Yang, Hai
Mu, Xin
author_facet Guo, Xuemin
Zeng, Shinuan
Ji, Xiaoxin
Meng, Xiaobin
Lei, Nanfeng
Yang, Hai
Mu, Xin
author_sort Guo, Xuemin
collection PubMed
description Enterovirus A71 (EV-A71) and Coxsackievirus A16 (CV-A16) are the main causative agents of hand, foot and mouth disease (HFMD) worldwide. Studies showed that EV-A71 and CV-A16 antagonize the interferon (IFN) signaling pathway; however, how IFN controls this viral infection is largely unknown. Here, we identified an IFN-stimulated gene, Transmembrane Protein 106A (TMEM106A), encoding a protein that blocks EV-A71 and CV-A16 infection. Combined approaches measuring viral infection, gene expression, and protein interactions uncovered that TMEM106A is required for optimal IFN-mediated viral inhibition and interferes with EV-A71 binding to host cells on the receptor scavenger receptor class B member 2 (SCARB2). Our findings reveal a new mechanism contributing to the IFN-mediated defense against EV-A71 and CV-A16 infection and provide a potential strategy for HFMD treatment by using the antiviral role of TMEM106A against enterovirus.
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spelling pubmed-89634252022-03-30 Type I Interferon-Induced TMEM106A Blocks Attachment of EV-A71 Virus by Interacting With the Membrane Protein SCARB2 Guo, Xuemin Zeng, Shinuan Ji, Xiaoxin Meng, Xiaobin Lei, Nanfeng Yang, Hai Mu, Xin Front Immunol Immunology Enterovirus A71 (EV-A71) and Coxsackievirus A16 (CV-A16) are the main causative agents of hand, foot and mouth disease (HFMD) worldwide. Studies showed that EV-A71 and CV-A16 antagonize the interferon (IFN) signaling pathway; however, how IFN controls this viral infection is largely unknown. Here, we identified an IFN-stimulated gene, Transmembrane Protein 106A (TMEM106A), encoding a protein that blocks EV-A71 and CV-A16 infection. Combined approaches measuring viral infection, gene expression, and protein interactions uncovered that TMEM106A is required for optimal IFN-mediated viral inhibition and interferes with EV-A71 binding to host cells on the receptor scavenger receptor class B member 2 (SCARB2). Our findings reveal a new mechanism contributing to the IFN-mediated defense against EV-A71 and CV-A16 infection and provide a potential strategy for HFMD treatment by using the antiviral role of TMEM106A against enterovirus. Frontiers Media S.A. 2022-03-11 /pmc/articles/PMC8963425/ /pubmed/35359978 http://dx.doi.org/10.3389/fimmu.2022.817835 Text en Copyright © 2022 Guo, Zeng, Ji, Meng, Lei, Yang and Mu https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Immunology
Guo, Xuemin
Zeng, Shinuan
Ji, Xiaoxin
Meng, Xiaobin
Lei, Nanfeng
Yang, Hai
Mu, Xin
Type I Interferon-Induced TMEM106A Blocks Attachment of EV-A71 Virus by Interacting With the Membrane Protein SCARB2
title Type I Interferon-Induced TMEM106A Blocks Attachment of EV-A71 Virus by Interacting With the Membrane Protein SCARB2
title_full Type I Interferon-Induced TMEM106A Blocks Attachment of EV-A71 Virus by Interacting With the Membrane Protein SCARB2
title_fullStr Type I Interferon-Induced TMEM106A Blocks Attachment of EV-A71 Virus by Interacting With the Membrane Protein SCARB2
title_full_unstemmed Type I Interferon-Induced TMEM106A Blocks Attachment of EV-A71 Virus by Interacting With the Membrane Protein SCARB2
title_short Type I Interferon-Induced TMEM106A Blocks Attachment of EV-A71 Virus by Interacting With the Membrane Protein SCARB2
title_sort type i interferon-induced tmem106a blocks attachment of ev-a71 virus by interacting with the membrane protein scarb2
topic Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8963425/
https://www.ncbi.nlm.nih.gov/pubmed/35359978
http://dx.doi.org/10.3389/fimmu.2022.817835
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