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SAMHD1 Enhances Chikungunya and Zika Virus Replication in Human Skin Fibroblasts
Chikungunya virus (CHIKV) and Zika virus (ZIKV) are emerging arboviruses that pose a worldwide threat to human health. Currently, neither vaccine nor antiviral treatment to control their infections is available. As the skin is a major viral entry site for arboviruses in the human host, we determined...
Autores principales: | , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6480247/ https://www.ncbi.nlm.nih.gov/pubmed/30959732 http://dx.doi.org/10.3390/ijms20071695 |
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author | Wichit, Sineewanlaya Hamel, Rodolphe Zanzoni, Andreas Diop, Fodé Cribier, Alexandra Talignani, Loïc Diack, Abibatou Ferraris, Pauline Liegeois, Florian Urbach, Serge Ekchariyawat, Peeraya Merits, Andres Yssel, Hans Benkirane, Monsef Missé, Dorothée |
author_facet | Wichit, Sineewanlaya Hamel, Rodolphe Zanzoni, Andreas Diop, Fodé Cribier, Alexandra Talignani, Loïc Diack, Abibatou Ferraris, Pauline Liegeois, Florian Urbach, Serge Ekchariyawat, Peeraya Merits, Andres Yssel, Hans Benkirane, Monsef Missé, Dorothée |
author_sort | Wichit, Sineewanlaya |
collection | PubMed |
description | Chikungunya virus (CHIKV) and Zika virus (ZIKV) are emerging arboviruses that pose a worldwide threat to human health. Currently, neither vaccine nor antiviral treatment to control their infections is available. As the skin is a major viral entry site for arboviruses in the human host, we determined the global proteomic profile of CHIKV and ZIKV infections in human skin fibroblasts using Stable Isotope Labelling by Amino acids in Cell culture (SILAC)-based mass-spectrometry analysis. We show that the expression of the interferon-stimulated proteins MX1, IFIT1, IFIT3 and ISG15, as well as expression of defense response proteins DDX58, STAT1, OAS3, EIF2AK2 and SAMHD1 was significantly up-regulated in these cells upon infection with either virus. Exogenous expression of IFITs proteins markedly inhibited CHIKV and ZIKV replication which, accordingly, was restored following the abrogation of IFIT1 or IFIT3. Overexpression of SAMHD1 in cutaneous cells, or pretreatment of cells with the virus-like particles containing SAMHD1 restriction factor Vpx, resulted in a strong increase or inhibition, respectively, of both CHIKV and ZIKV replication. Moreover, silencing of SAMHD1 by specific SAMHD1-siRNA resulted in a marked decrease of viral RNA levels. Together, these results suggest that IFITs are involved in the restriction of replication of CHIKV and ZIKV and provide, as yet unreported, evidence for a proviral role of SAMHD1 in arbovirus infection of human skin cells. |
format | Online Article Text |
id | pubmed-6480247 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-64802472019-04-29 SAMHD1 Enhances Chikungunya and Zika Virus Replication in Human Skin Fibroblasts Wichit, Sineewanlaya Hamel, Rodolphe Zanzoni, Andreas Diop, Fodé Cribier, Alexandra Talignani, Loïc Diack, Abibatou Ferraris, Pauline Liegeois, Florian Urbach, Serge Ekchariyawat, Peeraya Merits, Andres Yssel, Hans Benkirane, Monsef Missé, Dorothée Int J Mol Sci Article Chikungunya virus (CHIKV) and Zika virus (ZIKV) are emerging arboviruses that pose a worldwide threat to human health. Currently, neither vaccine nor antiviral treatment to control their infections is available. As the skin is a major viral entry site for arboviruses in the human host, we determined the global proteomic profile of CHIKV and ZIKV infections in human skin fibroblasts using Stable Isotope Labelling by Amino acids in Cell culture (SILAC)-based mass-spectrometry analysis. We show that the expression of the interferon-stimulated proteins MX1, IFIT1, IFIT3 and ISG15, as well as expression of defense response proteins DDX58, STAT1, OAS3, EIF2AK2 and SAMHD1 was significantly up-regulated in these cells upon infection with either virus. Exogenous expression of IFITs proteins markedly inhibited CHIKV and ZIKV replication which, accordingly, was restored following the abrogation of IFIT1 or IFIT3. Overexpression of SAMHD1 in cutaneous cells, or pretreatment of cells with the virus-like particles containing SAMHD1 restriction factor Vpx, resulted in a strong increase or inhibition, respectively, of both CHIKV and ZIKV replication. Moreover, silencing of SAMHD1 by specific SAMHD1-siRNA resulted in a marked decrease of viral RNA levels. Together, these results suggest that IFITs are involved in the restriction of replication of CHIKV and ZIKV and provide, as yet unreported, evidence for a proviral role of SAMHD1 in arbovirus infection of human skin cells. MDPI 2019-04-05 /pmc/articles/PMC6480247/ /pubmed/30959732 http://dx.doi.org/10.3390/ijms20071695 Text en © 2019 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Wichit, Sineewanlaya Hamel, Rodolphe Zanzoni, Andreas Diop, Fodé Cribier, Alexandra Talignani, Loïc Diack, Abibatou Ferraris, Pauline Liegeois, Florian Urbach, Serge Ekchariyawat, Peeraya Merits, Andres Yssel, Hans Benkirane, Monsef Missé, Dorothée SAMHD1 Enhances Chikungunya and Zika Virus Replication in Human Skin Fibroblasts |
title | SAMHD1 Enhances Chikungunya and Zika Virus Replication in Human Skin Fibroblasts |
title_full | SAMHD1 Enhances Chikungunya and Zika Virus Replication in Human Skin Fibroblasts |
title_fullStr | SAMHD1 Enhances Chikungunya and Zika Virus Replication in Human Skin Fibroblasts |
title_full_unstemmed | SAMHD1 Enhances Chikungunya and Zika Virus Replication in Human Skin Fibroblasts |
title_short | SAMHD1 Enhances Chikungunya and Zika Virus Replication in Human Skin Fibroblasts |
title_sort | samhd1 enhances chikungunya and zika virus replication in human skin fibroblasts |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6480247/ https://www.ncbi.nlm.nih.gov/pubmed/30959732 http://dx.doi.org/10.3390/ijms20071695 |
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