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An epidemic Zika virus isolate suppresses antiviral immunity by disrupting antigen presentation pathways
Zika virus (ZIKV) has emerged as an important global health threat, with the recently acquired capacity to cause severe neurological symptoms and to persist within host tissues. We previously demonstrated that an early Asian lineage ZIKV isolate induces a highly activated CD8 T cell response specifi...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8245533/ https://www.ncbi.nlm.nih.gov/pubmed/34193875 http://dx.doi.org/10.1038/s41467-021-24340-0 |
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author | Pardy, Ryan D. Valbon, Stefanie F. Cordeiro, Brendan Krawczyk, Connie M. Richer, Martin J. |
author_facet | Pardy, Ryan D. Valbon, Stefanie F. Cordeiro, Brendan Krawczyk, Connie M. Richer, Martin J. |
author_sort | Pardy, Ryan D. |
collection | PubMed |
description | Zika virus (ZIKV) has emerged as an important global health threat, with the recently acquired capacity to cause severe neurological symptoms and to persist within host tissues. We previously demonstrated that an early Asian lineage ZIKV isolate induces a highly activated CD8 T cell response specific for an immunodominant epitope in the ZIKV envelope protein in wild-type mice. Here we show that a contemporary ZIKV isolate from the Brazilian outbreak severely limits CD8 T cell immunity in mice and blocks generation of the immunodominant CD8 T cell response. This is associated with a more sustained infection that is cleared between 7- and 14-days post-infection. Mechanistically, we demonstrate that infection with the Brazilian ZIKV isolate reduces the cross-presentation capacity of dendritic cells and fails to fully activate the immunoproteasome. Thus, our study provides an isolate-specific mechanism of host immune evasion by one Brazilian ZIKV isolate, which differs from the early Asian lineage isolate and provides potential insight into viral persistence associated with recent ZIKV outbreaks. |
format | Online Article Text |
id | pubmed-8245533 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-82455332021-07-20 An epidemic Zika virus isolate suppresses antiviral immunity by disrupting antigen presentation pathways Pardy, Ryan D. Valbon, Stefanie F. Cordeiro, Brendan Krawczyk, Connie M. Richer, Martin J. Nat Commun Article Zika virus (ZIKV) has emerged as an important global health threat, with the recently acquired capacity to cause severe neurological symptoms and to persist within host tissues. We previously demonstrated that an early Asian lineage ZIKV isolate induces a highly activated CD8 T cell response specific for an immunodominant epitope in the ZIKV envelope protein in wild-type mice. Here we show that a contemporary ZIKV isolate from the Brazilian outbreak severely limits CD8 T cell immunity in mice and blocks generation of the immunodominant CD8 T cell response. This is associated with a more sustained infection that is cleared between 7- and 14-days post-infection. Mechanistically, we demonstrate that infection with the Brazilian ZIKV isolate reduces the cross-presentation capacity of dendritic cells and fails to fully activate the immunoproteasome. Thus, our study provides an isolate-specific mechanism of host immune evasion by one Brazilian ZIKV isolate, which differs from the early Asian lineage isolate and provides potential insight into viral persistence associated with recent ZIKV outbreaks. Nature Publishing Group UK 2021-06-30 /pmc/articles/PMC8245533/ /pubmed/34193875 http://dx.doi.org/10.1038/s41467-021-24340-0 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Pardy, Ryan D. Valbon, Stefanie F. Cordeiro, Brendan Krawczyk, Connie M. Richer, Martin J. An epidemic Zika virus isolate suppresses antiviral immunity by disrupting antigen presentation pathways |
title | An epidemic Zika virus isolate suppresses antiviral immunity by disrupting antigen presentation pathways |
title_full | An epidemic Zika virus isolate suppresses antiviral immunity by disrupting antigen presentation pathways |
title_fullStr | An epidemic Zika virus isolate suppresses antiviral immunity by disrupting antigen presentation pathways |
title_full_unstemmed | An epidemic Zika virus isolate suppresses antiviral immunity by disrupting antigen presentation pathways |
title_short | An epidemic Zika virus isolate suppresses antiviral immunity by disrupting antigen presentation pathways |
title_sort | epidemic zika virus isolate suppresses antiviral immunity by disrupting antigen presentation pathways |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8245533/ https://www.ncbi.nlm.nih.gov/pubmed/34193875 http://dx.doi.org/10.1038/s41467-021-24340-0 |
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