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Zika virus infection confers protection against West Nile virus challenge in mice
Flaviviruses are RNA viruses that constitute a worrisome threat to global human and animal health. Zika virus (ZIKV), which was initially reported to cause a mild disease, recently spread in the Americas, infecting millions of people. During this recent epidemic, ZIKV infection has been linked to se...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5625318/ https://www.ncbi.nlm.nih.gov/pubmed/28928416 http://dx.doi.org/10.1038/emi.2017.68 |
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author | Vázquez-Calvo, Ángela Blázquez, Ana-Belén Escribano-Romero, Estela Merino-Ramos, Teresa Saiz, Juan-Carlos Martín-Acebes, Miguel A Jiménez de Oya, Nereida |
author_facet | Vázquez-Calvo, Ángela Blázquez, Ana-Belén Escribano-Romero, Estela Merino-Ramos, Teresa Saiz, Juan-Carlos Martín-Acebes, Miguel A Jiménez de Oya, Nereida |
author_sort | Vázquez-Calvo, Ángela |
collection | PubMed |
description | Flaviviruses are RNA viruses that constitute a worrisome threat to global human and animal health. Zika virus (ZIKV), which was initially reported to cause a mild disease, recently spread in the Americas, infecting millions of people. During this recent epidemic, ZIKV infection has been linked to serious neurological diseases and birth defects, specifically Guillain-Barrè syndrome (GBS) and microcephaly. Because information about ZIKV immunity remains scarce, we assessed the humoral response of immunocompetent mice to infection with three viral strains of diverse geographical origin (Africa, Asia and America). No infected animals showed any sign of disease or died after infection. However, specific neutralizing antibodies were elicited in all infected mice. Considering the rapid expansion of ZIKV throughout the American continent and its co-circulation with other medically relevant flaviviruses, such as West Nile virus (WNV), the induction of protective immunity between ZIKV and WNV was analyzed. Remarkably, protection after challenge with WNV was observed in mice previously infected with ZIKV, as survival rates were significantly higher than in control mice. Moreover, previous ZIKV infection enhanced the humoral immune response against WNV. These findings may be relevant in geographical areas where both ZIKV and WNV co-circulate, as well as for the future development of broad-spectrum flavivirus vaccines. |
format | Online Article Text |
id | pubmed-5625318 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-56253182017-10-04 Zika virus infection confers protection against West Nile virus challenge in mice Vázquez-Calvo, Ángela Blázquez, Ana-Belén Escribano-Romero, Estela Merino-Ramos, Teresa Saiz, Juan-Carlos Martín-Acebes, Miguel A Jiménez de Oya, Nereida Emerg Microbes Infect Original Article Flaviviruses are RNA viruses that constitute a worrisome threat to global human and animal health. Zika virus (ZIKV), which was initially reported to cause a mild disease, recently spread in the Americas, infecting millions of people. During this recent epidemic, ZIKV infection has been linked to serious neurological diseases and birth defects, specifically Guillain-Barrè syndrome (GBS) and microcephaly. Because information about ZIKV immunity remains scarce, we assessed the humoral response of immunocompetent mice to infection with three viral strains of diverse geographical origin (Africa, Asia and America). No infected animals showed any sign of disease or died after infection. However, specific neutralizing antibodies were elicited in all infected mice. Considering the rapid expansion of ZIKV throughout the American continent and its co-circulation with other medically relevant flaviviruses, such as West Nile virus (WNV), the induction of protective immunity between ZIKV and WNV was analyzed. Remarkably, protection after challenge with WNV was observed in mice previously infected with ZIKV, as survival rates were significantly higher than in control mice. Moreover, previous ZIKV infection enhanced the humoral immune response against WNV. These findings may be relevant in geographical areas where both ZIKV and WNV co-circulate, as well as for the future development of broad-spectrum flavivirus vaccines. Nature Publishing Group 2017-09 2017-09-20 /pmc/articles/PMC5625318/ /pubmed/28928416 http://dx.doi.org/10.1038/emi.2017.68 Text en Copyright © 2017 The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Original Article Vázquez-Calvo, Ángela Blázquez, Ana-Belén Escribano-Romero, Estela Merino-Ramos, Teresa Saiz, Juan-Carlos Martín-Acebes, Miguel A Jiménez de Oya, Nereida Zika virus infection confers protection against West Nile virus challenge in mice |
title | Zika virus infection confers protection against West Nile virus challenge in mice |
title_full | Zika virus infection confers protection against West Nile virus challenge in mice |
title_fullStr | Zika virus infection confers protection against West Nile virus challenge in mice |
title_full_unstemmed | Zika virus infection confers protection against West Nile virus challenge in mice |
title_short | Zika virus infection confers protection against West Nile virus challenge in mice |
title_sort | zika virus infection confers protection against west nile virus challenge in mice |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5625318/ https://www.ncbi.nlm.nih.gov/pubmed/28928416 http://dx.doi.org/10.1038/emi.2017.68 |
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