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Mucosal Responses to Zika Virus Infection in Cynomolgus Macaques

Zika virus (ZIKV) cases continue to be reported, and no vaccine or specific antiviral agent has been approved for the prevention or treatment of infection. Though ZIKV is primarily transmitted by mosquitos, cases of sexual transmission and prolonged viral RNA presence in semen have been reported. In...

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Autores principales: Berry, Neil, Stein, Monja, Ferguson, Deborah, Ham, Claire, Hall, Jo, Giles, Elaine, Kempster, Sarah, Adedeji, Yemisi, Almond, Neil, Herrera, Carolina
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9503824/
https://www.ncbi.nlm.nih.gov/pubmed/36145466
http://dx.doi.org/10.3390/pathogens11091033
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author Berry, Neil
Stein, Monja
Ferguson, Deborah
Ham, Claire
Hall, Jo
Giles, Elaine
Kempster, Sarah
Adedeji, Yemisi
Almond, Neil
Herrera, Carolina
author_facet Berry, Neil
Stein, Monja
Ferguson, Deborah
Ham, Claire
Hall, Jo
Giles, Elaine
Kempster, Sarah
Adedeji, Yemisi
Almond, Neil
Herrera, Carolina
author_sort Berry, Neil
collection PubMed
description Zika virus (ZIKV) cases continue to be reported, and no vaccine or specific antiviral agent has been approved for the prevention or treatment of infection. Though ZIKV is primarily transmitted by mosquitos, cases of sexual transmission and prolonged viral RNA presence in semen have been reported. In this observational study, we report the mucosal responses to sub-cutaneous and mucosal ZIKV exposure in cynomolgus macaques during acute and late chronic infection. Subcutaneous challenge induced a decrease in the growth factor VEGF in colorectal and cervicovaginal tissues 100 days post-challenge, in contrast to the observed increase in these tissues following vaginal infection. This different pattern was not observed in the uterus, where VEGF was upregulated independently of the challenge route. Vaginal challenge induced a pro-inflammatory profile in all mucosal tissues during late chronic infection. Similar responses were already observed during acute infection in a vaginal tissue explant model of ex vivo challenge. Non-productive and productive infection 100 days post-in vivo vaginal challenge induced distinct proteomic profiles which were characterized by further VEGF increase and IL-10 decrease in non-infected animals. Ex vivo challenge of mucosal explants revealed tissue-specific modulation of cytokine levels during the acute phase of infection. Mucosal cytokine profiles could represent biosignatures of persistent ZIKV infection.
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spelling pubmed-95038242022-09-24 Mucosal Responses to Zika Virus Infection in Cynomolgus Macaques Berry, Neil Stein, Monja Ferguson, Deborah Ham, Claire Hall, Jo Giles, Elaine Kempster, Sarah Adedeji, Yemisi Almond, Neil Herrera, Carolina Pathogens Article Zika virus (ZIKV) cases continue to be reported, and no vaccine or specific antiviral agent has been approved for the prevention or treatment of infection. Though ZIKV is primarily transmitted by mosquitos, cases of sexual transmission and prolonged viral RNA presence in semen have been reported. In this observational study, we report the mucosal responses to sub-cutaneous and mucosal ZIKV exposure in cynomolgus macaques during acute and late chronic infection. Subcutaneous challenge induced a decrease in the growth factor VEGF in colorectal and cervicovaginal tissues 100 days post-challenge, in contrast to the observed increase in these tissues following vaginal infection. This different pattern was not observed in the uterus, where VEGF was upregulated independently of the challenge route. Vaginal challenge induced a pro-inflammatory profile in all mucosal tissues during late chronic infection. Similar responses were already observed during acute infection in a vaginal tissue explant model of ex vivo challenge. Non-productive and productive infection 100 days post-in vivo vaginal challenge induced distinct proteomic profiles which were characterized by further VEGF increase and IL-10 decrease in non-infected animals. Ex vivo challenge of mucosal explants revealed tissue-specific modulation of cytokine levels during the acute phase of infection. Mucosal cytokine profiles could represent biosignatures of persistent ZIKV infection. MDPI 2022-09-12 /pmc/articles/PMC9503824/ /pubmed/36145466 http://dx.doi.org/10.3390/pathogens11091033 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/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 (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Berry, Neil
Stein, Monja
Ferguson, Deborah
Ham, Claire
Hall, Jo
Giles, Elaine
Kempster, Sarah
Adedeji, Yemisi
Almond, Neil
Herrera, Carolina
Mucosal Responses to Zika Virus Infection in Cynomolgus Macaques
title Mucosal Responses to Zika Virus Infection in Cynomolgus Macaques
title_full Mucosal Responses to Zika Virus Infection in Cynomolgus Macaques
title_fullStr Mucosal Responses to Zika Virus Infection in Cynomolgus Macaques
title_full_unstemmed Mucosal Responses to Zika Virus Infection in Cynomolgus Macaques
title_short Mucosal Responses to Zika Virus Infection in Cynomolgus Macaques
title_sort mucosal responses to zika virus infection in cynomolgus macaques
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9503824/
https://www.ncbi.nlm.nih.gov/pubmed/36145466
http://dx.doi.org/10.3390/pathogens11091033
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