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Zika virus noncoding RNA suppresses apoptosis and is required for virus transmission by mosquitoes
Flaviviruses, including Zika virus (ZIKV), utilise host mRNA degradation machinery to produce subgenomic flaviviral RNA (sfRNA). In mammalian hosts, this noncoding RNA facilitates replication and pathogenesis of flaviviruses by inhibiting IFN-signalling, whereas the function of sfRNA in mosquitoes r...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7200751/ https://www.ncbi.nlm.nih.gov/pubmed/32371874 http://dx.doi.org/10.1038/s41467-020-16086-y |
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author | Slonchak, Andrii Hugo, Leon E. Freney, Morgan E. Hall-Mendelin, Sonja Amarilla, Alberto A. Torres, Francisco J. Setoh, Yin Xiang Peng, Nias Y. G. Sng, Julian D. J. Hall, Roy A. van den Hurk, Andrew F. Devine, Gregor J. Khromykh, Alexander A. |
author_facet | Slonchak, Andrii Hugo, Leon E. Freney, Morgan E. Hall-Mendelin, Sonja Amarilla, Alberto A. Torres, Francisco J. Setoh, Yin Xiang Peng, Nias Y. G. Sng, Julian D. J. Hall, Roy A. van den Hurk, Andrew F. Devine, Gregor J. Khromykh, Alexander A. |
author_sort | Slonchak, Andrii |
collection | PubMed |
description | Flaviviruses, including Zika virus (ZIKV), utilise host mRNA degradation machinery to produce subgenomic flaviviral RNA (sfRNA). In mammalian hosts, this noncoding RNA facilitates replication and pathogenesis of flaviviruses by inhibiting IFN-signalling, whereas the function of sfRNA in mosquitoes remains largely elusive. Herein, we conduct a series of in vitro and in vivo experiments to define the role of ZIKV sfRNA in infected Aedes aegypti employing viruses deficient in production of sfRNA. We show that sfRNA-deficient viruses have reduced ability to disseminate and reach saliva, thus implicating the role for sfRNA in productive infection and transmission. We also demonstrate that production of sfRNA alters the expression of mosquito genes related to cell death pathways, and prevents apoptosis in mosquito tissues. Inhibition of apoptosis restored replication and transmission of sfRNA-deficient mutants. Hence, we propose anti-apoptotic activity of sfRNA as the mechanism defining its role in ZIKV transmission. |
format | Online Article Text |
id | pubmed-7200751 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-72007512020-05-07 Zika virus noncoding RNA suppresses apoptosis and is required for virus transmission by mosquitoes Slonchak, Andrii Hugo, Leon E. Freney, Morgan E. Hall-Mendelin, Sonja Amarilla, Alberto A. Torres, Francisco J. Setoh, Yin Xiang Peng, Nias Y. G. Sng, Julian D. J. Hall, Roy A. van den Hurk, Andrew F. Devine, Gregor J. Khromykh, Alexander A. Nat Commun Article Flaviviruses, including Zika virus (ZIKV), utilise host mRNA degradation machinery to produce subgenomic flaviviral RNA (sfRNA). In mammalian hosts, this noncoding RNA facilitates replication and pathogenesis of flaviviruses by inhibiting IFN-signalling, whereas the function of sfRNA in mosquitoes remains largely elusive. Herein, we conduct a series of in vitro and in vivo experiments to define the role of ZIKV sfRNA in infected Aedes aegypti employing viruses deficient in production of sfRNA. We show that sfRNA-deficient viruses have reduced ability to disseminate and reach saliva, thus implicating the role for sfRNA in productive infection and transmission. We also demonstrate that production of sfRNA alters the expression of mosquito genes related to cell death pathways, and prevents apoptosis in mosquito tissues. Inhibition of apoptosis restored replication and transmission of sfRNA-deficient mutants. Hence, we propose anti-apoptotic activity of sfRNA as the mechanism defining its role in ZIKV transmission. Nature Publishing Group UK 2020-05-05 /pmc/articles/PMC7200751/ /pubmed/32371874 http://dx.doi.org/10.1038/s41467-020-16086-y Text en © The Author(s) 2020 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/. |
spellingShingle | Article Slonchak, Andrii Hugo, Leon E. Freney, Morgan E. Hall-Mendelin, Sonja Amarilla, Alberto A. Torres, Francisco J. Setoh, Yin Xiang Peng, Nias Y. G. Sng, Julian D. J. Hall, Roy A. van den Hurk, Andrew F. Devine, Gregor J. Khromykh, Alexander A. Zika virus noncoding RNA suppresses apoptosis and is required for virus transmission by mosquitoes |
title | Zika virus noncoding RNA suppresses apoptosis and is required for virus transmission by mosquitoes |
title_full | Zika virus noncoding RNA suppresses apoptosis and is required for virus transmission by mosquitoes |
title_fullStr | Zika virus noncoding RNA suppresses apoptosis and is required for virus transmission by mosquitoes |
title_full_unstemmed | Zika virus noncoding RNA suppresses apoptosis and is required for virus transmission by mosquitoes |
title_short | Zika virus noncoding RNA suppresses apoptosis and is required for virus transmission by mosquitoes |
title_sort | zika virus noncoding rna suppresses apoptosis and is required for virus transmission by mosquitoes |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7200751/ https://www.ncbi.nlm.nih.gov/pubmed/32371874 http://dx.doi.org/10.1038/s41467-020-16086-y |
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