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Low expression of RNA sensors impacts Zika virus infection in the lower female reproductive tract
Innate immune responses to Zika virus (ZIKV) are dampened in the lower female reproductive tract (LFRT) compared to other tissues, but the mechanism that underlies this vulnerability is poorly understood. Using tissues from uninfected and vaginally ZIKV-infected macaques and mice, we show that low b...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6761111/ https://www.ncbi.nlm.nih.gov/pubmed/31554802 http://dx.doi.org/10.1038/s41467-019-12371-7 |
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author | Khan, Shahzada Lew, Irene Wu, Frank Fritts, Linda Fontaine, Krystal A. Tomar, Sakshi Trapecar, Martin Shehata, Hesham M. Ott, Melanie Miller, Christopher J. Sanjabi, Shomyseh |
author_facet | Khan, Shahzada Lew, Irene Wu, Frank Fritts, Linda Fontaine, Krystal A. Tomar, Sakshi Trapecar, Martin Shehata, Hesham M. Ott, Melanie Miller, Christopher J. Sanjabi, Shomyseh |
author_sort | Khan, Shahzada |
collection | PubMed |
description | Innate immune responses to Zika virus (ZIKV) are dampened in the lower female reproductive tract (LFRT) compared to other tissues, but the mechanism that underlies this vulnerability is poorly understood. Using tissues from uninfected and vaginally ZIKV-infected macaques and mice, we show that low basal expression of RNA-sensing pattern recognition receptors (PRRs), or their co-receptors, in the LFRT contributes to high viral replication in this tissue. In the LFRT, ZIKV sensing provides limited protection against viral replication, and the sensors are also minimally induced after vaginal infection. While IFNα/β receptor signaling offers minimal protection in the LFRT, it is required to prevent dissemination of ZIKV to other tissues, including the upper FRT. Our findings support a role for RNA-sensing PRRs in the dampened innate immunity against ZIKV in the LFRT compared to other tissues and underlie potential implications for systemic dissemination upon heterosexual transmission of ZIKV in women. |
format | Online Article Text |
id | pubmed-6761111 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-67611112019-09-27 Low expression of RNA sensors impacts Zika virus infection in the lower female reproductive tract Khan, Shahzada Lew, Irene Wu, Frank Fritts, Linda Fontaine, Krystal A. Tomar, Sakshi Trapecar, Martin Shehata, Hesham M. Ott, Melanie Miller, Christopher J. Sanjabi, Shomyseh Nat Commun Article Innate immune responses to Zika virus (ZIKV) are dampened in the lower female reproductive tract (LFRT) compared to other tissues, but the mechanism that underlies this vulnerability is poorly understood. Using tissues from uninfected and vaginally ZIKV-infected macaques and mice, we show that low basal expression of RNA-sensing pattern recognition receptors (PRRs), or their co-receptors, in the LFRT contributes to high viral replication in this tissue. In the LFRT, ZIKV sensing provides limited protection against viral replication, and the sensors are also minimally induced after vaginal infection. While IFNα/β receptor signaling offers minimal protection in the LFRT, it is required to prevent dissemination of ZIKV to other tissues, including the upper FRT. Our findings support a role for RNA-sensing PRRs in the dampened innate immunity against ZIKV in the LFRT compared to other tissues and underlie potential implications for systemic dissemination upon heterosexual transmission of ZIKV in women. Nature Publishing Group UK 2019-09-25 /pmc/articles/PMC6761111/ /pubmed/31554802 http://dx.doi.org/10.1038/s41467-019-12371-7 Text en © The Author(s) 2019 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 Khan, Shahzada Lew, Irene Wu, Frank Fritts, Linda Fontaine, Krystal A. Tomar, Sakshi Trapecar, Martin Shehata, Hesham M. Ott, Melanie Miller, Christopher J. Sanjabi, Shomyseh Low expression of RNA sensors impacts Zika virus infection in the lower female reproductive tract |
title | Low expression of RNA sensors impacts Zika virus infection in the lower female reproductive tract |
title_full | Low expression of RNA sensors impacts Zika virus infection in the lower female reproductive tract |
title_fullStr | Low expression of RNA sensors impacts Zika virus infection in the lower female reproductive tract |
title_full_unstemmed | Low expression of RNA sensors impacts Zika virus infection in the lower female reproductive tract |
title_short | Low expression of RNA sensors impacts Zika virus infection in the lower female reproductive tract |
title_sort | low expression of rna sensors impacts zika virus infection in the lower female reproductive tract |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6761111/ https://www.ncbi.nlm.nih.gov/pubmed/31554802 http://dx.doi.org/10.1038/s41467-019-12371-7 |
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