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Sexual and Vertical Transmission of Zika Virus in anti-interferon receptor-treated Rag1-deficient mice
Although Zika virus (ZIKV) is primarily transmitted to humans by the Aedes aegypti mosquito, human-to-human transmission has also been observed from males-to-females as well as mother-to-offspring. In the current study, we studied both sexual transmission (STx) and vertical transmission (VTx) of ZIK...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5543051/ https://www.ncbi.nlm.nih.gov/pubmed/28775298 http://dx.doi.org/10.1038/s41598-017-07099-7 |
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author | Winkler, Clayton W. Woods, Tyson A. Rosenke, Rebecca Scott, Dana P. Best, Sonja M. Peterson, Karin E. |
author_facet | Winkler, Clayton W. Woods, Tyson A. Rosenke, Rebecca Scott, Dana P. Best, Sonja M. Peterson, Karin E. |
author_sort | Winkler, Clayton W. |
collection | PubMed |
description | Although Zika virus (ZIKV) is primarily transmitted to humans by the Aedes aegypti mosquito, human-to-human transmission has also been observed from males-to-females as well as mother-to-offspring. In the current study, we studied both sexual transmission (STx) and vertical transmission (VTx) of ZIKV using anti-IFNAR1-treatment of Rag1 (−/−) (AIR) mice. These mice have suppressed type I IFN responses and lack adaptive immune responses, leading to a prolonged infection prior to clinical disease. STx of ZIKV from infected AIR males to naive Ifnar1 (−/−) females was observed with greater than 50% incidence, with infection observed in the vaginal tract at early time points. In the case of a resulting pregnancy, virus was also found in the uterus and placental tissue. In additional studies, VTx of virus was observed in AIR female mice. Specifically, peripheral ZIKV infection of pregnant AIR females resulted in detectable virus in brain and/or lymph nodes of fetuses and/or pups. VTx of ZIKV was stochastic, in that not all fetuses/pups within the same dam had detectable virus and infection was not associated with breakdown of maternal/fetal placental barrier. This provides a new model to study the barriers to STx and VTx of ZIKV and the immune responses essential to preventing transmission. |
format | Online Article Text |
id | pubmed-5543051 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-55430512017-08-07 Sexual and Vertical Transmission of Zika Virus in anti-interferon receptor-treated Rag1-deficient mice Winkler, Clayton W. Woods, Tyson A. Rosenke, Rebecca Scott, Dana P. Best, Sonja M. Peterson, Karin E. Sci Rep Article Although Zika virus (ZIKV) is primarily transmitted to humans by the Aedes aegypti mosquito, human-to-human transmission has also been observed from males-to-females as well as mother-to-offspring. In the current study, we studied both sexual transmission (STx) and vertical transmission (VTx) of ZIKV using anti-IFNAR1-treatment of Rag1 (−/−) (AIR) mice. These mice have suppressed type I IFN responses and lack adaptive immune responses, leading to a prolonged infection prior to clinical disease. STx of ZIKV from infected AIR males to naive Ifnar1 (−/−) females was observed with greater than 50% incidence, with infection observed in the vaginal tract at early time points. In the case of a resulting pregnancy, virus was also found in the uterus and placental tissue. In additional studies, VTx of virus was observed in AIR female mice. Specifically, peripheral ZIKV infection of pregnant AIR females resulted in detectable virus in brain and/or lymph nodes of fetuses and/or pups. VTx of ZIKV was stochastic, in that not all fetuses/pups within the same dam had detectable virus and infection was not associated with breakdown of maternal/fetal placental barrier. This provides a new model to study the barriers to STx and VTx of ZIKV and the immune responses essential to preventing transmission. Nature Publishing Group UK 2017-08-03 /pmc/articles/PMC5543051/ /pubmed/28775298 http://dx.doi.org/10.1038/s41598-017-07099-7 Text en © The Author(s) 2017 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 Winkler, Clayton W. Woods, Tyson A. Rosenke, Rebecca Scott, Dana P. Best, Sonja M. Peterson, Karin E. Sexual and Vertical Transmission of Zika Virus in anti-interferon receptor-treated Rag1-deficient mice |
title | Sexual and Vertical Transmission of Zika Virus in anti-interferon receptor-treated Rag1-deficient mice |
title_full | Sexual and Vertical Transmission of Zika Virus in anti-interferon receptor-treated Rag1-deficient mice |
title_fullStr | Sexual and Vertical Transmission of Zika Virus in anti-interferon receptor-treated Rag1-deficient mice |
title_full_unstemmed | Sexual and Vertical Transmission of Zika Virus in anti-interferon receptor-treated Rag1-deficient mice |
title_short | Sexual and Vertical Transmission of Zika Virus in anti-interferon receptor-treated Rag1-deficient mice |
title_sort | sexual and vertical transmission of zika virus in anti-interferon receptor-treated rag1-deficient mice |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5543051/ https://www.ncbi.nlm.nih.gov/pubmed/28775298 http://dx.doi.org/10.1038/s41598-017-07099-7 |
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