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Pre- and peri-implantation Zika virus infection impairs fetal development by targeting trophectoderm cells

Zika virus (ZIKV) infection results in an increased risk of spontaneous abortion and poor intrauterine growth although the underlying mechanisms remain undetermined. Little is known about the impact of ZIKV infection during the earliest stages of pregnancy, at pre- and peri-implantation, because mos...

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Autores principales: Tan, Lei, Lacko, Lauretta A., Zhou, Ting, Tomoiaga, Delia, Hurtado, Romulo, Zhang, Tuo, Sevilla, Ana, Zhong, Aaron, Mason, Christopher E, Noggle, Scott, Evans, Todd, Stuhlmann, Heidi, Schwartz, Robert E., Chen, Shuibing
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6744420/
https://www.ncbi.nlm.nih.gov/pubmed/31519912
http://dx.doi.org/10.1038/s41467-019-12063-2
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author Tan, Lei
Lacko, Lauretta A.
Zhou, Ting
Tomoiaga, Delia
Hurtado, Romulo
Zhang, Tuo
Sevilla, Ana
Zhong, Aaron
Mason, Christopher E
Noggle, Scott
Evans, Todd
Stuhlmann, Heidi
Schwartz, Robert E.
Chen, Shuibing
author_facet Tan, Lei
Lacko, Lauretta A.
Zhou, Ting
Tomoiaga, Delia
Hurtado, Romulo
Zhang, Tuo
Sevilla, Ana
Zhong, Aaron
Mason, Christopher E
Noggle, Scott
Evans, Todd
Stuhlmann, Heidi
Schwartz, Robert E.
Chen, Shuibing
author_sort Tan, Lei
collection PubMed
description Zika virus (ZIKV) infection results in an increased risk of spontaneous abortion and poor intrauterine growth although the underlying mechanisms remain undetermined. Little is known about the impact of ZIKV infection during the earliest stages of pregnancy, at pre- and peri-implantation, because most current ZIKV pregnancy studies have focused on post-implantation stages. Here, we demonstrate that trophectoderm cells of pre-implantation human and mouse embryos can be infected with ZIKV, and propagate virus causing neural progenitor cell death. These findings are corroborated by the dose-dependent nature of ZIKV susceptibility of hESC-derived trophectoderm cells. Single blastocyst RNA-seq reveals key transcriptional changes upon ZIKV infection, including nervous system development, prior to commitment to the neural lineage. The pregnancy rate of mice is >50% lower in pre-implantation infection than infection at E4.5, demonstrating that pre-implantation ZIKV infection leads to miscarriage. Cumulatively, these data elucidate a previously unappreciated association of pre- and peri-implantation ZIKV infection and microcephaly.
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spelling pubmed-67444202019-09-16 Pre- and peri-implantation Zika virus infection impairs fetal development by targeting trophectoderm cells Tan, Lei Lacko, Lauretta A. Zhou, Ting Tomoiaga, Delia Hurtado, Romulo Zhang, Tuo Sevilla, Ana Zhong, Aaron Mason, Christopher E Noggle, Scott Evans, Todd Stuhlmann, Heidi Schwartz, Robert E. Chen, Shuibing Nat Commun Article Zika virus (ZIKV) infection results in an increased risk of spontaneous abortion and poor intrauterine growth although the underlying mechanisms remain undetermined. Little is known about the impact of ZIKV infection during the earliest stages of pregnancy, at pre- and peri-implantation, because most current ZIKV pregnancy studies have focused on post-implantation stages. Here, we demonstrate that trophectoderm cells of pre-implantation human and mouse embryos can be infected with ZIKV, and propagate virus causing neural progenitor cell death. These findings are corroborated by the dose-dependent nature of ZIKV susceptibility of hESC-derived trophectoderm cells. Single blastocyst RNA-seq reveals key transcriptional changes upon ZIKV infection, including nervous system development, prior to commitment to the neural lineage. The pregnancy rate of mice is >50% lower in pre-implantation infection than infection at E4.5, demonstrating that pre-implantation ZIKV infection leads to miscarriage. Cumulatively, these data elucidate a previously unappreciated association of pre- and peri-implantation ZIKV infection and microcephaly. Nature Publishing Group UK 2019-09-13 /pmc/articles/PMC6744420/ /pubmed/31519912 http://dx.doi.org/10.1038/s41467-019-12063-2 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
Tan, Lei
Lacko, Lauretta A.
Zhou, Ting
Tomoiaga, Delia
Hurtado, Romulo
Zhang, Tuo
Sevilla, Ana
Zhong, Aaron
Mason, Christopher E
Noggle, Scott
Evans, Todd
Stuhlmann, Heidi
Schwartz, Robert E.
Chen, Shuibing
Pre- and peri-implantation Zika virus infection impairs fetal development by targeting trophectoderm cells
title Pre- and peri-implantation Zika virus infection impairs fetal development by targeting trophectoderm cells
title_full Pre- and peri-implantation Zika virus infection impairs fetal development by targeting trophectoderm cells
title_fullStr Pre- and peri-implantation Zika virus infection impairs fetal development by targeting trophectoderm cells
title_full_unstemmed Pre- and peri-implantation Zika virus infection impairs fetal development by targeting trophectoderm cells
title_short Pre- and peri-implantation Zika virus infection impairs fetal development by targeting trophectoderm cells
title_sort pre- and peri-implantation zika virus infection impairs fetal development by targeting trophectoderm cells
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6744420/
https://www.ncbi.nlm.nih.gov/pubmed/31519912
http://dx.doi.org/10.1038/s41467-019-12063-2
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