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Preconceptual Zika virus asymptomatic infection protects against secondary prenatal infection
Pregnant women, and their fetal offspring, are uniquely susceptible to Zika virus and other microbial pathogens capable of congenital fetal infection. Unavoidable exposure to Zika virus in endemic areas underscores the need for identifying at-risk individuals, and protecting expecting mothers and th...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5689831/ https://www.ncbi.nlm.nih.gov/pubmed/29145516 http://dx.doi.org/10.1371/journal.ppat.1006684 |
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author | Turner, Lucien H. Kinder, Jeremy M. Wilburn, Adrienne D’Mello, Rahul J. Braunlin, Makayla R. Jiang, Tony T. Pham, Giang Way, Sing Sing |
author_facet | Turner, Lucien H. Kinder, Jeremy M. Wilburn, Adrienne D’Mello, Rahul J. Braunlin, Makayla R. Jiang, Tony T. Pham, Giang Way, Sing Sing |
author_sort | Turner, Lucien H. |
collection | PubMed |
description | Pregnant women, and their fetal offspring, are uniquely susceptible to Zika virus and other microbial pathogens capable of congenital fetal infection. Unavoidable exposure to Zika virus in endemic areas underscores the need for identifying at-risk individuals, and protecting expecting mothers and their fetal offspring against prenatal infection. Here we show that primary Zika virus asymptomatic infection in mice confers protection against re-infection, and that these protective benefits are maintained during pregnancy. Zika virus recovery was sharply reduced in maternal tissues and amongst fetal concepti after prenatal challenge in mothers with resolved subclinical infection prior to pregnancy compared with mice undergoing primary prenatal infection. These benefits coincide with expanded accumulation of viral-specific antibodies in maternal serum and fetal tissues that protect against infection by the identical or heterologous Zika virus genotype strains. Thus, preconceptual infection primes Zika virus-specific antibodies that confer cross-genotype protection against re-infection during pregnancy. |
format | Online Article Text |
id | pubmed-5689831 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-56898312017-11-30 Preconceptual Zika virus asymptomatic infection protects against secondary prenatal infection Turner, Lucien H. Kinder, Jeremy M. Wilburn, Adrienne D’Mello, Rahul J. Braunlin, Makayla R. Jiang, Tony T. Pham, Giang Way, Sing Sing PLoS Pathog Research Article Pregnant women, and their fetal offspring, are uniquely susceptible to Zika virus and other microbial pathogens capable of congenital fetal infection. Unavoidable exposure to Zika virus in endemic areas underscores the need for identifying at-risk individuals, and protecting expecting mothers and their fetal offspring against prenatal infection. Here we show that primary Zika virus asymptomatic infection in mice confers protection against re-infection, and that these protective benefits are maintained during pregnancy. Zika virus recovery was sharply reduced in maternal tissues and amongst fetal concepti after prenatal challenge in mothers with resolved subclinical infection prior to pregnancy compared with mice undergoing primary prenatal infection. These benefits coincide with expanded accumulation of viral-specific antibodies in maternal serum and fetal tissues that protect against infection by the identical or heterologous Zika virus genotype strains. Thus, preconceptual infection primes Zika virus-specific antibodies that confer cross-genotype protection against re-infection during pregnancy. Public Library of Science 2017-11-16 /pmc/articles/PMC5689831/ /pubmed/29145516 http://dx.doi.org/10.1371/journal.ppat.1006684 Text en © 2017 Turner et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Turner, Lucien H. Kinder, Jeremy M. Wilburn, Adrienne D’Mello, Rahul J. Braunlin, Makayla R. Jiang, Tony T. Pham, Giang Way, Sing Sing Preconceptual Zika virus asymptomatic infection protects against secondary prenatal infection |
title | Preconceptual Zika virus asymptomatic infection protects against secondary prenatal infection |
title_full | Preconceptual Zika virus asymptomatic infection protects against secondary prenatal infection |
title_fullStr | Preconceptual Zika virus asymptomatic infection protects against secondary prenatal infection |
title_full_unstemmed | Preconceptual Zika virus asymptomatic infection protects against secondary prenatal infection |
title_short | Preconceptual Zika virus asymptomatic infection protects against secondary prenatal infection |
title_sort | preconceptual zika virus asymptomatic infection protects against secondary prenatal infection |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5689831/ https://www.ncbi.nlm.nih.gov/pubmed/29145516 http://dx.doi.org/10.1371/journal.ppat.1006684 |
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