Experimental Zika Virus Inoculation in a New World Monkey Model Reproduces Key Features of the Human Infection

Abstract A monkey model of Zika virus (ZIKV) infection is urgently needed to better understand transmission and pathogenesis, given its proven association with fetal brain defects in pregnant women and acute neurological illness. Here we experimentally infected 4 male marmosets with ZIKV (prototype...

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Autores principales: Charles Y. Chiu, Claudia Sánchez-San Martín, Jerome Bouquet, Tony Li, Shigeo Yagi, Manasi Tamhankar, Vida L. Hodara, Laura M. Parodi, Sneha Somasekar, Guixia Yu, Luis D. Giavedoni, Suzette Tardif, Jean Patterson
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Publicado: Nature Portfolio 2017
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Acceso en línea:https://doaj.org/article/294e2f7fb0544b8eaa8d9c5fdf5f2b6d
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spelling oai:doaj.org-article:294e2f7fb0544b8eaa8d9c5fdf5f2b6d2021-12-02T15:06:19ZExperimental Zika Virus Inoculation in a New World Monkey Model Reproduces Key Features of the Human Infection10.1038/s41598-017-17067-w2045-2322https://doaj.org/article/294e2f7fb0544b8eaa8d9c5fdf5f2b6d2017-12-01T00:00:00Zhttps://doi.org/10.1038/s41598-017-17067-whttps://doaj.org/toc/2045-2322Abstract A monkey model of Zika virus (ZIKV) infection is urgently needed to better understand transmission and pathogenesis, given its proven association with fetal brain defects in pregnant women and acute neurological illness. Here we experimentally infected 4 male marmosets with ZIKV (prototype 1947 African strain) and monitored them clinically with sampling of various body fluids and tissues for nearly 3 months. We show that the course of acute infection with ZIKV in these New World monkeys resembles the human illness in many respects, including (1) lack of apparent clinical symptoms in most cases, (2) persistence of the virus in body fluids such as semen and saliva for longer periods of time than in serum, and (3) generation of neutralizing antibodies as well as an antiviral immunological host response. Importantly, ZIKV-infected saliva samples (in addition to serum) were found to be infectious, suggesting potential capacity for viral transmission by the oral route. Re-challenge of a previously infected marmoset with a contemporary outbreak strain SPH2015 from Brazil resulted in continued protection against infection, no viral shedding, and boosting of the immune response. Given the key similarities to human infection, a marmoset model of ZIKV infection may be useful for testing of new drugs and vaccines.Charles Y. ChiuClaudia Sánchez-San MartínJerome BouquetTony LiShigeo YagiManasi TamhankarVida L. HodaraLaura M. ParodiSneha SomasekarGuixia YuLuis D. GiavedoniSuzette TardifJean PattersonNature PortfolioarticleMedicineRScienceQENScientific Reports, Vol 7, Iss 1, Pp 1-11 (2017)
institution DOAJ
collection DOAJ
language EN
topic Medicine
R
Science
Q
spellingShingle Medicine
R
Science
Q
Charles Y. Chiu
Claudia Sánchez-San Martín
Jerome Bouquet
Tony Li
Shigeo Yagi
Manasi Tamhankar
Vida L. Hodara
Laura M. Parodi
Sneha Somasekar
Guixia Yu
Luis D. Giavedoni
Suzette Tardif
Jean Patterson
Experimental Zika Virus Inoculation in a New World Monkey Model Reproduces Key Features of the Human Infection
description Abstract A monkey model of Zika virus (ZIKV) infection is urgently needed to better understand transmission and pathogenesis, given its proven association with fetal brain defects in pregnant women and acute neurological illness. Here we experimentally infected 4 male marmosets with ZIKV (prototype 1947 African strain) and monitored them clinically with sampling of various body fluids and tissues for nearly 3 months. We show that the course of acute infection with ZIKV in these New World monkeys resembles the human illness in many respects, including (1) lack of apparent clinical symptoms in most cases, (2) persistence of the virus in body fluids such as semen and saliva for longer periods of time than in serum, and (3) generation of neutralizing antibodies as well as an antiviral immunological host response. Importantly, ZIKV-infected saliva samples (in addition to serum) were found to be infectious, suggesting potential capacity for viral transmission by the oral route. Re-challenge of a previously infected marmoset with a contemporary outbreak strain SPH2015 from Brazil resulted in continued protection against infection, no viral shedding, and boosting of the immune response. Given the key similarities to human infection, a marmoset model of ZIKV infection may be useful for testing of new drugs and vaccines.
format article
author Charles Y. Chiu
Claudia Sánchez-San Martín
Jerome Bouquet
Tony Li
Shigeo Yagi
Manasi Tamhankar
Vida L. Hodara
Laura M. Parodi
Sneha Somasekar
Guixia Yu
Luis D. Giavedoni
Suzette Tardif
Jean Patterson
author_facet Charles Y. Chiu
Claudia Sánchez-San Martín
Jerome Bouquet
Tony Li
Shigeo Yagi
Manasi Tamhankar
Vida L. Hodara
Laura M. Parodi
Sneha Somasekar
Guixia Yu
Luis D. Giavedoni
Suzette Tardif
Jean Patterson
author_sort Charles Y. Chiu
title Experimental Zika Virus Inoculation in a New World Monkey Model Reproduces Key Features of the Human Infection
title_short Experimental Zika Virus Inoculation in a New World Monkey Model Reproduces Key Features of the Human Infection
title_full Experimental Zika Virus Inoculation in a New World Monkey Model Reproduces Key Features of the Human Infection
title_fullStr Experimental Zika Virus Inoculation in a New World Monkey Model Reproduces Key Features of the Human Infection
title_full_unstemmed Experimental Zika Virus Inoculation in a New World Monkey Model Reproduces Key Features of the Human Infection
title_sort experimental zika virus inoculation in a new world monkey model reproduces key features of the human infection
publisher Nature Portfolio
publishDate 2017
url https://doaj.org/article/294e2f7fb0544b8eaa8d9c5fdf5f2b6d
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