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Comparative Pathogenesis of Asian and African-Lineage Zika Virus in Indian Rhesus Macaque’s and Development of a Non-Human Primate Model Suitable for the Evaluation of New Drugs and Vaccines

The establishment of a well characterized non-human primate model of Zika virus (ZIKV) infection is critical for the development of medical interventions. In this study, challenging Indian rhesus macaques (IRMs) with ZIKV strains of the Asian lineage resulted in dose-dependent peak viral loads betwe...

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Autores principales: Rayner, Jonathan O., Kalkeri, Raj, Goebel, Scott, Cai, Zhaohui, Green, Brian, Lin, Shuling, Snyder, Beth, Hagelin, Kimberly, Walters, Kevin B., Koide, Fusataka
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5977222/
https://www.ncbi.nlm.nih.gov/pubmed/29723973
http://dx.doi.org/10.3390/v10050229
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author Rayner, Jonathan O.
Kalkeri, Raj
Goebel, Scott
Cai, Zhaohui
Green, Brian
Lin, Shuling
Snyder, Beth
Hagelin, Kimberly
Walters, Kevin B.
Koide, Fusataka
author_facet Rayner, Jonathan O.
Kalkeri, Raj
Goebel, Scott
Cai, Zhaohui
Green, Brian
Lin, Shuling
Snyder, Beth
Hagelin, Kimberly
Walters, Kevin B.
Koide, Fusataka
author_sort Rayner, Jonathan O.
collection PubMed
description The establishment of a well characterized non-human primate model of Zika virus (ZIKV) infection is critical for the development of medical interventions. In this study, challenging Indian rhesus macaques (IRMs) with ZIKV strains of the Asian lineage resulted in dose-dependent peak viral loads between days 2 and 5 post infection and a robust immune response which protected the animals from homologous and heterologous re-challenge. In contrast, viremia in IRMs challenged with an African lineage strain was below the assay’s lower limit of quantitation, and the immune response was insufficient to protect from re-challenge. These results corroborate previous observations but are contrary to reports using other African strains, obviating the need for additional studies to elucidate the variables contributing to the disparities. Nonetheless, the utility of an Asian lineage ZIKV IRM model for countermeasure development was verified by vaccinating animals with a formalin inactivated reference vaccine and demonstrating sterilizing immunity against a subsequent subcutaneous challenge.
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spelling pubmed-59772222018-06-01 Comparative Pathogenesis of Asian and African-Lineage Zika Virus in Indian Rhesus Macaque’s and Development of a Non-Human Primate Model Suitable for the Evaluation of New Drugs and Vaccines Rayner, Jonathan O. Kalkeri, Raj Goebel, Scott Cai, Zhaohui Green, Brian Lin, Shuling Snyder, Beth Hagelin, Kimberly Walters, Kevin B. Koide, Fusataka Viruses Article The establishment of a well characterized non-human primate model of Zika virus (ZIKV) infection is critical for the development of medical interventions. In this study, challenging Indian rhesus macaques (IRMs) with ZIKV strains of the Asian lineage resulted in dose-dependent peak viral loads between days 2 and 5 post infection and a robust immune response which protected the animals from homologous and heterologous re-challenge. In contrast, viremia in IRMs challenged with an African lineage strain was below the assay’s lower limit of quantitation, and the immune response was insufficient to protect from re-challenge. These results corroborate previous observations but are contrary to reports using other African strains, obviating the need for additional studies to elucidate the variables contributing to the disparities. Nonetheless, the utility of an Asian lineage ZIKV IRM model for countermeasure development was verified by vaccinating animals with a formalin inactivated reference vaccine and demonstrating sterilizing immunity against a subsequent subcutaneous challenge. MDPI 2018-05-01 /pmc/articles/PMC5977222/ /pubmed/29723973 http://dx.doi.org/10.3390/v10050229 Text en © 2018 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Rayner, Jonathan O.
Kalkeri, Raj
Goebel, Scott
Cai, Zhaohui
Green, Brian
Lin, Shuling
Snyder, Beth
Hagelin, Kimberly
Walters, Kevin B.
Koide, Fusataka
Comparative Pathogenesis of Asian and African-Lineage Zika Virus in Indian Rhesus Macaque’s and Development of a Non-Human Primate Model Suitable for the Evaluation of New Drugs and Vaccines
title Comparative Pathogenesis of Asian and African-Lineage Zika Virus in Indian Rhesus Macaque’s and Development of a Non-Human Primate Model Suitable for the Evaluation of New Drugs and Vaccines
title_full Comparative Pathogenesis of Asian and African-Lineage Zika Virus in Indian Rhesus Macaque’s and Development of a Non-Human Primate Model Suitable for the Evaluation of New Drugs and Vaccines
title_fullStr Comparative Pathogenesis of Asian and African-Lineage Zika Virus in Indian Rhesus Macaque’s and Development of a Non-Human Primate Model Suitable for the Evaluation of New Drugs and Vaccines
title_full_unstemmed Comparative Pathogenesis of Asian and African-Lineage Zika Virus in Indian Rhesus Macaque’s and Development of a Non-Human Primate Model Suitable for the Evaluation of New Drugs and Vaccines
title_short Comparative Pathogenesis of Asian and African-Lineage Zika Virus in Indian Rhesus Macaque’s and Development of a Non-Human Primate Model Suitable for the Evaluation of New Drugs and Vaccines
title_sort comparative pathogenesis of asian and african-lineage zika virus in indian rhesus macaque’s and development of a non-human primate model suitable for the evaluation of new drugs and vaccines
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5977222/
https://www.ncbi.nlm.nih.gov/pubmed/29723973
http://dx.doi.org/10.3390/v10050229
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