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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...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2018
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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. |
format | Online Article Text |
id | pubmed-5977222 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
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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