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Protective efficacy of Zika vaccine in AG129 mouse model
Zika virus (ZIKV) is a mosquito-borne flavivirus that causes asymptomatic infection or presents only mild symptoms in majority of those infected. However, vaccination for ZIKV is a public health priority due to serious congenital and neuropathological abnormalities observed as a sequelae of the viru...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5388871/ https://www.ncbi.nlm.nih.gov/pubmed/28401907 http://dx.doi.org/10.1038/srep46375 |
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author | Sumathy, K. Kulkarni, Bharathi Gondu, Ravi Kumar Ponnuru, Sampath Kumar Bonguram, Nagaraju Eligeti, Rakesh Gadiyaram, Sindhuja Praturi, Usha Chougule, Bhushan Karunakaran, Latha Ella, Krishna M. |
author_facet | Sumathy, K. Kulkarni, Bharathi Gondu, Ravi Kumar Ponnuru, Sampath Kumar Bonguram, Nagaraju Eligeti, Rakesh Gadiyaram, Sindhuja Praturi, Usha Chougule, Bhushan Karunakaran, Latha Ella, Krishna M. |
author_sort | Sumathy, K. |
collection | PubMed |
description | Zika virus (ZIKV) is a mosquito-borne flavivirus that causes asymptomatic infection or presents only mild symptoms in majority of those infected. However, vaccination for ZIKV is a public health priority due to serious congenital and neuropathological abnormalities observed as a sequelae of the virus infection in the recent epidemics. We have developed an inactivated virus vaccine with the African MR 766 strain. Here we show that two doses of the vaccine provided 100% efficacy against mortality and disease following challenge with homotypic MR 766 and the heterotypic FSS 13025 ZIKV strains in the Type I and Type II interferon deficient AG129 mice. Two doses of the vaccine elicited high titer of neutralizing antibodies in Balb/c mice, and the vaccine antisera conferred protection against virus challenge in passively immunized mice. The studies were useful to rationalize vaccine doses for protective efficacy. Furthermore, the vaccine antisera neutralized the homotypic and heterotypic ZIKV strains in vitro with equivalent efficiency. Our study suggests a single ZIKV serotype, and that the development of an effective vaccine may not be limited by the choice of virus strain. |
format | Online Article Text |
id | pubmed-5388871 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-53888712017-04-14 Protective efficacy of Zika vaccine in AG129 mouse model Sumathy, K. Kulkarni, Bharathi Gondu, Ravi Kumar Ponnuru, Sampath Kumar Bonguram, Nagaraju Eligeti, Rakesh Gadiyaram, Sindhuja Praturi, Usha Chougule, Bhushan Karunakaran, Latha Ella, Krishna M. Sci Rep Article Zika virus (ZIKV) is a mosquito-borne flavivirus that causes asymptomatic infection or presents only mild symptoms in majority of those infected. However, vaccination for ZIKV is a public health priority due to serious congenital and neuropathological abnormalities observed as a sequelae of the virus infection in the recent epidemics. We have developed an inactivated virus vaccine with the African MR 766 strain. Here we show that two doses of the vaccine provided 100% efficacy against mortality and disease following challenge with homotypic MR 766 and the heterotypic FSS 13025 ZIKV strains in the Type I and Type II interferon deficient AG129 mice. Two doses of the vaccine elicited high titer of neutralizing antibodies in Balb/c mice, and the vaccine antisera conferred protection against virus challenge in passively immunized mice. The studies were useful to rationalize vaccine doses for protective efficacy. Furthermore, the vaccine antisera neutralized the homotypic and heterotypic ZIKV strains in vitro with equivalent efficiency. Our study suggests a single ZIKV serotype, and that the development of an effective vaccine may not be limited by the choice of virus strain. Nature Publishing Group 2017-04-12 /pmc/articles/PMC5388871/ /pubmed/28401907 http://dx.doi.org/10.1038/srep46375 Text en Copyright © 2017, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Sumathy, K. Kulkarni, Bharathi Gondu, Ravi Kumar Ponnuru, Sampath Kumar Bonguram, Nagaraju Eligeti, Rakesh Gadiyaram, Sindhuja Praturi, Usha Chougule, Bhushan Karunakaran, Latha Ella, Krishna M. Protective efficacy of Zika vaccine in AG129 mouse model |
title | Protective efficacy of Zika vaccine in AG129 mouse model |
title_full | Protective efficacy of Zika vaccine in AG129 mouse model |
title_fullStr | Protective efficacy of Zika vaccine in AG129 mouse model |
title_full_unstemmed | Protective efficacy of Zika vaccine in AG129 mouse model |
title_short | Protective efficacy of Zika vaccine in AG129 mouse model |
title_sort | protective efficacy of zika vaccine in ag129 mouse model |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5388871/ https://www.ncbi.nlm.nih.gov/pubmed/28401907 http://dx.doi.org/10.1038/srep46375 |
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