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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...

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Autores principales: 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.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2017
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.
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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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