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A Zika Vaccine Generated Using the Chimeric Insect-Specific Binjari Virus Platform Protects against Fetal Brain Infection in Pregnant Mice
Zika virus (ZIKV) is the etiological agent of congenital Zika syndrome (CZS), a spectrum of birth defects that can lead to life-long disabilities. A range of vaccines are in development with the target population including pregnant women and women of child-bearing age. Using a recently described chi...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7564101/ https://www.ncbi.nlm.nih.gov/pubmed/32887302 http://dx.doi.org/10.3390/vaccines8030496 |
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author | Hazlewood, Jessamine E. Rawle, Daniel J. Tang, Bing Yan, Kexin Vet, Laura J. Nakayama, Eri Hobson-Peters, Jody Hall, Roy A. Suhrbier, Andreas |
author_facet | Hazlewood, Jessamine E. Rawle, Daniel J. Tang, Bing Yan, Kexin Vet, Laura J. Nakayama, Eri Hobson-Peters, Jody Hall, Roy A. Suhrbier, Andreas |
author_sort | Hazlewood, Jessamine E. |
collection | PubMed |
description | Zika virus (ZIKV) is the etiological agent of congenital Zika syndrome (CZS), a spectrum of birth defects that can lead to life-long disabilities. A range of vaccines are in development with the target population including pregnant women and women of child-bearing age. Using a recently described chimeric flavivirus vaccine technology based on the novel insect-specific Binjari virus (BinJV), we generated a ZIKV vaccine (BinJ/ZIKA-prME) and illustrate herein its ability to protect against fetal brain infection. Female IFNAR(−/−) mice were vaccinated once with unadjuvanted BinJ/ZIKA-prME, were mated, and at embryonic day 12.5 were challenged with ZIKV(PRVABC59). No infectious ZIKV was detected in maternal blood, placenta, or fetal heads in BinJ/ZIKA-prME-vaccinated mice. A similar result was obtained when the more sensitive qRT PCR methodology was used to measure the viral RNA. BinJ/ZIKA-prME vaccination also did not result in antibody-dependent enhancement of dengue virus infection or disease. BinJ/ZIKA-prME thus emerges as a potential vaccine candidate for the prevention of CSZ. |
format | Online Article Text |
id | pubmed-7564101 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-75641012020-10-27 A Zika Vaccine Generated Using the Chimeric Insect-Specific Binjari Virus Platform Protects against Fetal Brain Infection in Pregnant Mice Hazlewood, Jessamine E. Rawle, Daniel J. Tang, Bing Yan, Kexin Vet, Laura J. Nakayama, Eri Hobson-Peters, Jody Hall, Roy A. Suhrbier, Andreas Vaccines (Basel) Article Zika virus (ZIKV) is the etiological agent of congenital Zika syndrome (CZS), a spectrum of birth defects that can lead to life-long disabilities. A range of vaccines are in development with the target population including pregnant women and women of child-bearing age. Using a recently described chimeric flavivirus vaccine technology based on the novel insect-specific Binjari virus (BinJV), we generated a ZIKV vaccine (BinJ/ZIKA-prME) and illustrate herein its ability to protect against fetal brain infection. Female IFNAR(−/−) mice were vaccinated once with unadjuvanted BinJ/ZIKA-prME, were mated, and at embryonic day 12.5 were challenged with ZIKV(PRVABC59). No infectious ZIKV was detected in maternal blood, placenta, or fetal heads in BinJ/ZIKA-prME-vaccinated mice. A similar result was obtained when the more sensitive qRT PCR methodology was used to measure the viral RNA. BinJ/ZIKA-prME vaccination also did not result in antibody-dependent enhancement of dengue virus infection or disease. BinJ/ZIKA-prME thus emerges as a potential vaccine candidate for the prevention of CSZ. MDPI 2020-09-02 /pmc/articles/PMC7564101/ /pubmed/32887302 http://dx.doi.org/10.3390/vaccines8030496 Text en © 2020 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 Hazlewood, Jessamine E. Rawle, Daniel J. Tang, Bing Yan, Kexin Vet, Laura J. Nakayama, Eri Hobson-Peters, Jody Hall, Roy A. Suhrbier, Andreas A Zika Vaccine Generated Using the Chimeric Insect-Specific Binjari Virus Platform Protects against Fetal Brain Infection in Pregnant Mice |
title | A Zika Vaccine Generated Using the Chimeric Insect-Specific Binjari Virus Platform Protects against Fetal Brain Infection in Pregnant Mice |
title_full | A Zika Vaccine Generated Using the Chimeric Insect-Specific Binjari Virus Platform Protects against Fetal Brain Infection in Pregnant Mice |
title_fullStr | A Zika Vaccine Generated Using the Chimeric Insect-Specific Binjari Virus Platform Protects against Fetal Brain Infection in Pregnant Mice |
title_full_unstemmed | A Zika Vaccine Generated Using the Chimeric Insect-Specific Binjari Virus Platform Protects against Fetal Brain Infection in Pregnant Mice |
title_short | A Zika Vaccine Generated Using the Chimeric Insect-Specific Binjari Virus Platform Protects against Fetal Brain Infection in Pregnant Mice |
title_sort | zika vaccine generated using the chimeric insect-specific binjari virus platform protects against fetal brain infection in pregnant mice |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7564101/ https://www.ncbi.nlm.nih.gov/pubmed/32887302 http://dx.doi.org/10.3390/vaccines8030496 |
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