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Protective Efficacy of a Chimeric Insect-Specific Flavivirus Vaccine against West Nile Virus
Virulent strains of West Nile virus (WNV) are highly neuro-invasive and human infection is potentially lethal. However, no vaccine is currently available for human use. Here, we report the immunogenicity and protective efficacy of a vaccine derived from a chimeric virus, which was constructed using...
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/PMC7349994/ https://www.ncbi.nlm.nih.gov/pubmed/32485930 http://dx.doi.org/10.3390/vaccines8020258 |
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author | Vet, Laura J. Setoh, Yin Xiang Amarilla, Alberto A. Habarugira, Gervais Suen, Willy W. Newton, Natalee D. Harrison, Jessica J. Hobson-Peters, Jody Hall, Roy A. Bielefeldt-Ohmann, Helle |
author_facet | Vet, Laura J. Setoh, Yin Xiang Amarilla, Alberto A. Habarugira, Gervais Suen, Willy W. Newton, Natalee D. Harrison, Jessica J. Hobson-Peters, Jody Hall, Roy A. Bielefeldt-Ohmann, Helle |
author_sort | Vet, Laura J. |
collection | PubMed |
description | Virulent strains of West Nile virus (WNV) are highly neuro-invasive and human infection is potentially lethal. However, no vaccine is currently available for human use. Here, we report the immunogenicity and protective efficacy of a vaccine derived from a chimeric virus, which was constructed using the structural proteins (prM and E) of the Kunjin strain of WNV (WNV(KUN)) and the genome backbone of the insect-specific flavivirus Binjari virus (BinJV). This chimeric virus (BinJ/WNV(KUN)-prME) exhibits an insect-specific phenotype and does not replicate in vertebrate cells. Importantly, it authentically presents the prM-E proteins of WNV(KUN), which is antigenically very similar to other WNV strains and lineages. Therefore BinJ/WNV(KUN)-prME represents an excellent candidate to assess as a vaccine against virulent WNV strains, including the highly pathogenic WNV(NY99). When CD1 mice were immunized with purified BinJ/WNV(KUN)-prME, they developed robust neutralizing antibody responses after a single unadjuvanted dose of 1 to 5 μg. We further demonstrated complete protection against viremia and mortality after lethal challenge with WNV(NY99), with no clinical or subclinical pathology observed in vaccinated animals. These data suggest that BinJ/WNV(KUN)-prME represents a safe and effective WNV vaccine candidate that warrants further investigation for use in humans or in veterinary applications. |
format | Online Article Text |
id | pubmed-7349994 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-73499942020-07-22 Protective Efficacy of a Chimeric Insect-Specific Flavivirus Vaccine against West Nile Virus Vet, Laura J. Setoh, Yin Xiang Amarilla, Alberto A. Habarugira, Gervais Suen, Willy W. Newton, Natalee D. Harrison, Jessica J. Hobson-Peters, Jody Hall, Roy A. Bielefeldt-Ohmann, Helle Vaccines (Basel) Article Virulent strains of West Nile virus (WNV) are highly neuro-invasive and human infection is potentially lethal. However, no vaccine is currently available for human use. Here, we report the immunogenicity and protective efficacy of a vaccine derived from a chimeric virus, which was constructed using the structural proteins (prM and E) of the Kunjin strain of WNV (WNV(KUN)) and the genome backbone of the insect-specific flavivirus Binjari virus (BinJV). This chimeric virus (BinJ/WNV(KUN)-prME) exhibits an insect-specific phenotype and does not replicate in vertebrate cells. Importantly, it authentically presents the prM-E proteins of WNV(KUN), which is antigenically very similar to other WNV strains and lineages. Therefore BinJ/WNV(KUN)-prME represents an excellent candidate to assess as a vaccine against virulent WNV strains, including the highly pathogenic WNV(NY99). When CD1 mice were immunized with purified BinJ/WNV(KUN)-prME, they developed robust neutralizing antibody responses after a single unadjuvanted dose of 1 to 5 μg. We further demonstrated complete protection against viremia and mortality after lethal challenge with WNV(NY99), with no clinical or subclinical pathology observed in vaccinated animals. These data suggest that BinJ/WNV(KUN)-prME represents a safe and effective WNV vaccine candidate that warrants further investigation for use in humans or in veterinary applications. MDPI 2020-05-29 /pmc/articles/PMC7349994/ /pubmed/32485930 http://dx.doi.org/10.3390/vaccines8020258 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 Vet, Laura J. Setoh, Yin Xiang Amarilla, Alberto A. Habarugira, Gervais Suen, Willy W. Newton, Natalee D. Harrison, Jessica J. Hobson-Peters, Jody Hall, Roy A. Bielefeldt-Ohmann, Helle Protective Efficacy of a Chimeric Insect-Specific Flavivirus Vaccine against West Nile Virus |
title | Protective Efficacy of a Chimeric Insect-Specific Flavivirus Vaccine against West Nile Virus |
title_full | Protective Efficacy of a Chimeric Insect-Specific Flavivirus Vaccine against West Nile Virus |
title_fullStr | Protective Efficacy of a Chimeric Insect-Specific Flavivirus Vaccine against West Nile Virus |
title_full_unstemmed | Protective Efficacy of a Chimeric Insect-Specific Flavivirus Vaccine against West Nile Virus |
title_short | Protective Efficacy of a Chimeric Insect-Specific Flavivirus Vaccine against West Nile Virus |
title_sort | protective efficacy of a chimeric insect-specific flavivirus vaccine against west nile virus |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7349994/ https://www.ncbi.nlm.nih.gov/pubmed/32485930 http://dx.doi.org/10.3390/vaccines8020258 |
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