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Development of a Viral-Like Particle Candidate Vaccine Against Novel Variant Infectious Bursal Disease Virus
Infectious bursal disease (IBD), an immunosuppressive disease of young chickens, is caused by infectious bursal disease virus (IBDV). Novel variant IBDV (nVarIBDV), a virus that can evade immune protection against very virulent IBDV (vvIBDV), is becoming a threat to the poultry industry. Therefore,...
Autores principales: | , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7916800/ https://www.ncbi.nlm.nih.gov/pubmed/33579020 http://dx.doi.org/10.3390/vaccines9020142 |
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author | Wang, Yulong Jiang, Nan Fan, Linjin Gao, Li Li, Kai Gao, Yulong Niu, Xinxin Zhang, Wenying Cui, Hongyu Liu, Aijing Pan, Qing Liu, Changjun Zhang, Yanping Wang, Xiaomei Qi, Xiaole |
author_facet | Wang, Yulong Jiang, Nan Fan, Linjin Gao, Li Li, Kai Gao, Yulong Niu, Xinxin Zhang, Wenying Cui, Hongyu Liu, Aijing Pan, Qing Liu, Changjun Zhang, Yanping Wang, Xiaomei Qi, Xiaole |
author_sort | Wang, Yulong |
collection | PubMed |
description | Infectious bursal disease (IBD), an immunosuppressive disease of young chickens, is caused by infectious bursal disease virus (IBDV). Novel variant IBDV (nVarIBDV), a virus that can evade immune protection against very virulent IBDV (vvIBDV), is becoming a threat to the poultry industry. Therefore, nVarIBDV-specific vaccine is much needed for nVarIBDV control. In this study, the VP2 protein of SHG19 (a representative strain of nVarIBDV) was successfully expressed using an Escherichia coli expression system and further purified via ammonium sulfate precipitation and size-exclusion chromatography. The purified protein SHG19-VP2-466 could self-assemble into 25-nm virus-like particle (VLP). Subsequently, the immunogenicity and protective effect of the SHG19-VLP vaccine were evaluated using animal experiments, which indicated that the SHG19-VLP vaccine elicited neutralization antibodies and provided 100% protection against the nVarIBDV. Furthermore, the protective efficacy of the SHG19-VLP vaccine against the vvIBDV was evaluated. Although the SHG19-VLP vaccine induced a comparatively lower vvIBDV-specific neutralization antibody titer, it provided good protection against the lethal vvIBDV. In summary, the SHG19-VLP candidate vaccine could provide complete immune protection against the homologous nVarIBDV as well as the heterologous vvIBDV. This study is of significance to the comprehensive prevention and control of the recent atypical IBD epidemic. |
format | Online Article Text |
id | pubmed-7916800 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-79168002021-03-01 Development of a Viral-Like Particle Candidate Vaccine Against Novel Variant Infectious Bursal Disease Virus Wang, Yulong Jiang, Nan Fan, Linjin Gao, Li Li, Kai Gao, Yulong Niu, Xinxin Zhang, Wenying Cui, Hongyu Liu, Aijing Pan, Qing Liu, Changjun Zhang, Yanping Wang, Xiaomei Qi, Xiaole Vaccines (Basel) Article Infectious bursal disease (IBD), an immunosuppressive disease of young chickens, is caused by infectious bursal disease virus (IBDV). Novel variant IBDV (nVarIBDV), a virus that can evade immune protection against very virulent IBDV (vvIBDV), is becoming a threat to the poultry industry. Therefore, nVarIBDV-specific vaccine is much needed for nVarIBDV control. In this study, the VP2 protein of SHG19 (a representative strain of nVarIBDV) was successfully expressed using an Escherichia coli expression system and further purified via ammonium sulfate precipitation and size-exclusion chromatography. The purified protein SHG19-VP2-466 could self-assemble into 25-nm virus-like particle (VLP). Subsequently, the immunogenicity and protective effect of the SHG19-VLP vaccine were evaluated using animal experiments, which indicated that the SHG19-VLP vaccine elicited neutralization antibodies and provided 100% protection against the nVarIBDV. Furthermore, the protective efficacy of the SHG19-VLP vaccine against the vvIBDV was evaluated. Although the SHG19-VLP vaccine induced a comparatively lower vvIBDV-specific neutralization antibody titer, it provided good protection against the lethal vvIBDV. In summary, the SHG19-VLP candidate vaccine could provide complete immune protection against the homologous nVarIBDV as well as the heterologous vvIBDV. This study is of significance to the comprehensive prevention and control of the recent atypical IBD epidemic. MDPI 2021-02-10 /pmc/articles/PMC7916800/ /pubmed/33579020 http://dx.doi.org/10.3390/vaccines9020142 Text en © 2021 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 Wang, Yulong Jiang, Nan Fan, Linjin Gao, Li Li, Kai Gao, Yulong Niu, Xinxin Zhang, Wenying Cui, Hongyu Liu, Aijing Pan, Qing Liu, Changjun Zhang, Yanping Wang, Xiaomei Qi, Xiaole Development of a Viral-Like Particle Candidate Vaccine Against Novel Variant Infectious Bursal Disease Virus |
title | Development of a Viral-Like Particle Candidate Vaccine Against Novel Variant Infectious Bursal Disease Virus |
title_full | Development of a Viral-Like Particle Candidate Vaccine Against Novel Variant Infectious Bursal Disease Virus |
title_fullStr | Development of a Viral-Like Particle Candidate Vaccine Against Novel Variant Infectious Bursal Disease Virus |
title_full_unstemmed | Development of a Viral-Like Particle Candidate Vaccine Against Novel Variant Infectious Bursal Disease Virus |
title_short | Development of a Viral-Like Particle Candidate Vaccine Against Novel Variant Infectious Bursal Disease Virus |
title_sort | development of a viral-like particle candidate vaccine against novel variant infectious bursal disease virus |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7916800/ https://www.ncbi.nlm.nih.gov/pubmed/33579020 http://dx.doi.org/10.3390/vaccines9020142 |
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