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Protective efficacy of inactivated Newcastle disease virus vaccines prepared in two different oil-based adjuvants

Despite the availability of Newcastle disease (ND) vaccines for more than six decades, disease outbreaks continue to occur with huge economic consequences to the global poultry industry. The aim of this study is to develop a safe and effective inactivated vaccine based on a recently isolated Newcast...

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Autores principales: Aljumaili, Oday A., Bello, Muhammad B., Yeap, Swee K., Omar, Abdul R., Ideris, Aini
Formato: Online Artículo Texto
Lenguaje:English
Publicado: AOSIS 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7565102/
https://www.ncbi.nlm.nih.gov/pubmed/33054260
http://dx.doi.org/10.4102/ojvr.v87i1.1865
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author Aljumaili, Oday A.
Bello, Muhammad B.
Yeap, Swee K.
Omar, Abdul R.
Ideris, Aini
author_facet Aljumaili, Oday A.
Bello, Muhammad B.
Yeap, Swee K.
Omar, Abdul R.
Ideris, Aini
author_sort Aljumaili, Oday A.
collection PubMed
description Despite the availability of Newcastle disease (ND) vaccines for more than six decades, disease outbreaks continue to occur with huge economic consequences to the global poultry industry. The aim of this study is to develop a safe and effective inactivated vaccine based on a recently isolated Newcastle disease virus (NDV) strain IBS025/13 and evaluate its protective efficacy in chicken following challenge with a highly virulent genotype VII isolate. Firstly, high titre of IBS025/13 was exposed to various concentrations of binary ethylenimine (BEI) to determine the optimal conditions for complete inactivation of the virus. The inactivated virus was then prepared in form of a stable water-in-oil emulsion of black seed oil (BSO) or Freund’s incomplete adjuvant (FIA) and used as vaccines in specific pathogen-free chicken. Efficacy of various vaccine preparations was also evaluated based on the ability of the vaccine to protect against clinical disease, mortality and virus shedding following challenge with highly virulent genotype\VII NDV isolate. The results indicate that exposure of NDV IBS025/13 to 10 mM of BEI for 21 h at 37 °C could completely inactivate the virus without tempering with the structural integrity of the viral hemagglutin-neuraminidase protein. More so, the inactivated vaccines adjuvanted with either BSO- or FIA-induced high hemagglutination inhibition antibody titre that protected the vaccinated birds against clinical disease and in some cases virus shedding, especially when used together with live attenuated vaccines. Thus, genotype VII-based NDV-inactivated vaccines formulated in BSO could substantially improve poultry disease control particularly when combined with live attenuated vaccines.
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spelling pubmed-75651022020-10-22 Protective efficacy of inactivated Newcastle disease virus vaccines prepared in two different oil-based adjuvants Aljumaili, Oday A. Bello, Muhammad B. Yeap, Swee K. Omar, Abdul R. Ideris, Aini Onderstepoort J Vet Res Original Research Despite the availability of Newcastle disease (ND) vaccines for more than six decades, disease outbreaks continue to occur with huge economic consequences to the global poultry industry. The aim of this study is to develop a safe and effective inactivated vaccine based on a recently isolated Newcastle disease virus (NDV) strain IBS025/13 and evaluate its protective efficacy in chicken following challenge with a highly virulent genotype VII isolate. Firstly, high titre of IBS025/13 was exposed to various concentrations of binary ethylenimine (BEI) to determine the optimal conditions for complete inactivation of the virus. The inactivated virus was then prepared in form of a stable water-in-oil emulsion of black seed oil (BSO) or Freund’s incomplete adjuvant (FIA) and used as vaccines in specific pathogen-free chicken. Efficacy of various vaccine preparations was also evaluated based on the ability of the vaccine to protect against clinical disease, mortality and virus shedding following challenge with highly virulent genotype\VII NDV isolate. The results indicate that exposure of NDV IBS025/13 to 10 mM of BEI for 21 h at 37 °C could completely inactivate the virus without tempering with the structural integrity of the viral hemagglutin-neuraminidase protein. More so, the inactivated vaccines adjuvanted with either BSO- or FIA-induced high hemagglutination inhibition antibody titre that protected the vaccinated birds against clinical disease and in some cases virus shedding, especially when used together with live attenuated vaccines. Thus, genotype VII-based NDV-inactivated vaccines formulated in BSO could substantially improve poultry disease control particularly when combined with live attenuated vaccines. AOSIS 2020-09-28 /pmc/articles/PMC7565102/ /pubmed/33054260 http://dx.doi.org/10.4102/ojvr.v87i1.1865 Text en © 2020. The Authors https://creativecommons.org/licenses/by/4.0/ Licensee: AOSIS. This work is licensed under the Creative Commons Attribution License.
spellingShingle Original Research
Aljumaili, Oday A.
Bello, Muhammad B.
Yeap, Swee K.
Omar, Abdul R.
Ideris, Aini
Protective efficacy of inactivated Newcastle disease virus vaccines prepared in two different oil-based adjuvants
title Protective efficacy of inactivated Newcastle disease virus vaccines prepared in two different oil-based adjuvants
title_full Protective efficacy of inactivated Newcastle disease virus vaccines prepared in two different oil-based adjuvants
title_fullStr Protective efficacy of inactivated Newcastle disease virus vaccines prepared in two different oil-based adjuvants
title_full_unstemmed Protective efficacy of inactivated Newcastle disease virus vaccines prepared in two different oil-based adjuvants
title_short Protective efficacy of inactivated Newcastle disease virus vaccines prepared in two different oil-based adjuvants
title_sort protective efficacy of inactivated newcastle disease virus vaccines prepared in two different oil-based adjuvants
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7565102/
https://www.ncbi.nlm.nih.gov/pubmed/33054260
http://dx.doi.org/10.4102/ojvr.v87i1.1865
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