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Comparative innocuity and efficacy of live and inactivated sheeppox vaccines

BACKGROUND: Sheeppox (SPP) is one of the priorities, high-impact animal diseases in many developing countries, where live attenuated vaccines are routinely used against sheeppox virus (SPPV). In an event of an SPP outbreak, historically disease-free countries would hesitate to use of live vaccines a...

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Autores principales: Boumart, Zineb, Daouam, Samira, Belkourati, Imane, Rafi, Lamya, Tuppurainen, Eeva, Tadlaoui, Khalid Omari, El Harrak, Mehdi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4928353/
https://www.ncbi.nlm.nih.gov/pubmed/27357388
http://dx.doi.org/10.1186/s12917-016-0754-0
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author Boumart, Zineb
Daouam, Samira
Belkourati, Imane
Rafi, Lamya
Tuppurainen, Eeva
Tadlaoui, Khalid Omari
El Harrak, Mehdi
author_facet Boumart, Zineb
Daouam, Samira
Belkourati, Imane
Rafi, Lamya
Tuppurainen, Eeva
Tadlaoui, Khalid Omari
El Harrak, Mehdi
author_sort Boumart, Zineb
collection PubMed
description BACKGROUND: Sheeppox (SPP) is one of the priorities, high-impact animal diseases in many developing countries, where live attenuated vaccines are routinely used against sheeppox virus (SPPV). In an event of an SPP outbreak, historically disease-free countries would hesitate to use of live vaccines against SPPVdue to the safety and trade reasons. Currently no killed SPPV vaccines are commercially available. In this study, we developed an inactivated Romanian SPPVvaccine and assessed its efficacy and potency in comparison with a live attenuated Romanian SPPV vaccine. Four naïve sheep were vaccinated once with the Romanian SPPV live attenuated vaccine and16 sheep were vaccinated twice with the inactivated vaccine. All sheep in the live vaccine group were included in the challenge trial, which was conducted using a highly virulent Moroccan SPPV field strain. Eight sheep of the inactivated vaccine group were challenged and the remaining sheep were monitored for seroconversion. Experimental animals were closely monitored for the appearance of clinical signs, body temperature and inflammation at the injection site. Two naïve sheep were used as unvaccinated controls. RESULTS: The inactivated Romanian SPPV vaccine was found to be safe and confer a good protection, similar to the live vaccine. Specific antibodies appeared from seven days post vaccination and remained up to nine months. CONCLUSION: This study showed that the developed inactivated Romanian SPPV vaccine has a potential to replace attenuated vaccine to control and prevent sheep pox in disease-free or endemic countries.
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spelling pubmed-49283532016-06-30 Comparative innocuity and efficacy of live and inactivated sheeppox vaccines Boumart, Zineb Daouam, Samira Belkourati, Imane Rafi, Lamya Tuppurainen, Eeva Tadlaoui, Khalid Omari El Harrak, Mehdi BMC Vet Res Research Article BACKGROUND: Sheeppox (SPP) is one of the priorities, high-impact animal diseases in many developing countries, where live attenuated vaccines are routinely used against sheeppox virus (SPPV). In an event of an SPP outbreak, historically disease-free countries would hesitate to use of live vaccines against SPPVdue to the safety and trade reasons. Currently no killed SPPV vaccines are commercially available. In this study, we developed an inactivated Romanian SPPVvaccine and assessed its efficacy and potency in comparison with a live attenuated Romanian SPPV vaccine. Four naïve sheep were vaccinated once with the Romanian SPPV live attenuated vaccine and16 sheep were vaccinated twice with the inactivated vaccine. All sheep in the live vaccine group were included in the challenge trial, which was conducted using a highly virulent Moroccan SPPV field strain. Eight sheep of the inactivated vaccine group were challenged and the remaining sheep were monitored for seroconversion. Experimental animals were closely monitored for the appearance of clinical signs, body temperature and inflammation at the injection site. Two naïve sheep were used as unvaccinated controls. RESULTS: The inactivated Romanian SPPV vaccine was found to be safe and confer a good protection, similar to the live vaccine. Specific antibodies appeared from seven days post vaccination and remained up to nine months. CONCLUSION: This study showed that the developed inactivated Romanian SPPV vaccine has a potential to replace attenuated vaccine to control and prevent sheep pox in disease-free or endemic countries. BioMed Central 2016-06-29 /pmc/articles/PMC4928353/ /pubmed/27357388 http://dx.doi.org/10.1186/s12917-016-0754-0 Text en © The Author(s). 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Boumart, Zineb
Daouam, Samira
Belkourati, Imane
Rafi, Lamya
Tuppurainen, Eeva
Tadlaoui, Khalid Omari
El Harrak, Mehdi
Comparative innocuity and efficacy of live and inactivated sheeppox vaccines
title Comparative innocuity and efficacy of live and inactivated sheeppox vaccines
title_full Comparative innocuity and efficacy of live and inactivated sheeppox vaccines
title_fullStr Comparative innocuity and efficacy of live and inactivated sheeppox vaccines
title_full_unstemmed Comparative innocuity and efficacy of live and inactivated sheeppox vaccines
title_short Comparative innocuity and efficacy of live and inactivated sheeppox vaccines
title_sort comparative innocuity and efficacy of live and inactivated sheeppox vaccines
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4928353/
https://www.ncbi.nlm.nih.gov/pubmed/27357388
http://dx.doi.org/10.1186/s12917-016-0754-0
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