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Efficacy of a Commercial PCV2a Vaccine with a Two-Dose Regimen Against PCV2d
Porcine circovirus type 2, the causative agent of porcine circovirus associated diseases (PCVAD), consists of three major genotypes PCV2a, 2b and 2d. Current commercial vaccines contain the first-identified PCV2a’s capsid protein or whole virions. Outbreaks of PCVAD, caused by the recently identifie...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6789767/ https://www.ncbi.nlm.nih.gov/pubmed/31261743 http://dx.doi.org/10.3390/vetsci6030061 |
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author | Kolyvushko, Oleksandr Rakibuzzaman, AGM Pillatzki, Angela Webb, Brett Ramamoorthy, Sheela |
author_facet | Kolyvushko, Oleksandr Rakibuzzaman, AGM Pillatzki, Angela Webb, Brett Ramamoorthy, Sheela |
author_sort | Kolyvushko, Oleksandr |
collection | PubMed |
description | Porcine circovirus type 2, the causative agent of porcine circovirus associated diseases (PCVAD), consists of three major genotypes PCV2a, 2b and 2d. Current commercial vaccines contain the first-identified PCV2a’s capsid protein or whole virions. Outbreaks of PCVAD, caused by the recently identified PCV2d in vaccinated herds have raised concerns regarding the efficacy of current PCV2a vaccines against PCV2d. Thus, the primary objective of this study was to assess the efficacy of a two-dose regimen for the recently reformulated Fostera PCV MetaStim vaccine, to determine if reformulation with the squalene oil adjuvant and two-dose regimen improves the threshold of protection enough to eliminate viremia in a vaccination and challenge model. Two groups of seven pigs each were vaccinated with the commercial vaccine or PBS, and challenged with the PCV2d virus. Strong pre-challenge virus neutralizing responses were detected against all three genotypes. Post-challenge viremia was not completely eliminated as expected but a 2 log(10) mean reduction in viral load was achieved in vaccinated pigs. Vaccinated pigs had a mean score of 0 for pathological evaluation, while unvaccinated pigs had a score of 6.6. In conclusion, the reformulated Fostera PCV MetaStim PCV2a-based vaccine provided significant heterologous protection and was effective against PCV2d. |
format | Online Article Text |
id | pubmed-6789767 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-67897672019-10-16 Efficacy of a Commercial PCV2a Vaccine with a Two-Dose Regimen Against PCV2d Kolyvushko, Oleksandr Rakibuzzaman, AGM Pillatzki, Angela Webb, Brett Ramamoorthy, Sheela Vet Sci Article Porcine circovirus type 2, the causative agent of porcine circovirus associated diseases (PCVAD), consists of three major genotypes PCV2a, 2b and 2d. Current commercial vaccines contain the first-identified PCV2a’s capsid protein or whole virions. Outbreaks of PCVAD, caused by the recently identified PCV2d in vaccinated herds have raised concerns regarding the efficacy of current PCV2a vaccines against PCV2d. Thus, the primary objective of this study was to assess the efficacy of a two-dose regimen for the recently reformulated Fostera PCV MetaStim vaccine, to determine if reformulation with the squalene oil adjuvant and two-dose regimen improves the threshold of protection enough to eliminate viremia in a vaccination and challenge model. Two groups of seven pigs each were vaccinated with the commercial vaccine or PBS, and challenged with the PCV2d virus. Strong pre-challenge virus neutralizing responses were detected against all three genotypes. Post-challenge viremia was not completely eliminated as expected but a 2 log(10) mean reduction in viral load was achieved in vaccinated pigs. Vaccinated pigs had a mean score of 0 for pathological evaluation, while unvaccinated pigs had a score of 6.6. In conclusion, the reformulated Fostera PCV MetaStim PCV2a-based vaccine provided significant heterologous protection and was effective against PCV2d. MDPI 2019-06-28 /pmc/articles/PMC6789767/ /pubmed/31261743 http://dx.doi.org/10.3390/vetsci6030061 Text en © 2019 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 Kolyvushko, Oleksandr Rakibuzzaman, AGM Pillatzki, Angela Webb, Brett Ramamoorthy, Sheela Efficacy of a Commercial PCV2a Vaccine with a Two-Dose Regimen Against PCV2d |
title | Efficacy of a Commercial PCV2a Vaccine with a Two-Dose Regimen Against PCV2d |
title_full | Efficacy of a Commercial PCV2a Vaccine with a Two-Dose Regimen Against PCV2d |
title_fullStr | Efficacy of a Commercial PCV2a Vaccine with a Two-Dose Regimen Against PCV2d |
title_full_unstemmed | Efficacy of a Commercial PCV2a Vaccine with a Two-Dose Regimen Against PCV2d |
title_short | Efficacy of a Commercial PCV2a Vaccine with a Two-Dose Regimen Against PCV2d |
title_sort | efficacy of a commercial pcv2a vaccine with a two-dose regimen against pcv2d |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6789767/ https://www.ncbi.nlm.nih.gov/pubmed/31261743 http://dx.doi.org/10.3390/vetsci6030061 |
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