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Non-Assembled ORF2 Capsid Protein of Porcine Circovirus 2b Does Not Confer Protective Immunity
Porcine Circovirus 2 (PCV2) vaccines are based on either inactivated whole virion, or recombinant ORF2 capsid protein assembled into Virus-like Particles (VLPs). No data are available about the immunizing properties of free, non-assembled capsid protein. To investigate this issue, ORF2 of a referenc...
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/PMC8466160/ https://www.ncbi.nlm.nih.gov/pubmed/34578193 http://dx.doi.org/10.3390/pathogens10091161 |
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author | Guarneri, Flavia Tonni, Matteo Sarli, Giuseppe Boniotti, Maria Beatrice Lelli, Davide Barbieri, Ilaria D’Annunzio, Giulia Alborali, Giovanni Loris Bacci, Barbara Amadori, Massimo |
author_facet | Guarneri, Flavia Tonni, Matteo Sarli, Giuseppe Boniotti, Maria Beatrice Lelli, Davide Barbieri, Ilaria D’Annunzio, Giulia Alborali, Giovanni Loris Bacci, Barbara Amadori, Massimo |
author_sort | Guarneri, Flavia |
collection | PubMed |
description | Porcine Circovirus 2 (PCV2) vaccines are based on either inactivated whole virion, or recombinant ORF2 capsid protein assembled into Virus-like Particles (VLPs). No data are available about the immunizing properties of free, non-assembled capsid protein. To investigate this issue, ORF2 of a reference PCV2b strain was expressed in a Baculovirus-based expression system without assembly into VLPs. The free purified protein was formulated into an oil vaccine at three distinct Ag payloads: 10.8/3.6/1.2 micrograms/dose. Each dose was injected intramuscularly into five, 37-day old piglets, carefully matched for maternally-derived antibody. Five control piglets were injected with sterile PBS in oil adjuvant. Twenty-eight days later, all the pigs were challenged intranasally with 10(5.3) TCID(50) of PCV2b strain DV6503. After challenge infection, all the pigs remained in good clinical conditions. The recombinant vaccine did not induce significant antibody and PCV2-specific IFN-γ responses. ELISPOT and lymphocyte proliferation data confirmed poor induction of cell-mediated immunity. In terms of PCV2 viremia, there was no significant difference between vaccinated and control animals. The histological data indicated the absence of a detectable viral load and of PCVAD lesions in both vaccinated and control animals, as well as of histiocytes and multi-nucleated giant cells. We conclude that free, non-assembled ORF2 capsid protein does not induce protective immunity. |
format | Online Article Text |
id | pubmed-8466160 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-84661602021-09-27 Non-Assembled ORF2 Capsid Protein of Porcine Circovirus 2b Does Not Confer Protective Immunity Guarneri, Flavia Tonni, Matteo Sarli, Giuseppe Boniotti, Maria Beatrice Lelli, Davide Barbieri, Ilaria D’Annunzio, Giulia Alborali, Giovanni Loris Bacci, Barbara Amadori, Massimo Pathogens Article Porcine Circovirus 2 (PCV2) vaccines are based on either inactivated whole virion, or recombinant ORF2 capsid protein assembled into Virus-like Particles (VLPs). No data are available about the immunizing properties of free, non-assembled capsid protein. To investigate this issue, ORF2 of a reference PCV2b strain was expressed in a Baculovirus-based expression system without assembly into VLPs. The free purified protein was formulated into an oil vaccine at three distinct Ag payloads: 10.8/3.6/1.2 micrograms/dose. Each dose was injected intramuscularly into five, 37-day old piglets, carefully matched for maternally-derived antibody. Five control piglets were injected with sterile PBS in oil adjuvant. Twenty-eight days later, all the pigs were challenged intranasally with 10(5.3) TCID(50) of PCV2b strain DV6503. After challenge infection, all the pigs remained in good clinical conditions. The recombinant vaccine did not induce significant antibody and PCV2-specific IFN-γ responses. ELISPOT and lymphocyte proliferation data confirmed poor induction of cell-mediated immunity. In terms of PCV2 viremia, there was no significant difference between vaccinated and control animals. The histological data indicated the absence of a detectable viral load and of PCVAD lesions in both vaccinated and control animals, as well as of histiocytes and multi-nucleated giant cells. We conclude that free, non-assembled ORF2 capsid protein does not induce protective immunity. MDPI 2021-09-09 /pmc/articles/PMC8466160/ /pubmed/34578193 http://dx.doi.org/10.3390/pathogens10091161 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/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 (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Guarneri, Flavia Tonni, Matteo Sarli, Giuseppe Boniotti, Maria Beatrice Lelli, Davide Barbieri, Ilaria D’Annunzio, Giulia Alborali, Giovanni Loris Bacci, Barbara Amadori, Massimo Non-Assembled ORF2 Capsid Protein of Porcine Circovirus 2b Does Not Confer Protective Immunity |
title | Non-Assembled ORF2 Capsid Protein of Porcine Circovirus 2b Does Not Confer Protective Immunity |
title_full | Non-Assembled ORF2 Capsid Protein of Porcine Circovirus 2b Does Not Confer Protective Immunity |
title_fullStr | Non-Assembled ORF2 Capsid Protein of Porcine Circovirus 2b Does Not Confer Protective Immunity |
title_full_unstemmed | Non-Assembled ORF2 Capsid Protein of Porcine Circovirus 2b Does Not Confer Protective Immunity |
title_short | Non-Assembled ORF2 Capsid Protein of Porcine Circovirus 2b Does Not Confer Protective Immunity |
title_sort | non-assembled orf2 capsid protein of porcine circovirus 2b does not confer protective immunity |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8466160/ https://www.ncbi.nlm.nih.gov/pubmed/34578193 http://dx.doi.org/10.3390/pathogens10091161 |
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