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Characterization of a PCV2d-2 isolate by experimental infection of pigs

Porcine circovirus type 2 (PCV2), a highly prevalent, economically important swine pathogen is classified into different genotypes (PCV2a-f) based on phylogenetic analysis. Since the introduction of extensive vaccination programs, at least two major shifts have been observed in the prevalence of PCV...

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Autores principales: Palya, Vilmos, Homonnay, Zalán G., Mató, Tamás, Kiss, István
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6260757/
https://www.ncbi.nlm.nih.gov/pubmed/30482219
http://dx.doi.org/10.1186/s12985-018-1098-0
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author Palya, Vilmos
Homonnay, Zalán G.
Mató, Tamás
Kiss, István
author_facet Palya, Vilmos
Homonnay, Zalán G.
Mató, Tamás
Kiss, István
author_sort Palya, Vilmos
collection PubMed
description Porcine circovirus type 2 (PCV2), a highly prevalent, economically important swine pathogen is classified into different genotypes (PCV2a-f) based on phylogenetic analysis. Since the introduction of extensive vaccination programs, at least two major shifts have been observed in the prevalence of PCV2 genotypes. The first genotype shift from 2a towards 2b occurred around 2003, while in recent years, we are witnessing the second change in genotype prevalence from the predominant 2b towards 2d. In this study, a PCV2d-2 isolate was characterized as a potential challenge virus for the evaluation of PCV2 vaccine efficacy. Ten-week-old pigs carrying low to moderate levels of maternally derived antibodies to PCV2 were infected with the isolate by the nasal route. Over the next 4 weeks post-infection, the pigs were monitored for the presence of viremia, fecal virus excretion, and humoral immune responses. At the end of the post-infection observation period, samples were taken from the mediastinal and mesenteric lymph nodes of the animals and tested for viral load. The gradual depletion of maternally derived antibodies in the sera of piglets was demonstrated by ELISA and virus neutralization tests. Following experimental infection by PCV2d-2, specific IgM antibodies were first detected at 14 days post challenge (dpch), while IgG class antibodies were first detected at 21 dpch. Both viremia and virus shedding could be detected at 7 dpch, in 36 and 50% of the pigs, respectively. The proportion of shedders reached 100% by 14 dpch and remained at this level, while viremia was demonstrated in 86, 100, and 100% of the pigs at 14, 21, and 28 dpch, respectively. Both the mediastinal and mesenteric lymph nodes contained high levels of virus (7.6 and 8.5 log(10) copies/mg tissue, respectively).
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spelling pubmed-62607572018-12-10 Characterization of a PCV2d-2 isolate by experimental infection of pigs Palya, Vilmos Homonnay, Zalán G. Mató, Tamás Kiss, István Virol J Short Report Porcine circovirus type 2 (PCV2), a highly prevalent, economically important swine pathogen is classified into different genotypes (PCV2a-f) based on phylogenetic analysis. Since the introduction of extensive vaccination programs, at least two major shifts have been observed in the prevalence of PCV2 genotypes. The first genotype shift from 2a towards 2b occurred around 2003, while in recent years, we are witnessing the second change in genotype prevalence from the predominant 2b towards 2d. In this study, a PCV2d-2 isolate was characterized as a potential challenge virus for the evaluation of PCV2 vaccine efficacy. Ten-week-old pigs carrying low to moderate levels of maternally derived antibodies to PCV2 were infected with the isolate by the nasal route. Over the next 4 weeks post-infection, the pigs were monitored for the presence of viremia, fecal virus excretion, and humoral immune responses. At the end of the post-infection observation period, samples were taken from the mediastinal and mesenteric lymph nodes of the animals and tested for viral load. The gradual depletion of maternally derived antibodies in the sera of piglets was demonstrated by ELISA and virus neutralization tests. Following experimental infection by PCV2d-2, specific IgM antibodies were first detected at 14 days post challenge (dpch), while IgG class antibodies were first detected at 21 dpch. Both viremia and virus shedding could be detected at 7 dpch, in 36 and 50% of the pigs, respectively. The proportion of shedders reached 100% by 14 dpch and remained at this level, while viremia was demonstrated in 86, 100, and 100% of the pigs at 14, 21, and 28 dpch, respectively. Both the mediastinal and mesenteric lymph nodes contained high levels of virus (7.6 and 8.5 log(10) copies/mg tissue, respectively). BioMed Central 2018-11-27 /pmc/articles/PMC6260757/ /pubmed/30482219 http://dx.doi.org/10.1186/s12985-018-1098-0 Text en © The Author(s). 2018 Open Access This 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 Short Report
Palya, Vilmos
Homonnay, Zalán G.
Mató, Tamás
Kiss, István
Characterization of a PCV2d-2 isolate by experimental infection of pigs
title Characterization of a PCV2d-2 isolate by experimental infection of pigs
title_full Characterization of a PCV2d-2 isolate by experimental infection of pigs
title_fullStr Characterization of a PCV2d-2 isolate by experimental infection of pigs
title_full_unstemmed Characterization of a PCV2d-2 isolate by experimental infection of pigs
title_short Characterization of a PCV2d-2 isolate by experimental infection of pigs
title_sort characterization of a pcv2d-2 isolate by experimental infection of pigs
topic Short Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6260757/
https://www.ncbi.nlm.nih.gov/pubmed/30482219
http://dx.doi.org/10.1186/s12985-018-1098-0
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