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Evaluation of porcine epidemic diarrhea virus transmission and the immune response in growing pigs
Clinical disease associated with porcine epidemic diarrhea virus (PEDV) infection in naïve pigs is well chronicled; however, information on endemic PEDV infection is limited. To characterize chronic PEDV infection, the duration of infectious virus shedding and development of protective immunity was...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4419466/ https://www.ncbi.nlm.nih.gov/pubmed/25943434 http://dx.doi.org/10.1186/s13567-015-0180-5 |
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author | Crawford, Kimberly Lager, Kelly Miller, Laura Opriessnig, Tanja Gerber, Priscilla Hesse, Richard |
author_facet | Crawford, Kimberly Lager, Kelly Miller, Laura Opriessnig, Tanja Gerber, Priscilla Hesse, Richard |
author_sort | Crawford, Kimberly |
collection | PubMed |
description | Clinical disease associated with porcine epidemic diarrhea virus (PEDV) infection in naïve pigs is well chronicled; however, information on endemic PEDV infection is limited. To characterize chronic PEDV infection, the duration of infectious virus shedding and development of protective immunity was determined. On Day 0 (D0), a growing pig was challenged with PEDV and 13 contacts were commingled. On D7, 9 contact pigs (principal virus group (PG)), were selected, moved to a separate room and commingled with one sentinel pig (S1). This process was repeated weekly with S2, S3 and S4. The PG was PEDV-positive by PCR from D3-11, with some pigs intermittently positive to D42. Pigs S1 and S2 were PEDV-positive within 24 hours of commingling. Antibodies were detected in all PG by D21 and by 7 days post-contact in S1 and S2. Pigs S3 and S4 were PCR and antibody negative following commingling. To evaluate protective immunity, 5 naïve pigs (N) and the PG were challenged (N/C, PG/C) with homologous virus on D49. All N/C pigs were PEDV PCR-positive by D52 with detection out to D62 in 3/5 N/C pigs. All PG/C pigs were PEDV PCR-negative post-challenge. By D63, all N/C seroconverted. Although PEDV RNA was demonstrated in pigs after primary infection until D42, infectious PEDV capable of horizontal transmission to naïve pigs was only shed 14–16 days after infection to age-matched pigs. Homologous re-challenge 49 days post initial PEDV exposure did not result in re-infection of the pigs. This demonstrates potential for an effective PEDV vaccine. |
format | Online Article Text |
id | pubmed-4419466 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-44194662015-05-06 Evaluation of porcine epidemic diarrhea virus transmission and the immune response in growing pigs Crawford, Kimberly Lager, Kelly Miller, Laura Opriessnig, Tanja Gerber, Priscilla Hesse, Richard Vet Res Research Article Clinical disease associated with porcine epidemic diarrhea virus (PEDV) infection in naïve pigs is well chronicled; however, information on endemic PEDV infection is limited. To characterize chronic PEDV infection, the duration of infectious virus shedding and development of protective immunity was determined. On Day 0 (D0), a growing pig was challenged with PEDV and 13 contacts were commingled. On D7, 9 contact pigs (principal virus group (PG)), were selected, moved to a separate room and commingled with one sentinel pig (S1). This process was repeated weekly with S2, S3 and S4. The PG was PEDV-positive by PCR from D3-11, with some pigs intermittently positive to D42. Pigs S1 and S2 were PEDV-positive within 24 hours of commingling. Antibodies were detected in all PG by D21 and by 7 days post-contact in S1 and S2. Pigs S3 and S4 were PCR and antibody negative following commingling. To evaluate protective immunity, 5 naïve pigs (N) and the PG were challenged (N/C, PG/C) with homologous virus on D49. All N/C pigs were PEDV PCR-positive by D52 with detection out to D62 in 3/5 N/C pigs. All PG/C pigs were PEDV PCR-negative post-challenge. By D63, all N/C seroconverted. Although PEDV RNA was demonstrated in pigs after primary infection until D42, infectious PEDV capable of horizontal transmission to naïve pigs was only shed 14–16 days after infection to age-matched pigs. Homologous re-challenge 49 days post initial PEDV exposure did not result in re-infection of the pigs. This demonstrates potential for an effective PEDV vaccine. BioMed Central 2015-05-06 2015 /pmc/articles/PMC4419466/ /pubmed/25943434 http://dx.doi.org/10.1186/s13567-015-0180-5 Text en © Crawford et al.; licensee BioMed Central. 2015 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. 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 Crawford, Kimberly Lager, Kelly Miller, Laura Opriessnig, Tanja Gerber, Priscilla Hesse, Richard Evaluation of porcine epidemic diarrhea virus transmission and the immune response in growing pigs |
title | Evaluation of porcine epidemic diarrhea virus transmission and the immune response in growing pigs |
title_full | Evaluation of porcine epidemic diarrhea virus transmission and the immune response in growing pigs |
title_fullStr | Evaluation of porcine epidemic diarrhea virus transmission and the immune response in growing pigs |
title_full_unstemmed | Evaluation of porcine epidemic diarrhea virus transmission and the immune response in growing pigs |
title_short | Evaluation of porcine epidemic diarrhea virus transmission and the immune response in growing pigs |
title_sort | evaluation of porcine epidemic diarrhea virus transmission and the immune response in growing pigs |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4419466/ https://www.ncbi.nlm.nih.gov/pubmed/25943434 http://dx.doi.org/10.1186/s13567-015-0180-5 |
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