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Effect of strain-specific maternally-derived antibodies on influenza A virus infection dynamics in nursery pigs

Reducing the number of influenza A virus (IAV) infected pigs at weaning is critical to minimize IAV spread to other farms. Sow vaccination is a common measure to reduce influenza levels at weaning. However, the impact of maternally-derived antibodies on IAV infection dynamics in growing pigs is poor...

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Autores principales: Chamba Pardo, Fabian Orlando, Wayne, Spencer, Culhane, Marie Rene, Perez, Andres, Allerson, Matthew, Torremorell, Montserrat
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6331129/
https://www.ncbi.nlm.nih.gov/pubmed/30640929
http://dx.doi.org/10.1371/journal.pone.0210700
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author Chamba Pardo, Fabian Orlando
Wayne, Spencer
Culhane, Marie Rene
Perez, Andres
Allerson, Matthew
Torremorell, Montserrat
author_facet Chamba Pardo, Fabian Orlando
Wayne, Spencer
Culhane, Marie Rene
Perez, Andres
Allerson, Matthew
Torremorell, Montserrat
author_sort Chamba Pardo, Fabian Orlando
collection PubMed
description Reducing the number of influenza A virus (IAV) infected pigs at weaning is critical to minimize IAV spread to other farms. Sow vaccination is a common measure to reduce influenza levels at weaning. However, the impact of maternally-derived antibodies on IAV infection dynamics in growing pigs is poorly understood. We evaluated the effect of maternally-derived antibodies at weaning on IAV prevalence at weaning, time of influenza infection, number of weeks that pigs tested IAV positive, and estimated quantity of IAV in nursery pigs. We evaluated 301 pigs within 10 cohorts for their influenza serological (seroprevalence estimated by hemagglutination inhibition (HI) test) and virological (prevalence) status. Nasal swabs were collected weekly and pigs were bled 3 times throughout the nursery period. There was significant variability in influenza seroprevalence, HI titers and influenza prevalence after weaning. Increase in influenza seroprevalence at weaning was associated with low influenza prevalence at weaning and delayed time to IAV infection throughout the nursery. Piglets with IAV HI titers of 40 or higher at weaning were also less likely to test IAV positive at weaning, took longer to become infected, tested IAV RT-PCR positive for fewer weeks, and had higher IAV RT-PCR cycle threshold values compared to piglets with HI titers less than 40. Our findings suggest that sow vaccination or infection status that results in high levels of IAV strain-specific maternally-derived antibodies may help to reduce IAV circulation in both suckling and nursery pigs.
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spelling pubmed-63311292019-02-01 Effect of strain-specific maternally-derived antibodies on influenza A virus infection dynamics in nursery pigs Chamba Pardo, Fabian Orlando Wayne, Spencer Culhane, Marie Rene Perez, Andres Allerson, Matthew Torremorell, Montserrat PLoS One Research Article Reducing the number of influenza A virus (IAV) infected pigs at weaning is critical to minimize IAV spread to other farms. Sow vaccination is a common measure to reduce influenza levels at weaning. However, the impact of maternally-derived antibodies on IAV infection dynamics in growing pigs is poorly understood. We evaluated the effect of maternally-derived antibodies at weaning on IAV prevalence at weaning, time of influenza infection, number of weeks that pigs tested IAV positive, and estimated quantity of IAV in nursery pigs. We evaluated 301 pigs within 10 cohorts for their influenza serological (seroprevalence estimated by hemagglutination inhibition (HI) test) and virological (prevalence) status. Nasal swabs were collected weekly and pigs were bled 3 times throughout the nursery period. There was significant variability in influenza seroprevalence, HI titers and influenza prevalence after weaning. Increase in influenza seroprevalence at weaning was associated with low influenza prevalence at weaning and delayed time to IAV infection throughout the nursery. Piglets with IAV HI titers of 40 or higher at weaning were also less likely to test IAV positive at weaning, took longer to become infected, tested IAV RT-PCR positive for fewer weeks, and had higher IAV RT-PCR cycle threshold values compared to piglets with HI titers less than 40. Our findings suggest that sow vaccination or infection status that results in high levels of IAV strain-specific maternally-derived antibodies may help to reduce IAV circulation in both suckling and nursery pigs. Public Library of Science 2019-01-14 /pmc/articles/PMC6331129/ /pubmed/30640929 http://dx.doi.org/10.1371/journal.pone.0210700 Text en © 2019 Chamba Pardo et al http://creativecommons.org/licenses/by/4.0/ 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 author and source are credited.
spellingShingle Research Article
Chamba Pardo, Fabian Orlando
Wayne, Spencer
Culhane, Marie Rene
Perez, Andres
Allerson, Matthew
Torremorell, Montserrat
Effect of strain-specific maternally-derived antibodies on influenza A virus infection dynamics in nursery pigs
title Effect of strain-specific maternally-derived antibodies on influenza A virus infection dynamics in nursery pigs
title_full Effect of strain-specific maternally-derived antibodies on influenza A virus infection dynamics in nursery pigs
title_fullStr Effect of strain-specific maternally-derived antibodies on influenza A virus infection dynamics in nursery pigs
title_full_unstemmed Effect of strain-specific maternally-derived antibodies on influenza A virus infection dynamics in nursery pigs
title_short Effect of strain-specific maternally-derived antibodies on influenza A virus infection dynamics in nursery pigs
title_sort effect of strain-specific maternally-derived antibodies on influenza a virus infection dynamics in nursery pigs
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6331129/
https://www.ncbi.nlm.nih.gov/pubmed/30640929
http://dx.doi.org/10.1371/journal.pone.0210700
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