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Using social interaction models for genetic analysis of skin damage in gilts

BACKGROUND: Skin damage is a trait of economic and welfare importance that results from social interactions between animals. These interactions may produce wound signs on the gilt’s skin as a result of damage behavior (i.e., fighting), biting syndromes (i.e., tail, vulva, or ear biting), and swine i...

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Autores principales: Leite, Natália Galoro, Knol, Egbert, Tsuruta, Shogo, Nuphaus, Stefanie, Vogelzang, Roos, Lourenco, Daniela
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10364388/
https://www.ncbi.nlm.nih.gov/pubmed/37488486
http://dx.doi.org/10.1186/s12711-023-00816-z
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author Leite, Natália Galoro
Knol, Egbert
Tsuruta, Shogo
Nuphaus, Stefanie
Vogelzang, Roos
Lourenco, Daniela
author_facet Leite, Natália Galoro
Knol, Egbert
Tsuruta, Shogo
Nuphaus, Stefanie
Vogelzang, Roos
Lourenco, Daniela
author_sort Leite, Natália Galoro
collection PubMed
description BACKGROUND: Skin damage is a trait of economic and welfare importance that results from social interactions between animals. These interactions may produce wound signs on the gilt’s skin as a result of damage behavior (i.e., fighting), biting syndromes (i.e., tail, vulva, or ear biting), and swine inflammation and necrosis syndrome. Although current selection for traits that are affected by social interactions primarily focuses on improving direct genetic effects, combined selection on direct and social genetic effects could increase genetic gain and avoid a negative response to selection in cases of competitive behavior. The objectives of this study were to (1) estimate variance components for combined skin damage (CSD), with or without accounting for social genetic effects, (2) investigate the impact of including genomic information on the prediction accuracy, bias, and dispersion of CSD estimated breeding values, and (3) perform a single-step genome-wide association study (ssGWAS) of CSD under a classical and a social interaction model. RESULTS: Our results show that CSD is heritable and affected by social genetic effects. Modeling CSD with social interaction models increased the total heritable variance relative to the phenotypic variance by three-fold compared to the classical model. Including genomic information increased the prediction accuracy of direct, social, and total estimated breeding values for purebred sires by at least 21.2%. Bias and dispersion of estimated breeding values were reduced by including genomic information in classical and social interaction models but remained present. The ssGWAS did not identify any single nucleotide polymorphism that was significantly associated with social or direct genetic effects for CSD. CONCLUSIONS: Combined skin damage is heritable, and genetic selection against this trait will increase the welfare of animals in the long term. Combined skin damage is affected by social genetic effects, and modeling this trait with a social interaction model increases the potential for genetic improvement. Including genomic information increases the prediction accuracy of estimated breeding values and reduces their bias and dispersion, although some biases persist. The results of the genome-wide association study indicate that CSD has a polygenic architecture and no major quantitative trait locus was detected.
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spelling pubmed-103643882023-07-25 Using social interaction models for genetic analysis of skin damage in gilts Leite, Natália Galoro Knol, Egbert Tsuruta, Shogo Nuphaus, Stefanie Vogelzang, Roos Lourenco, Daniela Genet Sel Evol Research Article BACKGROUND: Skin damage is a trait of economic and welfare importance that results from social interactions between animals. These interactions may produce wound signs on the gilt’s skin as a result of damage behavior (i.e., fighting), biting syndromes (i.e., tail, vulva, or ear biting), and swine inflammation and necrosis syndrome. Although current selection for traits that are affected by social interactions primarily focuses on improving direct genetic effects, combined selection on direct and social genetic effects could increase genetic gain and avoid a negative response to selection in cases of competitive behavior. The objectives of this study were to (1) estimate variance components for combined skin damage (CSD), with or without accounting for social genetic effects, (2) investigate the impact of including genomic information on the prediction accuracy, bias, and dispersion of CSD estimated breeding values, and (3) perform a single-step genome-wide association study (ssGWAS) of CSD under a classical and a social interaction model. RESULTS: Our results show that CSD is heritable and affected by social genetic effects. Modeling CSD with social interaction models increased the total heritable variance relative to the phenotypic variance by three-fold compared to the classical model. Including genomic information increased the prediction accuracy of direct, social, and total estimated breeding values for purebred sires by at least 21.2%. Bias and dispersion of estimated breeding values were reduced by including genomic information in classical and social interaction models but remained present. The ssGWAS did not identify any single nucleotide polymorphism that was significantly associated with social or direct genetic effects for CSD. CONCLUSIONS: Combined skin damage is heritable, and genetic selection against this trait will increase the welfare of animals in the long term. Combined skin damage is affected by social genetic effects, and modeling this trait with a social interaction model increases the potential for genetic improvement. Including genomic information increases the prediction accuracy of estimated breeding values and reduces their bias and dispersion, although some biases persist. The results of the genome-wide association study indicate that CSD has a polygenic architecture and no major quantitative trait locus was detected. BioMed Central 2023-07-24 /pmc/articles/PMC10364388/ /pubmed/37488486 http://dx.doi.org/10.1186/s12711-023-00816-z Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research Article
Leite, Natália Galoro
Knol, Egbert
Tsuruta, Shogo
Nuphaus, Stefanie
Vogelzang, Roos
Lourenco, Daniela
Using social interaction models for genetic analysis of skin damage in gilts
title Using social interaction models for genetic analysis of skin damage in gilts
title_full Using social interaction models for genetic analysis of skin damage in gilts
title_fullStr Using social interaction models for genetic analysis of skin damage in gilts
title_full_unstemmed Using social interaction models for genetic analysis of skin damage in gilts
title_short Using social interaction models for genetic analysis of skin damage in gilts
title_sort using social interaction models for genetic analysis of skin damage in gilts
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10364388/
https://www.ncbi.nlm.nih.gov/pubmed/37488486
http://dx.doi.org/10.1186/s12711-023-00816-z
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