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Genetic variation in Japanese Holstein cattle for EBL development
BACKGROUND: Infection with bovine leukemia virus (BLV), the causative agent for enzootic bovine leukosis (EBL), is increasing in dairy farms of Japan. The tendency of tumor development following BLV infection in certain cow families and bull lines has previously been described. We therefore hypothes...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7594299/ https://www.ncbi.nlm.nih.gov/pubmed/33115449 http://dx.doi.org/10.1186/s12917-020-02625-8 |
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author | Inagaki, Yasuko Kobayashi, Tomoko Suda, Yoshihito Kusama, Kazuya Imakawa, Kazuhiko |
author_facet | Inagaki, Yasuko Kobayashi, Tomoko Suda, Yoshihito Kusama, Kazuya Imakawa, Kazuhiko |
author_sort | Inagaki, Yasuko |
collection | PubMed |
description | BACKGROUND: Infection with bovine leukemia virus (BLV), the causative agent for enzootic bovine leukosis (EBL), is increasing in dairy farms of Japan. The tendency of tumor development following BLV infection in certain cow families and bull lines has previously been described. We therefore hypothesized the existence of a genetic component which differentiates cattle susceptibility to the disease. RESULTS: We analyzed routinely collected large-scale data including postmortem inspection data, which were combined with pedigree information and epidemiological data of BLV infection. A total of 6,022 postmortem inspection records of Holstein cattle, raised on 226 farms served by a regional abattoir over 10 years from 2004 to 2015, were analyzed for associations between sire information and EBL development. We then identified statistically the relative susceptibility to EBL development for the progeny of specific sires and paternal grandsires (PGSs). The heritability of EBL development was calculated as 0.19. Similarly, proviral loads (PVLs) of progeny from identified sires and PGSs were analyzed, but no significant differences were found. CONCLUSIONS: These observations suggest that because EBL development in our Holstein population is, at least in part, influenced by genetic factors independent of PVL levels, genetic improvement for lower incidence of EBL development in cattle notwithstanding BLV infection is possible. |
format | Online Article Text |
id | pubmed-7594299 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-75942992020-10-30 Genetic variation in Japanese Holstein cattle for EBL development Inagaki, Yasuko Kobayashi, Tomoko Suda, Yoshihito Kusama, Kazuya Imakawa, Kazuhiko BMC Vet Res Research Article BACKGROUND: Infection with bovine leukemia virus (BLV), the causative agent for enzootic bovine leukosis (EBL), is increasing in dairy farms of Japan. The tendency of tumor development following BLV infection in certain cow families and bull lines has previously been described. We therefore hypothesized the existence of a genetic component which differentiates cattle susceptibility to the disease. RESULTS: We analyzed routinely collected large-scale data including postmortem inspection data, which were combined with pedigree information and epidemiological data of BLV infection. A total of 6,022 postmortem inspection records of Holstein cattle, raised on 226 farms served by a regional abattoir over 10 years from 2004 to 2015, were analyzed for associations between sire information and EBL development. We then identified statistically the relative susceptibility to EBL development for the progeny of specific sires and paternal grandsires (PGSs). The heritability of EBL development was calculated as 0.19. Similarly, proviral loads (PVLs) of progeny from identified sires and PGSs were analyzed, but no significant differences were found. CONCLUSIONS: These observations suggest that because EBL development in our Holstein population is, at least in part, influenced by genetic factors independent of PVL levels, genetic improvement for lower incidence of EBL development in cattle notwithstanding BLV infection is possible. BioMed Central 2020-10-28 /pmc/articles/PMC7594299/ /pubmed/33115449 http://dx.doi.org/10.1186/s12917-020-02625-8 Text en © The Author(s) 2020 Open AccessThis 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/. 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 in a credit line to the data. |
spellingShingle | Research Article Inagaki, Yasuko Kobayashi, Tomoko Suda, Yoshihito Kusama, Kazuya Imakawa, Kazuhiko Genetic variation in Japanese Holstein cattle for EBL development |
title | Genetic variation in Japanese Holstein cattle for EBL development |
title_full | Genetic variation in Japanese Holstein cattle for EBL development |
title_fullStr | Genetic variation in Japanese Holstein cattle for EBL development |
title_full_unstemmed | Genetic variation in Japanese Holstein cattle for EBL development |
title_short | Genetic variation in Japanese Holstein cattle for EBL development |
title_sort | genetic variation in japanese holstein cattle for ebl development |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7594299/ https://www.ncbi.nlm.nih.gov/pubmed/33115449 http://dx.doi.org/10.1186/s12917-020-02625-8 |
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