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Systemic epigenome-wide association study of elk treponeme-associated hoof disease

Treponeme-associated hoof disease (TAHD) is an emerging disease of elk (Cervus canadensis) in the U.S. Pacific West. Because environmental epigenetics is the primary molecular process that mediates environmental factor impacts on a host organism and disease, the role of epigenetics in TAHD etiology...

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Autores principales: Wild, Margaret A., Taylor, Kyle R., Nilsson, Eric E., Beck, Daniel, Skinner, Michael K.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10505176/
https://www.ncbi.nlm.nih.gov/pubmed/37717058
http://dx.doi.org/10.1038/s41598-023-42546-8
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author Wild, Margaret A.
Taylor, Kyle R.
Nilsson, Eric E.
Beck, Daniel
Skinner, Michael K.
author_facet Wild, Margaret A.
Taylor, Kyle R.
Nilsson, Eric E.
Beck, Daniel
Skinner, Michael K.
author_sort Wild, Margaret A.
collection PubMed
description Treponeme-associated hoof disease (TAHD) is an emerging disease of elk (Cervus canadensis) in the U.S. Pacific West. Because environmental epigenetics is the primary molecular process that mediates environmental factor impacts on a host organism and disease, the role of epigenetics in TAHD etiology was examined. The current study was designed to examine potential effects of TAHD on systemic epigenetic modifications in infected elk over a range of TAHD lesion severity. Leg tendons that contain predominantly fibroblast connective tissue cells were used to isolate fibroblast cells for epigenetic analysis in unaffected and TAHD-positive male and female Roosevelt and Rocky Mountain elk. Differential DNA methylation regions (DMRs) between the unaffected and TAHD-positive elk were identified for both female and male elk. The presence of TAHD was associated with alteration of the connective tissue cell epigenetics, and DMR associated genes identified. Therefore, the infected elk were found to have a systemic epigenetic alteration that was associated with the disease, despite pathology being generally limited to feet. If the elk germline epigenetics is altered then generational transmission of susceptibility to TAHD may impact subsequent generations through epigenetic inheritance. This first study of epigenetic changes associated with disease in elk suggests that TAHD promotes a systemic effect on the elk epigenetics which could exert health impacts on the elk.
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spelling pubmed-105051762023-09-18 Systemic epigenome-wide association study of elk treponeme-associated hoof disease Wild, Margaret A. Taylor, Kyle R. Nilsson, Eric E. Beck, Daniel Skinner, Michael K. Sci Rep Article Treponeme-associated hoof disease (TAHD) is an emerging disease of elk (Cervus canadensis) in the U.S. Pacific West. Because environmental epigenetics is the primary molecular process that mediates environmental factor impacts on a host organism and disease, the role of epigenetics in TAHD etiology was examined. The current study was designed to examine potential effects of TAHD on systemic epigenetic modifications in infected elk over a range of TAHD lesion severity. Leg tendons that contain predominantly fibroblast connective tissue cells were used to isolate fibroblast cells for epigenetic analysis in unaffected and TAHD-positive male and female Roosevelt and Rocky Mountain elk. Differential DNA methylation regions (DMRs) between the unaffected and TAHD-positive elk were identified for both female and male elk. The presence of TAHD was associated with alteration of the connective tissue cell epigenetics, and DMR associated genes identified. Therefore, the infected elk were found to have a systemic epigenetic alteration that was associated with the disease, despite pathology being generally limited to feet. If the elk germline epigenetics is altered then generational transmission of susceptibility to TAHD may impact subsequent generations through epigenetic inheritance. This first study of epigenetic changes associated with disease in elk suggests that TAHD promotes a systemic effect on the elk epigenetics which could exert health impacts on the elk. Nature Publishing Group UK 2023-09-16 /pmc/articles/PMC10505176/ /pubmed/37717058 http://dx.doi.org/10.1038/s41598-023-42546-8 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/) .
spellingShingle Article
Wild, Margaret A.
Taylor, Kyle R.
Nilsson, Eric E.
Beck, Daniel
Skinner, Michael K.
Systemic epigenome-wide association study of elk treponeme-associated hoof disease
title Systemic epigenome-wide association study of elk treponeme-associated hoof disease
title_full Systemic epigenome-wide association study of elk treponeme-associated hoof disease
title_fullStr Systemic epigenome-wide association study of elk treponeme-associated hoof disease
title_full_unstemmed Systemic epigenome-wide association study of elk treponeme-associated hoof disease
title_short Systemic epigenome-wide association study of elk treponeme-associated hoof disease
title_sort systemic epigenome-wide association study of elk treponeme-associated hoof disease
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10505176/
https://www.ncbi.nlm.nih.gov/pubmed/37717058
http://dx.doi.org/10.1038/s41598-023-42546-8
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