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Detection of selection signatures for response to Aleutian mink disease virus infection in American mink
Aleutian disease (AD) is the most significant health issue for farmed American mink. The objective of this study was to identify the genomic regions subjected to selection for response to infection with Aleutian mink disease virus (AMDV) in American mink using genotyping by sequencing (GBS) data. A...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7859209/ https://www.ncbi.nlm.nih.gov/pubmed/33536540 http://dx.doi.org/10.1038/s41598-021-82522-8 |
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author | Karimi, Karim Farid, A. Hossain Myles, Sean Miar, Younes |
author_facet | Karimi, Karim Farid, A. Hossain Myles, Sean Miar, Younes |
author_sort | Karimi, Karim |
collection | PubMed |
description | Aleutian disease (AD) is the most significant health issue for farmed American mink. The objective of this study was to identify the genomic regions subjected to selection for response to infection with Aleutian mink disease virus (AMDV) in American mink using genotyping by sequencing (GBS) data. A total of 225 black mink were inoculated with AMDV and genotyped using a GBS assay based on the sequencing of ApeKI-digested libraries. Five AD-characterized phenotypes were used to assign animals to pairwise groups. Signatures of selection were detected using integrated measurement of fixation index (F(ST)) and nucleotide diversity (θπ), that were validated by haplotype-based (hap-FLK) test. The total of 99 putatively selected regions harbouring 63 genes were detected in different groups. The gene ontology revealed numerous genes related to immune response (e.g. TRAF3IP2, WDR7, SWAP70, CBFB, and GPR65), liver development (e.g. SULF2, SRSF5) and reproduction process (e.g. FBXO5, CatSperβ, CATSPER4, and IGF2R). The hapFLK test supported two strongly selected regions that contained five candidate genes related to immune response, virus–host interaction, reproduction and liver regeneration. This study provided the first map of putative selection signals of response to AMDV infection in American mink, bringing new insights into genomic regions controlling the AD phenotypes. |
format | Online Article Text |
id | pubmed-7859209 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-78592092021-02-04 Detection of selection signatures for response to Aleutian mink disease virus infection in American mink Karimi, Karim Farid, A. Hossain Myles, Sean Miar, Younes Sci Rep Article Aleutian disease (AD) is the most significant health issue for farmed American mink. The objective of this study was to identify the genomic regions subjected to selection for response to infection with Aleutian mink disease virus (AMDV) in American mink using genotyping by sequencing (GBS) data. A total of 225 black mink were inoculated with AMDV and genotyped using a GBS assay based on the sequencing of ApeKI-digested libraries. Five AD-characterized phenotypes were used to assign animals to pairwise groups. Signatures of selection were detected using integrated measurement of fixation index (F(ST)) and nucleotide diversity (θπ), that were validated by haplotype-based (hap-FLK) test. The total of 99 putatively selected regions harbouring 63 genes were detected in different groups. The gene ontology revealed numerous genes related to immune response (e.g. TRAF3IP2, WDR7, SWAP70, CBFB, and GPR65), liver development (e.g. SULF2, SRSF5) and reproduction process (e.g. FBXO5, CatSperβ, CATSPER4, and IGF2R). The hapFLK test supported two strongly selected regions that contained five candidate genes related to immune response, virus–host interaction, reproduction and liver regeneration. This study provided the first map of putative selection signals of response to AMDV infection in American mink, bringing new insights into genomic regions controlling the AD phenotypes. Nature Publishing Group UK 2021-02-03 /pmc/articles/PMC7859209/ /pubmed/33536540 http://dx.doi.org/10.1038/s41598-021-82522-8 Text en © The Author(s) 2021 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/. |
spellingShingle | Article Karimi, Karim Farid, A. Hossain Myles, Sean Miar, Younes Detection of selection signatures for response to Aleutian mink disease virus infection in American mink |
title | Detection of selection signatures for response to Aleutian mink disease virus infection in American mink |
title_full | Detection of selection signatures for response to Aleutian mink disease virus infection in American mink |
title_fullStr | Detection of selection signatures for response to Aleutian mink disease virus infection in American mink |
title_full_unstemmed | Detection of selection signatures for response to Aleutian mink disease virus infection in American mink |
title_short | Detection of selection signatures for response to Aleutian mink disease virus infection in American mink |
title_sort | detection of selection signatures for response to aleutian mink disease virus infection in american mink |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7859209/ https://www.ncbi.nlm.nih.gov/pubmed/33536540 http://dx.doi.org/10.1038/s41598-021-82522-8 |
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