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Whole genome resequencing reveals signatures of rapid selection in a virus‐affected commercial fishery
Infectious diseases are recognized as one of the greatest global threats to biodiversity and ecosystem functioning. Consequently, there is a growing urgency to understand the speed at which adaptive phenotypes can evolve and spread in natural populations to inform future management. Here we provide...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9327721/ https://www.ncbi.nlm.nih.gov/pubmed/35555938 http://dx.doi.org/10.1111/mec.16499 |
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author | Holland, Owen J. Toomey, Madeline Ahrens, Collin Hoffmann, Ary A. Croft, Laurence J. Sherman, Craig D. H. Miller, Adam D. |
author_facet | Holland, Owen J. Toomey, Madeline Ahrens, Collin Hoffmann, Ary A. Croft, Laurence J. Sherman, Craig D. H. Miller, Adam D. |
author_sort | Holland, Owen J. |
collection | PubMed |
description | Infectious diseases are recognized as one of the greatest global threats to biodiversity and ecosystem functioning. Consequently, there is a growing urgency to understand the speed at which adaptive phenotypes can evolve and spread in natural populations to inform future management. Here we provide evidence of rapid genomic changes in wild Australian blacklip abalone (Haliotis rubra) following a major population crash associated with an infectious disease. Genome scans on H. rubra were performed using pooled whole genome resequencing data from commercial fishing stocks varying in historical exposure to haliotid herpesvirus‐1 (HaHV‐1). Approximately 25,000 single nucleotide polymorphism loci associated with virus exposure were identified, many of which mapped to genes known to contribute to HaHV‐1 immunity in the New Zealand pāua (Haliotis iris) and herpesvirus response pathways in haliotids and other animal systems. These findings indicate genetic changes across a single generation in H. rubra fishing stocks decimated by HaHV‐1, with stock recovery potentially determined by rapid evolutionary changes leading to virus resistance. This is a novel example of apparently rapid adaptation in natural populations of a nonmodel marine organism, highlighting the pace at which selection can potentially act to counter disease in wildlife communities. |
format | Online Article Text |
id | pubmed-9327721 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-93277212022-07-30 Whole genome resequencing reveals signatures of rapid selection in a virus‐affected commercial fishery Holland, Owen J. Toomey, Madeline Ahrens, Collin Hoffmann, Ary A. Croft, Laurence J. Sherman, Craig D. H. Miller, Adam D. Mol Ecol ORIGINAL ARTICLES Infectious diseases are recognized as one of the greatest global threats to biodiversity and ecosystem functioning. Consequently, there is a growing urgency to understand the speed at which adaptive phenotypes can evolve and spread in natural populations to inform future management. Here we provide evidence of rapid genomic changes in wild Australian blacklip abalone (Haliotis rubra) following a major population crash associated with an infectious disease. Genome scans on H. rubra were performed using pooled whole genome resequencing data from commercial fishing stocks varying in historical exposure to haliotid herpesvirus‐1 (HaHV‐1). Approximately 25,000 single nucleotide polymorphism loci associated with virus exposure were identified, many of which mapped to genes known to contribute to HaHV‐1 immunity in the New Zealand pāua (Haliotis iris) and herpesvirus response pathways in haliotids and other animal systems. These findings indicate genetic changes across a single generation in H. rubra fishing stocks decimated by HaHV‐1, with stock recovery potentially determined by rapid evolutionary changes leading to virus resistance. This is a novel example of apparently rapid adaptation in natural populations of a nonmodel marine organism, highlighting the pace at which selection can potentially act to counter disease in wildlife communities. John Wiley and Sons Inc. 2022-05-31 2022-07 /pmc/articles/PMC9327721/ /pubmed/35555938 http://dx.doi.org/10.1111/mec.16499 Text en © 2022 The Authors. Molecular Ecology published by John Wiley & Sons Ltd. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | ORIGINAL ARTICLES Holland, Owen J. Toomey, Madeline Ahrens, Collin Hoffmann, Ary A. Croft, Laurence J. Sherman, Craig D. H. Miller, Adam D. Whole genome resequencing reveals signatures of rapid selection in a virus‐affected commercial fishery |
title | Whole genome resequencing reveals signatures of rapid selection in a virus‐affected commercial fishery |
title_full | Whole genome resequencing reveals signatures of rapid selection in a virus‐affected commercial fishery |
title_fullStr | Whole genome resequencing reveals signatures of rapid selection in a virus‐affected commercial fishery |
title_full_unstemmed | Whole genome resequencing reveals signatures of rapid selection in a virus‐affected commercial fishery |
title_short | Whole genome resequencing reveals signatures of rapid selection in a virus‐affected commercial fishery |
title_sort | whole genome resequencing reveals signatures of rapid selection in a virus‐affected commercial fishery |
topic | ORIGINAL ARTICLES |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9327721/ https://www.ncbi.nlm.nih.gov/pubmed/35555938 http://dx.doi.org/10.1111/mec.16499 |
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