Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: Holland, Owen J., Toomey, Madeline, Ahrens, Collin, Hoffmann, Ary A., Croft, Laurence J., Sherman, Craig D. H., Miller, Adam D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
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
_version_ 1784757566992023552
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
work_keys_str_mv AT hollandowenj wholegenomeresequencingrevealssignaturesofrapidselectioninavirusaffectedcommercialfishery
AT toomeymadeline wholegenomeresequencingrevealssignaturesofrapidselectioninavirusaffectedcommercialfishery
AT ahrenscollin wholegenomeresequencingrevealssignaturesofrapidselectioninavirusaffectedcommercialfishery
AT hoffmannarya wholegenomeresequencingrevealssignaturesofrapidselectioninavirusaffectedcommercialfishery
AT croftlaurencej wholegenomeresequencingrevealssignaturesofrapidselectioninavirusaffectedcommercialfishery
AT shermancraigdh wholegenomeresequencingrevealssignaturesofrapidselectioninavirusaffectedcommercialfishery
AT milleradamd wholegenomeresequencingrevealssignaturesofrapidselectioninavirusaffectedcommercialfishery