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Adaptive population structure shifts in invasive parasitic mites, Varroa destructor
Comparative studies of genetic diversity and population structure can shed light on the ecological and evolutionary factors governing host–parasite interactions. Even though invasive parasites are considered of major biological importance, little is known about their adaptative potential when infest...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8207383/ https://www.ncbi.nlm.nih.gov/pubmed/34141194 http://dx.doi.org/10.1002/ece3.7272 |
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author | Moro, Arrigo Blacquière, Tjeerd Dahle, Bjørn Dietemann, Vincent Le Conte, Yves Locke, Barbara Neumann, Peter Beaurepaire, Alexis |
author_facet | Moro, Arrigo Blacquière, Tjeerd Dahle, Bjørn Dietemann, Vincent Le Conte, Yves Locke, Barbara Neumann, Peter Beaurepaire, Alexis |
author_sort | Moro, Arrigo |
collection | PubMed |
description | Comparative studies of genetic diversity and population structure can shed light on the ecological and evolutionary factors governing host–parasite interactions. Even though invasive parasites are considered of major biological importance, little is known about their adaptative potential when infesting the new hosts. Here, the genetic diversification of Varroa destructor, a novel parasite of Apis mellifera originating from Asia, was investigated using population genetics to determine how the genetic structure of the parasite changed in distinct European populations of its new host. To do so, mites infesting two categories of hosts in four European regions were compared: (a) adapted hosts surviving through means of natural selection, thereby expected to impose strong selective pressure on the mites, and (b) treated host populations, surviving mite infestations because acaricides are applied, therefore characterized by a relaxed selection imposed by the host on the mites. Significant genetic divergence was found across regions, partially reflecting the invasion pattern of V. destructor throughout Europe and indicating local adaptation of the mite to the host populations. Additionally, varying degrees of genotypic changes were found between mites from adapted and treated colonies. Altogether, these results indicate that V. destructor managed to overcome the genetic bottlenecks following its introduction in Europe and that host‐mediated selection fostered changes in the genetic structure of this mite at diverse geographic scales. These findings highlight the potential of parasites to adapt to their local host populations and confirm that adaptations developed within coevolutionary dynamics are a major determinant of population genetic changes. |
format | Online Article Text |
id | pubmed-8207383 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-82073832021-06-16 Adaptive population structure shifts in invasive parasitic mites, Varroa destructor Moro, Arrigo Blacquière, Tjeerd Dahle, Bjørn Dietemann, Vincent Le Conte, Yves Locke, Barbara Neumann, Peter Beaurepaire, Alexis Ecol Evol Original Research Comparative studies of genetic diversity and population structure can shed light on the ecological and evolutionary factors governing host–parasite interactions. Even though invasive parasites are considered of major biological importance, little is known about their adaptative potential when infesting the new hosts. Here, the genetic diversification of Varroa destructor, a novel parasite of Apis mellifera originating from Asia, was investigated using population genetics to determine how the genetic structure of the parasite changed in distinct European populations of its new host. To do so, mites infesting two categories of hosts in four European regions were compared: (a) adapted hosts surviving through means of natural selection, thereby expected to impose strong selective pressure on the mites, and (b) treated host populations, surviving mite infestations because acaricides are applied, therefore characterized by a relaxed selection imposed by the host on the mites. Significant genetic divergence was found across regions, partially reflecting the invasion pattern of V. destructor throughout Europe and indicating local adaptation of the mite to the host populations. Additionally, varying degrees of genotypic changes were found between mites from adapted and treated colonies. Altogether, these results indicate that V. destructor managed to overcome the genetic bottlenecks following its introduction in Europe and that host‐mediated selection fostered changes in the genetic structure of this mite at diverse geographic scales. These findings highlight the potential of parasites to adapt to their local host populations and confirm that adaptations developed within coevolutionary dynamics are a major determinant of population genetic changes. John Wiley and Sons Inc. 2021-05-01 /pmc/articles/PMC8207383/ /pubmed/34141194 http://dx.doi.org/10.1002/ece3.7272 Text en © 2021 The Authors. Ecology and Evolution 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 Research Moro, Arrigo Blacquière, Tjeerd Dahle, Bjørn Dietemann, Vincent Le Conte, Yves Locke, Barbara Neumann, Peter Beaurepaire, Alexis Adaptive population structure shifts in invasive parasitic mites, Varroa destructor |
title | Adaptive population structure shifts in invasive parasitic mites, Varroa destructor
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title_full | Adaptive population structure shifts in invasive parasitic mites, Varroa destructor
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title_fullStr | Adaptive population structure shifts in invasive parasitic mites, Varroa destructor
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title_full_unstemmed | Adaptive population structure shifts in invasive parasitic mites, Varroa destructor
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title_short | Adaptive population structure shifts in invasive parasitic mites, Varroa destructor
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title_sort | adaptive population structure shifts in invasive parasitic mites, varroa destructor |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8207383/ https://www.ncbi.nlm.nih.gov/pubmed/34141194 http://dx.doi.org/10.1002/ece3.7272 |
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