Cargando…
Adaptive divergence and post-zygotic barriers to gene flow between sympatric populations of a herbivorous mite
Plant-herbivore interactions promote the generation and maintenance of both plant and herbivore biodiversity. The antagonistic interactions between plants and herbivores lead to host race formation: the evolution of herbivore types specializing on different plant species, with restricted gene flow b...
Autores principales: | , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8270941/ https://www.ncbi.nlm.nih.gov/pubmed/34244609 http://dx.doi.org/10.1038/s42003-021-02380-y |
_version_ | 1783720901179604992 |
---|---|
author | Villacis-Perez, Ernesto Snoeck, Simon Kurlovs, Andre H. Clark, Richard M. Breeuwer, Johannes A. J. Van Leeuwen, Thomas |
author_facet | Villacis-Perez, Ernesto Snoeck, Simon Kurlovs, Andre H. Clark, Richard M. Breeuwer, Johannes A. J. Van Leeuwen, Thomas |
author_sort | Villacis-Perez, Ernesto |
collection | PubMed |
description | Plant-herbivore interactions promote the generation and maintenance of both plant and herbivore biodiversity. The antagonistic interactions between plants and herbivores lead to host race formation: the evolution of herbivore types specializing on different plant species, with restricted gene flow between them. Understanding how ecological specialization promotes host race formation usually depends on artificial approaches, using laboratory experiments on populations associated with agricultural crops. However, evidence on how host races are formed and maintained in a natural setting remains scarce. Here, we take a multidisciplinary approach to understand whether populations of the generalist spider mite Tetranychus urticae form host races in nature. We demonstrate that a host race co-occurs among generalist conspecifics in the dune ecosystem of The Netherlands. Extensive field sampling and genotyping of individuals over three consecutive years showed a clear pattern of host associations. Genome-wide differences between the host race and generalist conspecifics were found using a dense set of SNPs on field-derived iso-female lines and previously sequenced genomes of T. urticae. Hybridization between lines of the host race and sympatric generalist lines is restricted by post-zygotic breakdown, and selection negatively impacts the survival of generalists on the native host of the host race. Our description of a host race among conspecifics with a larger diet breadth shows how ecological and reproductive isolation aid in maintaining intra-specific variation in sympatry, despite the opportunity for homogenization through gene flow. Our findings highlight the importance of explicitly considering the spatial and temporal scale on which plant-herbivore interactions occur in order to identify herbivore populations associated with different plant species in nature. This system can be used to study the underlying genetic architecture and mechanisms that facilitate the use of a large range of host plant taxa by extreme generalist herbivores. In addition, it offers the chance to investigate the prevalence and mechanisms of ecological specialization in nature. |
format | Online Article Text |
id | pubmed-8270941 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-82709412021-07-23 Adaptive divergence and post-zygotic barriers to gene flow between sympatric populations of a herbivorous mite Villacis-Perez, Ernesto Snoeck, Simon Kurlovs, Andre H. Clark, Richard M. Breeuwer, Johannes A. J. Van Leeuwen, Thomas Commun Biol Article Plant-herbivore interactions promote the generation and maintenance of both plant and herbivore biodiversity. The antagonistic interactions between plants and herbivores lead to host race formation: the evolution of herbivore types specializing on different plant species, with restricted gene flow between them. Understanding how ecological specialization promotes host race formation usually depends on artificial approaches, using laboratory experiments on populations associated with agricultural crops. However, evidence on how host races are formed and maintained in a natural setting remains scarce. Here, we take a multidisciplinary approach to understand whether populations of the generalist spider mite Tetranychus urticae form host races in nature. We demonstrate that a host race co-occurs among generalist conspecifics in the dune ecosystem of The Netherlands. Extensive field sampling and genotyping of individuals over three consecutive years showed a clear pattern of host associations. Genome-wide differences between the host race and generalist conspecifics were found using a dense set of SNPs on field-derived iso-female lines and previously sequenced genomes of T. urticae. Hybridization between lines of the host race and sympatric generalist lines is restricted by post-zygotic breakdown, and selection negatively impacts the survival of generalists on the native host of the host race. Our description of a host race among conspecifics with a larger diet breadth shows how ecological and reproductive isolation aid in maintaining intra-specific variation in sympatry, despite the opportunity for homogenization through gene flow. Our findings highlight the importance of explicitly considering the spatial and temporal scale on which plant-herbivore interactions occur in order to identify herbivore populations associated with different plant species in nature. This system can be used to study the underlying genetic architecture and mechanisms that facilitate the use of a large range of host plant taxa by extreme generalist herbivores. In addition, it offers the chance to investigate the prevalence and mechanisms of ecological specialization in nature. Nature Publishing Group UK 2021-07-09 /pmc/articles/PMC8270941/ /pubmed/34244609 http://dx.doi.org/10.1038/s42003-021-02380-y Text en © The Author(s) 2021 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Villacis-Perez, Ernesto Snoeck, Simon Kurlovs, Andre H. Clark, Richard M. Breeuwer, Johannes A. J. Van Leeuwen, Thomas Adaptive divergence and post-zygotic barriers to gene flow between sympatric populations of a herbivorous mite |
title | Adaptive divergence and post-zygotic barriers to gene flow between sympatric populations of a herbivorous mite |
title_full | Adaptive divergence and post-zygotic barriers to gene flow between sympatric populations of a herbivorous mite |
title_fullStr | Adaptive divergence and post-zygotic barriers to gene flow between sympatric populations of a herbivorous mite |
title_full_unstemmed | Adaptive divergence and post-zygotic barriers to gene flow between sympatric populations of a herbivorous mite |
title_short | Adaptive divergence and post-zygotic barriers to gene flow between sympatric populations of a herbivorous mite |
title_sort | adaptive divergence and post-zygotic barriers to gene flow between sympatric populations of a herbivorous mite |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8270941/ https://www.ncbi.nlm.nih.gov/pubmed/34244609 http://dx.doi.org/10.1038/s42003-021-02380-y |
work_keys_str_mv | AT villacisperezernesto adaptivedivergenceandpostzygoticbarrierstogeneflowbetweensympatricpopulationsofaherbivorousmite AT snoecksimon adaptivedivergenceandpostzygoticbarrierstogeneflowbetweensympatricpopulationsofaherbivorousmite AT kurlovsandreh adaptivedivergenceandpostzygoticbarrierstogeneflowbetweensympatricpopulationsofaherbivorousmite AT clarkrichardm adaptivedivergenceandpostzygoticbarrierstogeneflowbetweensympatricpopulationsofaherbivorousmite AT breeuwerjohannesaj adaptivedivergenceandpostzygoticbarrierstogeneflowbetweensympatricpopulationsofaherbivorousmite AT vanleeuwenthomas adaptivedivergenceandpostzygoticbarrierstogeneflowbetweensympatricpopulationsofaherbivorousmite |