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Spatially structured eco-evolutionary dynamics in a host-pathogen interaction render isolated populations vulnerable to disease
While the negative effects that pathogens have on their hosts are well-documented in humans and agricultural systems, direct evidence of pathogen-driven impacts in wild host populations is scarce and mixed. Here, to determine how the strength of pathogen-imposed selection depends on spatial structur...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9561709/ https://www.ncbi.nlm.nih.gov/pubmed/36229442 http://dx.doi.org/10.1038/s41467-022-33665-3 |
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author | Höckerstedt, Layla Numminen, Elina Ashby, Ben Boots, Mike Norberg, Anna Laine, Anna-Liisa |
author_facet | Höckerstedt, Layla Numminen, Elina Ashby, Ben Boots, Mike Norberg, Anna Laine, Anna-Liisa |
author_sort | Höckerstedt, Layla |
collection | PubMed |
description | While the negative effects that pathogens have on their hosts are well-documented in humans and agricultural systems, direct evidence of pathogen-driven impacts in wild host populations is scarce and mixed. Here, to determine how the strength of pathogen-imposed selection depends on spatial structure, we analyze growth rates across approximately 4000 host populations of a perennial plant through time coupled with data on pathogen presence-absence. We find that infection decreases growth more in the isolated than well-connected host populations. Our inoculation study reveals isolated populations to be highly susceptible to disease while connected host populations support the highest levels of resistance diversity, regardless of their disease history. A spatial eco-evolutionary model predicts that non-linearity in the costs to resistance may be critical in determining this pattern. Overall, evolutionary feedbacks define the ecological impacts of disease in spatially structured systems with host gene flow being more important than disease history in determining the outcome. |
format | Online Article Text |
id | pubmed-9561709 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-95617092022-10-15 Spatially structured eco-evolutionary dynamics in a host-pathogen interaction render isolated populations vulnerable to disease Höckerstedt, Layla Numminen, Elina Ashby, Ben Boots, Mike Norberg, Anna Laine, Anna-Liisa Nat Commun Article While the negative effects that pathogens have on their hosts are well-documented in humans and agricultural systems, direct evidence of pathogen-driven impacts in wild host populations is scarce and mixed. Here, to determine how the strength of pathogen-imposed selection depends on spatial structure, we analyze growth rates across approximately 4000 host populations of a perennial plant through time coupled with data on pathogen presence-absence. We find that infection decreases growth more in the isolated than well-connected host populations. Our inoculation study reveals isolated populations to be highly susceptible to disease while connected host populations support the highest levels of resistance diversity, regardless of their disease history. A spatial eco-evolutionary model predicts that non-linearity in the costs to resistance may be critical in determining this pattern. Overall, evolutionary feedbacks define the ecological impacts of disease in spatially structured systems with host gene flow being more important than disease history in determining the outcome. Nature Publishing Group UK 2022-10-13 /pmc/articles/PMC9561709/ /pubmed/36229442 http://dx.doi.org/10.1038/s41467-022-33665-3 Text en © The Author(s) 2022 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 Höckerstedt, Layla Numminen, Elina Ashby, Ben Boots, Mike Norberg, Anna Laine, Anna-Liisa Spatially structured eco-evolutionary dynamics in a host-pathogen interaction render isolated populations vulnerable to disease |
title | Spatially structured eco-evolutionary dynamics in a host-pathogen interaction render isolated populations vulnerable to disease |
title_full | Spatially structured eco-evolutionary dynamics in a host-pathogen interaction render isolated populations vulnerable to disease |
title_fullStr | Spatially structured eco-evolutionary dynamics in a host-pathogen interaction render isolated populations vulnerable to disease |
title_full_unstemmed | Spatially structured eco-evolutionary dynamics in a host-pathogen interaction render isolated populations vulnerable to disease |
title_short | Spatially structured eco-evolutionary dynamics in a host-pathogen interaction render isolated populations vulnerable to disease |
title_sort | spatially structured eco-evolutionary dynamics in a host-pathogen interaction render isolated populations vulnerable to disease |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9561709/ https://www.ncbi.nlm.nih.gov/pubmed/36229442 http://dx.doi.org/10.1038/s41467-022-33665-3 |
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