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Variation and correlations between sexual, asexual and natural enemy resistance life-history traits in a natural plant pathogen population
BACKGROUND: Understanding the mechanisms by which diversity is maintained in pathogen populations is critical for epidemiological predictions. Life-history trade-offs have been proposed as a hypothesis for explaining long-term maintenance of variation in pathogen populations, yet the empirical evide...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6624897/ https://www.ncbi.nlm.nih.gov/pubmed/31299905 http://dx.doi.org/10.1186/s12862-019-1468-2 |
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author | Numminen, Elina Vaumourin, Elise Parratt, Steven R. Poulin, Lucie Laine, Anna-Liisa |
author_facet | Numminen, Elina Vaumourin, Elise Parratt, Steven R. Poulin, Lucie Laine, Anna-Liisa |
author_sort | Numminen, Elina |
collection | PubMed |
description | BACKGROUND: Understanding the mechanisms by which diversity is maintained in pathogen populations is critical for epidemiological predictions. Life-history trade-offs have been proposed as a hypothesis for explaining long-term maintenance of variation in pathogen populations, yet the empirical evidence supporting trade-offs has remained mixed. This is in part due to the challenges of documenting successive pathogen life-history stages in many pathosystems. Moreover, little is understood of the role of natural enemies of pathogens on their life-history evolution. RESULTS: We characterize life-history-trait variation and possible trade-offs in fungal pathogen Podosphaera plantaginis infecting the host plant Plantago lanceolata. We measured the timing of both asexual and sexual stages, as well as resistance to a hyperparasite of seven pathogen strains that vary in their prevalence in nature. We find significant variation among the strains in their life-history traits that constitute the infection cycle, but no evidence for trade-offs among pathogen development stages, apart from fast pathogen growth coninciding with fast hyperparasite growth. Also, the seemingly least fit pathogen strain was the most prevalent in the nature. CONCLUSIONS: We conclude that in the nature environmental variation, and interactions with the antagonists of pathogens themselves may maintain variation in pathogen populations. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12862-019-1468-2) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-6624897 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-66248972019-07-23 Variation and correlations between sexual, asexual and natural enemy resistance life-history traits in a natural plant pathogen population Numminen, Elina Vaumourin, Elise Parratt, Steven R. Poulin, Lucie Laine, Anna-Liisa BMC Evol Biol Research Article BACKGROUND: Understanding the mechanisms by which diversity is maintained in pathogen populations is critical for epidemiological predictions. Life-history trade-offs have been proposed as a hypothesis for explaining long-term maintenance of variation in pathogen populations, yet the empirical evidence supporting trade-offs has remained mixed. This is in part due to the challenges of documenting successive pathogen life-history stages in many pathosystems. Moreover, little is understood of the role of natural enemies of pathogens on their life-history evolution. RESULTS: We characterize life-history-trait variation and possible trade-offs in fungal pathogen Podosphaera plantaginis infecting the host plant Plantago lanceolata. We measured the timing of both asexual and sexual stages, as well as resistance to a hyperparasite of seven pathogen strains that vary in their prevalence in nature. We find significant variation among the strains in their life-history traits that constitute the infection cycle, but no evidence for trade-offs among pathogen development stages, apart from fast pathogen growth coninciding with fast hyperparasite growth. Also, the seemingly least fit pathogen strain was the most prevalent in the nature. CONCLUSIONS: We conclude that in the nature environmental variation, and interactions with the antagonists of pathogens themselves may maintain variation in pathogen populations. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12862-019-1468-2) contains supplementary material, which is available to authorized users. BioMed Central 2019-07-12 /pmc/articles/PMC6624897/ /pubmed/31299905 http://dx.doi.org/10.1186/s12862-019-1468-2 Text en © The Author(s). 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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 Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Article Numminen, Elina Vaumourin, Elise Parratt, Steven R. Poulin, Lucie Laine, Anna-Liisa Variation and correlations between sexual, asexual and natural enemy resistance life-history traits in a natural plant pathogen population |
title | Variation and correlations between sexual, asexual and natural enemy resistance life-history traits in a natural plant pathogen population |
title_full | Variation and correlations between sexual, asexual and natural enemy resistance life-history traits in a natural plant pathogen population |
title_fullStr | Variation and correlations between sexual, asexual and natural enemy resistance life-history traits in a natural plant pathogen population |
title_full_unstemmed | Variation and correlations between sexual, asexual and natural enemy resistance life-history traits in a natural plant pathogen population |
title_short | Variation and correlations between sexual, asexual and natural enemy resistance life-history traits in a natural plant pathogen population |
title_sort | variation and correlations between sexual, asexual and natural enemy resistance life-history traits in a natural plant pathogen population |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6624897/ https://www.ncbi.nlm.nih.gov/pubmed/31299905 http://dx.doi.org/10.1186/s12862-019-1468-2 |
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