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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...

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Autores principales: Numminen, Elina, Vaumourin, Elise, Parratt, Steven R., Poulin, Lucie, Laine, Anna-Liisa
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
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.
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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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