Variation and correlations between sexual, asexual and natural enemy resistance life-history traits in a natural plant pathogen population

Abstract 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 empiric...

Full description

Bibliographic Details
Main Authors: Elina Numminen, Elise Vaumourin, Steven R. Parratt, Lucie Poulin, Anna-Liisa Laine
Format: Article
Language:English
Published: BMC 2019-07-01
Series:BMC Evolutionary Biology
Subjects:
Online Access:http://link.springer.com/article/10.1186/s12862-019-1468-2
id doaj-b7d433b43c6242bebcbf418ee087fd3a
record_format Article
spelling doaj-b7d433b43c6242bebcbf418ee087fd3a2021-09-02T14:49:13ZengBMCBMC Evolutionary Biology1471-21482019-07-0119111110.1186/s12862-019-1468-2Variation and correlations between sexual, asexual and natural enemy resistance life-history traits in a natural plant pathogen populationElina Numminen0Elise Vaumourin1Steven R. Parratt2Lucie Poulin3Anna-Liisa Laine4Department of Biosciences, University of HelsinkiDepartment of Biosciences, University of HelsinkiDepartment of Biosciences, University of HelsinkiDepartment of Biosciences, University of HelsinkiDepartment of Biosciences, University of HelsinkiAbstract 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.http://link.springer.com/article/10.1186/s12862-019-1468-2Ampelomyces spp.DiversityEpidemiologyFitnessHost-pathogen interactionPlantago lanceolata
collection DOAJ
language English
format Article
sources DOAJ
author Elina Numminen
Elise Vaumourin
Steven R. Parratt
Lucie Poulin
Anna-Liisa Laine
spellingShingle Elina Numminen
Elise Vaumourin
Steven R. Parratt
Lucie Poulin
Anna-Liisa Laine
Variation and correlations between sexual, asexual and natural enemy resistance life-history traits in a natural plant pathogen population
BMC Evolutionary Biology
Ampelomyces spp.
Diversity
Epidemiology
Fitness
Host-pathogen interaction
Plantago lanceolata
author_facet Elina Numminen
Elise Vaumourin
Steven R. Parratt
Lucie Poulin
Anna-Liisa Laine
author_sort Elina Numminen
title 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_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_sort variation and correlations between sexual, asexual and natural enemy resistance life-history traits in a natural plant pathogen population
publisher BMC
series BMC Evolutionary Biology
issn 1471-2148
publishDate 2019-07-01
description Abstract 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.
topic Ampelomyces spp.
Diversity
Epidemiology
Fitness
Host-pathogen interaction
Plantago lanceolata
url http://link.springer.com/article/10.1186/s12862-019-1468-2
work_keys_str_mv AT elinanumminen variationandcorrelationsbetweensexualasexualandnaturalenemyresistancelifehistorytraitsinanaturalplantpathogenpopulation
AT elisevaumourin variationandcorrelationsbetweensexualasexualandnaturalenemyresistancelifehistorytraitsinanaturalplantpathogenpopulation
AT stevenrparratt variationandcorrelationsbetweensexualasexualandnaturalenemyresistancelifehistorytraitsinanaturalplantpathogenpopulation
AT luciepoulin variationandcorrelationsbetweensexualasexualandnaturalenemyresistancelifehistorytraitsinanaturalplantpathogenpopulation
AT annaliisalaine variationandcorrelationsbetweensexualasexualandnaturalenemyresistancelifehistorytraitsinanaturalplantpathogenpopulation
_version_ 1721174278278217728