Cargando…

Temporal changes in pathogen diversity in a perennial plant–pathogen–hyperparasite system

Hyperparasites can affect the evolution of pathosystems by influencing the stability of both pathogen and host populations. However, how pathogens of perennial hosts evolve in the presence of a hyperparasite has rarely been studied. Here, we investigated temporal changes in genetic diversity of the...

Descripción completa

Detalles Bibliográficos
Autores principales: Stauber, Lea, Croll, Daniel, Prospero, Simone
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9540319/
https://www.ncbi.nlm.nih.gov/pubmed/35122694
http://dx.doi.org/10.1111/mec.16386
_version_ 1784803684430905344
author Stauber, Lea
Croll, Daniel
Prospero, Simone
author_facet Stauber, Lea
Croll, Daniel
Prospero, Simone
author_sort Stauber, Lea
collection PubMed
description Hyperparasites can affect the evolution of pathosystems by influencing the stability of both pathogen and host populations. However, how pathogens of perennial hosts evolve in the presence of a hyperparasite has rarely been studied. Here, we investigated temporal changes in genetic diversity of the invasive chestnut blight pathogen Cryphonectria parasitica in the presence of its parasitic mycovirus Cryphonectria hypovirus 1 (CHV1). The virus reduces fungal virulence and represents an effective natural biocontrol agent against chestnut blight in Europe. We analysed genome‐wide diversity and CHV1 prevalence in C. parasitica populations in southern Switzerland that were sampled twice at an interval of about 30 years. Overall, we found that both pathogen population structure and CHV1 prevalence were retained over time. The results suggest that recent bottlenecks have influenced the structure of C. parasitica populations in southern Switzerland. Strong balancing selection signals were found at a single vegetative incompatibility (vic) locus, consistent with negative frequency‐dependent selection imposed by the vegetative incompatibility system. High levels of mating among related individuals (i.e., inbreeding) and genetic drift are probably at the origin of imbalanced allele ratios at vic loci and subsequently low vc type diversity. Virus infection rates were stable at ~30% over the study period and we found no significant impact of the virus on fungal population diversity. Consequently, the efficacy of CHV1‐mediated biocontrol was probably retained.
format Online
Article
Text
id pubmed-9540319
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher John Wiley and Sons Inc.
record_format MEDLINE/PubMed
spelling pubmed-95403192022-10-14 Temporal changes in pathogen diversity in a perennial plant–pathogen–hyperparasite system Stauber, Lea Croll, Daniel Prospero, Simone Mol Ecol ORIGINAL ARTICLES Hyperparasites can affect the evolution of pathosystems by influencing the stability of both pathogen and host populations. However, how pathogens of perennial hosts evolve in the presence of a hyperparasite has rarely been studied. Here, we investigated temporal changes in genetic diversity of the invasive chestnut blight pathogen Cryphonectria parasitica in the presence of its parasitic mycovirus Cryphonectria hypovirus 1 (CHV1). The virus reduces fungal virulence and represents an effective natural biocontrol agent against chestnut blight in Europe. We analysed genome‐wide diversity and CHV1 prevalence in C. parasitica populations in southern Switzerland that were sampled twice at an interval of about 30 years. Overall, we found that both pathogen population structure and CHV1 prevalence were retained over time. The results suggest that recent bottlenecks have influenced the structure of C. parasitica populations in southern Switzerland. Strong balancing selection signals were found at a single vegetative incompatibility (vic) locus, consistent with negative frequency‐dependent selection imposed by the vegetative incompatibility system. High levels of mating among related individuals (i.e., inbreeding) and genetic drift are probably at the origin of imbalanced allele ratios at vic loci and subsequently low vc type diversity. Virus infection rates were stable at ~30% over the study period and we found no significant impact of the virus on fungal population diversity. Consequently, the efficacy of CHV1‐mediated biocontrol was probably retained. John Wiley and Sons Inc. 2022-02-16 2022-04 /pmc/articles/PMC9540319/ /pubmed/35122694 http://dx.doi.org/10.1111/mec.16386 Text en © 2022 The Authors. Molecular Ecology published by John Wiley & Sons Ltd. https://creativecommons.org/licenses/by-nc/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.
spellingShingle ORIGINAL ARTICLES
Stauber, Lea
Croll, Daniel
Prospero, Simone
Temporal changes in pathogen diversity in a perennial plant–pathogen–hyperparasite system
title Temporal changes in pathogen diversity in a perennial plant–pathogen–hyperparasite system
title_full Temporal changes in pathogen diversity in a perennial plant–pathogen–hyperparasite system
title_fullStr Temporal changes in pathogen diversity in a perennial plant–pathogen–hyperparasite system
title_full_unstemmed Temporal changes in pathogen diversity in a perennial plant–pathogen–hyperparasite system
title_short Temporal changes in pathogen diversity in a perennial plant–pathogen–hyperparasite system
title_sort temporal changes in pathogen diversity in a perennial plant–pathogen–hyperparasite system
topic ORIGINAL ARTICLES
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9540319/
https://www.ncbi.nlm.nih.gov/pubmed/35122694
http://dx.doi.org/10.1111/mec.16386
work_keys_str_mv AT stauberlea temporalchangesinpathogendiversityinaperennialplantpathogenhyperparasitesystem
AT crolldaniel temporalchangesinpathogendiversityinaperennialplantpathogenhyperparasitesystem
AT prosperosimone temporalchangesinpathogendiversityinaperennialplantpathogenhyperparasitesystem