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The relationship between pathogen life‐history traits and metapopulation dynamics

Plant pathogen traits, such as transmission mode and overwintering strategy, may have important effects on dispersal and persistence, and drive disease dynamics. Still, we lack insights into how life‐history traits influence spatiotemporal disease dynamics. We adopted a multifaceted approach, combin...

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Autores principales: van Dijk, Laura J. A., Ehrlén, Johan, Tack, Ayco J. M.
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/PMC9306763/
https://www.ncbi.nlm.nih.gov/pubmed/34997974
http://dx.doi.org/10.1111/nph.17948
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author van Dijk, Laura J. A.
Ehrlén, Johan
Tack, Ayco J. M.
author_facet van Dijk, Laura J. A.
Ehrlén, Johan
Tack, Ayco J. M.
author_sort van Dijk, Laura J. A.
collection PubMed
description Plant pathogen traits, such as transmission mode and overwintering strategy, may have important effects on dispersal and persistence, and drive disease dynamics. Still, we lack insights into how life‐history traits influence spatiotemporal disease dynamics. We adopted a multifaceted approach, combining experimental assays, theory and field surveys, to investigate whether information about two pathogen life‐history traits – infectivity and overwintering strategy – can predict pathogen metapopulation dynamics in natural systems. For this, we focused on four fungal pathogens (two rust fungi, one chytrid fungus and one smut fungus) on the forest herb Anemone nemorosa. Pathogens infecting new plants mostly via spores (the chytrid and smut fungi) had higher patch occupancies and colonization rates than pathogens causing mainly systemic infections and overwintering in the rhizomes (the two rust fungi). Although the rust fungi more often occupied well‐connected plant patches, the chytrid and smut fungi were equally or more common in isolated patches. Host patch size was positively related to patch occupancy and colonization rates for all pathogens. Predicting disease dynamics is crucial for understanding the ecological and evolutionary dynamics of host–pathogen interactions, and to prevent disease outbreaks. Our study shows that combining experiments, theory and field observations is a useful way to predict disease dynamics.
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spelling pubmed-93067632022-07-28 The relationship between pathogen life‐history traits and metapopulation dynamics van Dijk, Laura J. A. Ehrlén, Johan Tack, Ayco J. M. New Phytol Research Plant pathogen traits, such as transmission mode and overwintering strategy, may have important effects on dispersal and persistence, and drive disease dynamics. Still, we lack insights into how life‐history traits influence spatiotemporal disease dynamics. We adopted a multifaceted approach, combining experimental assays, theory and field surveys, to investigate whether information about two pathogen life‐history traits – infectivity and overwintering strategy – can predict pathogen metapopulation dynamics in natural systems. For this, we focused on four fungal pathogens (two rust fungi, one chytrid fungus and one smut fungus) on the forest herb Anemone nemorosa. Pathogens infecting new plants mostly via spores (the chytrid and smut fungi) had higher patch occupancies and colonization rates than pathogens causing mainly systemic infections and overwintering in the rhizomes (the two rust fungi). Although the rust fungi more often occupied well‐connected plant patches, the chytrid and smut fungi were equally or more common in isolated patches. Host patch size was positively related to patch occupancy and colonization rates for all pathogens. Predicting disease dynamics is crucial for understanding the ecological and evolutionary dynamics of host–pathogen interactions, and to prevent disease outbreaks. Our study shows that combining experiments, theory and field observations is a useful way to predict disease dynamics. John Wiley and Sons Inc. 2022-01-22 2022-03 /pmc/articles/PMC9306763/ /pubmed/34997974 http://dx.doi.org/10.1111/nph.17948 Text en © 2022 The Authors. New Phytologist © 2022 New Phytologist Foundation https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
van Dijk, Laura J. A.
Ehrlén, Johan
Tack, Ayco J. M.
The relationship between pathogen life‐history traits and metapopulation dynamics
title The relationship between pathogen life‐history traits and metapopulation dynamics
title_full The relationship between pathogen life‐history traits and metapopulation dynamics
title_fullStr The relationship between pathogen life‐history traits and metapopulation dynamics
title_full_unstemmed The relationship between pathogen life‐history traits and metapopulation dynamics
title_short The relationship between pathogen life‐history traits and metapopulation dynamics
title_sort relationship between pathogen life‐history traits and metapopulation dynamics
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9306763/
https://www.ncbi.nlm.nih.gov/pubmed/34997974
http://dx.doi.org/10.1111/nph.17948
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