Cargando…

Insect herbivory facilitates the establishment of an invasive plant pathogen

Plants can be severely affected by insect herbivores and phytopathogenic fungi, but interactions between these plant antagonists are poorly understood. We analysed the impact of feeding damage by the abundant herbivore Orchestes fagi on infection rates of beech (Fagus sylvatica) leaves with Petrakia...

Descripción completa

Detalles Bibliográficos
Autores principales: Gossner, Martin M., Beenken, Ludwig, Arend, Kirstin, Begerow, Dominik, Peršoh, Derek
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9723786/
https://www.ncbi.nlm.nih.gov/pubmed/37938649
http://dx.doi.org/10.1038/s43705-021-00004-4
_version_ 1784844266394091520
author Gossner, Martin M.
Beenken, Ludwig
Arend, Kirstin
Begerow, Dominik
Peršoh, Derek
author_facet Gossner, Martin M.
Beenken, Ludwig
Arend, Kirstin
Begerow, Dominik
Peršoh, Derek
author_sort Gossner, Martin M.
collection PubMed
description Plants can be severely affected by insect herbivores and phytopathogenic fungi, but interactions between these plant antagonists are poorly understood. We analysed the impact of feeding damage by the abundant herbivore Orchestes fagi on infection rates of beech (Fagus sylvatica) leaves with Petrakia liobae, an invasive plant pathogenic fungus. The fungus was not detected in hibernating beetles, indicating that O. fagi does not serve as vector for P. liobae, at least not between growing seasons. Abundance of the fungus in beech leaves increased with feeding damage of the beetle and this relationship was stronger for sun-exposed than for shaded leaves. A laboratory experiment revealed sun-exposed leaves to have thicker cell walls and to be more resistant to pathogen infection than shaded leaves. Mechanical damage significantly increased frequency and size of necroses in the sun, but not in shade leaves. Our findings indicate that feeding damage of adult beetles provides entry ports for fungal colonization by removal of physical barriers and thus promotes infection success by pathogenic fungi. Feeding activity by larvae probably provides additional nutrient sources or eases access to substrates for the necrotrophic fungus. Our study exemplifies that invasive pathogens may benefit from herbivore activity, which may challenge forest health in light of climate change.
format Online
Article
Text
id pubmed-9723786
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher Nature Publishing Group UK
record_format MEDLINE/PubMed
spelling pubmed-97237862023-01-04 Insect herbivory facilitates the establishment of an invasive plant pathogen Gossner, Martin M. Beenken, Ludwig Arend, Kirstin Begerow, Dominik Peršoh, Derek ISME Commun Article Plants can be severely affected by insect herbivores and phytopathogenic fungi, but interactions between these plant antagonists are poorly understood. We analysed the impact of feeding damage by the abundant herbivore Orchestes fagi on infection rates of beech (Fagus sylvatica) leaves with Petrakia liobae, an invasive plant pathogenic fungus. The fungus was not detected in hibernating beetles, indicating that O. fagi does not serve as vector for P. liobae, at least not between growing seasons. Abundance of the fungus in beech leaves increased with feeding damage of the beetle and this relationship was stronger for sun-exposed than for shaded leaves. A laboratory experiment revealed sun-exposed leaves to have thicker cell walls and to be more resistant to pathogen infection than shaded leaves. Mechanical damage significantly increased frequency and size of necroses in the sun, but not in shade leaves. Our findings indicate that feeding damage of adult beetles provides entry ports for fungal colonization by removal of physical barriers and thus promotes infection success by pathogenic fungi. Feeding activity by larvae probably provides additional nutrient sources or eases access to substrates for the necrotrophic fungus. Our study exemplifies that invasive pathogens may benefit from herbivore activity, which may challenge forest health in light of climate change. Nature Publishing Group UK 2021-03-22 /pmc/articles/PMC9723786/ /pubmed/37938649 http://dx.doi.org/10.1038/s43705-021-00004-4 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as 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 images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Gossner, Martin M.
Beenken, Ludwig
Arend, Kirstin
Begerow, Dominik
Peršoh, Derek
Insect herbivory facilitates the establishment of an invasive plant pathogen
title Insect herbivory facilitates the establishment of an invasive plant pathogen
title_full Insect herbivory facilitates the establishment of an invasive plant pathogen
title_fullStr Insect herbivory facilitates the establishment of an invasive plant pathogen
title_full_unstemmed Insect herbivory facilitates the establishment of an invasive plant pathogen
title_short Insect herbivory facilitates the establishment of an invasive plant pathogen
title_sort insect herbivory facilitates the establishment of an invasive plant pathogen
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9723786/
https://www.ncbi.nlm.nih.gov/pubmed/37938649
http://dx.doi.org/10.1038/s43705-021-00004-4
work_keys_str_mv AT gossnermartinm insectherbivoryfacilitatestheestablishmentofaninvasiveplantpathogen
AT beenkenludwig insectherbivoryfacilitatestheestablishmentofaninvasiveplantpathogen
AT arendkirstin insectherbivoryfacilitatestheestablishmentofaninvasiveplantpathogen
AT begerowdominik insectherbivoryfacilitatestheestablishmentofaninvasiveplantpathogen
AT persohderek insectherbivoryfacilitatestheestablishmentofaninvasiveplantpathogen