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Host evolutionary relationships explain tree mortality caused by a generalist pest–pathogen complex
The phylogenetic signal of transmissibility (competence) and attack severity among hosts of generalist pests is poorly understood. In this study, we examined the phylogenetic effects on hosts differentially affected by an emergent generalist beetle–pathogen complex in California and South Africa. Ho...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8061262/ https://www.ncbi.nlm.nih.gov/pubmed/33897822 http://dx.doi.org/10.1111/eva.13182 |
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author | Lynch, Shannon Colleen Eskalen, Akif Gilbert, Gregory S. |
author_facet | Lynch, Shannon Colleen Eskalen, Akif Gilbert, Gregory S. |
author_sort | Lynch, Shannon Colleen |
collection | PubMed |
description | The phylogenetic signal of transmissibility (competence) and attack severity among hosts of generalist pests is poorly understood. In this study, we examined the phylogenetic effects on hosts differentially affected by an emergent generalist beetle–pathogen complex in California and South Africa. Host types (non‐competent, competent and killed‐competent) are based on nested types of outcomes of interactions between host plants, the beetles and the fungal pathogens. Phylogenetic dispersion analysis of each host type revealed that the phylogenetic preferences of beetle attack and fungal growth were a nonrandom subset of all available tree and shrub species. Competent hosts were phylogenetically narrower by 62 Myr than the set of all potential hosts, and those with devastating impacts were the most constrained by 107 Myr. Our results show a strong phylogenetic signal in the relative effects of a generalist pest–pathogen complex on host species, demonstrating that the strength of multi‐host pest impacts in plants can be predicted by host evolutionary relationships. This study presents a unifying theoretical approach to identifying likely disease outcomes across multiple host‐pest combinations. |
format | Online Article Text |
id | pubmed-8061262 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-80612622021-04-23 Host evolutionary relationships explain tree mortality caused by a generalist pest–pathogen complex Lynch, Shannon Colleen Eskalen, Akif Gilbert, Gregory S. Evol Appl Original Articles The phylogenetic signal of transmissibility (competence) and attack severity among hosts of generalist pests is poorly understood. In this study, we examined the phylogenetic effects on hosts differentially affected by an emergent generalist beetle–pathogen complex in California and South Africa. Host types (non‐competent, competent and killed‐competent) are based on nested types of outcomes of interactions between host plants, the beetles and the fungal pathogens. Phylogenetic dispersion analysis of each host type revealed that the phylogenetic preferences of beetle attack and fungal growth were a nonrandom subset of all available tree and shrub species. Competent hosts were phylogenetically narrower by 62 Myr than the set of all potential hosts, and those with devastating impacts were the most constrained by 107 Myr. Our results show a strong phylogenetic signal in the relative effects of a generalist pest–pathogen complex on host species, demonstrating that the strength of multi‐host pest impacts in plants can be predicted by host evolutionary relationships. This study presents a unifying theoretical approach to identifying likely disease outcomes across multiple host‐pest combinations. John Wiley and Sons Inc. 2021-01-05 /pmc/articles/PMC8061262/ /pubmed/33897822 http://dx.doi.org/10.1111/eva.13182 Text en © 2021 The Authors. Evolutionary Applications published by John Wiley & Sons Ltd 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 | Original Articles Lynch, Shannon Colleen Eskalen, Akif Gilbert, Gregory S. Host evolutionary relationships explain tree mortality caused by a generalist pest–pathogen complex |
title | Host evolutionary relationships explain tree mortality caused by a generalist pest–pathogen complex |
title_full | Host evolutionary relationships explain tree mortality caused by a generalist pest–pathogen complex |
title_fullStr | Host evolutionary relationships explain tree mortality caused by a generalist pest–pathogen complex |
title_full_unstemmed | Host evolutionary relationships explain tree mortality caused by a generalist pest–pathogen complex |
title_short | Host evolutionary relationships explain tree mortality caused by a generalist pest–pathogen complex |
title_sort | host evolutionary relationships explain tree mortality caused by a generalist pest–pathogen complex |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8061262/ https://www.ncbi.nlm.nih.gov/pubmed/33897822 http://dx.doi.org/10.1111/eva.13182 |
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