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Root-associated fungal community reflects host spatial co-occurrence patterns in a subtropical forest
Plant roots harbor and interact with diverse fungal species. By changing these belowground fungal communities, focal plants can affect the performance of surrounding individuals and the outcome of coexistence. Although highly host related, the roles of these root-associated fungal communities per se...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9723750/ https://www.ncbi.nlm.nih.gov/pubmed/36755184 http://dx.doi.org/10.1038/s43705-021-00072-6 |
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author | Kuang, Jialiang Han, Shun Chen, Yongjian Bates, Colin T. Wang, Pandeng Shu, Wensheng |
author_facet | Kuang, Jialiang Han, Shun Chen, Yongjian Bates, Colin T. Wang, Pandeng Shu, Wensheng |
author_sort | Kuang, Jialiang |
collection | PubMed |
description | Plant roots harbor and interact with diverse fungal species. By changing these belowground fungal communities, focal plants can affect the performance of surrounding individuals and the outcome of coexistence. Although highly host related, the roles of these root-associated fungal communities per se in host plant spatial co-occurrence is largely unknown. Here, we evaluated the host dependency of root-associated communities for 39-plant species spatially mapped throughout a 50-ha subtropical forest plot with relevant environmental properties. In addition, we explored whether the differentiation in root fungal associations among plant species can reflect their observed co-occurrence patterns. We demonstrated a strong host-dependency by discriminating the differentiation of root-associated fungal communities regardless of background soil heterogeneity. Furthermore, Random Forest modeling indicated that these nonrandom root fungal associations significantly increased our ability to explain spatial co-occurrence patterns, and to a greater degree than the relative abundance, phylogenetic relatedness, and functional traits of the host plants. Our results further suggested that plants harbor more abundant shared, “generalist” pathogens are likely segregated, while hosting more abundant unique, “specialist” ectomycorrhizal fungi might be an important strategy for promoting spatial aggregation, particularly between early established trees and the heterospecific adults. Together, we provide a conceptual and testable approach to integrate this host-dependent root fungal “fingerprinting” into the plant diversity patterns. We highlight that this approach is complementary to the classic cultivation-based scheme and can deepen our understanding of the community-level effect from overall fungi and its contribution to the pairwise plant dynamics in local species-rich communities. |
format | Online Article Text |
id | pubmed-9723750 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-97237502023-01-04 Root-associated fungal community reflects host spatial co-occurrence patterns in a subtropical forest Kuang, Jialiang Han, Shun Chen, Yongjian Bates, Colin T. Wang, Pandeng Shu, Wensheng ISME Commun Article Plant roots harbor and interact with diverse fungal species. By changing these belowground fungal communities, focal plants can affect the performance of surrounding individuals and the outcome of coexistence. Although highly host related, the roles of these root-associated fungal communities per se in host plant spatial co-occurrence is largely unknown. Here, we evaluated the host dependency of root-associated communities for 39-plant species spatially mapped throughout a 50-ha subtropical forest plot with relevant environmental properties. In addition, we explored whether the differentiation in root fungal associations among plant species can reflect their observed co-occurrence patterns. We demonstrated a strong host-dependency by discriminating the differentiation of root-associated fungal communities regardless of background soil heterogeneity. Furthermore, Random Forest modeling indicated that these nonrandom root fungal associations significantly increased our ability to explain spatial co-occurrence patterns, and to a greater degree than the relative abundance, phylogenetic relatedness, and functional traits of the host plants. Our results further suggested that plants harbor more abundant shared, “generalist” pathogens are likely segregated, while hosting more abundant unique, “specialist” ectomycorrhizal fungi might be an important strategy for promoting spatial aggregation, particularly between early established trees and the heterospecific adults. Together, we provide a conceptual and testable approach to integrate this host-dependent root fungal “fingerprinting” into the plant diversity patterns. We highlight that this approach is complementary to the classic cultivation-based scheme and can deepen our understanding of the community-level effect from overall fungi and its contribution to the pairwise plant dynamics in local species-rich communities. Nature Publishing Group UK 2021-11-06 /pmc/articles/PMC9723750/ /pubmed/36755184 http://dx.doi.org/10.1038/s43705-021-00072-6 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 Kuang, Jialiang Han, Shun Chen, Yongjian Bates, Colin T. Wang, Pandeng Shu, Wensheng Root-associated fungal community reflects host spatial co-occurrence patterns in a subtropical forest |
title | Root-associated fungal community reflects host spatial co-occurrence patterns in a subtropical forest |
title_full | Root-associated fungal community reflects host spatial co-occurrence patterns in a subtropical forest |
title_fullStr | Root-associated fungal community reflects host spatial co-occurrence patterns in a subtropical forest |
title_full_unstemmed | Root-associated fungal community reflects host spatial co-occurrence patterns in a subtropical forest |
title_short | Root-associated fungal community reflects host spatial co-occurrence patterns in a subtropical forest |
title_sort | root-associated fungal community reflects host spatial co-occurrence patterns in a subtropical forest |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9723750/ https://www.ncbi.nlm.nih.gov/pubmed/36755184 http://dx.doi.org/10.1038/s43705-021-00072-6 |
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