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Manipulating atmospheric CO(2) concentration induces shifts in wheat leaf and spike microbiomes and in Fusarium pathogen communities
Changing atmospheric composition represents a source of uncertainty in our assessment of future disease risks, particularly in the context of mycotoxin producing fungal pathogens which are predicted to be more problematic with climate change. To address this uncertainty, we profiled microbiomes asso...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10595150/ https://www.ncbi.nlm.nih.gov/pubmed/37881249 http://dx.doi.org/10.3389/fmicb.2023.1271219 |
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author | Bakker, Matthew G. Whitaker, Briana K. McCormick, Susan P. Ainsworth, Elizabeth A. Vaughan, Martha M. |
author_facet | Bakker, Matthew G. Whitaker, Briana K. McCormick, Susan P. Ainsworth, Elizabeth A. Vaughan, Martha M. |
author_sort | Bakker, Matthew G. |
collection | PubMed |
description | Changing atmospheric composition represents a source of uncertainty in our assessment of future disease risks, particularly in the context of mycotoxin producing fungal pathogens which are predicted to be more problematic with climate change. To address this uncertainty, we profiled microbiomes associated with wheat plants grown under ambient vs. elevated atmospheric carbon dioxide concentration [CO(2)] in a field setting over 2 years. We also compared the dynamics of naturally infecting versus artificially introduced Fusarium spp. We found that the well-known temporal dynamics of plant-associated microbiomes were affected by [CO(2)]. The abundances of many amplicon sequence variants significantly differed in response to [CO(2)], often in an interactive manner with date of sample collection or with tissue type. In addition, we found evidence that two strains within Fusarium – an important group of mycotoxin producing fungal pathogens of plants – responded to changes in [CO(2)]. The two sequence variants mapped to different phylogenetic subgroups within the genus Fusarium, and had differential [CO(2)] responses. This work informs our understanding of how plant-associated microbiomes and pathogens may respond to changing atmospheric compositions. |
format | Online Article Text |
id | pubmed-10595150 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-105951502023-10-25 Manipulating atmospheric CO(2) concentration induces shifts in wheat leaf and spike microbiomes and in Fusarium pathogen communities Bakker, Matthew G. Whitaker, Briana K. McCormick, Susan P. Ainsworth, Elizabeth A. Vaughan, Martha M. Front Microbiol Microbiology Changing atmospheric composition represents a source of uncertainty in our assessment of future disease risks, particularly in the context of mycotoxin producing fungal pathogens which are predicted to be more problematic with climate change. To address this uncertainty, we profiled microbiomes associated with wheat plants grown under ambient vs. elevated atmospheric carbon dioxide concentration [CO(2)] in a field setting over 2 years. We also compared the dynamics of naturally infecting versus artificially introduced Fusarium spp. We found that the well-known temporal dynamics of plant-associated microbiomes were affected by [CO(2)]. The abundances of many amplicon sequence variants significantly differed in response to [CO(2)], often in an interactive manner with date of sample collection or with tissue type. In addition, we found evidence that two strains within Fusarium – an important group of mycotoxin producing fungal pathogens of plants – responded to changes in [CO(2)]. The two sequence variants mapped to different phylogenetic subgroups within the genus Fusarium, and had differential [CO(2)] responses. This work informs our understanding of how plant-associated microbiomes and pathogens may respond to changing atmospheric compositions. Frontiers Media S.A. 2023-10-10 /pmc/articles/PMC10595150/ /pubmed/37881249 http://dx.doi.org/10.3389/fmicb.2023.1271219 Text en Copyright © 2023 Bakker, Whitaker, McCormick, Ainsworth and Vaughan. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Microbiology Bakker, Matthew G. Whitaker, Briana K. McCormick, Susan P. Ainsworth, Elizabeth A. Vaughan, Martha M. Manipulating atmospheric CO(2) concentration induces shifts in wheat leaf and spike microbiomes and in Fusarium pathogen communities |
title | Manipulating atmospheric CO(2) concentration induces shifts in wheat leaf and spike microbiomes and in Fusarium pathogen communities |
title_full | Manipulating atmospheric CO(2) concentration induces shifts in wheat leaf and spike microbiomes and in Fusarium pathogen communities |
title_fullStr | Manipulating atmospheric CO(2) concentration induces shifts in wheat leaf and spike microbiomes and in Fusarium pathogen communities |
title_full_unstemmed | Manipulating atmospheric CO(2) concentration induces shifts in wheat leaf and spike microbiomes and in Fusarium pathogen communities |
title_short | Manipulating atmospheric CO(2) concentration induces shifts in wheat leaf and spike microbiomes and in Fusarium pathogen communities |
title_sort | manipulating atmospheric co(2) concentration induces shifts in wheat leaf and spike microbiomes and in fusarium pathogen communities |
topic | Microbiology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10595150/ https://www.ncbi.nlm.nih.gov/pubmed/37881249 http://dx.doi.org/10.3389/fmicb.2023.1271219 |
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