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Seasonal activities of the phyllosphere microbiome of perennial crops

Understanding the interactions between plants and microorganisms can inform microbiome management to enhance crop productivity and resilience to stress. Here, we apply a genome-centric approach to identify ecologically important leaf microbiome members on replicated plots of field-grown switchgrass...

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Autores principales: Howe, Adina, Stopnisek, Nejc, Dooley, Shane K., Yang, Fan, Grady, Keara L., Shade, Ashley
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9950430/
https://www.ncbi.nlm.nih.gov/pubmed/36823152
http://dx.doi.org/10.1038/s41467-023-36515-y
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author Howe, Adina
Stopnisek, Nejc
Dooley, Shane K.
Yang, Fan
Grady, Keara L.
Shade, Ashley
author_facet Howe, Adina
Stopnisek, Nejc
Dooley, Shane K.
Yang, Fan
Grady, Keara L.
Shade, Ashley
author_sort Howe, Adina
collection PubMed
description Understanding the interactions between plants and microorganisms can inform microbiome management to enhance crop productivity and resilience to stress. Here, we apply a genome-centric approach to identify ecologically important leaf microbiome members on replicated plots of field-grown switchgrass and miscanthus, and to quantify their activities over two growing seasons for switchgrass. We use metagenome and metatranscriptome sequencing and curate 40 medium- and high-quality metagenome-assembled-genomes (MAGs). We find that classes represented by these MAGs (Actinomycetia, Alpha- and Gamma- Proteobacteria, and Bacteroidota) are active in the late season, and upregulate transcripts for short-chain dehydrogenase, molybdopterin oxidoreductase, and polyketide cyclase. Stress-associated pathways are expressed for most MAGs, suggesting engagement with the host environment. We also detect seasonally activated biosynthetic pathways for terpenes and various non-ribosomal peptide pathways that are poorly annotated. Our findings support that leaf-associated bacterial populations are seasonally dynamic and responsive to host cues.
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spelling pubmed-99504302023-02-25 Seasonal activities of the phyllosphere microbiome of perennial crops Howe, Adina Stopnisek, Nejc Dooley, Shane K. Yang, Fan Grady, Keara L. Shade, Ashley Nat Commun Article Understanding the interactions between plants and microorganisms can inform microbiome management to enhance crop productivity and resilience to stress. Here, we apply a genome-centric approach to identify ecologically important leaf microbiome members on replicated plots of field-grown switchgrass and miscanthus, and to quantify their activities over two growing seasons for switchgrass. We use metagenome and metatranscriptome sequencing and curate 40 medium- and high-quality metagenome-assembled-genomes (MAGs). We find that classes represented by these MAGs (Actinomycetia, Alpha- and Gamma- Proteobacteria, and Bacteroidota) are active in the late season, and upregulate transcripts for short-chain dehydrogenase, molybdopterin oxidoreductase, and polyketide cyclase. Stress-associated pathways are expressed for most MAGs, suggesting engagement with the host environment. We also detect seasonally activated biosynthetic pathways for terpenes and various non-ribosomal peptide pathways that are poorly annotated. Our findings support that leaf-associated bacterial populations are seasonally dynamic and responsive to host cues. Nature Publishing Group UK 2023-02-23 /pmc/articles/PMC9950430/ /pubmed/36823152 http://dx.doi.org/10.1038/s41467-023-36515-y Text en © The Author(s) 2023 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
Howe, Adina
Stopnisek, Nejc
Dooley, Shane K.
Yang, Fan
Grady, Keara L.
Shade, Ashley
Seasonal activities of the phyllosphere microbiome of perennial crops
title Seasonal activities of the phyllosphere microbiome of perennial crops
title_full Seasonal activities of the phyllosphere microbiome of perennial crops
title_fullStr Seasonal activities of the phyllosphere microbiome of perennial crops
title_full_unstemmed Seasonal activities of the phyllosphere microbiome of perennial crops
title_short Seasonal activities of the phyllosphere microbiome of perennial crops
title_sort seasonal activities of the phyllosphere microbiome of perennial crops
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9950430/
https://www.ncbi.nlm.nih.gov/pubmed/36823152
http://dx.doi.org/10.1038/s41467-023-36515-y
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