Arabidopsis assemble distinct root-associated microbiomes through the synthesis of an array of defense metabolites.

Plant associated microbiomes are known to confer fitness advantages to the host. Understanding how plant factors including biochemical traits influence host associated microbiome assembly could facilitate the development of microbiome-mediated solutions for sustainable plant production. Here, we exa...

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Autores principales: Enoch Narh Kudjordjie, Rumakanta Sapkota, Mogens Nicolaisen
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Publicado: Public Library of Science (PLoS) 2021
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Acceso en línea:https://doaj.org/article/1ff29637b1614ec585b5ebe90c4880ad
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spelling oai:doaj.org-article:1ff29637b1614ec585b5ebe90c4880ad2021-12-02T20:19:11ZArabidopsis assemble distinct root-associated microbiomes through the synthesis of an array of defense metabolites.1932-620310.1371/journal.pone.0259171https://doaj.org/article/1ff29637b1614ec585b5ebe90c4880ad2021-01-01T00:00:00Zhttps://doi.org/10.1371/journal.pone.0259171https://doaj.org/toc/1932-6203Plant associated microbiomes are known to confer fitness advantages to the host. Understanding how plant factors including biochemical traits influence host associated microbiome assembly could facilitate the development of microbiome-mediated solutions for sustainable plant production. Here, we examined microbial community structures of a set of well-characterized Arabidopsis thaliana mutants disrupted in metabolic pathways for the production of glucosinolates, flavonoids, or a number of defense signalling molecules. A. thaliana lines were grown in a natural soil and maintained under greenhouse conditions for 4 weeks before collection of roots for bacterial and fungal community profiling. We found distinct relative abundances and diversities of bacterial and fungal communities assembled in the individual A. thaliana mutants compared to their parental lines. Bacterial and fungal genera were mostly enriched than depleted in secondary metabolite and defense signaling mutants, except for flavonoid mutations on fungi communities. Bacterial genera Azospirillum and Flavobacterium were significantly enriched in most of the glucosinolate, flavonoid and signalling mutants while the fungal taxa Sporobolomyces and Emericellopsis were enriched in several glucosinolates and signalling mutants. Whilst the present study revealed marked differences in microbiomes of Arabidopsis mutants and their parental lines, it is suggestive that unknown enzymatic and pleiotropic activities of the mutated genes could contribute to the identified host-associated microbiomes. Notwithstanding, this study revealed interesting gene-microbiota links, and thus represents valuable resource data for selecting candidate A. thaliana mutants for analyzing the links between host genetics and the associated microbiome.Enoch Narh KudjordjieRumakanta SapkotaMogens NicolaisenPublic Library of Science (PLoS)articleMedicineRScienceQENPLoS ONE, Vol 16, Iss 10, p e0259171 (2021)
institution DOAJ
collection DOAJ
language EN
topic Medicine
R
Science
Q
spellingShingle Medicine
R
Science
Q
Enoch Narh Kudjordjie
Rumakanta Sapkota
Mogens Nicolaisen
Arabidopsis assemble distinct root-associated microbiomes through the synthesis of an array of defense metabolites.
description Plant associated microbiomes are known to confer fitness advantages to the host. Understanding how plant factors including biochemical traits influence host associated microbiome assembly could facilitate the development of microbiome-mediated solutions for sustainable plant production. Here, we examined microbial community structures of a set of well-characterized Arabidopsis thaliana mutants disrupted in metabolic pathways for the production of glucosinolates, flavonoids, or a number of defense signalling molecules. A. thaliana lines were grown in a natural soil and maintained under greenhouse conditions for 4 weeks before collection of roots for bacterial and fungal community profiling. We found distinct relative abundances and diversities of bacterial and fungal communities assembled in the individual A. thaliana mutants compared to their parental lines. Bacterial and fungal genera were mostly enriched than depleted in secondary metabolite and defense signaling mutants, except for flavonoid mutations on fungi communities. Bacterial genera Azospirillum and Flavobacterium were significantly enriched in most of the glucosinolate, flavonoid and signalling mutants while the fungal taxa Sporobolomyces and Emericellopsis were enriched in several glucosinolates and signalling mutants. Whilst the present study revealed marked differences in microbiomes of Arabidopsis mutants and their parental lines, it is suggestive that unknown enzymatic and pleiotropic activities of the mutated genes could contribute to the identified host-associated microbiomes. Notwithstanding, this study revealed interesting gene-microbiota links, and thus represents valuable resource data for selecting candidate A. thaliana mutants for analyzing the links between host genetics and the associated microbiome.
format article
author Enoch Narh Kudjordjie
Rumakanta Sapkota
Mogens Nicolaisen
author_facet Enoch Narh Kudjordjie
Rumakanta Sapkota
Mogens Nicolaisen
author_sort Enoch Narh Kudjordjie
title Arabidopsis assemble distinct root-associated microbiomes through the synthesis of an array of defense metabolites.
title_short Arabidopsis assemble distinct root-associated microbiomes through the synthesis of an array of defense metabolites.
title_full Arabidopsis assemble distinct root-associated microbiomes through the synthesis of an array of defense metabolites.
title_fullStr Arabidopsis assemble distinct root-associated microbiomes through the synthesis of an array of defense metabolites.
title_full_unstemmed Arabidopsis assemble distinct root-associated microbiomes through the synthesis of an array of defense metabolites.
title_sort arabidopsis assemble distinct root-associated microbiomes through the synthesis of an array of defense metabolites.
publisher Public Library of Science (PLoS)
publishDate 2021
url https://doaj.org/article/1ff29637b1614ec585b5ebe90c4880ad
work_keys_str_mv AT enochnarhkudjordjie arabidopsisassembledistinctrootassociatedmicrobiomesthroughthesynthesisofanarrayofdefensemetabolites
AT rumakantasapkota arabidopsisassembledistinctrootassociatedmicrobiomesthroughthesynthesisofanarrayofdefensemetabolites
AT mogensnicolaisen arabidopsisassembledistinctrootassociatedmicrobiomesthroughthesynthesisofanarrayofdefensemetabolites
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