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Taxonomic and Functional Diversity of Rhizosphere Microbiome Recruited From Compost Synergistically Determined by Plant Species and Compost

Compost is frequently served as the first reservoir for plants to recruit rhizosphere microbiome when used as growing substrate in the seedling nursery. In the present study, recruitment of rhizosphere microbiome from two composts by tomato, pepper, or maize was addressed by shotgun metagenomics and...

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Autores principales: Wang, Ning, Li, Huixiu, Wang, Bo, Ding, Jia, Liu, Yingjie, Wei, Yuquan, Li, Ji, Ding, Guo-Chun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8792965/
https://www.ncbi.nlm.nih.gov/pubmed/35095808
http://dx.doi.org/10.3389/fmicb.2021.798476
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author Wang, Ning
Li, Huixiu
Wang, Bo
Ding, Jia
Liu, Yingjie
Wei, Yuquan
Li, Ji
Ding, Guo-Chun
author_facet Wang, Ning
Li, Huixiu
Wang, Bo
Ding, Jia
Liu, Yingjie
Wei, Yuquan
Li, Ji
Ding, Guo-Chun
author_sort Wang, Ning
collection PubMed
description Compost is frequently served as the first reservoir for plants to recruit rhizosphere microbiome when used as growing substrate in the seedling nursery. In the present study, recruitment of rhizosphere microbiome from two composts by tomato, pepper, or maize was addressed by shotgun metagenomics and 16S rRNA amplicon sequencing. The 16S rRNA amplicon sequencing analysis showed that 41% of variation in the rhizosphere bacterial community was explained by compost, in contrast to 23% by plant species. Proteobacterial genera were commonly recruited by all three plant species with specific selections for Ralstonia by tomato and Enterobacteria by maize. These findings were confirmed by analysis of 16S rRNA retrieved from the shotgun metagenomics library. Approximately 70% of functional gene clusters differed more than sevenfold in abundance between rhizosphere and compost. Functional groups associated with the sensing and up-taking of C3 and C4 carboxylic acids, amino acids, monosaccharide, production of antimicrobial substances, and antibiotic resistance were over-represented in the rhizosphere. In summary, compost and plant species synergistically shaped the composition of the rhizosphere microbiome and selected for functional traits associated with the competition on root exudates.
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spelling pubmed-87929652022-01-28 Taxonomic and Functional Diversity of Rhizosphere Microbiome Recruited From Compost Synergistically Determined by Plant Species and Compost Wang, Ning Li, Huixiu Wang, Bo Ding, Jia Liu, Yingjie Wei, Yuquan Li, Ji Ding, Guo-Chun Front Microbiol Microbiology Compost is frequently served as the first reservoir for plants to recruit rhizosphere microbiome when used as growing substrate in the seedling nursery. In the present study, recruitment of rhizosphere microbiome from two composts by tomato, pepper, or maize was addressed by shotgun metagenomics and 16S rRNA amplicon sequencing. The 16S rRNA amplicon sequencing analysis showed that 41% of variation in the rhizosphere bacterial community was explained by compost, in contrast to 23% by plant species. Proteobacterial genera were commonly recruited by all three plant species with specific selections for Ralstonia by tomato and Enterobacteria by maize. These findings were confirmed by analysis of 16S rRNA retrieved from the shotgun metagenomics library. Approximately 70% of functional gene clusters differed more than sevenfold in abundance between rhizosphere and compost. Functional groups associated with the sensing and up-taking of C3 and C4 carboxylic acids, amino acids, monosaccharide, production of antimicrobial substances, and antibiotic resistance were over-represented in the rhizosphere. In summary, compost and plant species synergistically shaped the composition of the rhizosphere microbiome and selected for functional traits associated with the competition on root exudates. Frontiers Media S.A. 2022-01-13 /pmc/articles/PMC8792965/ /pubmed/35095808 http://dx.doi.org/10.3389/fmicb.2021.798476 Text en Copyright © 2022 Wang, Li, Wang, Ding, Liu, Wei, Li and Ding. 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
Wang, Ning
Li, Huixiu
Wang, Bo
Ding, Jia
Liu, Yingjie
Wei, Yuquan
Li, Ji
Ding, Guo-Chun
Taxonomic and Functional Diversity of Rhizosphere Microbiome Recruited From Compost Synergistically Determined by Plant Species and Compost
title Taxonomic and Functional Diversity of Rhizosphere Microbiome Recruited From Compost Synergistically Determined by Plant Species and Compost
title_full Taxonomic and Functional Diversity of Rhizosphere Microbiome Recruited From Compost Synergistically Determined by Plant Species and Compost
title_fullStr Taxonomic and Functional Diversity of Rhizosphere Microbiome Recruited From Compost Synergistically Determined by Plant Species and Compost
title_full_unstemmed Taxonomic and Functional Diversity of Rhizosphere Microbiome Recruited From Compost Synergistically Determined by Plant Species and Compost
title_short Taxonomic and Functional Diversity of Rhizosphere Microbiome Recruited From Compost Synergistically Determined by Plant Species and Compost
title_sort taxonomic and functional diversity of rhizosphere microbiome recruited from compost synergistically determined by plant species and compost
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8792965/
https://www.ncbi.nlm.nih.gov/pubmed/35095808
http://dx.doi.org/10.3389/fmicb.2021.798476
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