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Comparative metagenomic analysis reveals rhizosphere microbial community composition and functions help protect grapevines against salt stress

INTRODUCTION: Soil salinization is a serious abiotic stress for grapevines. The rhizosphere microbiota of plants can help counter the negative effects caused by salt stress, but the distinction between rhizosphere microbes of salt-tolerant and salt-sensitive varieties remains unclear. METHODS: This...

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Autores principales: Wang, Bo, Wang, Xicheng, Wang, Zhuangwei, Zhu, Kefeng, Wu, Weimin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9987714/
https://www.ncbi.nlm.nih.gov/pubmed/36891384
http://dx.doi.org/10.3389/fmicb.2023.1102547
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author Wang, Bo
Wang, Xicheng
Wang, Zhuangwei
Zhu, Kefeng
Wu, Weimin
author_facet Wang, Bo
Wang, Xicheng
Wang, Zhuangwei
Zhu, Kefeng
Wu, Weimin
author_sort Wang, Bo
collection PubMed
description INTRODUCTION: Soil salinization is a serious abiotic stress for grapevines. The rhizosphere microbiota of plants can help counter the negative effects caused by salt stress, but the distinction between rhizosphere microbes of salt-tolerant and salt-sensitive varieties remains unclear. METHODS: This study employed metagenomic sequencing to explore the rhizosphere microbial community of grapevine rootstocks 101-14 (salt tolerant) and 5BB (salt sensitive) with or without salt stress. RESULTS AND DISCUSSION: Compared to the control (treated with ddH(2)O), salt stress induced greater changes in the rhizosphere microbiota of 101-14 than in that of 5BB. The relative abundances of more plant growth-promoting bacteria, including Planctomycetes, Bacteroidetes, Verrucomicrobia, Cyanobacteria, Gemmatimonadetes, Chloroflexi, and Firmicutes, were increased in 101-14 under salt stress, whereas only the relative abundances of four phyla (Actinobacteria, Gemmatimonadetes, Chloroflexi, and Cyanobacteria) were increased in 5BB under salt stress while those of three phyla (Acidobacteria, Verrucomicrobia, and Firmicutes) were depleted. The differentially enriched functions (KEGG level 2) in 101-14 were mainly associated with pathways related to cell motility; folding, sorting, and degradation functions; glycan biosynthesis and metabolism; xenobiotics biodegradation and metabolism; and metabolism of cofactors and vitamins, whereas only the translation function was differentially enriched in 5BB. Under salt stress, the rhizosphere microbiota functions of 101-14 and 5BB differed greatly, especially pathways related to metabolism. Further analysis revealed that pathways associated with sulfur and glutathione metabolism as well as bacterial chemotaxis were uniquely enriched in 101-14 under salt stress and therefore might play vital roles in the mitigation of salt stress on grapevines. In addition, the abundance of various sulfur cycle-related genes, including genes involved in assimilatory sulfate reduction (cysNC, cysQ, sat, and sir), sulfur reduction (fsr), SOX systems (soxB), sulfur oxidation (sqr), organic sulfur transformation (tpa, mdh, gdh, and betC), increased significantly in 101-14 after treatment with NaCl; these genes might mitigate the harmful effects of salt on grapevine. In short, the study findings indicate that both the composition and functions of the rhizosphere microbial community contribute to the enhanced tolerance of some grapevines to salt stress.
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spelling pubmed-99877142023-03-07 Comparative metagenomic analysis reveals rhizosphere microbial community composition and functions help protect grapevines against salt stress Wang, Bo Wang, Xicheng Wang, Zhuangwei Zhu, Kefeng Wu, Weimin Front Microbiol Microbiology INTRODUCTION: Soil salinization is a serious abiotic stress for grapevines. The rhizosphere microbiota of plants can help counter the negative effects caused by salt stress, but the distinction between rhizosphere microbes of salt-tolerant and salt-sensitive varieties remains unclear. METHODS: This study employed metagenomic sequencing to explore the rhizosphere microbial community of grapevine rootstocks 101-14 (salt tolerant) and 5BB (salt sensitive) with or without salt stress. RESULTS AND DISCUSSION: Compared to the control (treated with ddH(2)O), salt stress induced greater changes in the rhizosphere microbiota of 101-14 than in that of 5BB. The relative abundances of more plant growth-promoting bacteria, including Planctomycetes, Bacteroidetes, Verrucomicrobia, Cyanobacteria, Gemmatimonadetes, Chloroflexi, and Firmicutes, were increased in 101-14 under salt stress, whereas only the relative abundances of four phyla (Actinobacteria, Gemmatimonadetes, Chloroflexi, and Cyanobacteria) were increased in 5BB under salt stress while those of three phyla (Acidobacteria, Verrucomicrobia, and Firmicutes) were depleted. The differentially enriched functions (KEGG level 2) in 101-14 were mainly associated with pathways related to cell motility; folding, sorting, and degradation functions; glycan biosynthesis and metabolism; xenobiotics biodegradation and metabolism; and metabolism of cofactors and vitamins, whereas only the translation function was differentially enriched in 5BB. Under salt stress, the rhizosphere microbiota functions of 101-14 and 5BB differed greatly, especially pathways related to metabolism. Further analysis revealed that pathways associated with sulfur and glutathione metabolism as well as bacterial chemotaxis were uniquely enriched in 101-14 under salt stress and therefore might play vital roles in the mitigation of salt stress on grapevines. In addition, the abundance of various sulfur cycle-related genes, including genes involved in assimilatory sulfate reduction (cysNC, cysQ, sat, and sir), sulfur reduction (fsr), SOX systems (soxB), sulfur oxidation (sqr), organic sulfur transformation (tpa, mdh, gdh, and betC), increased significantly in 101-14 after treatment with NaCl; these genes might mitigate the harmful effects of salt on grapevine. In short, the study findings indicate that both the composition and functions of the rhizosphere microbial community contribute to the enhanced tolerance of some grapevines to salt stress. Frontiers Media S.A. 2023-02-20 /pmc/articles/PMC9987714/ /pubmed/36891384 http://dx.doi.org/10.3389/fmicb.2023.1102547 Text en Copyright © 2023 Wang, Wang, Wang, Zhu and Wu. 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, Bo
Wang, Xicheng
Wang, Zhuangwei
Zhu, Kefeng
Wu, Weimin
Comparative metagenomic analysis reveals rhizosphere microbial community composition and functions help protect grapevines against salt stress
title Comparative metagenomic analysis reveals rhizosphere microbial community composition and functions help protect grapevines against salt stress
title_full Comparative metagenomic analysis reveals rhizosphere microbial community composition and functions help protect grapevines against salt stress
title_fullStr Comparative metagenomic analysis reveals rhizosphere microbial community composition and functions help protect grapevines against salt stress
title_full_unstemmed Comparative metagenomic analysis reveals rhizosphere microbial community composition and functions help protect grapevines against salt stress
title_short Comparative metagenomic analysis reveals rhizosphere microbial community composition and functions help protect grapevines against salt stress
title_sort comparative metagenomic analysis reveals rhizosphere microbial community composition and functions help protect grapevines against salt stress
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9987714/
https://www.ncbi.nlm.nih.gov/pubmed/36891384
http://dx.doi.org/10.3389/fmicb.2023.1102547
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