Analysis of microbial dynamics in the soybean root-associated environments from community to single-cell levels

IF 2.3 4区 生物学 Q3 BIOTECHNOLOGY & APPLIED MICROBIOLOGY
Masako Kifushi , Yohei Nishikawa , Masahito Hosokawa , Keigo Ide , Masato Kogawa , Toyoaki Anai , Haruko Takeyama
{"title":"Analysis of microbial dynamics in the soybean root-associated environments from community to single-cell levels","authors":"Masako Kifushi ,&nbsp;Yohei Nishikawa ,&nbsp;Masahito Hosokawa ,&nbsp;Keigo Ide ,&nbsp;Masato Kogawa ,&nbsp;Toyoaki Anai ,&nbsp;Haruko Takeyama","doi":"10.1016/j.jbiosc.2024.02.007","DOIUrl":null,"url":null,"abstract":"<div><p>Plant root-associated environments such as the rhizosphere, rhizoplane, and endosphere, are notably different from non-root-associated soil environments. However, the microbial dynamics in these spatially divided compartments remain unexplored. In this study, we propose a combinational analysis of single-cell genomics with 16S rRNA gene sequencing. This method enabled us to understand the entire soil microbiome and individual root-associated microorganisms. We applied this method to soybean microbiomes and revealed that their composition was different between the rhizoplane and rhizosphere in the early growth stages, but became more similar as growth progressed. In addition, a total of 610 medium- to high-quality single-amplified genomes (SAGs) were acquired, including plant growth-promoting rhizobacteria (PGPR) candidates while genomes with high GC content tended to be missed by SAGs. The whole-genome analyses of the SAGs suggested that rhizoplane-enriched <em>Flavobacterium</em> solubilizes organophosphate actively and <em>Bacillus</em> colonizes roots more efficiently. Single-cell genomics, together with 16S rRNA gene sequencing, enabled us to connect microbial taxonomy and function, and assess microorganisms at a strain resolution even in the complex soil microbiome.</p></div>","PeriodicalId":15199,"journal":{"name":"Journal of bioscience and bioengineering","volume":"137 6","pages":"Pages 429-436"},"PeriodicalIF":2.3000,"publicationDate":"2024-04-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of bioscience and bioengineering","FirstCategoryId":"5","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S138917232400077X","RegionNum":4,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"BIOTECHNOLOGY & APPLIED MICROBIOLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

Plant root-associated environments such as the rhizosphere, rhizoplane, and endosphere, are notably different from non-root-associated soil environments. However, the microbial dynamics in these spatially divided compartments remain unexplored. In this study, we propose a combinational analysis of single-cell genomics with 16S rRNA gene sequencing. This method enabled us to understand the entire soil microbiome and individual root-associated microorganisms. We applied this method to soybean microbiomes and revealed that their composition was different between the rhizoplane and rhizosphere in the early growth stages, but became more similar as growth progressed. In addition, a total of 610 medium- to high-quality single-amplified genomes (SAGs) were acquired, including plant growth-promoting rhizobacteria (PGPR) candidates while genomes with high GC content tended to be missed by SAGs. The whole-genome analyses of the SAGs suggested that rhizoplane-enriched Flavobacterium solubilizes organophosphate actively and Bacillus colonizes roots more efficiently. Single-cell genomics, together with 16S rRNA gene sequencing, enabled us to connect microbial taxonomy and function, and assess microorganisms at a strain resolution even in the complex soil microbiome.

从群落到单细胞水平分析大豆根相关环境中的微生物动态。
与植物根系相关的环境,如根圈、根面和内圈,与不与根系相关的土壤环境有明显不同。然而,这些空间分区中的微生物动态仍未得到探索。在本研究中,我们提出了单细胞基因组学与 16S rRNA 基因测序相结合的分析方法。这种方法使我们能够了解整个土壤微生物组和单个根相关微生物。我们将这种方法应用于大豆微生物群,结果发现,在大豆生长初期,根瘤层和根瘤层的微生物组成不同,但随着生长的进行,微生物组成变得越来越相似。此外,共获得了 610 个中高质量的单体扩增基因组(SAG),其中包括候选的植物生长促进根瘤菌(PGPR),而 GC 含量高的基因组往往会被 SAG 遗漏。对 SAG 的全基因组分析表明,富含根瘤的黄杆菌能积极溶解有机磷,而芽孢杆菌则能更有效地定植于根部。单细胞基因组学与 16S rRNA 基因测序相结合,使我们能够将微生物分类与功能联系起来,即使在复杂的土壤微生物群中也能以菌株分辨率评估微生物。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
Journal of bioscience and bioengineering
Journal of bioscience and bioengineering 生物-生物工程与应用微生物
CiteScore
5.90
自引率
3.60%
发文量
144
审稿时长
51 days
期刊介绍: The Journal of Bioscience and Bioengineering is a research journal publishing original full-length research papers, reviews, and Letters to the Editor. The Journal is devoted to the advancement and dissemination of knowledge concerning fermentation technology, biochemical engineering, food technology and microbiology.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信