Comparative analysis of rhizosphere microbiomes of cultivated and wild rice under contrasting field water regimes.

IF 3.8 2区 生物学 Q2 MICROBIOLOGY
Yuhong Luo, Xiaolong Xu, Renfei Qiao, Ru-Peng Zhao, Zu-Wen Zhou, Dong-Ao Li, Yuhao Wen, Jia-Ming Song, Ling-Ling Chen
{"title":"Comparative analysis of rhizosphere microbiomes of cultivated and wild rice under contrasting field water regimes.","authors":"Yuhong Luo, Xiaolong Xu, Renfei Qiao, Ru-Peng Zhao, Zu-Wen Zhou, Dong-Ao Li, Yuhao Wen, Jia-Ming Song, Ling-Ling Chen","doi":"10.1128/spectrum.00263-25","DOIUrl":null,"url":null,"abstract":"<p><p>Asian cultivated rice (<i>Oryza sativa L</i>.) is domesticated from the common wild rice (<i>Oryza rufipogon Griff</i>.). However, the increasing water stress caused by climate change in recent years has become a major threat to rice growth and yield. To explore the adaptive changes of rhizosphere microbiomes in annual cultivated and perennial wild rice under different water limitation conditions, we conducted metagenomic sequencing analysis on rice rhizosphere soil samples from natural environments with varying water conditions. In particular, the genus <i>Pseudomonas</i> plays a dominant role in the rhizosphere microbiome of wild rice under non-irrigated condition. For archaea, we found that, compared to non-irrigated condition, submergence condition enriched methanogenic <i>Methanosarcina</i>. In comparison to cultivated rice, wild rice showed significant enrichment of <i>Nitrosarchaeum</i>, as ammonia-oxidizing archaea play a key role in the nitrogen cycle, whereas cultivated rice tends to enrich methanogenic archaea (<i>Methanosarcina</i>), which may increase methane emissions and have adverse environmental impacts. The rhizosphere metabolites of wild rice also enriched DL-Norleucine, L-Phenylalanine, and Palmitic acid, which may enhance root water absorption and provide essential nutrients to help rice resist water-limiting stress. In terms of rhizosphere microbiome function, <i>asnB</i> and <i>nirK</i> were particularly enriched in wild rice under non-irrigated condition, suggesting that wild rice may exhibit higher ecological adaptability to water stress by enhancing nitrogen assimilation and denitrification processes. Excavating these microbiome communities and functional changes in rice rhizospheres is crucial for optimizing water-limiting resistance, protecting the environment, and improving rice yield.</p><p><strong>Importance: </strong>This study highlights the differences in rhizosphere microbiomes and metabolites between wild and cultivated rice, providing new insights into how water limitation impacts their interaction with the rhizosphere microbiome. These findings are crucial for advancing rice cultivation under submergence and non-irrigated conditions, offering strategies to optimize farming practices, manage water scarcity, and reduce methane emissions. In contrast to cultivated rice, wild rice may regulate its rhizosphere microbial community to enhance resistance to water stress. This discovery offers valuable theoretical support for improving rice growth and adaptation across diverse ecological environments.</p>","PeriodicalId":18670,"journal":{"name":"Microbiology spectrum","volume":" ","pages":"e0026325"},"PeriodicalIF":3.8000,"publicationDate":"2025-09-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Microbiology spectrum","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1128/spectrum.00263-25","RegionNum":2,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"MICROBIOLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

Asian cultivated rice (Oryza sativa L.) is domesticated from the common wild rice (Oryza rufipogon Griff.). However, the increasing water stress caused by climate change in recent years has become a major threat to rice growth and yield. To explore the adaptive changes of rhizosphere microbiomes in annual cultivated and perennial wild rice under different water limitation conditions, we conducted metagenomic sequencing analysis on rice rhizosphere soil samples from natural environments with varying water conditions. In particular, the genus Pseudomonas plays a dominant role in the rhizosphere microbiome of wild rice under non-irrigated condition. For archaea, we found that, compared to non-irrigated condition, submergence condition enriched methanogenic Methanosarcina. In comparison to cultivated rice, wild rice showed significant enrichment of Nitrosarchaeum, as ammonia-oxidizing archaea play a key role in the nitrogen cycle, whereas cultivated rice tends to enrich methanogenic archaea (Methanosarcina), which may increase methane emissions and have adverse environmental impacts. The rhizosphere metabolites of wild rice also enriched DL-Norleucine, L-Phenylalanine, and Palmitic acid, which may enhance root water absorption and provide essential nutrients to help rice resist water-limiting stress. In terms of rhizosphere microbiome function, asnB and nirK were particularly enriched in wild rice under non-irrigated condition, suggesting that wild rice may exhibit higher ecological adaptability to water stress by enhancing nitrogen assimilation and denitrification processes. Excavating these microbiome communities and functional changes in rice rhizospheres is crucial for optimizing water-limiting resistance, protecting the environment, and improving rice yield.

Importance: This study highlights the differences in rhizosphere microbiomes and metabolites between wild and cultivated rice, providing new insights into how water limitation impacts their interaction with the rhizosphere microbiome. These findings are crucial for advancing rice cultivation under submergence and non-irrigated conditions, offering strategies to optimize farming practices, manage water scarcity, and reduce methane emissions. In contrast to cultivated rice, wild rice may regulate its rhizosphere microbial community to enhance resistance to water stress. This discovery offers valuable theoretical support for improving rice growth and adaptation across diverse ecological environments.

不同田间水分条件下栽培稻与野生稻根际微生物组的比较分析。
亚洲栽培稻(Oryza sativa L.)是由普通野生稻(Oryza rufipogon Griff.)驯化而成的。然而,近年来气候变化造成的日益严重的水分胁迫已成为水稻生长和产量的主要威胁。为了探究不同水分限制条件下一年生栽培稻和多年生野生稻根际微生物组的适应性变化,我们对不同水分条件自然环境下的水稻根际土壤样品进行了宏基因组测序分析。特别是在非灌溉条件下,假单胞菌属在野生水稻根际微生物群中起主导作用。对于古细菌,我们发现,与不灌溉条件相比,淹没条件丰富了产甲烷的甲烷菌。与栽培稻相比,野生稻氮古菌富集显著,因为氨氧化古菌在氮循环中起关键作用,而栽培稻则倾向于富集产甲烷古菌(Methanosarcina),这可能增加甲烷排放,对环境产生不利影响。野生水稻根际代谢物还富含dl -去甲亮氨酸、l -苯丙氨酸和棕榈酸,这些物质可能促进根系水分吸收,为水稻抵御限水胁迫提供必需的营养物质。在根际微生物组功能方面,asnB和nirK在非灌溉条件下尤其富集,表明野生水稻可能通过加强氮同化和反硝化过程对水分胁迫表现出更高的生态适应性。挖掘这些微生物群落及其在水稻根际的功能变化,对优化水稻的限水抗性、保护环境和提高产量具有重要意义。重要性:本研究强调了野生稻和栽培稻根际微生物群和代谢物的差异,为水分限制如何影响它们与根际微生物群的相互作用提供了新的见解。这些发现对于推进淹水和非灌溉条件下的水稻种植至关重要,为优化耕作方式、管理水资源短缺和减少甲烷排放提供了策略。与栽培稻相比,野生稻可以通过调节根际微生物群落来增强对水分胁迫的抵抗力。这一发现为改善水稻生长和适应不同生态环境提供了有价值的理论支持。
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
Microbiology spectrum
Microbiology spectrum Biochemistry, Genetics and Molecular Biology-Genetics
CiteScore
3.20
自引率
5.40%
发文量
1800
期刊介绍: Microbiology Spectrum publishes commissioned review articles on topics in microbiology representing ten content areas: Archaea; Food Microbiology; Bacterial Genetics, Cell Biology, and Physiology; Clinical Microbiology; Environmental Microbiology and Ecology; Eukaryotic Microbes; Genomics, Computational, and Synthetic Microbiology; Immunology; Pathogenesis; and Virology. Reviews are interrelated, with each review linking to other related content. A large board of Microbiology Spectrum editors aids in the development of topics for potential reviews and in the identification of an editor, or editors, who shepherd each collection.
×
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:604180095
Book学术官方微信