Host Genetic Variation Is Associated with Root-Associated Microbiome Assembly and Resistance to Fusarium oxysporum in Tobacco

IF 8.2 1区 生物学 Q1 PLANT SCIENCES
Huan Su, Huabing Liu, Jiemeng Tao, Zechao Qu, Qiao Wang, Peng Lu, Xinhua Tian, Shizhou Yu, Kaiyan Li, Heli Shi, Mei Zuo, Bikun Xiang, Jizhong Wu, Peijian Cao, Jingjing Jin
{"title":"Host Genetic Variation Is Associated with Root-Associated Microbiome Assembly and Resistance to Fusarium oxysporum in Tobacco","authors":"Huan Su, Huabing Liu, Jiemeng Tao, Zechao Qu, Qiao Wang, Peng Lu, Xinhua Tian, Shizhou Yu, Kaiyan Li, Heli Shi, Mei Zuo, Bikun Xiang, Jizhong Wu, Peijian Cao, Jingjing Jin","doi":"10.1093/plphys/kiag727","DOIUrl":null,"url":null,"abstract":"Plant–microbe interactions are essential for plant health, yet the genetic basis of host control over root-associated microbiome assembly in Nicotiana tabacum remains unclear. We integrated whole-genome resequencing, amplicon sequencing, and metabolomics across 50 tobacco cultivars, together with microbial genome-wide association and mediation analyses, to investigate host–microbiome covariation. Host genotype significantly influenced the diversity and composition of root-associated microbial communities, particularly in the rhizosphere. Several host loci were associated with heritable microbial taxa linked to nutrient acquisition and stress responses. Mediation analysis suggested that associations between host genetic variation and Pseudomonadaceae abundance were partly transmitted through secondary metabolites variation, particularly terpenoids, whereas this mediating effect was less pronounced for other taxa. Functional assays further showed that several genotype-associated bacterial isolates antagonized Fusarium oxysporum. Among them, Pseudomonas aeruginosa FZ1 suppressed pathogen growth, enhanced host defense responses, and reduced disease severity in greenhouse experiments. These findings suggest that host genetic variation is associated with shifts in the tobacco root microbiome and that secondary metabolites may contribute to the assembly of specific microbial taxa. The study provides a basis for future mechanistic and breeding-oriented investigations of microbiome-associated traits.","PeriodicalId":20101,"journal":{"name":"Plant Physiology","volume":"111 1","pages":""},"PeriodicalIF":8.2000,"publicationDate":"2026-09-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Plant Physiology","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1093/plphys/kiag727","RegionNum":1,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"PLANT SCIENCES","Score":null,"Total":0}
引用次数: 0

Abstract

Plant–microbe interactions are essential for plant health, yet the genetic basis of host control over root-associated microbiome assembly in Nicotiana tabacum remains unclear. We integrated whole-genome resequencing, amplicon sequencing, and metabolomics across 50 tobacco cultivars, together with microbial genome-wide association and mediation analyses, to investigate host–microbiome covariation. Host genotype significantly influenced the diversity and composition of root-associated microbial communities, particularly in the rhizosphere. Several host loci were associated with heritable microbial taxa linked to nutrient acquisition and stress responses. Mediation analysis suggested that associations between host genetic variation and Pseudomonadaceae abundance were partly transmitted through secondary metabolites variation, particularly terpenoids, whereas this mediating effect was less pronounced for other taxa. Functional assays further showed that several genotype-associated bacterial isolates antagonized Fusarium oxysporum. Among them, Pseudomonas aeruginosa FZ1 suppressed pathogen growth, enhanced host defense responses, and reduced disease severity in greenhouse experiments. These findings suggest that host genetic variation is associated with shifts in the tobacco root microbiome and that secondary metabolites may contribute to the assembly of specific microbial taxa. The study provides a basis for future mechanistic and breeding-oriented investigations of microbiome-associated traits.
烟草寄主遗传变异与根相关菌群组合及对尖孢镰刀菌抗性的关系
植物与微生物的相互作用对植物健康至关重要,但寄主控制烟草根相关微生物组组装的遗传基础尚不清楚。我们整合了50个烟草品种的全基因组重测序、扩增子测序和代谢组学,以及微生物全基因组关联和中介分析,以研究宿主-微生物组共变。寄主基因型显著影响根相关微生物群落的多样性和组成,特别是在根际。一些宿主基因座与与养分获取和胁迫反应相关的可遗传微生物类群有关。中介分析表明,寄主遗传变异与假单胞菌科植物丰度之间的关联部分是通过次生代谢物变异(尤其是萜类)传递的,而这种中介作用在其他类群中不太明显。功能分析进一步表明,几种基因型相关的分离菌对尖孢镰刀菌有拮抗作用。其中铜绿假单胞菌FZ1在温室试验中抑制病原菌生长,增强宿主防御反应,降低病害严重程度。这些发现表明,寄主遗传变异与烟草根微生物组的变化有关,次生代谢物可能有助于特定微生物类群的聚集。该研究为今后微生物组相关性状的机理和育种研究奠定了基础。
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
Plant Physiology
Plant Physiology 生物-植物科学
CiteScore
12.20
自引率
5.40%
发文量
535
审稿时长
2.3 months
期刊介绍: Plant Physiology® is a distinguished and highly respected journal with a rich history dating back to its establishment in 1926. It stands as a leading international publication in the field of plant biology, covering a comprehensive range of topics from the molecular and structural aspects of plant life to systems biology and ecophysiology. Recognized as the most highly cited journal in plant sciences, Plant Physiology® is a testament to its commitment to excellence and the dissemination of groundbreaking research. As the official publication of the American Society of Plant Biologists, Plant Physiology® upholds rigorous peer-review standards, ensuring that the scientific community receives the highest quality research. The journal releases 12 issues annually, providing a steady stream of new findings and insights to its readership.
×
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
小红书