Turning antagonists into allies: Bacterial-fungal interactions enhance the efficacy of controlling Fusarium wilt disease

IF 11.7 1区 综合性期刊 Q1 MULTIDISCIPLINARY SCIENCES
Tuo Li, Xiaoteng Shi, Jiaguo Wang, Yihao Zhou, Tuokai Wang, Yan Xu, Zhihui Xu, Waseem Raza, Dongyang Liu, Qirong Shen
{"title":"Turning antagonists into allies: Bacterial-fungal interactions enhance the efficacy of controlling Fusarium wilt disease","authors":"Tuo Li, Xiaoteng Shi, Jiaguo Wang, Yihao Zhou, Tuokai Wang, Yan Xu, Zhihui Xu, Waseem Raza, Dongyang Liu, Qirong Shen","doi":"10.1126/sciadv.ads5089","DOIUrl":null,"url":null,"abstract":"Intense microbial competition in soil has driven the evolution of resistance mechanisms, yet the implications of such evolution on plant health remain unclear. Our study explored the conversion from antagonism to coexistence between <jats:italic>Bacillus velezensis</jats:italic> ( <jats:italic>Bv</jats:italic> ) and <jats:italic>Trichoderma guizhouense</jats:italic> ( <jats:italic>Tg</jats:italic> ) and its effects on <jats:italic>Fusarium</jats:italic> wilt disease (FWD) control. We found a bacilysin transmembrane transporter ( <jats:italic>Tg</jats:italic> MFS4) in <jats:italic>Tg</jats:italic> , critical during cross-kingdom dialogue with <jats:italic>B</jats:italic> v. Deleting <jats:italic>Tgmfs4</jats:italic> (Δ <jats:italic>Tgmfs4</jats:italic> ) mitigated <jats:italic>Bv</jats:italic> - <jats:italic>Tg</jats:italic> antagonism, reduced bacilysin import into <jats:italic>Tg</jats:italic> , and elevated its level in the coculture environment. This increase acted as a feedback regulator, limiting overproduction and enhancing <jats:italic>Bv</jats:italic> biomass. Δ <jats:italic>Tgmfs4</jats:italic> coinoculation with <jats:italic>Bv</jats:italic> demonstrated enhanced FWD control relative to wild-type <jats:italic>Tg</jats:italic> ( <jats:italic>Tg</jats:italic> -WT). In addition, the <jats:italic>Tg</jats:italic> -WT+ <jats:italic>Bv</jats:italic> consortium up-regulated antimycotic secretion pathways, whereas the Δ <jats:italic>Tgmfs4</jats:italic> + <jats:italic>Bv</jats:italic> consortium enriched the CAZyme (carbohydrate-active enzyme) family gene expression in the rhizosphere, potentiating plant immune responses. This study elucidates the intricacies of bacterial-fungal interactions and their ramifications for plant health.","PeriodicalId":21609,"journal":{"name":"Science Advances","volume":"20 1","pages":""},"PeriodicalIF":11.7000,"publicationDate":"2025-02-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Science Advances","FirstCategoryId":"103","ListUrlMain":"https://doi.org/10.1126/sciadv.ads5089","RegionNum":1,"RegionCategory":"综合性期刊","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"MULTIDISCIPLINARY SCIENCES","Score":null,"Total":0}
引用次数: 0

Abstract

Intense microbial competition in soil has driven the evolution of resistance mechanisms, yet the implications of such evolution on plant health remain unclear. Our study explored the conversion from antagonism to coexistence between Bacillus velezensis ( Bv ) and Trichoderma guizhouense ( Tg ) and its effects on Fusarium wilt disease (FWD) control. We found a bacilysin transmembrane transporter ( Tg MFS4) in Tg , critical during cross-kingdom dialogue with B v. Deleting Tgmfs4Tgmfs4 ) mitigated Bv - Tg antagonism, reduced bacilysin import into Tg , and elevated its level in the coculture environment. This increase acted as a feedback regulator, limiting overproduction and enhancing Bv biomass. Δ Tgmfs4 coinoculation with Bv demonstrated enhanced FWD control relative to wild-type Tg ( Tg -WT). In addition, the Tg -WT+ Bv consortium up-regulated antimycotic secretion pathways, whereas the Δ Tgmfs4 + Bv consortium enriched the CAZyme (carbohydrate-active enzyme) family gene expression in the rhizosphere, potentiating plant immune responses. This study elucidates the intricacies of bacterial-fungal interactions and their ramifications for plant health.
化敌为友:细菌与真菌的相互作用提高了镰刀菌枯萎病的防治效果
土壤中激烈的微生物竞争推动了抗性机制的进化,但这种进化对植物健康的影响尚不清楚。本研究探讨了芽孢杆菌(Bacillus velezensis, Bv)与贵州木霉(Trichoderma guizhouense, Tg)从拮抗到共存的转化及其对枯萎病(Fusarium wilt disease, FWD)的防治效果。我们在Tg中发现了一个杆菌素跨膜转运蛋白(Tg MFS4),在与Bv的跨界对话中起关键作用。删除Tgmfs4 (Δ Tgmfs4)可以减轻Bv - Tg的拮抗作用,减少细菌素输入Tg,并提高其在共培养环境中的水平。这种增加起到了反馈调节器的作用,限制了生产过剩,提高了生物量。Δ Tgmfs4与Bv共接种显示出相对于野生型Tg (Tg -WT)增强的FWD控制。此外,Tg -WT+ Bv联合体上调了抗真菌分泌途径,而Δ Tgmfs4 + Bv联合体则增加了根际CAZyme(碳水化合物活性酶)家族基因的表达,增强了植物的免疫应答。本研究阐明了细菌-真菌相互作用的复杂性及其对植物健康的影响。
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
Science Advances
Science Advances 综合性期刊-综合性期刊
CiteScore
21.40
自引率
1.50%
发文量
1937
审稿时长
29 weeks
期刊介绍: Science Advances, an open-access journal by AAAS, publishes impactful research in diverse scientific areas. It aims for fair, fast, and expert peer review, providing freely accessible research to readers. Led by distinguished scientists, the journal supports AAAS's mission by extending Science magazine's capacity to identify and promote significant advances. Evolving digital publishing technologies play a crucial role in advancing AAAS's global mission for science communication and benefitting humankind.
×
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