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芽孢杆菌与溶杆菌之间的协同相互作用增强了联合体稳定性并抑制黄瓜枯萎病

Cooperative Interactions Between Bacillus and Lysobacter Enhance Consortium Stability and Fusarium Wilt Suppression in Cucumber.

作者信息

Sun Xinli, Xia Riyan, Xie Jiyu, Duan Kun, Xun Weibing, Zhang Nan, Huang Guidong, Zhang Ruifu, Shen Qirong, Wu Kai, Xu Zhihui

机构信息

Jiangsu Provincial Key Lab for Solid Organic Waste Utilization, Key Lab of Organic-Based Fertilizers of China, Jiangsu Collaborative Innovation Center for Solid Organic Wastes, Educational Ministry Engineering Center of Resource-Saving Fertilizers, Nanjing Agricultural University, Nanjing, 210095, China.

Department of Food Science, Foshan University, Foshan, 528231, China.

出版信息

Microb Ecol. 2025 Aug 29;88(1):92. doi: 10.1007/s00248-025-02592-3.

Abstract

The rhizosphere microbiome plays a pivotal role in plant health by mediating interactions between hosts, beneficial microbes, and pathogens. However, the ecological mechanisms underlying microbial consortia that suppress soil-borne diseases remain largely unexplored. In this study, we investigated how the biocontrol bacterium Bacillus velezensis SQR9 influences the assembly of the cucumber rhizosphere bacterial community in the presence of the pathogenic fungus Fusarium oxysporum f. sp. cucumerinum (FOC). Inoculation with B. velezensis SQR9 significantly enriched the genus Lysobacter, a known biocontrol taxon. Meta-analysis revealed a positive correlation between Bacillus and Lysobacter abundances in healthy plant rhizospheres-a relationship absent in Fusarium wilt-diseased soils-suggesting a conserved ecological association linked to disease suppression. Mechanistic assays demonstrated that Lysobacter enzymogenes XL8, an antifungal bacterium isolated from the cucumber rhizosphere, formed synergistic biofilms with B. velezensis SQR9. Spent medium growth assays indicated that strain SQR9 facilitated the growth of L. enzymogenes XL8 through metabolic interactions. Targeted RT-qPCR and UHPLC-MS/MS analyses confirmed that treatment with spent medium of the partner strain enhanced the expression and production of antifungal metabolites bacillomycin D and heat-stable antifungal factor (HSAF), both antagonistic to F. oxysporum. Greenhouse trials confirmed that this dual-species consortium more effectively suppressed Fusarium wilt than single-species inoculations, as evidenced by reduced pathogen abundance and enhanced plant growth. Together, our findings underscore the importance of microbial metabolic cooperation and biofilm-mediated coexistence in shaping rhizosphere community assembly and function, providing ecological insights for the development of synthetic microbial consortia aimed at sustainable plant disease management.

摘要

根际微生物群通过介导宿主、有益微生物和病原体之间的相互作用,在植物健康中发挥着关键作用。然而,抑制土传病害的微生物群落的生态机制在很大程度上仍未得到探索。在本研究中,我们调查了生防细菌贝莱斯芽孢杆菌SQR9在致病真菌尖孢镰刀菌黄瓜专化型(FOC)存在的情况下,如何影响黄瓜根际细菌群落的组装。接种贝莱斯芽孢杆菌SQR9显著富集了溶杆菌属,这是一个已知的生防分类群。荟萃分析显示,在健康植物根际中,芽孢杆菌属和溶杆菌属的丰度呈正相关——在枯萎病土壤中不存在这种关系——这表明存在与病害抑制相关的保守生态关联。机制分析表明,从黄瓜根际分离出的抗真菌细菌溶杆菌XL8与贝莱斯芽孢杆菌SQR9形成了协同生物膜。用过的培养基生长试验表明,菌株SQR9通过代谢相互作用促进了溶杆菌XL8的生长。靶向RT-qPCR和UHPLC-MS/MS分析证实,用伙伴菌株的用过的培养基处理可增强抗真菌代谢物杆菌霉素D和热稳定抗真菌因子(HSAF)的表达和产生,这两种物质均对尖孢镰刀菌具有拮抗作用。温室试验证实,这种双物种群落比单物种接种更有效地抑制了枯萎病,病原体丰度降低和植物生长增强证明了这一点。总之,我们的研究结果强调了微生物代谢合作和生物膜介导的共存对塑造根际群落组装和功能的重要性,为旨在实现可持续植物病害管理的合成微生物群落的开发提供了生态见解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/12e7/12397161/9c5bc456ae70/248_2025_2592_Fig1_HTML.jpg

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