Interactions with native microbial keystone taxa enhance the biocontrol efficiency of Streptomyces.

IF 13.8 1区 生物学 Q1 MICROBIOLOGY
Tianyu Sun, Hongwei Liu, Ningqi Wang, Mingcong Huang, Samiran Banerjee, Alexandre Jousset, Yangchun Xu, Qirong Shen, Shimei Wang, Xiaofang Wang, Zhong Wei
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引用次数: 0

Abstract

Background: Streptomyces spp. are known for producing bioactive compounds that suppress phytopathogens. However, previous studies have largely focused on their direct interactions with pathogens and plants, often neglecting their interactions with the broader soil microbiome. In this study, we hypothesized that these interactions are critical for effective pathogen control. We investigated a diverse collection of Streptomyces strains to select those with strong protective capabilities against tomato wilt disease caused by Ralstonia solanacearum. Leveraging a synthetic community (SynCom) established in our lab, alongside multiple in planta and in vitro co-cultivation experiments, as well as transcriptomic and metabolomic analyses, we explored the synergistic inhibitory mechanisms underlying bacterial wilt resistance facilitated by both Streptomyces and the soil microbiome.

Results: Our findings indicate that direct antagonism by Streptomyces is not sufficient for their biocontrol efficacy. Instead, the efficacy was associated with shifts in the rhizosphere microbiome, particularly the promotion of two native keystone taxa, CSC98 (Stenotrophomonas maltophilia) and CSC13 (Paenibacillus cellulositrophicus). In vitro co-cultivation experiments revealed that CSC98 and CSC13 did not directly inhibit the pathogen. Instead, the metabolite of CSC13 significantly enhanced the inhibition efficiency of Streptomyces R02, a highly effective biocontrol strain in natural soil. Transcriptomic and metabolomic analyses revealed that CSC13's metabolites induced the production of Erythromycin E in Streptomyces R02, a key compound that directly suppressed R. solanacearum, as demonstrated by our antagonism tests.

Conclusions: Collectively, our study reveals how beneficial microbes engage with the native soil microbiome to combat pathogens, suggesting the potential of leveraging microbial interactions to enhance biocontrol efficiency. These findings highlight the significance of intricate microbial interactions within the microbiome in regulating plant diseases and provide a theoretical foundation for devising efficacious biocontrol strategies in sustainable agriculture. Video Abstract.

与本地微生物基石类群的相互作用增强了链霉菌的生物防治效果。
背景:链霉菌以产生抑制植物病原体的生物活性化合物而闻名。然而,以往的研究主要集中在它们与病原体和植物的直接相互作用上,往往忽略了它们与更广泛的土壤微生物群的相互作用。在这项研究中,我们假设这些相互作用对有效的病原体控制至关重要。为了筛选出对番茄枯萎病具有较强防护能力的链霉菌菌株,我们对不同种类的链霉菌进行了研究。利用我们实验室建立的合成群落(SynCom),结合多种植物和体外共培养实验,以及转录组学和代谢组学分析,我们探索了链霉菌和土壤微生物组共同促进的细菌枯萎抗性的协同抑制机制。结果:链霉菌的直接拮抗作用不足以发挥其生物防治效果。相反,这种效果与根际微生物群的变化有关,特别是促进了两个本地关键分类群CSC98(嗜麦芽窄养单胞菌)和CSC13(嗜纤维素芽孢杆菌)。体外共培养实验表明,CSC98和CSC13对病原菌没有直接抑制作用。相反,CSC13的代谢物显著提高了天然土壤中高效生物防治菌株Streptomyces R02的抑制效率。转录组学和代谢组学分析显示,CSC13的代谢物诱导Streptomyces R02产生红霉素E,这是直接抑制番茄红霉的关键化合物,我们的拮抗实验证实了这一点。结论:总的来说,我们的研究揭示了有益微生物如何与原生土壤微生物群相互作用以对抗病原体,这表明利用微生物相互作用来提高生物防治效率的潜力。这些发现强调了微生物组内复杂的微生物相互作用在调控植物病害中的重要性,并为制定有效的可持续农业生物防治策略提供了理论基础。视频摘要。
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来源期刊
Microbiome
Microbiome MICROBIOLOGY-
CiteScore
21.90
自引率
2.60%
发文量
198
审稿时长
4 weeks
期刊介绍: Microbiome is a journal that focuses on studies of microbiomes in humans, animals, plants, and the environment. It covers both natural and manipulated microbiomes, such as those in agriculture. The journal is interested in research that uses meta-omics approaches or novel bioinformatics tools and emphasizes the community/host interaction and structure-function relationship within the microbiome. Studies that go beyond descriptive omics surveys and include experimental or theoretical approaches will be considered for publication. The journal also encourages research that establishes cause and effect relationships and supports proposed microbiome functions. However, studies of individual microbial isolates/species without exploring their impact on the host or the complex microbiome structures and functions will not be considered for publication. Microbiome is indexed in BIOSIS, Current Contents, DOAJ, Embase, MEDLINE, PubMed, PubMed Central, and Science Citations Index Expanded.
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