Antibacterial mechanism of hypocrellin against Ralstonia solanacearum in tobacco and its modulation of the endophytic microbiome.

IF 4.1 2区 生物学 Q2 MICROBIOLOGY
Wen Du, Chunlong Sun, Jun Wang, Jingtao Liu, Yanmei Wang, Wenwen Huang, Guolan Liu, Jian Li, Ran Wang, Zhiwei Su, Wenjuan Zhao, Chenzhao Wang
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引用次数: 0

Abstract

The photosensitive compound hypocrellin, derived from the traditional Chinese medicinal fungus Shiraia bambusicola Henn., shows potential as a novel pesticide. To evaluate its efficacy against bacterial wilt disease caused by Ralstonia solanacearum in tobacco, this study examined its antibacterial mechanisms through in vitro experiments and analyzed their impact on tobacco endophytic microbiota. An optimized hypocrellin offering a promising sustainable formulation-with a 2:3 ratio of hypocrellin A to hypocrellin B-was developed for enhanced antibacterial activity, and its interaction with bacterial DNA, intracellular components, and membrane integrity was systematically investigated. Hypocrellins exhibited strong antibacterial effects by disrupting the cell wall and membrane integrity of R. solanacearum, increasing membrane permeability, and inducing the leakage of intracellular K+, soluble proteins, and reducing sugars. Dual DNA-binding mechanisms were suggested: electrostatic adsorption to phosphate groups, followed by groove insertion, and intercalation between base pairs. In tobacco plants, hypocrellin treatment significantly altered the endophytic microbial community, increasing microbial richness and diversity, increasing the proportion of Bacillota and Pseudomonadota, and significantly reducing pathogen abundance. Predictive functional analysis based on PICRUSt2 suggested that hypocrellin may have influenced metabolic pathways associated with microbial basal metabolic activity and proliferation potential. Hypocrellins mitigate R. solanacearum infection through multi-target mechanisms: physical disruption of bacterial membranes and DNA, restoration of beneficial endophytic microbiota, and activation of metabolic pathways critical for plant defense.IMPORTANCEThis study highlights the multi-target antibacterial mechanisms and microbiome-modulating effects of hypocrellin, offering a promising candidate for a sustainable strategy for controlling soil-borne diseases. Unlike conventional chemical pesticides, hypocrellin acts through physical disruption of bacterial membranes and DNA interaction, while simultaneously restoring beneficial endophytic microbiota and activating metabolic pathways critical for plant defense in tobacco. Its ability to suppress Ralstonia solanacearum and enhance microbial ecological balance positions hypocrellin as both an effective antibacterial agent and a microbiome regulator. These findings provide a scientific basis for developing hypocrellin-based bio-pesticides and support further research into its application in eco-friendly agricultural practices.

丁香素对烟草青枯病菌的抑菌机制及其对内生菌群的调节作用。
从传统中药真菌白竹菌中提取的光敏化合物下丘脑素。显示出作为一种新型杀虫剂的潜力。为评价其对烟草青枯病的抑菌效果,本研究通过体外实验考察其抑菌机制,并分析其对烟草内生菌群的影响。我们开发了一种优化的下皮草素,其具有良好的可持续性,下皮草素a与下皮草素b的比例为2:3,以增强抗菌活性,并系统地研究了其与细菌DNA、细胞内成分和膜完整性的相互作用。Hypocrellins通过破坏茄枯细胞壁和膜的完整性,增加膜的通透性,诱导细胞内K+、可溶性蛋白和还原糖的渗漏,表现出较强的抗菌作用。提出了双重dna结合机制:磷酸基团的静电吸附,随后的凹槽插入和碱基对之间的插入。在烟草植株中,次香菇素处理显著改变了内生微生物群落,增加了微生物的丰富度和多样性,增加了杆菌门和假单胞菌门的比例,显著降低了病原菌的丰度。基于PICRUSt2的预测功能分析表明,hypocrellin可能影响与微生物基础代谢活性和增殖潜力相关的代谢途径。Hypocrellins通过多靶点机制减轻番茄红霉感染:物理破坏细菌膜和DNA,恢复有益的内生微生物群,激活对植物防御至关重要的代谢途径。重要意义:本研究强调了下蒿素的多靶点抗菌机制和微生物调节作用,为控制土传疾病的可持续策略提供了有希望的候选物。与传统化学农药不同,hypocrellin通过物理破坏细菌膜和DNA相互作用发挥作用,同时恢复有益的内生微生物群并激活烟草中对植物防御至关重要的代谢途径。它具有抑制茄枯菌和促进微生物生态平衡的作用,是一种有效的抗菌剂和微生物组调节剂。这些发现为开发次氯酸酯类生物农药提供了科学依据,并为其在生态农业实践中的进一步研究提供了支持。
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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.
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