Antifungal Efficacy and Mechanisms of Methyleugenol from Asarum Essential Oil Against Rhizoctonia solani Causing Ginseng Damping-Off Disease

IF 4.5 2区 农林科学 Q1 AGRONOMY
Rui Zhang, Xiaolin Chen, Xueqian Yan, Zhongliang Yang, Dandan Zhang, Yingping Wang, Baohui Lu
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Abstract

Damping-off disease caused by Rhizoctonia solani is a devastating soilborne disease that poses a serious threat to sustainable ginseng (Panax ginseng) production. In an effort to develop environmentally friendly control alternatives, we investigated the volatile constituents of Asarum heterotropoides essential oil using GC-MS in 2023 and identified methyleugenol as the predominant bioactive component, accounting for 21.32% of the total volatile fraction. Mycelial growth rate assays demonstrated that methyleugenol exerted pronounced antifungal activity against R. solani, with EC50 and EC90 values of 60 mg/L and 800 mg/L, respectively. Treatment at 0.1 mg/mL resulted in 51% growth inhibition after 4 days of incubation. To elucidate the underlying mechanisms of action, R. solani mycelia exposed to 0.1 mg/mL methyleugenol were harvested at 4 and 6 days post-treatment for integrated transcriptomic and untargeted metabolomic profiling. Transcriptome analysis revealed 1444 and 1157 significantly downregulated genes at 4 and 6 days, respectively, with 836 genes consistently repressed at both time points. GO and KEGG enrichment analyses indicated that these persistently suppressed genes were predominantly associated with protein processing in the endoplasmic reticulum, protein export, tyrosine metabolism, and peroxisome biogenesis. Metabolomic profiling identified 95 differentially accumulated metabolites that were commonly reduced across both time points, with KEGG pathway enrichment highlighting significant suppression of starch and sucrose metabolism and galactose metabolism pathways central to carbon source utilization. Integrative transcriptome–metabolome correlation analysis further uncovered three key transcription factors (gene-RDB_LOCUS74145, gene-RDB_LOCUS26344, and gene-RDB_LOCUS52181) implicated in the regulation of carbohydrate metabolism and tricarboxylic acid cycle-related metabolite production. Collectively, our findings indicate that methyleugenol suppresses R. solani growth through a multi-target mechanism involving impairment of carbon source metabolism, disruption of protein processing and secretion, and attenuation of cellular energy supply. These results provide a mechanistic foundation for the development of botanical fungicide-based strategies for the green management of ginseng damping-off disease.
细辛精油中甲基丁香酚对人参萎蔫病的拮抗作用及机制研究
枯枯病是由枯枯菌引起的一种破坏性土传病害,严重威胁人参可持续生产。为了开发环境友好的防治替代品,我们于2023年采用气相色谱-质谱法对细辛挥发油的挥发性成分进行了研究,鉴定出甲基丁香酚为主要的生物活性成分,占总挥发分的21.32%。菌丝生长速率测定表明,甲基丁香酚对茄枯病菌具有明显的抑菌活性,EC50和EC90分别为60 mg/L和800 mg/L。在0.1 mg/mL的浓度下,培养4天后,生长抑制率达到51%。为了阐明潜在的作用机制,在处理后4天和6天采集暴露于0.1 mg/mL甲基丁香酚的茄茄菌丝体,进行综合转录组学和非靶向代谢组学分析。转录组分析显示,1444个和1157个基因分别在第4天和第6天显著下调,836个基因在两个时间点都持续被抑制。GO和KEGG富集分析表明,这些持续抑制的基因主要与内质网的蛋白质加工、蛋白质输出、酪氨酸代谢和过氧化物酶体的生物发生有关。代谢组学分析确定了95种不同积累的代谢物,这些代谢物在两个时间点上都普遍减少,KEGG途径的富集突出了淀粉和蔗糖代谢以及对碳源利用至关重要的半乳糖代谢途径的显著抑制。整合转录组-代谢组相关分析进一步发现了三个关键转录因子(基因- rdb_locus74145,基因- rdb_locus26344和基因- rdb_locus52181)参与碳水化合物代谢和三羧酸循环相关代代谢产物的调节。综上所述,我们的研究结果表明,甲基丁香酚通过碳源代谢损伤、蛋白质加工和分泌中断以及细胞能量供应衰减等多靶点机制抑制茄茄的生长。这些结果为开发植物杀菌剂为基础的人参萎蔫病绿色治理策略提供了机理基础。
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来源期刊
Agriculture-Basel
Agriculture-Basel Agricultural and Biological Sciences-Food Science
CiteScore
4.90
自引率
13.90%
发文量
1793
审稿时长
11 weeks
期刊介绍: Agriculture (ISSN 2077-0472) is an international and cross-disciplinary scholarly and scientific open access journal on the science of cultivating the soil, growing, harvesting crops, and raising livestock. We will aim to look at production, processing, marketing and use of foods, fibers, plants and animals. The journal Agriculturewill publish reviews, regular research papers, communications and short notes, and there is no restriction on the length of the papers. Our aim is to encourage scientists to publish their experimental and theoretical research in as much detail as possible. Full experimental and/or methodical details must be provided for research articles.
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Agilent 2100 Bioanalyzer
2
AMPure XP beads
3
SPSS 26.0
4
Illumina HiSeq platform
6
ultrapure water
7732-18-5
7
NEB Fragmentation Buffer
8
DHP-9082 constant-temperature incubator
9
Total RNA Rapid Extraction Kit
10
BSA124S-CW analytical balance
11
D3024R refrigerated microcentrifuge
12
ZEISS SERIES 120 microscope
13
XFH-40CA vertical autoclave
14
DK-S24 thermostatic water bath
15
SW-CJ-2FD laminar flow clean bench
16
Hypersil Gold column
17
Q Exactive HF-X hybrid quadrupole-Orbitrap mass spectrometer
18
Vanquish UHPLC system
19
ammonium acetate
631-61-8
20
formic acid
64-18-6
21
Hypersil Gold column
22
methanol
67-56-1
23
NanoDrop ND-2000 spectrophotometer
24
Qubit 2.0 Fluorometer
25
22
Methyleugenol
93-15-2
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