Methyl-2,4-dihydroxybenzoate induces transcriptomic reprogramming in Fusarium oxysporum f. sp. cubense and defense gene responses in Kadali banana

IF 3.5 3区 医学 Q3 IMMUNOLOGY
B.R. Ajesh , S. Nakkeeran , P. Renukadevi , R.U. Krishna Nayana , Suhail Ashraf , R. Udhayakumar , Khalid E. Hamed
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Abstract

The emergence of fungicide resistance and environmental concerns with conventional chemicals necessitate the identification of novel antifungal compounds. Methyl-2,4-dihydroxybenzoate (MDHB), a hydroxybenzoate derivative, exhibits potent antifungal activity against Fusarium oxysporum f. sp. cubense, the causative agent of Panama disease in bananas. To uncover its molecular mechanism of action, we performed comprehensive transcriptomic profiling of Foc treated with 100 ppm MDHB using RNA sequencing technology. The analysis revealed 173 differentially expressed genes (DEGs), comprising 121 upregulated and 52 downregulated genes (|log2FC| > 1, FDR <0.05). Gene Ontology analysis showed that MDHB exerts multifaceted antifungal activity through membrane destabilization (47 membrane-associated genes affected), suppression of energy metabolism via downregulation of ATP-binding proteins and proton-pumping ATPases, oxidative stress induction through impairment of superoxide dismutase (SOD2) and antioxidant systems. It also disrupted protein synthesis machinery including ribosomal proteins and elongation factors. MDHB further compromised cellular transport by downregulating ABC transporters (STE6) and major facilitator superfamily transporters (PTR2), and disrupted N-glycosylation via repression of SRD5A3 and RFT1 genes. Plant defense gene expression analysis revealed enhanced immune responses in banana, with significant upregulation of WRKY transcription factors (5.9-fold), LECTIN receptors (5.3-fold), and MAPK signaling components (5.5-fold). Glasshouse trials confirmed MDHB's efficacy, reducing disease severity from 100 % to 4.4 % and limiting disease incidence to 16 % compared to 100 % in pathogen-inoculated controls. This study provides the first transcriptomic insights into Foc's response to MDHB, revealing a multi-target mechanism disrupting key cellular functions while enhancing plant defense, establishing MDHB as a promising antifungal candidate for sustainable Fusarium wilt management.

Abstract Image

甲基-2,4-二羟基苯甲酸盐诱导古巴尖孢镰刀菌转录组重编程及防御基因响应
杀菌剂耐药性的出现和传统化学品的环境问题要求鉴定新的抗真菌化合物。甲基-2,4-二羟基苯甲酸酯(MDHB)是一种羟基苯甲酸酯衍生物,对香蕉巴拿马病病原菌古巴镰刀菌(Fusarium oxysporum f. sp. cubense)具有较强的抗真菌活性。为了揭示其作用的分子机制,我们使用RNA测序技术对100 ppm MDHB处理的Foc进行了全面的转录组学分析。分析发现173个差异表达基因(DEGs),其中121个表达上调,52个表达下调(|log2FC| > 1, FDR <0.05)。基因本体分析表明,MDHB通过破坏膜稳定(影响47个膜相关基因),通过下调atp结合蛋白和质子泵送atp酶抑制能量代谢,通过损伤超氧化物歧化酶(SOD2)和抗氧化系统诱导氧化应激,发挥多方面的抗真菌活性。它还破坏了蛋白质合成机制,包括核糖体蛋白和延伸因子。MDHB通过下调ABC转运蛋白(STE6)和主要促进剂超家族转运蛋白(PTR2)进一步损害细胞运输,并通过抑制SRD5A3和RFT1基因破坏n -糖基化。植物防御基因表达分析显示,香蕉的免疫应答增强,WRKY转录因子(5.9倍)、凝集素受体(5.3倍)和MAPK信号成分(5.5倍)显著上调。温室试验证实了MDHB的有效性,将疾病严重程度从100%降低到4.4%,将疾病发病率限制在16%,而接种病原体的对照为100%。本研究首次提供了Foc对MDHB反应的转录组学见解,揭示了在增强植物防御的同时破坏关键细胞功能的多靶点机制,确立了MDHB作为可持续管理枯萎病的有前途的抗真菌候选物。
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来源期刊
Microbial pathogenesis
Microbial pathogenesis 医学-免疫学
CiteScore
7.40
自引率
2.60%
发文量
472
审稿时长
56 days
期刊介绍: Microbial Pathogenesis publishes original contributions and reviews about the molecular and cellular mechanisms of infectious diseases. It covers microbiology, host-pathogen interaction and immunology related to infectious agents, including bacteria, fungi, viruses and protozoa. It also accepts papers in the field of clinical microbiology, with the exception of case reports. Research Areas Include: -Pathogenesis -Virulence factors -Host susceptibility or resistance -Immune mechanisms -Identification, cloning and sequencing of relevant genes -Genetic studies -Viruses, prokaryotic organisms and protozoa -Microbiota -Systems biology related to infectious diseases -Targets for vaccine design (pre-clinical studies)
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