Wild mungbean resistance to the nematode Meloidogyne enterolobii involves the induction of phenylpropanoid metabolism and lignification.

IF 5.4 2区 生物学 Q1 PLANT SCIENCES Physiologia plantarum Pub Date : 2024-09-01 DOI:10.1111/ppl.14533
Sook-Kuan Lee, Pin-Zhe Liao, Chih-Yu Lin, Hung-Wei Chen, Meng-Shan Hsieh, Ya-Ping Lin, Yi-Ju Chen, Jia-Heng Hong, Yi-Ling Chiang, Chiu-Ping Cheng, Pei-Chen Janet Chen, Cheng-Ruei Lee, Jiue-In Yang, Hieng-Ming Ting
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Abstract

Root-knot nematodes (Meloidogyne spp.) are plant parasites causing annual economic losses amounting to several billion US dollars worldwide. One of the most aggressive species is M. enterolobii, a growing threat to agriculture due to its broad host range and ability to overcome many known resistance genes. Mungbean, a nutritionally and economically valuable crop, is particularly vulnerable to nematodes and pathogens. However, research focusing on mungbean resistance to M. enterolobii is scarce, and the corresponding defense mechanisms are poorly understood. Here, we screened mungbean accessions and identified an accession strongly resistant to M. enterolobii. Transcriptome analysis revealed 2730 differentially expressed genes (DEGs) in this resistant accession (CPI106939) compared to 1777 in the susceptible accession (Crystal) 7 days after nematode inoculation. The gene ontology (GO) upregulated in CPI106939 with functions related to plant-pathogen interactions, plant hormone signaling, oxidative stress, and plant immunity. Plant defense-related genes (WRKY, PAL, MAPK, POD and PR) were also significantly induced in CPI106939. Metabolome analysis showed that four secondary metabolites related to phenylpropanoid metabolism and lignification were significantly enriched in CPI106939. The induced immune response and secondary metabolites may underpin the enhanced resistance to M. enterolobii, providing insight into the resistance mechanisms in accession CPI106939 as well as candidate genes controlling the interaction between mungbean and its nematode parasite. Our study therefore provides foundations for the breeding of new varieties with intrinsic M. enterolobii resistance.

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野生绿豆对线虫 Meloidogyne enterolobii 的抗性涉及诱导苯丙素代谢和木质化。
根结线虫(Meloidogyne spp.)肠结线虫是最具攻击性的物种之一,由于其寄主范围广泛,并能克服许多已知的抗性基因,因此对农业的威胁日益严重。绿豆是一种具有营养和经济价值的作物,特别容易受到线虫和病原体的侵害。然而,有关绿豆对肠道线虫抗性的研究很少,人们对相应的防御机制也知之甚少。在此,我们对绿豆品种进行了筛选,发现了一个对肠孢霉具有强抗性的品种。转录组分析显示,在接种线虫 7 天后,该抗性品种(CPI106939)与易感品种(Crystal)相比,有 2730 个差异表达基因(DEGs),而易感品种只有 1777 个。CPI106939 中基因本体(GO)上调的功能与植物-病原体相互作用、植物激素信号转导、氧化应激和植物免疫有关。CPI106939 中的植物防御相关基因(WRKY、PAL、MAPK、POD 和 PR)也被显著诱导。代谢组分析表明,CPI106939 中明显富集了四种与苯丙类代谢和木质化有关的次生代谢物。诱导的免疫反应和次生代谢物可能是增强对肠道线虫抗性的基础,这有助于深入了解 CPI106939 的抗性机制以及控制绿豆与其线虫寄生体之间相互作用的候选基因。因此,我们的研究为培育具有内在肠道线虫抗性的新品种奠定了基础。
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来源期刊
Physiologia plantarum
Physiologia plantarum 生物-植物科学
CiteScore
11.00
自引率
3.10%
发文量
224
审稿时长
3.9 months
期刊介绍: Physiologia Plantarum is an international journal committed to publishing the best full-length original research papers that advance our understanding of primary mechanisms of plant development, growth and productivity as well as plant interactions with the biotic and abiotic environment. All organisational levels of experimental plant biology – from molecular and cell biology, biochemistry and biophysics to ecophysiology and global change biology – fall within the scope of the journal. The content is distributed between 5 main subject areas supervised by Subject Editors specialised in the respective domain: (1) biochemistry and metabolism, (2) ecophysiology, stress and adaptation, (3) uptake, transport and assimilation, (4) development, growth and differentiation, (5) photobiology and photosynthesis.
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