Trichoderma asperellum 152-42 enhances growth of perennial ryegrass (Lolium perenne L.) by modulation of plant hormones and carbon-nitrogen metabolism

IF 4.2 2区 农林科学 Q1 HORTICULTURE Scientia Horticulturae Pub Date : 2025-04-01 Epub Date: 2025-04-18 DOI:10.1016/j.scienta.2025.114138
Xin Wen , Hongyin Qi , Qichen Niu , Ruoyi Tang , Shuxia Yin
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Abstract

This study elucidates the growth-enhancing mechanisms underlying Trichoderma asperellum 152-42 mediated growth enhancement in perennial ryegrass (Lolium perenne L.) through integrated physiological and transcriptomic analyses. T. asperellum 152-42 inoculation induced significant biomass augmentation, with treated plants exhibiting 26.36 % increased shoot height, 64.96 % roots elongation, 42.02 % shoot fresh weight and 40.65 % shoot dry weight gain versus controls. Notably, root systems displayed sensitivity to fungal symbiosis, correlating with 14.53 % auxin (IAA) elevation and 39.30 % abscisic acid (ABA) reduction. Molecular dissection revealed multilevel regulatory networks: (1) auxin biosynthesis via 2.45-fold transcription factor bHLH128 upregulation and shikimate pathway activation; (2) metabolic restructuring is through expression of gene LOC124653768 encoding phosphoenolpyruvate carboxylase (PEPC) was upregulated by 2.45-fold, and the PEPC enzyme activity increased by 135.60 % enhancing carbon flux. And metabolic restructuring toward increased glycolytic flux through PDC-mediated pyruvate conversion and enhanced anaplerotic carbon fixation via PEPC activity; (3) nitrogen assimilation with 4.1-fold and 2.3-fold upregulation of gene LOC127318565 and gene LOC127305933, respectively, correlating with 23.78 % nitrate reductase (NR) and 8.81 % nitrite reductase (NiR) enzymatic activity increases. The T. asperellum 152-42's growth-promotive effects stem from synergistic hormonal modulation and substrate channeling, where PEPC-derived carbon skeletons fuel NR-mediated nitrogen assimilation. This synergistic integration of hormonal regulation and metabolic network optimization demonstrates microbe-plant partnership.
Our findings advance microbe-plant interaction by delineating the multilevel network through which T. asperellum 152-42 enhances perennial ryegrass productivity. The results offer novel perspectives on microbial-mediated modulation of plant metabolic coordination, with potential applications in sustainable forage cultivation and biofertilizer development.

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曲霉152-42通过调节植物激素和碳氮代谢促进多年生黑麦草的生长
本研究通过综合生理和转录组学分析,阐明了曲霉152-42介导的多年生黑麦草(Lolium perenne L.)生长促进机制。接种曲霉152-42后,植株生物量显著增加,与对照相比,茎高增加26.36%,根系伸长增加64.96%,鲜重增加42.02%,干重增加40.65%。值得注意的是,根系对真菌共生表现出敏感性,生长素(IAA)升高14.53%,脱落酸(ABA)减少39.30%。分子解剖揭示了生长素的多水平调控网络:(1)通过2.45倍转录因子bHLH128的上调和莽草酸途径的激活实现生长素的生物合成;(2)代谢重组是通过表达编码磷酸烯醇丙酮酸羧化酶(phosphoenolpyruvate carboxylase, PEPC)的LOC124653768基因上调2.45倍,PEPC酶活性提高135.60%,增强碳通量。代谢重组通过pdc介导的丙酮酸转化增加糖酵解通量,并通过PEPC活性增强反旋碳固定;(3)氮同化使LOC127318565和LOC127305933基因分别上调4.1倍和2.3倍,与23.78%的硝酸还原酶(NR)和8.81%的亚硝酸盐还原酶(NiR)酶活性升高相关。曲霉152-42的生长促进作用源于协同激素调节和底物通道,其中pepc衍生的碳骨架为nr介导的氮同化提供燃料。这种激素调节和代谢网络优化的协同整合证明了微生物与植物的伙伴关系。我们的研究结果通过描述T. asperellum 152-42提高多年生黑麦草生产力的多层次网络,推进了微生物与植物的相互作用。该结果为微生物介导的植物代谢协调调节提供了新的视角,在可持续饲料栽培和生物肥料开发中具有潜在的应用前景。
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来源期刊
Scientia Horticulturae
Scientia Horticulturae 农林科学-园艺
CiteScore
8.60
自引率
4.70%
发文量
796
审稿时长
47 days
期刊介绍: Scientia Horticulturae is an international journal publishing research related to horticultural crops. Articles in the journal deal with open or protected production of vegetables, fruits, edible fungi and ornamentals under temperate, subtropical and tropical conditions. Papers in related areas (biochemistry, micropropagation, soil science, plant breeding, plant physiology, phytopathology, etc.) are considered, if they contain information of direct significance to horticulture. Papers on the technical aspects of horticulture (engineering, crop processing, storage, transport etc.) are accepted for publication only if they relate directly to the living product. In the case of plantation crops, those yielding a product that may be used fresh (e.g. tropical vegetables, citrus, bananas, and other fruits) will be considered, while those papers describing the processing of the product (e.g. rubber, tobacco, and quinine) will not. The scope of the journal includes all horticultural crops but does not include speciality crops such as, medicinal crops or forestry crops, such as bamboo. Basic molecular studies without any direct application in horticulture will not be considered for this journal.
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