{"title":"Trichoderma asperellum 152-42 enhances growth of perennial ryegrass (Lolium perenne L.) by modulation of plant hormones and carbon-nitrogen metabolism","authors":"Xin Wen , Hongyin Qi , Qichen Niu , Ruoyi Tang , Shuxia Yin","doi":"10.1016/j.scienta.2025.114138","DOIUrl":null,"url":null,"abstract":"<div><div>This study elucidates the growth-enhancing mechanisms underlying <em>Trichoderma asperellum</em> 152-42 mediated growth enhancement in perennial ryegrass (<em>Lolium perenne</em> L.) through integrated physiological and transcriptomic analyses. <em>T. asperellum</em> 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 <em>bHLH128</em> upregulation and shikimate pathway activation; (2) metabolic restructuring is through expression of gene <em>LOC124653768</em> 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 <em>LOC127318565</em> and gene <em>LOC127305933,</em> respectively, correlating with 23.78 % nitrate reductase (NR) and 8.81 % nitrite reductase (NiR) enzymatic activity increases. The <em>T. asperellu</em>m 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.</div><div>Our findings advance microbe-plant interaction by delineating the multilevel network through which <em>T. asperellum</em> 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.</div></div>","PeriodicalId":21679,"journal":{"name":"Scientia Horticulturae","volume":"345 ","pages":"Article 114138"},"PeriodicalIF":4.2000,"publicationDate":"2025-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Scientia Horticulturae","FirstCategoryId":"97","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0304423825001876","RegionNum":2,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/4/18 0:00:00","PubModel":"Epub","JCR":"Q1","JCRName":"HORTICULTURE","Score":null,"Total":0}
引用次数: 0
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.
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.