Yaping Yin, Zhen Liu, Ming Xue, Xuewei Zhang, Raja Asad Ali Khan, Rui Wang, Jumei Hou, Tong Liu
{"title":"A Trichoderma milRNA cross-species targeting chitin synthases genes is delivered by carbon nanomaterials to suppress Botrytis cinerea","authors":"Yaping Yin, Zhen Liu, Ming Xue, Xuewei Zhang, Raja Asad Ali Khan, Rui Wang, Jumei Hou, Tong Liu","doi":"10.1093/plphys/kiag715","DOIUrl":null,"url":null,"abstract":"Botrytis cinerea is a globally destructive plant pathogen that threatens major agricultural crops. Although biocontrol agents are widely used against this fungus, their inconsistent efficacy reflects a limited mechanistic understanding, hindering the development of effective disease management strategies. In this study, we investigated the in-depth biocontrol mechanism of Trichoderma breve against B. cinerea on tomato plants and various fruits. We identified a new microRNA Tri-milR29 from T. breve. Tri-milR29 is delivered into B. cinerea via extracellular vesicles, enabling cross-species RNA interference (RNAi). Once inside B. cinerea, Tri-milR29 targets the chitin synthase genes BcCHS7 and BcCHS6, thereby impairing fungal growth and reducing its pathogenicity. This cross-species miRNA phenomenon significantly enhanced the antifungal and disease-suppressing efficacy of T. breve against B. cinerea. Moreover, to optimize the antifungal and disease-control effects of Tri-milR29, we engineered polyethyleneimine-modified carbon dot nanocomposites (CPP) as nanocarriers using coconut water as a raw material. This green, biomass-based nanocarrier system improved the delivery and uptake of Tri-milR29 in B. cinerea. Pot experiments indicated that CPP-loaded Tri-milR29 improved disease control efficacy by 37.5%. A six-month field trial further confirmed that its field control rate reached 78.71%, which was close to the commercial fungicide procymidone (82.84%). Understanding the targets and mechanism of Tri-milR29, along with its enhanced performance via CPP facilitation, could support the broader application of dsRNA-CPP in other plant-pathogen systems, leading to reduced chemical inputs and encouraging safer, more environmentally-friendly alternatives.","PeriodicalId":20101,"journal":{"name":"Plant Physiology","volume":"83 1","pages":""},"PeriodicalIF":8.2000,"publicationDate":"2026-09-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Plant Physiology","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1093/plphys/kiag715","RegionNum":1,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"PLANT SCIENCES","Score":null,"Total":0}
引用次数: 0
Abstract
Botrytis cinerea is a globally destructive plant pathogen that threatens major agricultural crops. Although biocontrol agents are widely used against this fungus, their inconsistent efficacy reflects a limited mechanistic understanding, hindering the development of effective disease management strategies. In this study, we investigated the in-depth biocontrol mechanism of Trichoderma breve against B. cinerea on tomato plants and various fruits. We identified a new microRNA Tri-milR29 from T. breve. Tri-milR29 is delivered into B. cinerea via extracellular vesicles, enabling cross-species RNA interference (RNAi). Once inside B. cinerea, Tri-milR29 targets the chitin synthase genes BcCHS7 and BcCHS6, thereby impairing fungal growth and reducing its pathogenicity. This cross-species miRNA phenomenon significantly enhanced the antifungal and disease-suppressing efficacy of T. breve against B. cinerea. Moreover, to optimize the antifungal and disease-control effects of Tri-milR29, we engineered polyethyleneimine-modified carbon dot nanocomposites (CPP) as nanocarriers using coconut water as a raw material. This green, biomass-based nanocarrier system improved the delivery and uptake of Tri-milR29 in B. cinerea. Pot experiments indicated that CPP-loaded Tri-milR29 improved disease control efficacy by 37.5%. A six-month field trial further confirmed that its field control rate reached 78.71%, which was close to the commercial fungicide procymidone (82.84%). Understanding the targets and mechanism of Tri-milR29, along with its enhanced performance via CPP facilitation, could support the broader application of dsRNA-CPP in other plant-pathogen systems, leading to reduced chemical inputs and encouraging safer, more environmentally-friendly alternatives.
期刊介绍:
Plant Physiology® is a distinguished and highly respected journal with a rich history dating back to its establishment in 1926. It stands as a leading international publication in the field of plant biology, covering a comprehensive range of topics from the molecular and structural aspects of plant life to systems biology and ecophysiology. Recognized as the most highly cited journal in plant sciences, Plant Physiology® is a testament to its commitment to excellence and the dissemination of groundbreaking research.
As the official publication of the American Society of Plant Biologists, Plant Physiology® upholds rigorous peer-review standards, ensuring that the scientific community receives the highest quality research. The journal releases 12 issues annually, providing a steady stream of new findings and insights to its readership.