A Trichoderma milRNA cross-species targeting chitin synthases genes is delivered by carbon nanomaterials to suppress Botrytis cinerea

IF 8.2 1区 生物学 Q1 PLANT SCIENCES
Yaping Yin, Zhen Liu, Ming Xue, Xuewei Zhang, Raja Asad Ali Khan, Rui Wang, Jumei Hou, Tong Liu
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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.
利用碳纳米材料传递一种靶向几丁质合成酶基因的木霉milRNA以抑制灰葡萄孢
灰霉病是一种全球性的破坏性植物病原体,威胁着主要的农作物。尽管生物防治剂被广泛用于对抗这种真菌,但它们不一致的效果反映了对其机理的有限理解,阻碍了有效疾病管理策略的发展。在本研究中,我们深入研究了短木霉(Trichoderma breve)对番茄植株和各种果实的番茄灰霉(b.c ineea)的生物防治机制。我们从T. breve中鉴定出一个新的microRNA Tri-milR29。Tri-milR29通过胞外囊泡被递送到灰芽孢杆菌中,从而实现跨物种RNA干扰(RNAi)。一旦进入灰葡萄球菌,Tri-milR29靶向几丁质合成酶基因BcCHS7和BcCHS6,从而抑制真菌生长,降低致病性。这种跨种miRNA现象显著增强了短链梭菌对灰绿杆菌的抗真菌和抑病效果。此外,为了优化Tri-milR29的抗真菌和疾病控制效果,我们以椰子水为原料,设计了聚乙烯亚胺修饰碳点纳米复合材料(CPP)作为纳米载体。这种绿色的、基于生物质的纳米载体系统改善了Tri-milR29在绿莓中的传递和吸收。盆栽试验表明,载cpp的Tri-milR29防治效果提高了37.5%。6个月的田间试验进一步证实,其田间防制率为78.71%,接近市售杀菌剂丙嘧米酮(82.84%)。了解Tri-milR29的靶点和机制,以及其通过CPP促进而增强的性能,可以支持dsRNA-CPP在其他植物-病原体系统中的更广泛应用,从而减少化学投入,并鼓励更安全、更环保的替代品。
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来源期刊
Plant Physiology
Plant Physiology 生物-植物科学
CiteScore
12.20
自引率
5.40%
发文量
535
审稿时长
2.3 months
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.
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