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Summary Spray‐induced gene silencing (SIGS) is an innovative and eco‐friendly technology where topical application of pathogen gene‐targeting RNAs to plant material can enable disease control. SIGS applications remain limited because of the instability of RNA, which can be rapidly degraded when exposed to various environmental conditions. Inspired by the natural mechanism of cross‐kingdom RNAi through extracellular vesicle trafficking, we describe herein the use of artificial nanovesicles (AVs) for RNA encapsulation and control against the fungal pathogen, Botrytis cinerea . AVs were synthesized using three different cationic lipid formulations, DOTAP + PEG, DOTAP and DODMA, and examined for their ability to protect and deliver double stranded RNA (dsRNA). All three formulations enabled dsRNA delivery and uptake by B . cinerea . Further, encapsulating dsRNA in AVs provided strong protection from nuclease degradation and from removal by leaf washing. This improved stability led to prolonged RNAi‐mediated protection against B . cinerea both on pre‐ and post‐harvest plant material using AVs. Specifically, the AVs extended the protection duration conferred by dsRNA to 10 days on tomato and grape fruits and to 21 days on grape leaves. The results of this work demonstrate how AVs can be used as a new nanocarrier to overcome RNA instability in SIGS for crop protection.
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This content will become publicly available on November 13, 2026
Cross-kingdom RNA trafficking from bacteria to fungi enables plant protection against fungal pathogens
Fungal pathogens pose escalating challenges to global food security, as resistance has emerged against nearly all major fungicides used in agriculture. RNA-based antifungals offer a sustainable and environmentally friendly alternative for disease control, but their deployment is hindered by RNA instability under environmental conditions, especially in soil. In this study, we engineered two plant-beneficial soil bacteria-Bacillus subtilis (Gram-positive) and Pseudomonas putida (Gram-negative)-to produce double-stranded RNAs (dsRNAs) targeting fungal genes in the foliar and postharvest pathogen Botrytis cinerea and the soilborne pathogen Verticillium dahliae. We found that both bacterial species secrete RNA through extracellular vesicles (EVs) and that these RNAs are transported into fungal cells, demonstrating cross-kingdom RNA trafficking from bacteria to fungi. Application of dsRNA-containing bacterial EVs to plant leaves suppressed B. cinerea infection. In addition, direct treatment with dsRNA-producing bacteria protected both Arabidopsis thaliana and tomato plants from infections by B. cinerea and V. dahliae. Our findings establish beneficial bacteria as a scalable platform for continuous production and delivery of antifungal RNAs, enabling a cost-effective strategy for sustainable crop protection.
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- Award ID(s):
- 2020731
- PAR ID:
- 10657756
- Publisher / Repository:
- Cell Press
- Date Published:
- Journal Name:
- Molecular Plant
- Volume:
- 19
- Issue:
- 1
- ISSN:
- 1674-2052
- Page Range / eLocation ID:
- 100 to 115
- Format(s):
- Medium: X
- Sponsoring Org:
- National Science Foundation
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