Evidence map›Paper›PMID 42237611›Full record

ArticleThe plant pathology journal2026

Chitosan-Tripolyphosphate Nanoparticles Enhance Foliar dsRNA Delivery and Suppress Turnip Crinkle Virus in Arabidopsis.

Min-Jae Kim, Nam-Yeon Kim, Rae-Dong Jeong

Abstract read
In one paragraph

Article in The plant pathology journal, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
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0citing papers in PubMed
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1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

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3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

3 authors.

Min-Jae KimDepartment of Applied Biology, Chonnam National University, Gwangju 61185, Korea.
Nam-Yeon KimResearch & Development Center, Invirustech Co., Inc., Gwangju 61011, Korea.
Rae-Dong JeongDepartment of Applied Biology, Chonnam National University, Gwangju 61185, Korea. jraed2@jnu.ac.kr.

Funding

Rural Development Administration RS-2025-02263567
6 · The paper itself

Abstract

Topically applied double-stranded RNA (dsRNA) can trigger antiviral RNA interference in plants, but naked dsRNA is unstable and poorly taken up after foliar application. Here, we developed an eco-friendly chitosan- tripolyphosphate (CS-TPP) nanocarrier to enhance dsRNA delivery using turnip crinkle virus (TCV) as a model and tested it in Arabidopsis thaliana. A dsRNA targeting the TCV-coat protein (CP) gene was produced in Escherichia coli, and complexation with CS-TPP was induced by ionic gelation. Complete complexation occurred at a 1:1 CS-TPP:dsRNA ratio, producing cationic nanoparticles that protected dsRNA from RNase digestion and maintained its integrity during incubation at 37°C. Using Cy3 fluorescence imaging, we observed stronger epidermis-associated fluorescence in plants treated with the CS-TPP@dsRNA complex than in those treated with naked dsRNA, and RT-qPCR confirmed higher CP-target RNA fragment accumulation in planta. Small RNA sequencing revealed increased levels of TCV-derived, 21-24 nt siRNA molecules targeting the CP region, suggesting the applied dsRNA was processed in planta. Importantly, a CS-TPP@ TCV-dsRNA foliar spray application reduced systemic CP RNA levels at 7 and 14 days post-treatment and alleviated disease symptoms more effectively than naked dsRNA. These results demonstrate that CS-TPP nanocomplexation improves dsRNA stability and delivery, enabling improved and more durable antiviral protection.

Indexed as

chitosan–tripolyphosphate nanoparticlesdouble-stranded RNARNA interferenceturnip crinkle virus

Identifiers

PMID42237611
PMCPMC13462810

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.