Evidence map›Paper›PMID 40811070›Full record

ArticlePlant biotechnology journal2025

An Ultra-Sensitive Quarantine Pathogen On-Site Detection Based on a One-Pot Asymmetric Recombinase Polymerase Amplification and MNAzyme-Assisted Target Recycling Biosensor (OAR-MNA).

Lei Yang, Guanwei Chen, Yongming Bo, Cheng Peng, Jiatong Yan, Xiaoyun Chen, Xiaoli Xu, Wei Wei, Xiaoxue Fang, Jian Wu and 3 more

Abstract read
In one paragraph

Article in Plant biotechnology journal, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
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

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Article
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

13 authors.

Lei YangState Key Laboratory for Quality and Safety of Agro-Products, Key Laboratory of Traceability for Agricultural Genetically Modified Organisms, Ministry of Agriculture and Rural Affairs, People's Republic of China, Zhejiang Key Laboratory of Crop Germplasm Innovation and Utilization, Zhejiang Academy of Agricultural Sciences, Hangzhou, China.
Guanwei ChenCollege of Life Sciences, Zhejiang Normal University, Jinhua, China.ORCID https://orcid.org/0009-0009-6771-6218
Yongming BoKey Laboratory of Watermelon and Cabbage Digital Seed Industry, Ministry of Agriculture and Rural Affairs, Ningbo Weimeng Seed Industry Co. Ltd., Ningbo, China.
Cheng PengState Key Laboratory for Quality and Safety of Agro-Products, Key Laboratory of Traceability for Agricultural Genetically Modified Organisms, Ministry of Agriculture and Rural Affairs, People's Republic of China, Zhejiang Key Laboratory of Crop Germplasm Innovation and Utilization, Zhejiang Academy of Agricultural Sciences, Hangzhou, China.ORCID https://orcid.org/0000-0003-1782-1350
Jiatong YanCollege of Life Sciences, Zhejiang Normal University, Jinhua, China.
Xiaoyun ChenState Key Laboratory for Quality and Safety of Agro-Products, Key Laboratory of Traceability for Agricultural Genetically Modified Organisms, Ministry of Agriculture and Rural Affairs, People's Republic of China, Zhejiang Key Laboratory of Crop Germplasm Innovation and Utilization, Zhejiang Academy of Agricultural Sciences, Hangzhou, China.
Xiaoli XuState Key Laboratory for Quality and Safety of Agro-Products, Key Laboratory of Traceability for Agricultural Genetically Modified Organisms, Ministry of Agriculture and Rural Affairs, People's Republic of China, Zhejiang Key Laboratory of Crop Germplasm Innovation and Utilization, Zhejiang Academy of Agricultural Sciences, Hangzhou, China.
Wei WeiState Key Laboratory for Quality and Safety of Agro-Products, Key Laboratory of Traceability for Agricultural Genetically Modified Organisms, Ministry of Agriculture and Rural Affairs, People's Republic of China, Zhejiang Key Laboratory of Crop Germplasm Innovation and Utilization, Zhejiang Academy of Agricultural Sciences, Hangzhou, China.
Xiaoxue FangKey Laboratory of Watermelon and Cabbage Digital Seed Industry, Ministry of Agriculture and Rural Affairs, Ningbo Weimeng Seed Industry Co. Ltd., Ningbo, China.
Jian WuCollege of Biosystems Engineering and Food Science, Zhejiang University, Hangzhou, China.
Xiaofu WangState Key Laboratory for Quality and Safety of Agro-Products, Key Laboratory of Traceability for Agricultural Genetically Modified Organisms, Ministry of Agriculture and Rural Affairs, People's Republic of China, Zhejiang Key Laboratory of Crop Germplasm Innovation and Utilization, Zhejiang Academy of Agricultural Sciences, Hangzhou, China.ORCID https://orcid.org/0000-0001-9323-4022
Meihao SunCollege of Life Sciences, Zhejiang Normal University, Jinhua, China.
Junfeng XuState Key Laboratory for Quality and Safety of Agro-Products, Key Laboratory of Traceability for Agricultural Genetically Modified Organisms, Ministry of Agriculture and Rural Affairs, People's Republic of China, Zhejiang Key Laboratory of Crop Germplasm Innovation and Utilization, Zhejiang Academy of Agricultural Sciences, Hangzhou, China.

Funding

Department of Agriculture and Rural Affairs of Zhejiang Province, China 2023SNJF043Department of Science and Technology of Zhejiang Province, China 2021R52046Natural Science Foundation of Zhejiang Province LMS25C200002
6 · The paper itself

Abstract

The dissemination of quarantine pathogens poses a significant risk to global crop production, threatening crop health and disrupting agroecosystems. Timely and accurate on-site detection is crucial to prevent outbreaks. Recombinase polymerase amplification (RPA) and multicomponent DNAzyme (MNAzyme) are promising isothermal detection technologies; however, their integration has been hindered by the requirement of single-stranded DNA (ssDNA) for MNAzyme activation, as RPA generates double-stranded DNA (dsDNA). To address this, we developed the OAR-MNA biosensor, an innovative one-pot platform coupling asymmetric RPA (aRPA) with MNAzyme-assisted target recycling. The biosensor was applied to detect Acidovorax citrulli, the causative agent of bacterial fruit blotch (BFB) in cucurbits. By adjusting RPA primer concentrations, aRPA generates abundant ssDNA, enabling visual detection of A. citrulli with a detection limit of 20 copies/μL and perfect specificity, surpassing the performance of fluorescent RPA. The biosensor demonstrated 100% concordance with qPCR in seed samples and maintained robust performance in spiked melon homogenate. Our comparative analysis revealed advantages of the OAR-MNA system, including reduced detection costs and enhanced field applicability. When coupled with a portable DNA analyser, the biosensor provides user-friendly results (+/-), making it ideal for on-site deployment. Beyond BFB detection, OAR-MNA has been successfully applied to the detection of Cucumber green mottle mosaic virus (CGMMV), an RNA quarantine pathogen that causes severe losses to cucurbit crop production. By enabling early, accurate on-site diagnosis, the OAR-MNA biosensor represents an advancement in plant pathogen detection technology, offering a promising tool for safeguarding global crop production.

Indexed as

Biosensing TechniquesComamonadaceaeNucleic Acid Amplification TechniquesPlant DiseasesCucurbitaDNA, CatalyticDNA, Single-StrandedRecombinasesDNA, CatalyticDNA, Single-StrandedRecombinasesasymmetric RPAbacterial fruit blotchcucumber green mottle mosaic virusMNAzymeone‐potssDNA

Identifiers

PMID40811070
PMCPMC12665056

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Registered trials

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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.