# A multi-channel CRISPR-based method for rapid, sensitive detection of four diseases of Brassica rapa in the field

**Authors:** Xiaojing Liu, Tongbing Su, Xiaoyun Xin, Peirong Li, Weihong Wang, Cancan Song, Xiuyun Zhao, Deshuang Zhang, Yangjun Yu, Jiao Wang, Ning Li, Miao Wang, Fenglan Zhang, Shuancang Yu

PMC · DOI: 10.1093/hr/uhae351 · Horticulture Research · 2024-12-12

## TL;DR

This paper introduces a CRISPR-based field test that can quickly and accurately detect four diseases in Brassica rapa, helping farmers manage crop health more effectively.

## Contribution

A novel multi-channel CRISPR-based biosensor platform, Cas-AIRPA, for rapid and sensitive on-site detection of four Brassica rapa diseases.

## Key findings

- The method achieves high sensitivity, detecting pathogens at concentrations as low as 1.5 pg/μl.
- Optimized parameters for the CRISPR/Cas12a system and lateral flow biosensor enable reliable visual detection.
- The Cas-AIRPA platform successfully detected four diseases in Brassica rapa within 25 minutes in field conditions.

## Abstract

Pathogens significantly restrict the production of Brassica rapa (B. rapa L. ssp. Pekinensis), with climate change and evolving planting patterns exacerbating disease prevalence. Multichannel rapid diagnostic methods in the field can facilitate the early detection and control of diseases in B. rapa. Here, we established a multichannel lateral flow biosensor (LFB) combined with a CRISPR/Cas12a cleavage assay for the simultaneous detection of four B. rapa diseases. Key innovations of this study include: (1) High specificity and sensitivity, down to pathogen concentrations of 1.5 pg/μl—due to the optimization of crRNA secondary structure: the more stable the crRNA, the higher its detection sensitivity. (2) Optimized visual detection parameters. We identified ideal concentration ratios for the visual fluorescence detection system: 50 nM Cas12a, 50 nM crRNA, and 500 nM ssDNA fluorescent probe. Furthermore, the optimal concentrations of components on the LFB detection system were 3 μl SA-GNPs, 500 nM ssDNA test strip probe, 0.5 mg/ml biotin-BSA as the test line, and 1 mg/ml anti-FITC as the control line. (3) Field-Ready Cas-AIRPA Platform. We developed the on-site Cas-AIRPA platform for the simultaneous detection of B. rapa pathogens by combining rapid nucleic acid extraction and a four-channel lateral flow biosensor (4-LFB), which quickly provides disease-related information through a specific 2D barcode. Analysis of B. rapa samples in the field confirmed the suitability of the Cas-AIRPA platform for rapid (~25 min) and simultaneous on-site detection of four diseases of B. rapa. This platform can also be adapted to detect other plant diseases in the field.

## Linked entities

- **Species:** Brassica rapa (taxon 3711)

## Full-text entities

- **Diseases:** B. rapa diseases (MESH:D006509)
- **Species:** Brassica rapa (field mustard, species) [taxon 3711], Brassica rapa subsp. pekinensis (bai cai, subspecies) [taxon 51351]

## Full text

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## Figures

6 figures with captions in the complete paper: https://tomesphere.com/paper/PMC11890027/full.md

## References

36 references — full list in the complete paper: https://tomesphere.com/paper/PMC11890027/full.md

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Source: https://tomesphere.com/paper/PMC11890027