Rapid Visual Detection of on Lychees Using Recombinase Polymerase Amplification Combined with Lateral Flow Assay Based on the Unique Target Gene .

Rongbo Wang, Benjin Li, Mingyue Shi, Yumei Zhao, Jinlong Lin, Qinghe Chen, Peiqing Liu
Author Information
  1. Rongbo Wang: Fujian Key Laboratory for Monitoring and Integrated Management of Crop Pests, Institute of Plant Protection, Fujian Academy of Agricultural Sciences, Fuzhou 350003, China.
  2. Benjin Li: Fujian Key Laboratory for Monitoring and Integrated Management of Crop Pests, Institute of Plant Protection, Fujian Academy of Agricultural Sciences, Fuzhou 350003, China.
  3. Mingyue Shi: Fujian Key Laboratory for Monitoring and Integrated Management of Crop Pests, Institute of Plant Protection, Fujian Academy of Agricultural Sciences, Fuzhou 350003, China.
  4. Yumei Zhao: Fujian Key Laboratory for Monitoring and Integrated Management of Crop Pests, Institute of Plant Protection, Fujian Academy of Agricultural Sciences, Fuzhou 350003, China.
  5. Jinlong Lin: Fujian Key Laboratory for Monitoring and Integrated Management of Crop Pests, Institute of Plant Protection, Fujian Academy of Agricultural Sciences, Fuzhou 350003, China.
  6. Qinghe Chen: Sanya Institute of Breeding and Multiplication, School of Tropical Agriculture and Forestry, Hainan University, Sanya 572000, China. ORCID
  7. Peiqing Liu: Fujian Key Laboratory for Monitoring and Integrated Management of Crop Pests, Institute of Plant Protection, Fujian Academy of Agricultural Sciences, Fuzhou 350003, China.

Abstract

Downy blight, caused by , is a destructive disease that impacts lychee fruit throughout the pre-harvest, post-harvest, and transportation phases. Therefore, the prompt and precise identification of is crucial for the effective management of the disease. A novel gene encoding a Rh-type ammonium transporter, , was identified in through bioinformatic analysis in this study. Based on this gene, a coupled recombinase polymerase amplification-lateral flow (RPA-LF) assay for the rapid visual detection of was developed. The assay has been shown to detect accurately, without cross-reactivity to related pathogenic oomycetes or fungi. Moreover, it can be performed effectively within 15 to 25 min at temperatures ranging from 28 to 46 °C. Under optimized conditions, the RPA-LF assay could detect as low as 1 pg of genomic DNA in a 25 μL reaction system. Furthermore, the RPA-LF assay successfully detected in infected lychee samples within a 30 min timeframe. These attributes establish the RPA-LF assay as a rapid, sensitive, and specific method for diagnosing early; it is particularly suitable for applications in resource-limited settings.

Keywords

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Grants

  1. 32072400/National Natural Science Foundation of China
  2. 2022J01460/Natural Science Foundation of Fujian Province
  3. 2023R1070/the Basic R & D Special Fund Business of Fujian Province
  4. XTCXGC2021011, XTCXGC2021017, GJYS202204/the Basic Research Projects of Fujian Academy of Agricultural Sciences

Word Cloud

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