New and rapid visual detection assay for Trogoderma granarium everts based on recombinase polymerase amplification and CRISPR/Cas12a

Author:

Zeng Lingyu12ORCID,Zheng Sizhu3,Stejskal Vaclav45,Opit George6,Aulicky Radek4,Li Zhihong12ORCID

Affiliation:

1. Department of Plant Biosecurity, College of Plant Protection China Agricultural University Beijing P. R. China

2. Key Laboratory of Surveillance and Management for Plant Quarantine Pests Ministry of Agriculture and Rural Affairs Beijing P. R. China

3. Suzhou Customs District Suzhou P. R. China

4. Crop Research Institute, Drnovská, Prague Czech Republic

5. Faculty of Agrobiology, Food and Natural Resources Czech University of Life Sciences Prague Czech Republic

6. Department of Entomology and Plant Pathology Oklahoma State University, 127 Noble Research Center Stillwater USA

Abstract

AbstractBACKGROUNDKhapra beetle (Trogoderma granarium Everts), one of the most important quarantine pests globally, is capable of causing severe infestation and huge economic loss to stored grain, and its interception rate has increased in major global trade countries over the past few years. However, difficulties remain in distinguishing this species with similar ones. In order to assist border ports and warehouses in khapra beetle's effective rapid identification as well as pest control at the early stages of monitoring or interception, we herein developed a new and rapid visual detection assay for T. granarium based on recombinase polymerase amplification (RPA) and the CRISPR/Cas12a system.RESULTSWe designed and selected the first khapra beetle‐specific RPA primers and crRNA, and optimized the visualization reaction system (Cas12a/CrRNA = 100 nM/500 nM). With only a 37 °C‐heat‐source and a blue light torch, RPA and CRISPR/CAS12a‐based visualization assays can be completed within 40 min to differentiate between khapra beetle and nine similar Dermestidae species. After DNA extraction using a kit (4–5 h) or a simple method (5 min), the specific amplicons were obtained after a 15 min RPA reaction at 37 °C, followed by a 15 min color reaction under 37 °C in dark conditions using a CRISPR/CAS12a system and a fluorescent probe (5′‐FAM/3′‐BHQ1 labeled). This method is ingenious to low levels of DNA (10−1 ng μL−1) and meets the sensitivity requirements for detecting a single khapra beetle's egg (≈0.7 mm).CONCLUSIONOur specificity and sensitivity analysis inferred that the present visualization system is effective to quickly and uniquely detect khapra beetle at room temperature (37 °C), thereby preventing this species before they spread widely. Our study is suitable for being pushed forward in storage pest management, and provides value as a reference for monitoring and identification of other pests. © 2023 Society of Chemical Industry.

Funder

National Key Research and Development Program of China

Publisher

Wiley

Subject

Insect Science,Agronomy and Crop Science,General Medicine

Reference51 articles.

1. Quarantine importance of Trogoderma pests;Liu HF;Plant Quar,2009

2. PM 7/13 (2)Trogoderma granarium

3. Biology and Control of the Khapra Beetle, Trogoderma granarium, a Major Quarantine Threat to Global Food Security

4. AthanassiouCG Trogoderma granarium(khapra beetle).https://www.cabidigitallibrary.org/doi/epdf/10.1079/cabicompendium.55010[10 March 2023].

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