CRISPR‐based diagnostics detects invasive insect pests

Author:

Shashank Pathour R.12,Parker Brandon M.134,Rananaware Santosh R.5,Plotkin David1,Couch Christian1,Yang Lilia G.5,Nguyen Long T.5,Prasannakumar N. R.6,Braswell W. Evan7,Jain Piyush K.589,Kawahara Akito Y.1ORCID

Affiliation:

1. McGuire Center for Lepidoptera and Biodiversity, Florida Museum of Natural History University of Florida Gainesville Florida USA

2. Division of Entomology ICAR‐Indian Agricultural Research Institution New Delhi India

3. Oak Ridge Institute for Science and Education Oak Ridge Tennessee USA

4. Office of Research and Development U.S. Environmental Protection Agency Research Triangle Park North Carolina USA

5. Department of Chemical Engineering University of Florida Gainesville Florida USA

6. Division of Crop Protection ICAR‐Indian Institute of Horticultural Research Bengaluru India

7. Insect Management and Molecular Diagnostics Laboratory USDA APHIS PPQ S&T Edinburg Texas USA

8. Department of Molecular Genetics and Microbiology University of Florida Gainesville Florida USA

9. UF Health Cancer Center University of Florida Gainesville Florida USA

Abstract

AbstractRapid identification of organisms is essential for many biological and medical disciplines, from understanding basic ecosystem processes, disease diagnosis, to the detection of invasive pests. CRISPR‐based diagnostics offers a novel and rapid alternative to other identification methods and can revolutionize our ability to detect organisms with high accuracy. Here we describe a CRISPR‐based diagnostic developed with the universal cytochrome‐oxidase 1 gene (CO1). The CO1 gene is the most sequenced gene among Animalia, and therefore our approach can be adopted to detect nearly any animal. We tested the approach on three difficult‐to‐identify moth species (Keiferia lycopersicella, Phthorimaea absoluta and Scrobipalpa atriplicella) that are major invasive pests globally. We designed an assay that combines recombinase polymerase amplification (RPA) with CRISPR for signal generation. Our approach has a much higher sensitivity than real‐time PCR assays and achieved 100% accuracy for identification of all three species, with a detection limit of up to 120 fM for P. absoluta and 400 fM for the other two species. Our approach does not require a sophisticated laboratory, reduces the risk of cross‐contamination, and can be completed in less than 1 h. This work serves as a proof of concept that has the potential to revolutionize animal detection and monitoring.

Funder

National Institutes of Health

Publisher

Wiley

Subject

Genetics,Ecology, Evolution, Behavior and Systematics,Biotechnology

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