Abstract

Global trade and climate change are responsible for a surge in foreign invasive species and emerging pests and pathogens across the world. Early detection and surveillance activities are essential to monitor the environment and prevent or mitigate future ecosystem impacts. Molecular diagnostics by DNA testing has become an integral part of this process. However, for environmental applications, there is a need for cost-effective and efficient point-of-use DNA testing to obtain accurate results from remote sites in real-time. This requires the development of simple and fast sample processing and DNA extraction, room-temperature stable reagents and a portable instrument. We developed a point-of-use real-time Polymerase Chain Reaction system using a crude buffer-based DNA extraction protocol and lyophilized, pre-made, reactions for on-site applications. We demonstrate the use of this approach with pathogens and pests covering a broad spectrum of known undesirable forest enemies: the fungi Sphaerulina musiva, Cronartium ribicola and Cronartium comandrae, the oomycete Phytophthora ramorum and the insect Lymantria dispar. We obtained positive DNA identification from a variety of different tissues, including infected leaves, pathogen spores, or insect legs and antenna. The assays were accurate and yielded no false positive nor negative. The shelf-life of the lyophilized reactions was confirmed after one year at room temperature. Finally, successful tests conducted with portable thermocyclers and disposable instruments demonstrate the suitability of the method, named in Situ Processing and Efficient Environmental Detection (iSPEED), for field testing. This kit fits in a backpack and can be carried to remote locations for accurate and rapid detection of pests and pathogens.

Highlights

  • A leaf disk was cut out from a poplar hybrid (P. trichocarpa x P. deltoides) leaf infected with the pathogen S. musiva and further cut in two halves (Fig 1A); each half was used for comparison of two DNA extraction methods

  • We compared field-ready and column-based extractions as well as fresh and lyophilized reagents in order to assess the performance of the Polymerase Chain Reaction (PCR) field kit

  • In this proof-of-concept study, we demonstrated the rapid development of real-time PCR assays for point-of-use pest and pathogen detection

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Summary

Introduction

We describe the development of a complete sample-to-data, point-of-use, real-time PCR system to provide in situ Processing and Efficient Environmental Detection (iSPEED) of pests and pathogens. This system can be carried in a backpack and is ideal for environmental applications. It comprises a minimal DNA extraction method to process environmental samples without centrifuge or homogenizer instruments and room-temperature stable ready-to-use real-time PCR reagents that we used in portable instruments. As a show-case, we demonstrate successful detection and identification of a variety of forest pests and pathogens: the fungi Sphaerulina musiva, Cronartium comandrae and Cronartium ribicola, the oomycete Phytopththora ramorum and the insects Lymantria dispar dispar and Lymantria dispar asiatica

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