Detection of living Bursaphelenchus xylophilus in wood, using reverse transcriptase loop‐mediated isothermal amplification (RT‐LAMP). Issue 2 (8th October 2014)

• Record Type: Journal Article
• Authors: Leal, I.; Allen, E.; Foord, B.; Anema, J.; Reisle, C.; Uzunovic, A.; Varga, A.; James, D.; Sturrock, R. N.
• Is Part Of: Forest pathology. Volume 45:Issue 2(2015:Apr.)
• Page Start: 134
• Page End: 148
• Publication Date: 2014-10-08
• Subjects: Trees -- Diseases and pests -- Periodicals; Trees -- Effect of air pollution on -- Periodicals; Forests and forestry -- Environmental aspects -- Periodicals; 634.9
• DOI: 10.1111/efp.12149
• Languages: English
• ISSNs: 1437-4781

Abstract

<abstract abstract-type="main" id="efp12149-abs-0001"> <title>Summary</title> <p>Pinewood nematode (PWN), <italic>Bursaphelenchus xylophilus</italic>, the causal agent of pine wilt disease, is an inhabitant of native pine species of North America, where its presence has minor impact. In contrast, the introduction of this nematode to forests in Asia and Europe has devastated some pine stands and is recognized as a pest of significant phytosanitary concern by the National Plant Protection Organizations of several countries. The ability to detect PWN in internationally traded wood products is crucial to reduce the spread of this organism. Currently, the majority of molecular techniques for the detection of PWN rely on the presence of genomic DNA and thus fail to differentiate between living and dead PWN. The detection of dead nematodes could lead to unnecessary trade disruption. Therefore, accurate techniques for the detection of and differentiation between living and dead PWN are critical. We have developed a reverse transcription loop‐mediated isothermal amplification (RT‐LAMP) assay, which specifically identifies living PWN in wood by detecting the presence of mRNA encoding an expansin gene as a viability marker. This diagnostic method was found to be more sensitive, faster and less dependent on expensive laboratory equipment than PCR. In addition, unlike PCR, it allows for simple colour detection of amplification products. This method will help resolve disputes over the detection of PWN by clarifying whether it originates from live or dead organisms. Where approved treatments are implemented, unnecessary trade disruption will be avoided, thus protecting market access of wood products from PWN‐infested areas.</p> </abstract>