Improved detection and identification of the sudden oak death pathogen Phytophthora ramorum and the Port Orford cedar root pathogen Phytophthora lateralis. (21st April 2019)

• Record Type: Journal Article
• Authors: Feau, N.; Ojeda, D. I.; Beauseigle, S.; Bilodeau, G. J.; Brar, A.; Cervantes‐Arango, S.; Dale, A. L.; Dhillon, B.; Hammett, C.; Herath, P.; Shamoun, S. F.; Tsui, C. K. M.; Tanguay, P.; Hamelin, R. C.
• Is Part Of: Plant pathology. Volume 68:Number 5(2019)
• Page Start: 878
• Page End: 888
• Publication Date: 2019-04-21
• Subjects: EU1 and EU2 lineages -- NA1 -- NA2 -- sudden oak death -- TaqMan probes -- unique genes; Agricultural pests -- Periodicals; Plant diseases -- Periodicals; 632
• DOI: 10.1111/ppa.13015
• Languages: English
• ISSNs: 0032-0862

Abstract

Abstract : Early detection provides the best way to prevent introduction and establishment of alien plant pathogens. Amplification of DNA by PCR has revolutionized the detection and monitoring of plant pathogens. Most of those assays rely on the amplification of a fraction of the genome of the targeted species. With the availability of whole genomes for a growing number of fungi and oomycetes it is becoming possible to compare genomes and discover regions that are unique to a target organism. This study has applied this pipeline to develop a set of hierarchical TaqMan real‐time PCR detection assays targeting DNA of all four Phytophthora ramorum lineages, and a closely related species, P. lateralis . Nine assays were generated: three targeting DNA of all P. ramorum lineages, one for each lineage of P. ramorum, one for P. lateralis and one targeting DNA of P. ramorum and P. lateralis . These assays were very accurate and sensitive, ranging from 98.7% to 100% detection accuracy of 2–10 gene copies of the targeted taxa from pure cultures or inoculated tissues. This level of sensitivity is within the lowest theoretical limit of detection of DNA. It is expected that these assays will be useful because of their high level of specificity and the ease with which they can be multiplexed because of the inherent flexibility in primer and probe design afforded by their lack of conservation in non‐target species.