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https://hdl.handle.net/20.500.14279/14029
Title: | Transferability of PCR-based diagnostic protocols: An international collaborative case study assessing protocols targeting the quarantine pine pathogen Fusarium circinatum | Authors: | Nowakowska, Justyna Anna Ioos, Renaud Mullett, Martin Vettraino, Anna Maria Douanla-Meli, Clovis Cornejo, Carolina Alves, Artur Diez, Julio J. Ahumada, Rodrigo Kanetis, Loukas Berbegal, Mónica Luchi, Nicola Pasquali, Matias Adamson, Kalev Aloi, Francesco Guinet, Cécile Kačergius, Audrius Dvořák, Miloň Baskarathevan, Jeyaseelan Fourie, Gerda Bragança, Helena Cacciola, Santa Olga Piškur, Barbara Martínez-Álvarez, Pablo Ghelardini, Luisa Sanz-Ros, Antonio Oskay, Funda Aguayo, Jaime |
Major Field of Science: | Agricultural Sciences | Field Category: | AGRICULTURAL SCIENCES;Agricultural Biotechnology;Other Agricultural Sciences | Keywords: | Gibberella circinata;Pinus radiata;Pitch canker | Issue Date: | 3-Jun-2019 | Source: | Scientific Reports, 2019, vol. 9, no.1 | Volume: | 9 | Issue: | 1 | Journal: | Scientific Reports | Abstract: | Fusarium circinatum is a harmful pathogenic fungus mostly attacking Pinus species and also Pseudotsuga menziesii, causing cankers in trees of all ages, damping-off in seedlings, and mortality in cuttings and mother plants for clonal production. This fungus is listed as a quarantine pest in several parts of the world and the trade of potentially contaminated pine material such as cuttings, seedlings or seeds is restricted in order to prevent its spread to disease-free areas. Inspection of plant material often relies on DNA testing and several conventional or real-time PCR based tests targeting F. circinatum are available in the literature. In this work, an international collaborative study joined 23 partners to assess the transferability and the performance of nine molecular protocols, using a wide panel of DNA from 71 representative strains of F. circinatum and related Fusarium species. Diagnostic sensitivity, specificity and accuracy of the nine protocols all reached values >80%, and the diagnostic specificity was the only parameter differing significantly between protocols. The rates of false positives and of false negatives were computed and only the false positive rates differed significantly, ranging from 3.0% to 17.3%. The difference between protocols for some of the performance values were mainly due to cross-reactions with DNA from non-target species, which were either not tested or documented in the original articles. Considering that participating laboratories were free to use their own reagents and equipment, this study demonstrated that the diagnostic protocols for F. circinatum were not easily transferable to end-users. More generally, our results suggest that the use of protocols using conventional or real-time PCR outside their initial development and validation conditions should require careful characterization of the performance data prior to use under modified conditions (i.e. reagents and equipment). Suggestions to improve the transfer are proposed. | ISSN: | 20452322 | DOI: | 10.1038/s41598-019-44672-8 | Rights: | © The Author(s). | Type: | Article | Affiliation : | Unité de Mycologie University of Catania Slovenian Forestry Institute Forest Research Alice Holt Lodge Universitat Politècnica de València Instituto Nacional de Investigação Agrária e Veterinária Çankırı Karatekin University Swiss Federal Institute for Forest Estonian University of Life Sciences Institute for National and International Plant Health Lithuanian Research Centre for Agriculture and Forestry University of Valladolid Cardinal Stefan Wyszynski University in Warsaw Institute for Sustainable Plant Protection University of Tuscia University of Milan University of Pretoria Cyprus University of Technology Universidade de Aveiro University of Florence Mendel University in Brno Forest Health Center of Calabazanos Università degli Studi di Palermo Ministry for Primary Industries |
Publication Type: | Peer Reviewed |
Appears in Collections: | Άρθρα/Articles |
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File | Description | Size | Format | |
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Transferability of PCR-based diagnostic protocols.pdf | 1.71 MB | Adobe PDF | View/Open |
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