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      Genome-enhanced detection and identification of fungal pathogens responsible for pine and poplar rust diseases

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          Abstract

          Biosurveillance is a proactive approach that may help to limit the spread of invasive fungal pathogens of trees, such as rust fungi which have caused some of the world’s most damaging diseases of pines and poplars. Most of these fungi have a complex life cycle, with up to five spore stages, which is completed on two different hosts. They have a biotrophic lifestyle and may be propagated by asymptomatic plant material, complicating their detection and identification. A bioinformatics approach, based on whole genome comparison, was used to identify genome regions that are unique to the white pine blister rust fungus, Cronartium ribicola, the poplar leaf rust fungi Melampsora medusae and Melampsora larici-populina or to members of either the Cronartium and Melampsora genera. Species- and genus-specific real-time PCR assays, targeting these unique regions, were designed with the aim of detecting each of these five taxonomic groups. In total, twelve assays were developed and tested over a wide range of samples, including different spore types, different infected plant parts on the pycnio-aecial or uredinio-telial host, and captured insect vectors. One hundred percent detection accuracy was achieved for the three targeted species and two genera with either a single assay or a combination of two assays. This proof of concept experiment on pine and poplar leaf rust fungi demonstrates that the genome-enhanced detection and identification approach can be translated into effective real-time PCR assays to monitor tree fungal pathogens.

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          Most cited references33

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          Biogeographical patterns and determinants of invasion by forest pathogens in Europe.

          A large database of invasive forest pathogens (IFPs) was developed to investigate the patterns and determinants of invasion in Europe. Detailed taxonomic and biological information on the invasive species was combined with country-specific data on land use, climate, and the time since invasion to identify the determinants of invasiveness, and to differentiate the class of environments which share territorial and climate features associated with a susceptibility to invasion. IFPs increased exponentially in the last four decades. Until 1919, IFPs already present moved across Europe. Then, new IFPs were introduced mainly from North America, and recently from Asia. Hybrid pathogens also appeared. Countries with a wider range of environments, higher human impact or international trade hosted more IFPs. Rainfall influenced the diffusion rates. Environmental conditions of the new and original ranges and systematic and ecological attributes affected invasiveness. Further spread of established IFPs is expected in countries that have experienced commercial isolation in the recent past. Densely populated countries with high environmental diversity may be the weakest links in attempts to prevent new arrivals. Tight coordination of actions against new arrivals is needed. Eradication seems impossible, and prevention seems the only reliable measure, although this will be difficult in the face of global mobility. © 2012 The Authors. New Phytologist © 2012 New Phytologist Trust.
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            Validation of a quantitative method for real time PCR kinetics.

            Real time RT-PCR is the most sensitive method for quantitation of gene expression levels. The accuracy can be dependent on the mathematical model on which the quantitative methods are based. The generally accepted mathematical model assumes that amplification efficiencies are equal at the exponential phase of the reactions for the same amplicon. However, no methods are available to test the assumptions regarding amplification efficiency before one starts the real time PCR quantitation. Here we further develop and test the validity of a new mathematical model which dynamically fits real time PCR data with good correlation (R(2)=0.9995+/-0.002, n=50). The method is capable of measuring cycle-by-cycle PCR amplification efficiencies and demonstrates that these change dynamically. Validation of the method revealed the intrinsic relationship between the initial amount of gene transcript and kinetic parameters. A new quantitative method is proposed which represents a simple but accurate quantitative method. (c) 2002 Elsevier Science (USA).
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              Phylogeny of the rust fungi: an approach using nuclear large subunit ribosomal DNA sequences

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                Author and article information

                Contributors
                Role: ConceptualizationRole: Formal analysisRole: MethodologyRole: ValidationRole: Writing – original draftRole: Writing – review & editing
                Role: ConceptualizationRole: Data curationRole: Formal analysisRole: SoftwareRole: Writing – original draftRole: Writing – review & editing
                Role: MethodologyRole: Writing – review & editing
                Role: ConceptualizationRole: Funding acquisitionRole: SupervisionRole: Writing – original draftRole: Writing – review & editing
                Role: ConceptualizationRole: Funding acquisitionRole: SupervisionRole: Writing – original draftRole: Writing – review & editing
                Role: Editor
                Journal
                PLoS One
                PLoS ONE
                plos
                plosone
                PLoS ONE
                Public Library of Science (San Francisco, CA USA )
                1932-6203
                6 February 2019
                2019
                : 14
                : 2
                : e0210952
                Affiliations
                [1 ] Laurentian Forestry Centre, Canadian Forest Service, Natural Resources Canada, Québec, Québec, Canada
                [2 ] Forest Sciences Centre, Department of Forest and Conservation Sciences, University of British Columbia, Vancouver, British Columbia, Canada
                [3 ] Institut de Biologie Intégrative des Systèmes, Université Laval, Québec, Québec, Canada
                University of Helsinki, FINLAND
                Author notes

                Competing Interests: The authors have declared that no competing interests exist.

                Author information
                http://orcid.org/0000-0002-4308-5695
                Article
                PONE-D-18-23330
                10.1371/journal.pone.0210952
                6364900
                30726264
                f33f0f88-b71d-4ce0-ac86-1014fb781c9a
                © 2019 Bergeron et al

                This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

                History
                : 7 August 2018
                : 6 January 2019
                Page count
                Figures: 3, Tables: 3, Pages: 20
                Funding
                Funded by: funder-id http://dx.doi.org/10.13039/100008762, Genome Canada;
                Award ID: 2112 and 10106
                Award Recipient :
                Funded by: funder-id http://dx.doi.org/10.13039/501100000233, Genome British Columbia;
                Award ID: 2112 and 10106
                Award Recipient :
                Funded by: Natural Resources Canada
                Award Recipient :
                This research was funded by Genome Canada, Genome British Columbia and Génome Québec Large-Scale Applied Research Program, projects #2112 and #10106 to RCH; https://www.genomecanada.ca/en/genomics-based-forest-health-diagnostics-and-monitoring; https://www.genomecanada.ca/en/biosurveillance-alien-forest-enemies-biosafe. Author PT received funding from the Government of Canada from the Genomic Research and Development Initiative program. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
                Categories
                Research Article
                Biology and Life Sciences
                Molecular Biology
                Molecular Biology Techniques
                Artificial Gene Amplification and Extension
                Polymerase Chain Reaction
                Research and Analysis Methods
                Molecular Biology Techniques
                Artificial Gene Amplification and Extension
                Polymerase Chain Reaction
                Biology and life sciences
                Molecular biology
                Molecular biology techniques
                Biomolecular isolation
                DNA isolation
                Research and analysis methods
                Molecular biology techniques
                Biomolecular isolation
                DNA isolation
                Biology and Life Sciences
                Organisms
                Eukaryota
                Plants
                Trees
                Pines
                Biology and Life Sciences
                Computational Biology
                Comparative Genomics
                Biology and Life Sciences
                Genetics
                Genomics
                Comparative Genomics
                Biology and Life Sciences
                Plant Science
                Plant Pathology
                Plant Pathogens
                Plant Fungal Pathogens
                Biology and life sciences
                Molecular biology
                Molecular biology techniques
                DNA barcoding
                Research and analysis methods
                Molecular biology techniques
                DNA barcoding
                Biology and life sciences
                Evolutionary biology
                Evolutionary systematics
                Molecular systematics
                DNA barcoding
                Biology and life sciences
                Taxonomy
                Evolutionary systematics
                Molecular systematics
                DNA barcoding
                Computer and information sciences
                Data management
                Taxonomy
                Evolutionary systematics
                Molecular systematics
                DNA barcoding
                Biology and Life Sciences
                Mycology
                Fungal Reproduction
                Fungal Spores
                Biology and Life Sciences
                Organisms
                Eukaryota
                Fungi
                Custom metadata
                Data are available at GenBank (accession numbers: MH171727-MH171903).

                Uncategorized
                Uncategorized

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