Genome-Enhanced Detection and Identification (GEDI) of plant pathogens

Author:

Feau Nicolas1,Beauseigle Stéphanie2,Bergeron Marie-Josée3,Bilodeau Guillaume J.4,Birol Inanc5,Cervantes-Arango Sandra1,Dhillon Braham6,Dale Angela L.17,Herath Padmini1,Jones Steven J.M.589,Lamarche Josyanne3,Ojeda Dario I.10,Sakalidis Monique L.11,Taylor Greg5,Tsui Clement K.M.12,Uzunovic Adnan7,Yueh Hesther1,Tanguay Philippe3,Hamelin Richard C.113

Affiliation:

1. Department of Forest and Conservation Sciences, Forest Sciences Centre, University of British Columbia, Vancouver, BC, Canada

2. Biopterre, Sainte-Anne-de-la-Pocatière, Quebec, Canada

3. Canadian Forest Service, Natural Resources Canada, Quebec city, Quebec, Canada

4. Ottawa Plant Laboratory, Canadian Food Inspection Agency, Ottawa, Ontario, Canada

5. BC Cancer agency, Genome Sciences Centre, Vancouver, BC, Canada

6. Department of Plant Pathology, University of Arkansas at Fayetteville, Fayetteville, AR, United States of America

7. FPInnovations, Vancouver, BC, Canada

8. Department of Medical Genetics, University of British Columbia, Vancouver, BC, Canada

9. Department of Molecular Biology and Biochemistry, Simon Fraser University, Burnaby, BC, Canada

10. Department of Biology Unit of Ecology and Genetics, University of Oulu, Oulu, Finland

11. Department of Plant, Soil & Microbial Sciences and Department of Forestry, Michigan State University, East Lansing, MI, United States of America

12. Faculty of Medicine, University of British Columbia, Vancouver, BC, Canada

13. Foresterie et géomatique, Institut de Biologie Intégrative des Systèmes, Laval University, Quebec city, Quebec, Canada

Abstract

Plant diseases caused by fungi and Oomycetes represent worldwide threats to crops and forest ecosystems. Effective prevention and appropriate management of emerging diseases rely on rapid detection and identification of the causal pathogens. The increase in genomic resources makes it possible to generate novel genome-enhanced DNA detection assays that can exploit whole genomes to discover candidate genes for pathogen detection. A pipeline was developed to identify genome regions that discriminate taxa or groups of taxa and can be converted into PCR assays. The modular pipeline is comprised of four components: (1) selection and genome sequencing of phylogenetically related taxa, (2) identification of clusters of orthologous genes, (3) elimination of false positives by filtering, and (4) assay design. This pipeline was applied to some of the most important plant pathogens across three broad taxonomic groups: Phytophthoras (Stramenopiles, Oomycota), Dothideomycetes (Fungi, Ascomycota) and Pucciniales (Fungi, Basidiomycota). Comparison of 73 fungal and Oomycete genomes led the discovery of 5,939 gene clusters that were unique to the targeted taxa and an additional 535 that were common at higher taxonomic levels. Approximately 28% of the 299 tested were converted into qPCR assays that met our set of specificity criteria. This work demonstrates that a genome-wide approach can efficiently identify multiple taxon-specific genome regions that can be converted into highly specific PCR assays. The possibility to easily obtain multiple alternative regions to design highly specific qPCR assays should be of great help in tackling challenging cases for which higher taxon-resolution is needed.

Funder

Genome Canada

Genome British Columbia

Canadian Forest Service

Genomics Research and Development Initiative, GRDI

Canadian Food Inspection Agency

Large Scale Applied Research Project (LSARP)

Publisher

PeerJ

Subject

General Agricultural and Biological Sciences,General Biochemistry, Genetics and Molecular Biology,General Medicine,General Neuroscience

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