Using Next-Generation Sequencing to Develop Molecular Diagnostics for Pseudoperonospora cubensis, the Cucurbit Downy Mildew Pathogen

被引:33
|
作者
Withers, S. [1 ]
Gongora-Castillo, E. [1 ]
Gent, D. [2 ,3 ]
Thomas, A. [1 ,4 ]
Ojiambo, P. S. [1 ,4 ]
Quesada-Ocampo, L. M. [1 ]
机构
[1] North Carolina State Univ, Dept Plant Pathol, Raleigh, NC 27695 USA
[2] USDA ARS, Forage Seed & Cereal Res Unit, Corvallis, OR 97331 USA
[3] Oregon State Univ, Corvallis, OR 97331 USA
[4] North Carolina State Univ, Ctr Integrated Fungal Res, Raleigh, NC 27695 USA
关键词
LINEAGE-SPECIFIC GENES; SWEET BASIL; PCR ASSAYS; 1ST REPORT; DNA; PLANT; GENOME; QUANTIFICATION; IDENTIFICATION; FUNGICIDES;
D O I
10.1094/PHYTO-10-15-0260-FI
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Advances in next-generation sequencing (NGS) allow for rapid development of genomics resources needed to generate molecular diagnostics assays for infectious agents. NGS approaches are particularly helpful for organisms that cannot be cultured, such as the downy mildew pathogens, a group of biotrophic obligate oomycetes that infect crops of economic importance. Unlike most downy mildew pathogens that are highly host-specific, Pseudoperonospora cubensis causes disease on a broad range of crops belonging to the family Cucurbitaceae. In this study, we identified candidate diagnostic markers for P. cubensis by comparing NGS data from a diverse panel of P. cubensis and P. humuli isolates, two very closely related oomycete species. P cubensis isolates from diverse hosts and geographical regions in the United States were selected for sequencing to ensure that candidates were conserved in P cubensis isolates infecting different cucurbit hosts. Genomic regions unique to and conserved in P cubensis isolates were identified through bioinformatics. These candidate regions were then validated using PCR against a larger collection of isolates from P cubensis, P. humuli, and other oomycetes. Overall seven diagnostic markers were found to be specific to P. cubensis. These markers could be used for pathogen diagnostics on infected tissue, or adapted for monitoring airborne inoculum with real-time PCR and spore traps.
引用
收藏
页码:1105 / 1116
页数:12
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