High-Resolution Melting (HRM) Curve Assay for the Identification of Eight Fusarium Species Causing Ear Rot in Maize

被引:26
作者
Schiwek, Simon [1 ]
Beule, Lukas [1 ]
Vinas, Maria [2 ]
Pfordt, Annette [3 ]
von Tiedemann, Andreas [3 ]
Karlovsky, Petr [1 ]
机构
[1] Univ Goettingen, Mol Phytopathol & Mycotoxin Res, D-37077 Gottingen, Germany
[2] Univ Costa Rica, Ctr Invest Granos & Semillas, San Jose 2060, Costa Rica
[3] Univ Goettingen, Plant Pathol & Crop Protect, D-37077 Gottingen, Germany
来源
PATHOGENS | 2020年 / 9卷 / 04期
关键词
Fusarium; high-resolution melting (HRM) curves; HRM analysis; maize ear rot; fungal colony PCR; RPB2; TEF-1; alpha; SYSTEMIC INFECTION; KERNEL INFECTION; HEAD BLIGHT; PCR ASSAYS; MYCOTOXINS; WHEAT; PROLIFERATUM; GRAMINEARUM; DISEASE; FUNGUS;
D O I
10.3390/pathogens9040270
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Maize plants are often infected with fungal pathogens of the genus Fusarium. Taxonomic characterization of these species by microscopic examination of pure cultures or assignment to mating populations is time-consuming and requires specific expertise. Reliable taxonomic assignment may be strengthened by the analysis of DNA sequences. Species-specific PCR assays are available for most Fusarium pathogens, but the number of species that infect maize increases the labor and costs required for analysis. In this work, a diagnostic assay for major Fusarium pathogens of maize based on the analysis of melting curves of PCR amplicons was established. Short segments of genes RPB2 and TEF-1 alpha, which have been widely used in molecular taxonomy of Fusarium, were amplified with universal primers in a real-time thermocycler and high-resolution melting (HRM) curves of the products were recorded. Among major Fusarium pathogens of maize ears, F. cerealis, F. culmorum, F. graminearum, F. equiseti, F. poae, F. temperatum, F. tricinctum, and F. verticillioides, all species except for the pair F. culmorum/F. graminearum could be distinguished by HRM analysis of a 304 bp segment of the RPB2 gene. The latter two species could be differentiated by HRM analysis of a 247 bp segment of the TEF-1 alpha gene. The assay was validated with DNA extracted from pure cultures of fungal strains, successfully applied to total DNA extracted from infected maize ears and also to fungal mycelium that was added directly to the PCR master mix ("colony PCR"). HRM analysis thus offers a cost-efficient method suitable for the diagnosis of multiple fungal pathogens.
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页数:13
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