A molecular diagnostic for tropical race 4 of the banana fusarium wilt pathogen

被引:212
作者
Dita, M. A. [1 ,2 ]
Waalwijk, C. [2 ]
Buddenhagen, I. W.
Souza, M. T., Jr. [2 ,3 ]
Kema, G. H. J. [2 ]
机构
[1] Embrapa Cassava & Trop Fruits, BR-44380000 Cruz Das Almas, BA, Brazil
[2] Plant Res Int BV, NL-6700 AA Wageningen, Netherlands
[3] Embrapa LABEX Europe, NL-6700 AA Wageningen, Netherlands
关键词
Fusarium oxysporum f. sp cubense in planta detection; Musa spp; Panama disease; PCR-based diagnostic; vegetative compatibility groups; F-SP CUBENSE; VEGETATIVE COMPATIBILITY GROUPS; GENETIC-VARIATION; PANAMA-DISEASE; OXYSPORUM; PCR; QUANTIFICATION; IDENTIFICATION; AUSTRALIA; TISSUE;
D O I
10.1111/j.1365-3059.2009.02221.x
中图分类号
S3 [农学(农艺学)];
学科分类号
0901 ;
摘要
This study analysed genomic variation of the translation elongation factor 1 alpha (TEF-1 alpha) and the intergenic spacer region (IGS) of the nuclear ribosomal operon of Fusarium oxysporum f. sp. cubense (Foc) isolates, from different banana production areas, representing strains within the known races, comprising 20 vegetative compatibility groups (VCG). Based on two single nucleotide polymorphisms present in the IGS region, a PCR-based diagnostic tool was developed to specifically detect isolates from VCG 01213, also called tropical race 4 (TR4), which is currently a major concern in global banana production. Validation involved TR4 isolates, as well as Foc isolates from 19 other VCGs, other fungal plant pathogens and DNA samples from infected tissues of the Cavendish banana cultivar Grand Naine (AAA). Subsequently, a multiplex PCR was developed for fungal or plant samples that also discriminated Musa acuminata and M. balbisiana genotypes. It was concluded that this diagnostic procedure is currently the best option for the rapid and reliable detection and monitoring of TR4 to support eradication and quarantine strategies.
引用
收藏
页码:348 / 357
页数:10
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