Simultaneous detection and identification of trichothecene- and moniliformin-producing Fusarium species based on multiplex SNP analysis

被引:20
作者
Kristensen, R. [1 ]
Berdal, K. G. [1 ]
Holst-Jensen, A. [1 ]
机构
[1] Natl Vet Inst, Sect Feed & Food Microbiol, N-0033 Oslo, Norway
关键词
diagnostics; fungi; Fusarium; mycotoxin; SNaPshot; translation elongation factor-1 alpha; trichothecene;
D O I
10.1111/j.1365-2672.2006.03166.x
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Aim: To develop a multiplex identification method for trichothecene- and moniliformin-producing Fusarium species. Method and Results: In this article, we present a single nucleotide polymorphism (SNP) assay to simultaneously detect and identify 16 trichothecene- and moniliformin-producing Fusarium species. A number of SNP primers are designed to detect clades of species with particular mycotoxigenic synthetic abilities. The assay is based on minisequencing using SNaPshot reactions and the SNP primers are designed based on motifs derived from phylogenetic analyses of translation elongation factor-1 alpha sequences. The present version of the Fusarium SNP assay can distinguish major groups of trichothecene producers; the strict-type-A, the strict-type-B, the type-A and type-B trichothecene producers and the putative moniliformin producers. The SNP assay was validated against five naturally infected cereal samples that previously had been analysed morphologically, chemically and by a multiplex DNA array hybridization. Conclusions: The Fusarium SNP assay reveals the advantages of using SNPs for multiplex species identification. Significance and Impact of the Study: The current assay may qualify as a high-throughput screening method for small-grain cereals in the feed and food chain, and may facilitate detection of new or introduced Fusarium species.
引用
收藏
页码:1071 / 1081
页数:11
相关论文
共 35 条
[1]   Morphological and molecular characterization of Fusarium pseudograminearum sp nov., formerly recognized as the Group 1 population of F-graminearum [J].
Aoki, T ;
O'Donnell, K .
MYCOLOGIA, 1999, 91 (04) :597-609
[2]  
*APPL BIOS, 2000, ABI PRISM SNAPSH MUL
[3]  
*APPL BIOS, 2002, US GEN MAPP SOFTW VE
[4]  
Booth C, 1971, GENUS FUSARIUM
[5]  
DYNAL, 1998, TECHNICAL HDB, V3
[6]   Identification of RNA editing sites in the SNP database [J].
Eisenberg, E ;
Adamsky, K ;
Cohen, L ;
Amariglio, N ;
Hirshberg, A ;
Rechavi, G ;
Levanon, EY .
NUCLEIC ACIDS RESEARCH, 2005, 33 (14) :4612-4617
[7]   Pharmacogenomics: Translating functional genomics into rational therapeutics [J].
Evans, WE ;
Relling, MV .
SCIENCE, 1999, 286 (5439) :487-491
[8]   Demonstration of loss of heterozygosity by single-nucleotide polymorphism microarray analysis and alterations in strain morphology in Candida albicansstrains during infection [J].
Forche, A ;
May, G ;
Magee, PT .
EUKARYOTIC CELL, 2005, 4 (01) :156-165
[9]   FUSARIUM-ID v. 1.0:: A DNA sequence database for identifying Fusarium [J].
Geiser, DM ;
Jiménez-Gasco, MD ;
Kang, SC ;
Makalowska, I ;
Veeraraghavan, N ;
Ward, TJ ;
Zhang, N ;
Kuldau, GA ;
O'Donnell, K .
EUROPEAN JOURNAL OF PLANT PATHOLOGY, 2004, 110 (5-6) :473-479
[10]  
Gerlach W, 1982, GENUS FUSARIUM PICTO