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区分禾谷丝核菌禾谷变种和禾谷丝核菌叶斑变种,即大麦网斑病病原菌的交配型座特异性聚合酶链反应标记。

Mating type locus-specific polymerase chain reaction markers for differentiation of Pyrenophora teres f. teres and P. teres f. maculata, the causal agents of barley net blotch.

机构信息

U.S. Department of Agriculture-Agricultural Research Service, Cereal Crops Research Unit, Northern Crop Science Laboratory, Fargo, ND 58102-2765, USA.

出版信息

Phytopathology. 2010 Dec;100(12):1298-306. doi: 10.1094/PHYTO-05-10-0135.

Abstract

Fourteen single nucleotide polymorphisms (SNPs) were identified at the mating type (MAT) loci of Pyrenophora teres f. teres (Ptt), which causes net form (NF) net blotch, and P. teres f. maculata (Ptm), which causes spot form (SF) net blotch of barley. MAT-specific SNP primers were developed for polymerase chain reaction (PCR) and the two forms were differentiated by distinct PCR products: PttMAT1-1 (1,143 bp) and PttMAT1-2 (1,421 bp) for NF MAT1-1 and MAT1-2 isolates; PtmMAT1-1 (194 bp) and PtmMAT1-2 (939 bp) for SF MAT1-1 and MAT1-2 isolates, respectively. Specificity was validated using 37 NF and 17 SF isolates collected from different geographic regions. Both MAT1-1 and MAT1-2 SNP primers retained respective specificity when used in duplex PCR. No cross-reactions were observed with DNA from P. graminea, P. tritici-repentis, or other ascomycetes, or barley. Single or mixed infections of the two different forms were also differentiated. This study provides the first evidence that the limited SNPs at the MAT locus are sufficient for distinguishing closely related heterothallic ascomycetes at subspecies levels, thus allowing pathogenicity and mating type characteristics of the fungus to be determined simultaneously. Methods presented will facilitate pathogen detection, disease management, and epidemiological studies.

摘要

鉴定出引起大麦网斑病的禾旋孢腔菌网斑变种(Pyrenophora teres f. teres,Ptt)和斑点变种(P. teres f. maculata,Ptm)交配型(MAT)基因座的 14 个单核苷酸多态性(SNP)。MAT 特异性 SNP 引物用于聚合酶链反应(PCR),通过不同的 PCR 产物区分两种形式:NF MAT1-1 和 MAT1-2 分离株的 PttMAT1-1(1143 bp)和 PttMAT1-2(1421 bp);SF MAT1-1 和 MAT1-2 分离株的 PtmMAT1-1(194 bp)和 PtmMAT1-2(939 bp)。使用来自不同地理区域的 37 个 NF 和 17 个 SF 分离株验证了特异性。在双重 PCR 中使用时,MAT1-1 和 MAT1-2 SNP 引物都保留了各自的特异性。与禾谷镰孢菌、禾旋孢腔菌或其他子囊菌或大麦的 DNA 没有交叉反应。还区分了两种不同形式的单一或混合感染。这项研究首次证明,MAT 基因座中的有限 SNP 足以区分亚种水平上密切相关的异宗配合子囊菌,从而能够同时确定真菌的致病性和交配型特征。所提出的方法将有助于病原体检测、疾病管理和流行病学研究。

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