Metagenomic analysis of fungal phytopathogens in birch planting material

V. Padutov
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Abstract

The data of the is presented. The technology allows to identify the entire spectrum of organisms in an experimental sample per one cycle, while separate study for each potentially contained component previously was required. An integrated approach is submitted as a method for early diagnosis of causative agents of the main fungal diseases during of silver birch (Betula pendula Roth) and downy birch (Betula pubescens Ehrh.) plants. It based on an estimation of the size of internal transcribed spacers (ITS1 and ITS2) in the 18S-5.8S-28S rDNA gene cluster. Identification of the dominant fungi species phytopathogenic for birch under in planta conditions is possible because of the the specificity of size of the rDNA operon internal transcribed spacers, which is constant for most micromycete species, as well as the possibility of electrophoretic analysis of the ITS1 and ITS2 loci.
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桦木种植材料中真菌植物病原菌的宏基因组分析
给出了实验数据。该技术允许在一个周期内识别实验样品中的整个生物光谱,而以前需要对每个可能包含的成分进行单独研究。本文提出了一种用于白桦(Betula pendula Roth)和毛桦(Betula pubescens Ehrh.)主要真菌病害病原早期诊断的综合方法。它基于对18S-5.8S-28S rDNA基因簇中内部转录间隔段(ITS1和ITS2)大小的估计。由于rDNA操纵子内部转录间隔子的大小的特异性,以及ITS1和ITS2位点的电泳分析的可能性,在植物条件下鉴定桦树的优势真菌物种是可能的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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