基于ITS区单核苷酸多态性的dothidea和Neofusicoccum sp .的区分

Q3 Agricultural and Biological Sciences
S. Palavouzis, A. Triantafyllopoulou, A. Tzima, E. Paplomatas
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引用次数: 1

摘要

真菌是许多被子植物的广泛病原体,在各种高价值作物上致病。希腊地区和其他地中海国家最重要的家族成员是Botryosphaeria dothidea、Neofusicoccum hellenicum、Neofusococcum mediteraneum和Neofusicoctum parvum。Botryosphaeriaceae物种经常同时从同一宿主中分离,以及B.dothidea的广泛宿主范围,需要开发快速可靠的检测方法。本研究提供了一种新的、强大的分子诊断工具,其形式是基于位于B.dothidea和Neofusicoccum物种ITS区(内部转录区)的SNP(单核苷酸多态性)设计的引物的PCR方法。将添加或不添加错配核苷酸构建的SNP引物与相同的上游通用引物组合以产生不同的扩增子。当在PCR分析中进行评估时,发现不匹配的引物具有最高的分化能力。目前正在评估进一步开发SNP分析以区分物种的潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Differentiation between Botryosphaeria dothidea and Neofusicoccum spp. based on a single nucleotide polymorphism in the ITS region
Summary Fungi belonging to the Botryosphaeriaceae family are widespread pathogens of many angiosperms, causing disease on various high value crops. The most important members of the family for the Greek region and other Mediterranean countries are Botryosphaeria dothidea, Neofusicoccum hellenicum, Neofusicoccum mediterraneum and Neofusicoccum parvum. The frequently concurrent isolation of Botryosphaeriaceae species from the same host, as well as the extensive host range of B. dothidea, necessitate the development of rapid and reliable detection methods. This study presents a new and robust molecular diagnostic tool, in the form of a PCR method based on primers designed on an SNP (single nucleotide polymorphism) located in the ITS region (Internal Transcribed Region) of B. dothidea and Neofusicoccum species. SNP primers constructed with or without added mismatch nucleotides were combined with the same upstream universal primer to generate distinct amplicons. When evaluated in PCR assays, mismatched primers were found to have the highest differentiation capability. The potential for further development of SNP assays in order to differentiate between species is being evaluated.
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来源期刊
Hellenic Plant Protection Journal
Hellenic Plant Protection Journal Agricultural and Biological Sciences-Agronomy and Crop Science
CiteScore
1.50
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