Canadian Forest Service, Pacific Forestry Centre, Natural Resources Canada, Victoria, BC, Canada.
Forest and Conservation Sciences, University of British Columbia, Vancouver, BC, Canada.
Methods Mol Biol. 2023;2659:37-49. doi: 10.1007/978-1-0716-3159-1_3.
The accurate identification of plant pathogens is a critical step to prevent their spread and attenuate their impact. Among the wide range of methods available, DNA-barcoding, i.e., the identification of an organism through the PCR amplification and sequencing of a single locus, remains one of the most straightforward and accurate plant-pathogen identification techniques that can be used in a generic molecular biology lab. This chapter provides a detailed protocol for the isolation of genomic DNA of fungal and oomycete pathogens from fresh field samples and the amplification and sequencing of the internal transcribed spacer (ITS) locus for DNA-barcoding purpose. Amendments to the protocol are provided to help in resolving issues related to the analysis of complicated samples and to the lack of species resolution that can be encountered with ITS barcodes.
准确鉴定植物病原体是防止其传播和减轻其影响的关键步骤。在众多可用方法中,DNA 条形码技术(即通过 PCR 扩增和测序单个基因座来鉴定生物体)仍然是最直接和准确的植物病原体鉴定技术之一,可在通用分子生物学实验室中使用。本章提供了从新鲜田间样本中分离真菌和卵菌病原体基因组 DNA 以及扩增和测序内部转录间隔区 (ITS) 基因座进行 DNA 条形码目的的详细方案。还提供了对该方案的修订,以帮助解决与复杂样本分析以及与 ITS 条形码可能遇到的物种分辨率不足相关的问题。