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A rapid fungal DNA extraction method suitable for PCR screening fungal mutants, infected plant tissue and spore trap samples

Paola Pilo, Anna M. M. Tiley, Colleen Lawless, Sujit Jung Karki, J. Burke, Angela Feechan

2021Physiological and Molecular Plant Pathology23 citationsDOIOpen Access PDF

Abstract

Current DNA extraction methods from filamentous fungi take from an hour to a full day. These methods require buffers and tools for grinding fungal tissues. Although commercial extraction kits can reduce the amount of time spent preparing and extracting genomic DNA from fungal samples, these can be expensive. Here we describe a quick and inexpensive sonication technique to extract genomic DNA from filamentous fungi without buffer which can be used to perform PCR in under an hour. DNA was extracted from Zymoseptoria tritici, Fusarium graminearum and Botrytis cinerea in vitro cultures, Z. tritici asexual fruiting bodies and directly from spore trap tapes.

Topics & Concepts

BiologyDNA extractionSporegenomic DNABotrytis cinereaDNAFusariumPolymerase chain reactionExtraction (chemistry)BotrytisMicrobiologyBotanyChromatographyGeneGeneticsChemistryPlant Pathogens and Fungal DiseasesMycotoxins in Agriculture and FoodFungal Plant Pathogen Control
A rapid fungal DNA extraction method suitable for PCR screening fungal mutants, infected plant tissue and spore trap samples | Litcius