The diverse mycoflora present on dried cannabis (Cannabis sativaL., marijuana) inflorescences in commercial production


Back to previous page
Authors: Punja, ZK
Year: 2020
Journal: Can. J. Plant Pathol.   Article Link (DOI)
Title: The diverse mycoflora present on dried cannabis (Cannabis sativaL., marijuana) inflorescences in commercial production
Abstract: The objective of this study was to assess harvested dried inflorescences (buds) of cannabis (Cannabis sativaL., marijuana) for fungal presence and diversity. Samples from drying rooms of three licenced facilities in British Columbia were tested repeatedly during 2017-2019. A swab method was used, wherein sterile cotton swabs were gently swabbed over bud surfaces and directly streaked onto potato dextrose agar containing 140 mg L(-1)streptomycin sulphate. Petri dishes were incubated at 21-24 degrees C for 5-6 days and the fungal colonies that developed were recorded. The testing was repeated to provide >40 cumulative sampling times over a 2-year period. Representative colonies of each unique morphological type were identified to genus and species by PCR of the ITS1-5.8-ITS2 region of rDNA and sequence analysis. Among 34 different fungal species identified, the most prevalent werePenicillium(comprising 17 different species), followed by species ofCladosporium, Botrytis, Aspergillus, Fusarium, TalaromycesandAlternaria. All samples had several fungal species present and the number and composition varied at different sampling times and within different facilities. The swab method provided a qualitative assessment of viable mould contaminants on cannabis buds and reflected the diversity of mycoflora present, many of which are previously unreported. Fungi on cannabis buds may originate from spores released from diseased or decomposing plant materials, from growing substrates used in cannabis production, or as airborne contaminants in post-harvest trimming and drying rooms. Samples of dried buds exposed to electrobeam (e-beam) radiation treatment had no detectable fungal contamination when assessed using the swab method.
Back to previous page
 

Please send suggestions for improving this publication database to sass-support@sfu.ca.
Departmental members may update their publication list.