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Identification of benzimidazole resistance in Cladobotryum dendroides using a PCR-based method

Published online by Cambridge University Press:  01 June 1998

GARETH J. McKAY
Affiliation:
Department of Applied Plant Science, The Queen's University of Belfast, Agriculture & Food Science Centre, Newforge Lane, Belfast, BT9 5PX, UK
DAMIAN EGAN
Affiliation:
Department of Environmental Resource Management, Faculty of Agriculture, University College Dublin, Ireland
ELIZABETH MORRIS
Affiliation:
Mushroom Research Group, National Agricultural and Veterinary Biotechnology Centre, University College Dublin, Ireland
AVERIL E. BROWN
Affiliation:
Department of Applied Plant Science, The Queen's University of Belfast, Agriculture & Food Science Centre, Newforge Lane, Belfast, BT9 5PX, UK
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Abstract

Cladobotryum dendroides, causal agent of cobweb disease of Agaricus bisporus, has become increasingly resistant to methylbenzimidazole carbamate (MBC) fungicides following the extensive use of MBC in cultivated mushroom production in Ireland. Of 38 isolates of C. dendroides obtained from Irish mushroom units, 34 were resistant to carbendazim. Primers based on conserved regions of the β-tubulin gene were used to amplify and sequence a portion of the β-tubulin gene in C. dendroides. A point mutation was detected at codon 50 in isolates resistant to benzimidazole fungicides, causing an amino acid substitution from tyrosine to cysteine. Species-specific PCR primers were designed to amplify the region of the β-tubulin gene containing this substitution. The point mutation removed an Acc I restriction site in the β-tubulin gene sequence of resistant isolates. Digestion of the PCR product with Acc I thus provides a rapid diagnostic test to differentiate sensitive and resistant isolates of this fungus. EMBL accession number: Y12256.

Type
Research Article
Copyright
© The British Mycological Society 1998

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