4.7 Article

Identification of the crayfish plague fungus Aphanomyces astaci by polymerase chain reaction and restriction enzyme analysis

Journal

VETERINARY MICROBIOLOGY
Volume 85, Issue 2, Pages 183-194

Publisher

ELSEVIER SCIENCE BV
DOI: 10.1016/S0378-1135(01)00505-3

Keywords

Aphanomyces astaci; crayfish plague; identification; large subunit rDNA, 28 S ribosomal DNA; PCR; restriction enzyme analysis

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To characterise the DNA of the crayfish plague fungus Aphanomyces astaci. Saprolegniales (Oomycetes), primers were developed to amplify a 1050 bp segment of the 28 S rDNA region. Restriction enzyme,, were applied to the amplicon obtained, to distinguish A. astaci from 12 fungal species belonging also to the Saprolegniales and five more distantly related fungi. Most of the fungal species included in the study are either known parasites of freshwater crayfish cuticle or can be found in their natural environment. A. astaci DNA was distinguishable from the DNA of other fungal species tested by using the primers developed plus restriction enzymes AluI, HindIII and AvaI. Prior to this study, methods for A. astaci-species determination. e.g. spore production and infection experiments. required a protracted period to yield results the method described in this study is quicker. (C) 2002 Elsevier Science B.V. All rights reserved.

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