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

被引:16
作者
Oidtmann, B
Bausewein, S
Hölzle, L
Hoffmann, R
Wittenbrink, M
机构
[1] Univ Munich, Inst Zool Fish Biol & Fish Dis, D-80539 Munich, Germany
[2] Univ Zurich, Inst Vet Bacteriol, CH-8057 Zurich, Switzerland
关键词
Aphanomyces astaci; crayfish plague; identification; large subunit rDNA; 28 S ribosomal DNA; PCR; restriction enzyme analysis;
D O I
10.1016/S0378-1135(01)00505-3
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
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.
引用
收藏
页码:183 / 194
页数:12
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