Identification and typing of Malassezia yeasts using amplified fragment length polymorphism (AFLPTm), random amplified polymorphic DNA (RAPD) and denaturing gradient gel electrophoresis (DGGE)

被引:58
作者
Theelen, Bart [1 ]
Silvestri, Massimiliano [1 ]
Gueho, Eveline [2 ]
van Belkum, Alex [3 ]
Boekhout, Teun [1 ]
机构
[1] Cent Bur Schimmelcultures, Yeast Div, NL-3854 CT Utrecht, Netherlands
[2] Inst Pasteur, Unite Mycol, F-75724 Paris 15, France
[3] Erasmus Univ, Med Ctr, Dept Med Microbiol & Infect Dis, Rotterdam, Netherlands
关键词
Malassezia; yeast; amplified fragment length polymorphism; denaturing gradient gel electrophoresis; random amplified polymorphic DNA; identification;
D O I
10.1016/S1567-1356(01)00015-0
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Three molecular tools, amplified fragment length polymorphism (AFLP(Tm)), denaturing gradient gel electrophoresis (DGGE) and random amplified polymorphic DNA (RAPD) analysis, were explored for their usefulness to identify isolates of Malassezia yeasts. All seven species could be separated by AFLP and DGGE. Using AFLP, four genotypes could be distinguished within M. furfur. AFLP genotype 4 contained only isolates from deep human sources, and ca. 80% of these isolates were from patients with systemic disease. Most of the systemic isolates belonged to a single RAPD genotype. This suggests that systemic conditions strongly select for a particular genotype. Although the clinical use of DGGE may be limited due to technical demands, it remains a powerful tool for the analysis of complex clinical samples. (C) 2001 Federation of European Microbiological Societies. Published by Elsevier Science B.V. All rights reserved.
引用
收藏
页码:79 / 86
页数:8
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