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pubmed-article:12517882pubmed:abstractTextBecause Candida species have innately highly variable antifungal susceptibilities, the availability of a fast and reliable species identification test is very important so that suitable and effective therapeutic measures may be taken. Using three oligonucleotide primers, we established a randomly amplified polymorphic DNA (RAPD) analysis method that enabled direct identification of the most common opportunistic pathogenic Candida species. RAPD analysis revealed a characteristic molecular fingerprint for each Candida species. Differences between the profiles for Candida albicans and C. dubliniensis were evident. RAPD analysis is a relatively easy, reproducible, and reliable technique that can be useful in providing genetic fingerprints for the identification of strains. In addition, a collection of different C. albicans strains was identified by a specific PCR based on multiple secreted aspartic proteinase (SAP) genes and the dipeptidyl aminopeptidase (DAP2) gene. Our findings demonstrate that PCR based upon the SAP and DAP2 sequences is a simple, rapid, clear, and direct technique for the identification and differentiation of C. albicans and C. dubliniensis.lld:pubmed
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pubmed-article:12517882pubmed:authorpubmed-author:Bautista-Muño...lld:pubmed
pubmed-article:12517882pubmed:authorpubmed-author:BoldoXavier...lld:pubmed
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pubmed-article:12517882pubmed:pagination414-20lld:pubmed
pubmed-article:12517882pubmed:dateRevised2009-11-18lld:pubmed
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pubmed-article:12517882pubmed:articleTitleIdentification of Candida spp. by randomly amplified polymorphic DNA analysis and differentiation between Candida albicans and Candida dubliniensis by direct PCR methods.lld:pubmed
pubmed-article:12517882pubmed:affiliationDepartamento de Microbiología, Escuela Nacional de Ciencias Biológicas, I.P.N., Mexico D.F., Mexico.lld:pubmed
pubmed-article:12517882pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:12517882pubmed:publicationTypeResearch Support, Non-U.S. Gov'tlld:pubmed
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