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Provedor de dados:  BJM
País:  Brazil
Título:  Identification of Candida spp. by phenotypic tests and PCR
Autores:  Marinho,Sandra Aparecida
Teixeira,Alice Becker
Santos,Otávio Silveira
Cazanova,Ricardo Flores
Ferreira,Carlos Alexandre Sanchez
Cherubini,Karen
Oliveira,Sílvia Dias de
Data:  2010-06-01
Ano:  2010
Palavras-chave:  Candida spp
Identification
PCR
Phenotypic tests
Resumo:  The correct identification of Candida species is of great importance, as it presents prognostic and therapeutical significance, allowing an early and appropriate antifungical therapy. The purpose of this study was to identify isolates of Candida spp. from oral mucosa of 38 patients with oral candidosis evaluated in 2004 by phenotypic methods and PCR, discriminating C. albicans from the other Candida species. The tests used for phenotypic analysis were germ-tube and chlamydoconidia production, culture in CHROMAgarTM Candida, carbohydrate assimilation test, growth at 45ºC and culture in Tween 80 agar. Genotypic confirmation was performed by PCR. Phenotypic tests showed that 63.2% strains formed germ-tubes, 73.7% produced chlamydoconidia, and 63.2% showed green colonies in chromogenic medium, presumptively indicating C. albicans or C. dubliniensis. The carbohydrate assimilation test confirmed these results. A total of 21% strains were identified as C. krusei and 13.2% were indicative of C. tropicalis. Of these later strains, three produced chlamydoconidia. The association of other phenotypic tests with culture in Tween 80 agar identified 95.8% of strains as C. albicans and 4.2% as C. dubliniensis. All 24 strains indicative of C. albicans and C. dubliniensis were confirmed by PCR as C. albicans.
Tipo:  Info:eu-repo/semantics/article
Idioma:  Inglês
Identificador:  http://www.scielo.br/scielo.php?script=sci_arttext&pid=S1517-83822010000200004
Editor:  Sociedade Brasileira de Microbiologia
Relação:  10.1590/S1517-83822010000200004
Formato:  text/html
Fonte:  Brazilian Journal of Microbiology v.41 n.2 2010
Direitos:  info:eu-repo/semantics/openAccess
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