Candida clinical species identification: molecular and biochemical methods

Detalhes bibliográficos
Autor(a) principal: Costa, AR
Data de Publicação: 2010
Outros Autores: Silva, F, Henriques, M, Azeredo, J, Oliveira, R, Faustino, A
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Texto Completo: http://hdl.handle.net/10400.23/215
Resumo: In the last decade, the number and diversity of nosocomial Candida infections has increased significantly, resulting in an emergent need for rapid and accurate methods for Candida identification. Therefore, the aim of this study was to evaluate the performance of three biochemical systems (Auxacolor, ID32C, and Vitek 2 YST) for the identification of Candida species, comparing them with molecular identification (polymerase chain reaction and gel agarose electrophoresis). These methods were used to assess Candida spp. (229 clinical isolates) prevalence and distribution among clinical specimens. The biochemical methods with higher percentages of correct identification were Vitek 2 YST (79.6%) and Auxacolor (78.6%). However, overall the biochemical methods assayed differed from the molecular identification. Thus, due to their rapid and precise identification, molecular methods are promising techniques for Candida species identification in clinical laboratories. Candida albicans and Non Candida albicans Candida species had a similar prevalence (50.4 and 49.6%, respectively), corroborating the epidemiological shift observed for these pathogens in the recent years.
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spelling Candida clinical species identification: molecular and biochemical methodsCandidaCandidíaseIn the last decade, the number and diversity of nosocomial Candida infections has increased significantly, resulting in an emergent need for rapid and accurate methods for Candida identification. Therefore, the aim of this study was to evaluate the performance of three biochemical systems (Auxacolor, ID32C, and Vitek 2 YST) for the identification of Candida species, comparing them with molecular identification (polymerase chain reaction and gel agarose electrophoresis). These methods were used to assess Candida spp. (229 clinical isolates) prevalence and distribution among clinical specimens. The biochemical methods with higher percentages of correct identification were Vitek 2 YST (79.6%) and Auxacolor (78.6%). However, overall the biochemical methods assayed differed from the molecular identification. Thus, due to their rapid and precise identification, molecular methods are promising techniques for Candida species identification in clinical laboratories. Candida albicans and Non Candida albicans Candida species had a similar prevalence (50.4 and 49.6%, respectively), corroborating the epidemiological shift observed for these pathogens in the recent years.SpringerRepositório Científico do Hospital de BragaCosta, ARSilva, FHenriques, MAzeredo, JOliveira, RFaustino, A2012-04-27T15:09:39Z2010-01-01T00:00:00Z2010-01-01T00:00:00Zinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfhttp://hdl.handle.net/10400.23/215engAnn Microbiol. 2010; 60:105-12info:eu-repo/semantics/openAccessreponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãoinstacron:RCAAP2022-09-21T09:01:45Zoai:repositorio.hospitaldebraga.pt:10400.23/215Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-19T15:54:27.470780Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãofalse
dc.title.none.fl_str_mv Candida clinical species identification: molecular and biochemical methods
title Candida clinical species identification: molecular and biochemical methods
spellingShingle Candida clinical species identification: molecular and biochemical methods
Costa, AR
Candida
Candidíase
title_short Candida clinical species identification: molecular and biochemical methods
title_full Candida clinical species identification: molecular and biochemical methods
title_fullStr Candida clinical species identification: molecular and biochemical methods
title_full_unstemmed Candida clinical species identification: molecular and biochemical methods
title_sort Candida clinical species identification: molecular and biochemical methods
author Costa, AR
author_facet Costa, AR
Silva, F
Henriques, M
Azeredo, J
Oliveira, R
Faustino, A
author_role author
author2 Silva, F
Henriques, M
Azeredo, J
Oliveira, R
Faustino, A
author2_role author
author
author
author
author
dc.contributor.none.fl_str_mv Repositório Científico do Hospital de Braga
dc.contributor.author.fl_str_mv Costa, AR
Silva, F
Henriques, M
Azeredo, J
Oliveira, R
Faustino, A
dc.subject.por.fl_str_mv Candida
Candidíase
topic Candida
Candidíase
description In the last decade, the number and diversity of nosocomial Candida infections has increased significantly, resulting in an emergent need for rapid and accurate methods for Candida identification. Therefore, the aim of this study was to evaluate the performance of three biochemical systems (Auxacolor, ID32C, and Vitek 2 YST) for the identification of Candida species, comparing them with molecular identification (polymerase chain reaction and gel agarose electrophoresis). These methods were used to assess Candida spp. (229 clinical isolates) prevalence and distribution among clinical specimens. The biochemical methods with higher percentages of correct identification were Vitek 2 YST (79.6%) and Auxacolor (78.6%). However, overall the biochemical methods assayed differed from the molecular identification. Thus, due to their rapid and precise identification, molecular methods are promising techniques for Candida species identification in clinical laboratories. Candida albicans and Non Candida albicans Candida species had a similar prevalence (50.4 and 49.6%, respectively), corroborating the epidemiological shift observed for these pathogens in the recent years.
publishDate 2010
dc.date.none.fl_str_mv 2010-01-01T00:00:00Z
2010-01-01T00:00:00Z
2012-04-27T15:09:39Z
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url http://hdl.handle.net/10400.23/215
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dc.relation.none.fl_str_mv Ann Microbiol. 2010; 60:105-12
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