Utilize este identificador para referenciar este registo: https://hdl.handle.net/1822/34882

TítuloMALDI-TOF ICMS: a proteomic method for identification of clinical Sporothrix complex isolates
Autor(es)Oliveira, M. M. E.
Santos, C.
Sampaio, Paula
Pais, Célia
Lima, Nelson
Zancopé-Oliveira, R. M.
Palavras-chaveSporothrix complex
MALDI-TOF
DataJun-2012
EditoraUniversidade do Minho. Micoteca
Resumo(s)Sporotrichosis is a subcutaneous mycosis of worldwide distribution. However, Latin America, South Africa, India and Japan are areas of high endemicity. Recently, a combination of phenotypic and genotypic features suggested that Sporothrix schenckii should not be considered as a single taxon causing sporotrichosis as 3 new species, S. brasiliensis, S. globosa and S. mexicana have recently been described. Sporothrix mexicana was related with environmental samples and apparently restricted to Mexico. However, our Research Group has recently described the first case of human sporotrichosis caused by S. mexicana in Portugal [1]. An identification key for the Sporothrix complex species has now been proposed which includes macro- and micro-morphology and auxonogram analyses using raffinose and sucrose as carbon sources. Nevertheless, identification based on this methodology could be ambiguous due to phenotypic variability within these species [2]. In addition, conclusive species identification is reached only after partial calmodulin gene (CAL) sequence analysis. In order to show the potential of the Matrix-Assisted Laser Desorption/Ionisation Time-Of-Flight Intact Cell Mass Spectrometry (MALDI-TOF ICMS) technique on the identification of Sporothrix complex species the aim of this study was to optimise the MALDI-TOF ICMS methodology for the 4 available Sporothrix isolates related with human sporotrichosis. For that proposal the type strain S. brasiliensis IPEC16490 (CBS 120339) and the reference strains S. globosa IPEC27135, S. schenckii IPEC27722 and S. mexicana MUM11.02 were used. Also were compared this isolates in two morphologic phases. The analysis demonstrated that optimal spectra and statistical clustering were obtained when the microbial cells were analysed on the yeast phase. The present methodology is simple, reliable, and rapid making it an ideal routine identification system for clinical mycology laboratories and culture collections.
TipoResumo em ata de conferência
DescriçãoPublicado em "Biological resource centres : closing the gap between science and society : abstracts book...". ISBN 978-972-97916-5-9
URIhttps://hdl.handle.net/1822/34882
Arbitragem científicayes
AcessoAcesso aberto
Aparece nas coleções:CEB - Resumos em Livros de Atas / Abstracts in Proceedings

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