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dc.contributor.authorSilva, Roberto Moreira da-
dc.contributor.authorSilva Neto, João Ricardo da-
dc.contributor.authorSantos, Carla Silvana-
dc.contributor.authorFrickmann, Hagen-
dc.contributor.authorPoppert, Sven-
dc.contributor.authorCruz, Kátia Santana-
dc.contributor.authorKoshikene, Daniela-
dc.contributor.authorSouza, João Vicente Braga de-
dc.date.accessioned2020-05-20T14:15:52Z-
dc.date.available2020-05-20T14:15:52Z-
dc.date.issued2015-
dc.identifier.urihttps://repositorio.inpa.gov.br/handle/1/15908-
dc.description.abstractThe aim of this study was to evaluate the diagnostic performance of in-house FISH (fluorescence in situ hybridisation) procedures for the direct identification of invasive fungal infections in blood cultures and cerebrospinal fluid (CSF) samples and to compare these FISH results with those obtained using traditional microbiological techniques and PCR targeting of the ITS1 region of the rRNA gene. In total, 112 CSF samples and 30 positive blood cultures were investigated by microscopic examination, culture, PCR-RFLP and FISH. The sensitivity of FISH for fungal infections in CSF proved to be slightly better than that of conventional microscopy (India ink) under the experimental conditions, detecting 48 (instead of 46) infections in 112 samples. The discriminatory powers of traditional microbiology, PCR-RFLP and FISH for fungal bloodstream infections were equivalent, with the detection of 14 fungal infections in 30 samples. However, the mean times to diagnosis after the detection of microbial growth by automated blood culture systems were 5 hours, 20 hours and 6 days for FISH, PCR-RFLP and traditional microbiology, respectively. The results demonstrate that FISH is a valuable tool for the identification of invasive mycoses that can be implemented in the diagnostic routine of hospital laboratories. © 2015 Da Silva et al.en
dc.language.isoenpt_BR
dc.relation.ispartofVolume 14, Número 1pt_BR
dc.rightsAttribution-NonCommercial-NoDerivs 3.0 Brazil*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/3.0/br/*
dc.subjectAdolescenten
dc.subjectAdulten
dc.subjectBlood Cultureen
dc.subjectBloodstream Infectionen
dc.subjectCerebrospinal Fluiden
dc.subjectChilden
dc.subjectControlled Studyen
dc.subjectCryptococcosisen
dc.subjectDiagnostic Test Accuracy Studyen
dc.subjectFemaleen
dc.subjectIn Situ Hybridization, Fluorescenceen
dc.subjectFungal Detectionen
dc.subjectHospital Laboratoryen
dc.subjectHumanen
dc.subjectMajor Clinical Studyen
dc.subjectMaleen
dc.subjectMicrobial Growthen
dc.subjectPolymorphism, Restriction Fragment Lengthen
dc.subjectSensitivity And Specificityen
dc.subjectSystemic Mycosisen
dc.subjectBlooden
dc.subjectClassificationen
dc.subjectEvaluation Studyen
dc.subjectIn Situ Hybridization, Fluorescenceen
dc.subjectFungusen
dc.subjectGeneticsen
dc.subjectIsolation And Purificationen
dc.subjectMicrobiologyen
dc.subjectMycosesen
dc.subjectPolymerase Chain Reactionen
dc.subjectProceduresen
dc.subjectDna, Fungalen
dc.subjectAdulten
dc.subjectBlooden
dc.subjectDna, Fungalen
dc.subjectFemaleen
dc.subjectFungien
dc.subjectHumansen
dc.subjectIn Situ Hybridization, Fluorescenceen
dc.subjectMaleen
dc.subjectMycosesen
dc.subjectPolymerase Chain Reactionen
dc.titleEvaluation of fluorescence in situ hybridisation (FISH) for the detection of fungi directly from blood cultures and cerebrospinal fluid from patients with suspected invasive mycosesen
dc.typeArtigopt_BR
dc.identifier.doi10.1186/s12941-015-0065-5-
dc.publisher.journalAnnals of Clinical Microbiology and Antimicrobialspt_BR
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