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1.
APMIS ; 122(4): 324-8, 2014 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-23919730

RESUMO

We tested the capacity of the Sysmex UF-1000i system to detect yeasts in urine by screening a total of 22 132 urine samples received for culture in our microbiology laboratory during 1 year. We also analyzed different dilutions of previously filtered urine inoculated with a strain of Candida albicans. With clinical samples, a single cut-off point of 50 yeast-like cells (YLCs)/µL detected candiduria ≥10 000 colony forming units (CFU)/mL and >100 000 CFU/mL with a sensitivity of 87.3%/95.4%, a specificity of 97%, a negative predictive value of 95.9%, and a positive predictive value of 9.3%/5.7%. With the simulated samples, a linear relationship was observed between the dilution factor and the number of cells detected by UF-1000i. This instrument appears to be able to reliably rule out candiduria of a magnitude of at least 10 000 CFU/mL and facilitate urine sample screening, thereby providing fast results. The Sysmex UF1000i system can be adapted for candiduria screening by the use of an appropriate YLCs/µL cut-off point that takes account of the prevalence of candiduria in the population.


Assuntos
Micologia/métodos , Infecções Urinárias/diagnóstico , Infecções Urinárias/microbiologia , Urina/microbiologia , Leveduras/isolamento & purificação , Adulto , Idoso , Automação Laboratorial , Candidíase/diagnóstico , Candidíase/microbiologia , Contagem de Colônia Microbiana/métodos , Contagem de Colônia Microbiana/estatística & dados numéricos , Feminino , Humanos , Lactente , Masculino , Micologia/estatística & dados numéricos , Micoses/diagnóstico , Micoses/microbiologia , Gravidez
2.
J Clin Microbiol ; 35(12): 3278-83, 1997 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-9399534

RESUMO

The precise diagnosis of paracoccidioidomycosis, in most cases, is established by direct methods and indirect immunological tests. The latter method is reliant on the identification of the host's humoral responses, which are usually impaired or absent in patients with severe juvenile forms of the disease and in immunocompromised patients. Determining disease activity or assessing treatment responses by measuring antibody levels is difficult, since antibody titer may remain elevated or persist at stationary levels, even in the presence of clinical improvement. Consequently, there is a need for alternative tests aimed at the identification of circulating antigens. A modification of the standard hybridoma production method was used to raise a panel of murine monoclonal antibodies (MAbs) against the yeast form of Paracoccidioides brasiliensis. Of these, MAb PIB, directed against an 87-kDa determinant, was used to develop an inhibition ELISA (inh-ELISA) capable of detecting as little as 5.8 ng of circulating antigen per ml of serum. Sera from 46 patients with paracoccidioidomycosis or other mycoses and sera from healthy individuals were evaluated by the inh-ELISA; overall sensitivity was 80.4% (37 of 46 paracoccidioidomycosis patients tested positive), and specificity compared with that of normal controls from areas of endemicity was 81.4%. The inh-ELISA detected circulating antigen in 100% of patients with the acute form of paracoccidioidomycosis and in 83.3 and 60% of patients with the chronic multifocal and unifocal forms of paracoccidioidomycosis according to the patients' clinical presentation. These results indicate that the inh-ELISA with MAb PIB is effective in the detection of circulating antigen and that this test may be useful for monitoring responses to treatment and establishing disease prognoses.


Assuntos
Anticorpos Antifúngicos , Anticorpos Monoclonais , Antígenos de Fungos/sangue , Paracoccidioides/imunologia , Paracoccidioidomicose/diagnóstico , Paracoccidioidomicose/microbiologia , Antígenos de Fungos/química , Ensaio de Imunoadsorção Enzimática/métodos , Ensaio de Imunoadsorção Enzimática/estatística & dados numéricos , Estudos de Avaliação como Assunto , Humanos , Peso Molecular , Micologia/métodos , Micologia/estatística & dados numéricos , Paracoccidioidomicose/imunologia , Sensibilidade e Especificidade
3.
Mycopathologia ; 137(3): 153-7, 1997.
Artigo em Inglês | MEDLINE | ID: mdl-9368409

RESUMO

In the last decade the number of systemic yeast infections has increased significantly. Although Candida albicans is the most frequently isolated yeast from clinical specimens, the emergence of non-albicans species has clearly been a recent concern. As a consequence, there is a greater need for rapid and accurate methods for yeast identification. The aim of this study was to evaluate the performance of the AUXACOLOR system (Sanofi Diagnostics Pasteur) for the identification of clinically relevant yeasts, as compared with the conventional method. Yeast isolates (n = 97) belonging to 12 species were identified by the commercial system and the classic method. Correct identifications were obtained by using AUXACOLOR system in 79.4% of the isolates tested. Misidentification occurred in 5.2% of the strains and 15.5% were not identified due to a failure in the manufacturer's data base. In order to improve its accuracy, there is a need for expanding the database or revamping the tests included in the system.


Assuntos
Micologia/métodos , Leveduras/classificação , Leveduras/isolamento & purificação , Candida/classificação , Candida/isolamento & purificação , Candida albicans/classificação , Candida albicans/isolamento & purificação , Cryptococcus neoformans/classificação , Cryptococcus neoformans/isolamento & purificação , Bases de Dados Factuais , Erros de Diagnóstico , Estudos de Avaliação como Assunto , Humanos , Micologia/estatística & dados numéricos , Micoses/diagnóstico , Micoses/microbiologia , Saccharomyces cerevisiae/classificação , Saccharomyces cerevisiae/isolamento & purificação , Especificidade da Espécie , Trichosporon/classificação , Trichosporon/isolamento & purificação , Leveduras/metabolismo
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