Literature DB >> 9764550

Evaluation of six commercial systems for identification of medically important yeasts.

L Buchaille1, A M Freydière, R Guinet, Y Gille.   

Abstract

Six commercially available systems for the identification of yeasts were evaluated using 133 clinical isolates and four reference strains that had been previously identified by conventional methods and 19 recent clinical isolates that had been identified by the ID32C system (bioMérieux, France). The total identification rates (TIR) established for the total number of strains tested and the database identification rates (DBIR) established for the strains included in the respective manufacturer databases were both determined. After incubation for 4 h, the TIR and DBIR were 78% and 84%, respectively, for the RapID Yeast Plus system (Innovative Diagnostic Systems, USA). After incubation for 24 h, the TIR and DBIR were 32% and 32%, respectively, for the ID32C, 65% and 67% for the Auxacolor system (Sanofi Diagnostics Pasteur, France), 62% and 65% for the Fungichrom I system (International Microbio, France), 52% and 65% for the Fungifast I twin system (International Microbio), and 62% and 68% for the API Candida system (bioMérieux). The maximum TIR and DBIR (+/- 1%) obtained after incubation for 48 h were 86% and 88% for the Auxacolor, 85% and 89% for the Fungichrom I, 78% and 98% for the Fungifast I twin, and 82% and 91% for the API Candida. For the ID32C, the maximum TIR and DBIR were 98% and 98%, respectively, but these values were obtained only after 72 h of incubation. In addition, the six systems varied in their ease of use and readings. In conclusion, based on results obtained with 156 strains, the Auxacolor and Fungichrom systems seem the most appropriate for use in a clinical microbiology laboratory, due to their ease of use and reading, their rapidity, their cost per test, and their relatively high TIR results, which indicated acceptable performance with strains frequently isolated in our hospital. For a reference identification, the ID32C remains the sole system usable.

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Year:  1998        PMID: 9764550     DOI: 10.1007/bf01691130

Source DB:  PubMed          Journal:  Eur J Clin Microbiol Infect Dis        ISSN: 0934-9723            Impact factor:   3.267


  27 in total

1.  Rapid methods for identification of the most frequent clinical yeasts.

Authors:  A M Freydière; R Guinet
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2.  Comparison of the new API Candida system to the ID 32C system for identification of clinically important yeast species.

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Journal:  J Clin Microbiol       Date:  1996-07       Impact factor: 5.948

3.  Ability of RapID Yeast Plus System to identify 304 clinically significant yeasts within 5 hours.

Authors:  T T Kitch; M R Jacobs; M R McGinnis; P C Appelbaum
Journal:  J Clin Microbiol       Date:  1996-05       Impact factor: 5.948

4.  Evaluation of the modified API 20C system for identification of clinically important yeasts.

Authors:  W J Buesching; K Kurek; G D Roberts
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5.  Evaluation of the updated Vitek yeast identification data base.

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Review 6.  Opportunistic mycoses in the immunocompromised host: experience at a cancer center and review.

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8.  Evaluation of the Baxter-MicroScan 4-hour enzyme-based yeast identification system.

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9.  Rapid identification of medically important yeasts by electrophoretic protein patterns.

Authors:  S Bruneau; R Guinet
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10.  Evaluation of four commercial biochemical test systems for identification of yeasts.

Authors:  T Bergan; A B Hollum; M Vangdal
Journal:  Eur J Clin Microbiol       Date:  1982-08       Impact factor: 3.267

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Review 4.  Are the Conventional Commercial Yeast Identification Methods Still Helpful in the Era of New Clinical Microbiology Diagnostics? A Meta-Analysis of Their Accuracy.

Authors:  Brunella Posteraro; Ljupcho Efremov; Emanuele Leoncini; Rosarita Amore; Patrizia Posteraro; Walter Ricciardi; Maurizio Sanguinetti
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Review 5.  Biology of the pathogenic yeast Candida glabrata.

Authors:  A Bialková; J Subík
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6.  Evaluation of the VITEK 2 system for rapid identification of yeasts and yeast-like organisms.

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Journal:  J Clin Microbiol       Date:  2000-05       Impact factor: 5.948

7.  Isolation and characterization of a species-specific DNA fragment for identification of Candida (Torulopsis) glabrata by PCR.

Authors:  K Becker; D Badehorn; B Keller; M Schulte; K H Böhm; G Peters; W Fegeler
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8.  Comparison of the API Candida system with the AUXACOLOR system for identification of common yeast pathogens.

Authors:  C K Campbell; K G Davey; A D Holmes; A Szekely; D W Warnock
Journal:  J Clin Microbiol       Date:  1999-03       Impact factor: 5.948

9.  Comparison of VITEK 2 with ITS2-fragment length polymorphism analysis for identification of yeast species.

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10.  Identification of medically important yeast species by sequence analysis of the internal transcribed spacer regions.

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Journal:  J Clin Microbiol       Date:  2006-03       Impact factor: 5.948

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