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Are Commercial Systems Used for the Identification of Yeasts Enough Alone?: A Case Report

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dc.contributor.author Altuncekic-Yildirim, Arzu
dc.contributor.author Atalay, Mustafa Altay
dc.contributor.author Calgin, Mustafa Kerem
dc.contributor.author Cetinkol, Yeliz
dc.contributor.author Koc, Ayse Nedret
dc.date.accessioned 2022-08-16T11:54:11Z
dc.date.available 2022-08-16T11:54:11Z
dc.date.issued 2016
dc.identifier.uri http://doi.org/10.5152/kd.2016.23
dc.identifier.uri https://www.klimikdergisi.org/en/2021/01/05/are-commercial-systems-used-for-the-identification-of-yeasts-enough-alone-a-case-report/
dc.identifier.uri http://earsiv.odu.edu.tr:8080/xmlui/handle/11489/2042
dc.description.abstract Infections developing due to Trichosporon species especially in immunosuppressed patients have started to increase also in our country as well as in the world. Some difficulties have been encountered in identification and treatment of Trichosporon spp. which are relatively more resistant to antifungal treatment. Accurate and rapid identification of yeast species is very important to ensure determination of the appropriate antifungal agent in treating these infections. Due to long time span and intense effort required, determination using conventional methods has recently been replaced by common use of commercial systems allowing rapid identification. However, the commercial systems used to determine yeasts are reported to have higher correct identification rates for frequently isolated species, whereas lower rates for rarer species. In this report, we aimed to address that the commercial systems are enough alone for identification by evaluating a case of urinary tract infection with a positive urine culture yielding yeasts. A urine culture revealed dry, wrinkled, waxy, pink, yeast-like colonies on blood agar and eosin-methylene blue agar after a 24-hour incubation. These colonies were identified as Cryptococcus sp. using VITEK (R) 2 (bioMerieux, Marcy l'Etoile, France) system. On the other hand, this isolate had been demonstrated as Trichosporon asahii by microscopic and macroscopic appearance, carbohydrate assimilation test results and urease positivity. Additionally, antifungal susceptibility of isolate was determined using microdilution (amphotericin B, voriconazole, fluconazole) and Etest (R) (AB Biodisk, Solna, Sweden) methods (caspofungin, anidulafungin) according to Clinical Laboratory Standards Institute M27-A3 standard. In conclusion, this case report demonstrated that there is a need for confirmation of results with conventional methods for determination of rare species such as Trichosporon spp. identified with commercial systems based on biochemical properties, and antifungal susceptibility tests should be performed in clinical microbiology laboratories. en_US
dc.language.iso eng en_US
dc.publisher AVES, BUYUKDERE CAD 105-9, MECIDIYEKOY, SISLI, ISTANBUL 34394, TURKEY en_US
dc.relation.isversionof 10.5152/kd.2016.23 en_US
dc.rights info:eu-repo/semantics/openAccess en_US
dc.subject Cryptococcus sp.; Trichosporon asahii; urinary tract infections; yeasts en_US
dc.subject URINARY-TRACT-INFECTIONS; TRICHOSPORON-ASAHII; MICROBIOLOGY LABORATORIES; MULTICENTER; DIAGNOSIS; COMMON en_US
dc.title Are Commercial Systems Used for the Identification of Yeasts Enough Alone?: A Case Report en_US
dc.type article en_US
dc.relation.journal KLIMIK JOURNAL en_US
dc.contributor.department Ordu Üniversitesi en_US
dc.contributor.authorID 0000-0003-1141-9838 en_US
dc.contributor.authorID 0000-0003-4236-6177 en_US
dc.contributor.authorID 0000-0003-4940-4498 en_US
dc.identifier.volume 29 en_US
dc.identifier.issue 2 en_US
dc.identifier.startpage 95 en_US
dc.identifier.endpage 98 en_US


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