Abstract

Background and Purpose: Candidemia is one of the most important fungal infections caused by Candida species. Infections and mortality caused by Candida species have been on a growing trend during the past two decades. The resistance of yeasts to antifungal drugs and their epidemiological issues have highlighted the importance of accurately distinguishing the yeasts at the species level. The technique applied for yeast identification should be fast enough to facilitate the imminent initiation of the appropriate therapy. Candidemia has not been studied comprehensively in Iran yet. Regarding this, the current study aimed to assess the epidemiology of candidemia at Tehran hospitals and compare the results with the previous fi ndings. Materials and Methods: This study was conducted on 204 positive blood cultures obtained from 125 patients hospitalized in several hospitals located in Tehran, Iran, within a period of 13 months. The yeast isolation and species identification were accomplished using several phenotypic methods (i.e., production of germ tube in human serum, culture on CHROMagar Candida, and Corn meal agar containing Tween 80) and molecular methods, such as polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP). In addition, unknown cases were subjected to PCR sequencing. These methods were then compared in terms of accuracy, sensitivity, and speed of identi fi cation. Results: According to the results, C. albicans (62.4) was the most common isolate, followed by C. parapsilosis (n=36, 17.5), C. glabrata (n=18, 8.8), C. tropicalis (n=13, 6.3), Trichosporon asahii (n=3, 1.5), C. kefyr (n=2, 1.0), C. lusitaniae (n=2, 1.0), C. intermedia (n=1, 0.5), C. guilliermondii (n=1, 0.5), and C. krusei (n=1, 0.5), respectively. Conclusion: As the findings indicated, the most common species causing candidemia were C. albicans, C. parapsilosis, and C. glabrata, respectively. Children less than one year old and people with cancer were at higher risk for candidemia, compared to other groups. Moreover, phenotypic and molecular methods resulted in the identification of 65.2 and 96.6 of the isolates, respectively. Consequently, PCR-RFLP could be concluded as a more favorable technique for species identification.