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Journal of Clinical Microbiology, August 2007, p. 2385-2391, Vol. 45, No. 8
0095-1137/07/$08.00+0     doi:10.1128/JCM.00381-07
Copyright © 2007, American Society for Microbiology. All Rights Reserved.

Changes in Karyotype and Azole Susceptibility of Sequential Bloodstream Isolates from Patients with Candida glabrata Candidemia{triangledown}

Jong Hee Shin,1* Myung Jong Chae,1 Jeong Won Song,1 Sook-In Jung,2 Duck Cho,1 Seung Jung Kee,1 Soo Hyun Kim,1 Myung Geun Shin,1 Soon Pal Suh,1 and Dong Wook Ryang1

Departments of Laboratory Medicine,1 Internal Medicine, Chonnam National University Medical School, Gwangju, South Korea2

Received 18 February 2007/ Returned for modification 10 April 2007/ Accepted 11 June 2007

We examined the changes in genotypes and azole susceptibilities among sequential bloodstream isolates of Candida glabrata during the course of fungemia and the relationship of these changes to antifungal therapy. Forty-one isolates were obtained from 15 patients (9 patients who received antifungal therapy and 6 patients who did not) over periods of up to 36 days. The isolates were analyzed using pulsed-field gel electrophoresis (PFGE) and multilocus sequence typing (MLST) and tested for antifungal susceptibility to fluconazole, itraconazole, and voriconazole. PFGE typing consisted of electrophoretic karyotyping and restriction endonuclease analysis of genomic DNA by use of NotI (REAG-N). The 41 isolates yielded 23 different karyotypes and 11 different REAG-N patterns but only 3 MLST types. The sequential strains from each patient had identical or similar REAG-N patterns. However, they had two or three different karyotypes in 6 (40%) of 15 patients. The isolates from these six patients exhibited the same or similar azole susceptibilities, and five patients did not receive antifungal therapy. Development of acquired azole resistance in sequential isolates was detected for only one patient. For this patient, an isolate of the same genotype obtained after azole therapy showed three- or fourfold increases in the MICs of all three azole antifungals and exhibited increased expression of the CgCDR1 efflux pump. This study shows that karyotypic changes can develop rapidly among sequential bloodstream strains of C. glabrata from the same patient without antifungal therapy. In addition, we confirmed that C. glabrata could acquire azole resistance during the course of fungemia in association with azole therapy.


* Corresponding author. Mailing address: Department of Laboratory Medicine, Chonnam National University Medical School, 8 Hakdong Dongku, Gwangju 501-757, South Korea. Phone: 82 (62) 220-5342. Fax: 82 (62) 224-2518. E-mail: shinjh{at}chonnam.ac.kr

{triangledown} Published ahead of print on 20 June 2007.


Journal of Clinical Microbiology, August 2007, p. 2385-2391, Vol. 45, No. 8
0095-1137/07/$08.00+0     doi:10.1128/JCM.00381-07
Copyright © 2007, American Society for Microbiology. All Rights Reserved.




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