TY - JOUR
T1 - Candida haemulonii and closely related species at 5 university hospitals in Korea
T2 - Identification, antifungal susceptibility, and clinical features
AU - Kim, Mi Na
AU - Shin, Jong Hee
AU - Sung, Heungsup
AU - Lee, Kyungwon
AU - Kim, Eui Chong
AU - Ryoo, Namhee
AU - Lee, Jin Sol
AU - Jung, Sook Ln
AU - Park, Kyung Hwa
AU - Kee, Seung Jung
AU - Kim, Soo Hyun
AU - Shin, Myung Geun
AU - Suh, Soon Pal
AU - Ryang, Dong Wook
N1 - Funding Information:
Financial support. The Korea Research Foundation Grant, funded by the Korean Government (MOEHRD) (KRF-2007-E00432). Potential conflicts of interest. All authors: no conflicts.
PY - 2009/3/15
Y1 - 2009/3/15
N2 - Background. Candida haemulonii, a yeast species that often exhibits antifungal resistance, rarely causes human infection. During 2004-2006, unusual yeast isolates with phenotypic similarity to C, haemulonii were recovered from 23 patients (8 patients with fungemia and 15 patients with chronic otitis media) in 5 hospitals in Korea. Methods. Isolates were characterized using D1/D2 domain and ITS gene sequencing, and the susceptibility of the isolates to 6 antifungal agents was tested in vitro. Results. Gene sequencing of the blood isolates confirmed C. haemulonii group I (in 1 patient) and Candida pseudohaemulonii (in 7 patients), whereas all isolates recovered from the ear were a novel species of which C. haemulonii is its closest relative. The minimum inhibitory concentration (MIC) ranges of amphotericin B, fluconazole, itraconazole, and voriconazole for all isolates were 0.5-32 μg/mL (MIC 50, 1 μg/mL), 2-128 μg/mL (MIC 50, 4 μg/mL), 0.125-4 μg/mL (MIC 50, 0.25 μg/mL), and 0.03-2 μg/mL (MIC 50, 0.06 μg/mL), respectively. All isolates were susceptible to caspofungin (MIC, 0.125-0.25 μg/mL) and micafungin (MIC, 0.03-0.06 μg/mL). All cases of fungemia occurred in patients with severe underlying diseases who had central venous catheters. Three patients developed breakthrough fungemia while receiving antifungal therapy, and amphotericin B therapeutic failure, which was associated with a high MIC of amphotericin B (32 μg/mL), was observed in 2 patients. Conclusions. Candida species that are closely related to C haemulonii are emerging sources of infection in Korea. These species show variable patterns of susceptibility to amphotericin B and azole antifungal agents.
AB - Background. Candida haemulonii, a yeast species that often exhibits antifungal resistance, rarely causes human infection. During 2004-2006, unusual yeast isolates with phenotypic similarity to C, haemulonii were recovered from 23 patients (8 patients with fungemia and 15 patients with chronic otitis media) in 5 hospitals in Korea. Methods. Isolates were characterized using D1/D2 domain and ITS gene sequencing, and the susceptibility of the isolates to 6 antifungal agents was tested in vitro. Results. Gene sequencing of the blood isolates confirmed C. haemulonii group I (in 1 patient) and Candida pseudohaemulonii (in 7 patients), whereas all isolates recovered from the ear were a novel species of which C. haemulonii is its closest relative. The minimum inhibitory concentration (MIC) ranges of amphotericin B, fluconazole, itraconazole, and voriconazole for all isolates were 0.5-32 μg/mL (MIC 50, 1 μg/mL), 2-128 μg/mL (MIC 50, 4 μg/mL), 0.125-4 μg/mL (MIC 50, 0.25 μg/mL), and 0.03-2 μg/mL (MIC 50, 0.06 μg/mL), respectively. All isolates were susceptible to caspofungin (MIC, 0.125-0.25 μg/mL) and micafungin (MIC, 0.03-0.06 μg/mL). All cases of fungemia occurred in patients with severe underlying diseases who had central venous catheters. Three patients developed breakthrough fungemia while receiving antifungal therapy, and amphotericin B therapeutic failure, which was associated with a high MIC of amphotericin B (32 μg/mL), was observed in 2 patients. Conclusions. Candida species that are closely related to C haemulonii are emerging sources of infection in Korea. These species show variable patterns of susceptibility to amphotericin B and azole antifungal agents.
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U2 - 10.1086/597108
DO - 10.1086/597108
M3 - Article
C2 - 19193113
AN - SCOPUS:62449106111
SN - 1058-4838
VL - 48
SP - e57-e61
JO - Clinical Infectious Diseases
JF - Clinical Infectious Diseases
IS - 6
ER -