Cited 0 times in
Cited 252 times in
Candida haemulonii and closely related species at 5 university hospitals in Korea: identification, antifungal susceptibility, and clinical features
DC Field | Value | Language |
---|---|---|
dc.contributor.author | 이경원 | - |
dc.date.accessioned | 2015-04-24T16:55:20Z | - |
dc.date.available | 2015-04-24T16:55:20Z | - |
dc.date.issued | 2009 | - |
dc.identifier.issn | 1058-4838 | - |
dc.identifier.uri | https://ir.ymlib.yonsei.ac.kr/handle/22282913/104423 | - |
dc.description.abstract | 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 microg/mL (MIC(50), 1 microg/mL), 2-128 microg/mL (MIC(50), 4 microg/mL), 0.125-4 microg/mL (MIC(50), 0.25 microg/mL), and 0.03-2 microg/mL (MIC(50), 0.06 microg/mL), respectively. All isolates were susceptible to caspofungin (MIC, 0.125-0.25 microg/mL) and micafungin (MIC, 0.03-0.06 microg/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 microg/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 | - |
dc.description.statementOfResponsibility | open | - |
dc.format.extent | e57~e61 | - |
dc.relation.isPartOf | CLINICAL INFECTIOUS DISEASES | - |
dc.rights | CC BY-NC-ND 2.0 KR | - |
dc.rights.uri | https://creativecommons.org/licenses/by-nc-nd/2.0/kr/ | - |
dc.subject.MESH | Aged | - |
dc.subject.MESH | Antifungal Agents/pharmacology* | - |
dc.subject.MESH | Blood/microbiology | - |
dc.subject.MESH | Candida/classification* | - |
dc.subject.MESH | Candida/drug effects* | - |
dc.subject.MESH | Candida/isolation & purification | - |
dc.subject.MESH | Candidiasis/epidemiology* | - |
dc.subject.MESH | Candidiasis/microbiology | - |
dc.subject.MESH | Candidiasis/pathology | - |
dc.subject.MESH | Candidiasis/physiopathology | - |
dc.subject.MESH | Child | - |
dc.subject.MESH | Child, Preschool | - |
dc.subject.MESH | Cross Infection/epidemiology* | - |
dc.subject.MESH | Cross Infection/microbiology* | - |
dc.subject.MESH | Cross Infection/pathology | - |
dc.subject.MESH | Cross Infection/physiopathology | - |
dc.subject.MESH | DNA, Fungal/chemistry | - |
dc.subject.MESH | DNA, Fungal/genetics | - |
dc.subject.MESH | DNA, Ribosomal/chemistry | - |
dc.subject.MESH | DNA, Ribosomal/genetics | - |
dc.subject.MESH | DNA, Ribosomal Spacer/chemistry | - |
dc.subject.MESH | DNA, Ribosomal Spacer/genetics | - |
dc.subject.MESH | Female | - |
dc.subject.MESH | Hospitals, University | - |
dc.subject.MESH | Humans | - |
dc.subject.MESH | Infant | - |
dc.subject.MESH | Korea/epidemiology | - |
dc.subject.MESH | Male | - |
dc.subject.MESH | Microbial Sensitivity Tests | - |
dc.subject.MESH | Middle Aged | - |
dc.subject.MESH | Molecular Sequence Data | - |
dc.subject.MESH | Sequence Analysis, DNA | - |
dc.title | Candida haemulonii and closely related species at 5 university hospitals in Korea: identification, antifungal susceptibility, and clinical features | - |
dc.type | Article | - |
dc.contributor.college | College of Medicine (의과대학) | - |
dc.contributor.department | Dept. of Laboratory Medicine (진단검사의학) | - |
dc.contributor.googleauthor | Mi-Na Kim | - |
dc.contributor.googleauthor | Jong Hee Shin | - |
dc.contributor.googleauthor | Heungsup Sung | - |
dc.contributor.googleauthor | Kyungwon Lee | - |
dc.contributor.googleauthor | Eui-Chong Kim | - |
dc.contributor.googleauthor | Namhee Ryoo | - |
dc.contributor.googleauthor | Jin-Sol Lee | - |
dc.contributor.googleauthor | Sook-In Jung | - |
dc.contributor.googleauthor | Kyung Hwa Park | - |
dc.contributor.googleauthor | Seung Jung Kee | - |
dc.contributor.googleauthor | Soo Hyun Kim | - |
dc.contributor.googleauthor | Myung Geun Shin | - |
dc.contributor.googleauthor | Soon Pal Suh | - |
dc.contributor.googleauthor | Dong Wook 꾜뭏 | - |
dc.identifier.doi | 10.1086/597108 | - |
dc.admin.author | false | - |
dc.admin.mapping | false | - |
dc.contributor.localId | A02649 | - |
dc.relation.journalcode | J00581 | - |
dc.identifier.eissn | 1537-6591 | - |
dc.identifier.pmid | 19193113 | - |
dc.contributor.alternativeName | Lee, Kyung Won | - |
dc.contributor.affiliatedAuthor | Lee, Kyung Won | - |
dc.citation.volume | 48 | - |
dc.citation.number | 6 | - |
dc.citation.startPage | 57 | - |
dc.citation.endPage | 61 | - |
dc.identifier.bibliographicCitation | CLINICAL INFECTIOUS DISEASES, Vol.48(6) : 57-61, 2009 | - |
dc.identifier.rimsid | 54104 | - |
dc.type.rims | ART | - |
Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.