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Candida haemulonii and closely related species at 5 university hospitals in Korea: identification, antifungal susceptibility, and clinical features

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dc.contributor.author이경원-
dc.date.accessioned2015-04-24T16:55:20Z-
dc.date.available2015-04-24T16:55:20Z-
dc.date.issued2009-
dc.identifier.issn1058-4838-
dc.identifier.urihttps://ir.ymlib.yonsei.ac.kr/handle/22282913/104423-
dc.description.abstractBackground. 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.statementOfResponsibilityopen-
dc.format.extente57~e61-
dc.relation.isPartOfCLINICAL INFECTIOUS DISEASES-
dc.rightsCC BY-NC-ND 2.0 KR-
dc.rights.urihttps://creativecommons.org/licenses/by-nc-nd/2.0/kr/-
dc.subject.MESHAged-
dc.subject.MESHAntifungal Agents/pharmacology*-
dc.subject.MESHBlood/microbiology-
dc.subject.MESHCandida/classification*-
dc.subject.MESHCandida/drug effects*-
dc.subject.MESHCandida/isolation & purification-
dc.subject.MESHCandidiasis/epidemiology*-
dc.subject.MESHCandidiasis/microbiology-
dc.subject.MESHCandidiasis/pathology-
dc.subject.MESHCandidiasis/physiopathology-
dc.subject.MESHChild-
dc.subject.MESHChild, Preschool-
dc.subject.MESHCross Infection/epidemiology*-
dc.subject.MESHCross Infection/microbiology*-
dc.subject.MESHCross Infection/pathology-
dc.subject.MESHCross Infection/physiopathology-
dc.subject.MESHDNA, Fungal/chemistry-
dc.subject.MESHDNA, Fungal/genetics-
dc.subject.MESHDNA, Ribosomal/chemistry-
dc.subject.MESHDNA, Ribosomal/genetics-
dc.subject.MESHDNA, Ribosomal Spacer/chemistry-
dc.subject.MESHDNA, Ribosomal Spacer/genetics-
dc.subject.MESHFemale-
dc.subject.MESHHospitals, University-
dc.subject.MESHHumans-
dc.subject.MESHInfant-
dc.subject.MESHKorea/epidemiology-
dc.subject.MESHMale-
dc.subject.MESHMicrobial Sensitivity Tests-
dc.subject.MESHMiddle Aged-
dc.subject.MESHMolecular Sequence Data-
dc.subject.MESHSequence Analysis, DNA-
dc.titleCandida haemulonii and closely related species at 5 university hospitals in Korea: identification, antifungal susceptibility, and clinical features-
dc.typeArticle-
dc.contributor.collegeCollege of Medicine (의과대학)-
dc.contributor.departmentDept. of Laboratory Medicine (진단검사의학)-
dc.contributor.googleauthorMi-Na Kim-
dc.contributor.googleauthorJong Hee Shin-
dc.contributor.googleauthorHeungsup Sung-
dc.contributor.googleauthorKyungwon Lee-
dc.contributor.googleauthorEui-Chong Kim-
dc.contributor.googleauthorNamhee Ryoo-
dc.contributor.googleauthorJin-Sol Lee-
dc.contributor.googleauthorSook-In Jung-
dc.contributor.googleauthorKyung Hwa Park-
dc.contributor.googleauthorSeung Jung Kee-
dc.contributor.googleauthorSoo Hyun Kim-
dc.contributor.googleauthorMyung Geun Shin-
dc.contributor.googleauthorSoon Pal Suh-
dc.contributor.googleauthorDong Wook 꾜뭏-
dc.identifier.doi10.1086/597108-
dc.admin.authorfalse-
dc.admin.mappingfalse-
dc.contributor.localIdA02649-
dc.relation.journalcodeJ00581-
dc.identifier.eissn1537-6591-
dc.identifier.pmid19193113-
dc.contributor.alternativeNameLee, Kyung Won-
dc.contributor.affiliatedAuthorLee, Kyung Won-
dc.citation.volume48-
dc.citation.number6-
dc.citation.startPage57-
dc.citation.endPage61-
dc.identifier.bibliographicCitationCLINICAL INFECTIOUS DISEASES, Vol.48(6) : 57-61, 2009-
dc.identifier.rimsid54104-
dc.type.rimsART-
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Laboratory Medicine (진단검사의학교실) > 1. Journal Papers

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