Publications

Detailed Information

Candida haemulonii and Closely Related Species at 5 University Hospitals in Korea: Identification, Antifungal Susceptibility, and Clinical Features

DC Field Value Language
dc.contributor.authorKim, Mi-Na-
dc.contributor.authorShin, Jong Hee-
dc.contributor.authorSung, Heungsup-
dc.contributor.authorLee, Kyungwon-
dc.contributor.authorRyoo, Namhee-
dc.contributor.authorJung, Sook-In-
dc.contributor.authorKee, Seung Jung-
dc.contributor.authorShin, Myung Geun-
dc.contributor.authorRyang, Dong Wook-
dc.contributor.authorSuh, Soon Pal-
dc.contributor.authorKim, Soo Hyun-
dc.contributor.authorPark, Kyung Hwa-
dc.contributor.authorLee, Jin-Sol-
dc.contributor.authorKim, Eui-Chong-
dc.date.accessioned2012-05-24T05:37:53Z-
dc.date.available2012-05-24T05:37:53Z-
dc.date.issued2009-03-15-
dc.identifier.citationCLINICAL INFECTIOUS DISEASES; Vol.48 6; e57-e61ko_KR
dc.identifier.issn1058-4838-
dc.identifier.urihttps://hdl.handle.net/10371/76409-
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 mu g/mL (MIC(50), 1 mu g/mL), 2-128 mu g/mL (MIC(50), 4 mu g/mL), 0.125-4 mu g/mL (MIC(50), 0.25 mu g/mL), and 0.03-2 mu g/mL (MIC(50), 0.06 mu g/mL), respectively. All isolates were susceptible to caspofungin (MIC, 0.125-0.25 mu g/mL) and micafungin (MIC, 0.03-0.06 mu g/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 mu g/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.ko_KR
dc.language.isoenko_KR
dc.publisherUNIV CHICAGO PRESSko_KR
dc.titleCandida haemulonii and Closely Related Species at 5 University Hospitals in Korea: Identification, Antifungal Susceptibility, and Clinical Featuresko_KR
dc.typeArticleko_KR
dc.contributor.AlternativeAuthor김미나-
dc.contributor.AlternativeAuthor신종희-
dc.contributor.AlternativeAuthor성흥섭-
dc.contributor.AlternativeAuthor이경원-
dc.contributor.AlternativeAuthor김의종-
dc.contributor.AlternativeAuthor류남희-
dc.contributor.AlternativeAuthor이진솔-
dc.contributor.AlternativeAuthor정숙인-
dc.contributor.AlternativeAuthor박경화-
dc.contributor.AlternativeAuthor기승정-
dc.contributor.AlternativeAuthor김수현-
dc.contributor.AlternativeAuthor신명근-
dc.contributor.AlternativeAuthor서순팔-
dc.contributor.AlternativeAuthor양동욱-
dc.identifier.doi10.1086/597108-
dc.citation.journaltitleCLINICAL INFECTIOUS DISEASES-
dc.description.citedreferenceShin JH, 2007, J CLIN MICROBIOL, V45, P2385, DOI 10.1128/JCM.00381-07-
dc.description.citedreferenceKhan ZU, 2007, J CLIN MICROBIOL, V45, P2025, DOI 10.1128/JCM.00222-07-
dc.description.citedreferenceLee JS, 2007, J CLIN MICROBIOL, V45, P1005, DOI 10.1128/JCM.02264-06-
dc.description.citedreferencePfaller MA, 2006, J CLIN MICROBIOL, V44, P819, DOI 10.1128/JCM.44.3.819-826.2006-
dc.description.citedreferenceSugita T, 2006, MICROBIOL IMMUNOL, V50, P469-
dc.description.citedreferenceClancy CJ, 2005, ANTIMICROB AGENTS CH, V49, P3171, DOI 10.1128/AAC.49.8.3171-3177.2005-
dc.description.citedreferenceOdds FC, 2004, J CLIN MICROBIOL, V42, P3475, DOI 10.1128/JCM.42.8.3475-3482.2004-
dc.description.citedreferenceRodero L, 2002, J CLIN MICROBIOL, V40, P2266, DOI 10.1128/JCM.40.6.2266-2269.2002-
dc.description.citedreference*CLSI, 2002, M27A2 CLSI-
dc.description.citedreferenceSugita T, 1999, J CLIN MICROBIOL, V37, P1985-
dc.description.citedreferencePfaller MA, 1998, DIAGN MICR INFEC DIS, V32, P223-
dc.description.citedreferenceNguyen MH, 1998, J INFECT DIS, V177, P425-
dc.description.citedreferenceKurtzman CP, 1997, J CLIN MICROBIOL, V35, P1216-
dc.description.citedreferenceLEHMANN PF, 1993, J CLIN MICROBIOL, V31, P1683-
dc.description.citedreferenceGARGEYA IB, 1991, J MED VET MYCOL, V29, P335-
dc.description.tc8-
Appears in Collections:
Files in This Item:

Altmetrics

Item View & Download Count

  • mendeley

Items in S-Space are protected by copyright, with all rights reserved, unless otherwise indicated.

Share