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Resistance Mechanisms and Clinical Features of Fluconazole-Nonsusceptible Candida tropicalis Isolates Compared with Fluconazole-Less-Susceptible Isolates

DC Field Value Language
dc.contributor.author이경원-
dc.date.accessioned2017-10-26T07:29:45Z-
dc.date.available2017-10-26T07:29:45Z-
dc.date.issued2016-
dc.identifier.issn0066-4804-
dc.identifier.urihttps://ir.ymlib.yonsei.ac.kr/handle/22282913/152105-
dc.description.abstractWe investigated the azole resistance mechanisms and clinical features of fluconazole-nonsusceptible (FNS) isolates of Candida tropicalis recovered from Korean surveillance cultures in comparison with fluconazole-less-susceptible (FLS) isolates. Thirty-five clinical isolates of C. tropicalis, comprising 9 FNS (fluconazole MIC, 4 to 64 μg/ml), 12 FLS (MIC, 1 to 2 μg/ml), and 14 control (MIC, 0.125 to 0.5 μg/ml) isolates, were assessed. CDR1, MDR1, and ERG11 expression was quantified, and the ERG11 and UPC2 genes were sequenced. Clinical features of 16 patients with FNS or FLS bloodstream isolates were analyzed. Both FNS and FLS isolates had >10-fold higher mean expression levels of CDR1, MDR1, and ERG11 genes than control isolates (P values of <0.02 for all). When FNS and FLS isolates were compared, FNS isolates had 3.4-fold higher mean ERG11 expression levels than FLS isolates (P = 0.004), but there were no differences in those of CDR1 or MDR1 Of all 35 isolates, 4 (2 FNS and 2 FLS) and 28 (8 FNS, 11 FLS, and 9 control) isolates exhibited amino acid substitutions in Erg11p and Upc2p, respectively. Both FNS and FLS bloodstream isolates were associated with azole therapeutic failure (3/4 versus 4/7) or uncleared fungemia (4/6 versus 4/10), but FNS isolates were identified more frequently from patients with previous azole exposure (6/6 versus 3/10; P = 0.011) and immunosuppression (6/6 versus 3/10; P = 0.011). These results reveal that the majority of FNS C. tropicalis isolates show overexpression of CDR1, MDR1, and ERG11 genes, and fungemia develops after azole exposure in patients with immunosuppression.-
dc.description.statementOfResponsibilityopen-
dc.publisherAmerican Society for Microbiology-
dc.relation.isPartOfANTIMICROBIAL AGENTS AND CHEMOTHERAPY-
dc.rightsCC BY-NC-ND 2.0 KR-
dc.rights.urihttps://creativecommons.org/licenses/by-nc-nd/2.0/kr/-
dc.subject.MESHATP-Binding Cassette Transporters/genetics-
dc.subject.MESHATP-Binding Cassette Transporters/metabolism-
dc.subject.MESHATP-Binding Cassette, Sub-Family B, Member 1/genetics-
dc.subject.MESHATP-Binding Cassette, Sub-Family B, Member 1/metabolism-
dc.subject.MESHAmino Acid Substitution-
dc.subject.MESHAntifungal Agents/pharmacology-
dc.subject.MESHCandida tropicalis/drug effects-
dc.subject.MESHCandida tropicalis/genetics*-
dc.subject.MESHCandida tropicalis/growth & development-
dc.subject.MESHCandida tropicalis/isolation & purification-
dc.subject.MESHCandidiasis/drug therapy-
dc.subject.MESHCandidiasis/etiology-
dc.subject.MESHCandidiasis/immunology-
dc.subject.MESHCandidiasis/microbiology*-
dc.subject.MESHCytochrome P-450 Enzyme System/genetics-
dc.subject.MESHCytochrome P-450 Enzyme System/metabolism-
dc.subject.MESHDrug Resistance, Fungal/genetics*-
dc.subject.MESHFemale-
dc.subject.MESHFluconazole/pharmacology-
dc.subject.MESHFungal Proteins/genetics*-
dc.subject.MESHFungal Proteins/metabolism-
dc.subject.MESHFungemia/drug therapy-
dc.subject.MESHFungemia/etiology-
dc.subject.MESHFungemia/immunology-
dc.subject.MESHFungemia/microbiology*-
dc.subject.MESHGene Expression-
dc.subject.MESHHumans-
dc.subject.MESHImmunosuppressive Agents/adverse effects-
dc.subject.MESHMale-
dc.subject.MESHMicrobial Sensitivity Tests-
dc.subject.MESHMutation*-
dc.subject.MESHPublic Health Surveillance-
dc.subject.MESHRepublic of Korea-
dc.subject.MESHSequence Analysis, DNA-
dc.subject.MESHTrans-Activators/genetics-
dc.subject.MESHTrans-Activators/metabolism-
dc.titleResistance Mechanisms and Clinical Features of Fluconazole-Nonsusceptible Candida tropicalis Isolates Compared with Fluconazole-Less-Susceptible Isolates-
dc.typeArticle-
dc.publisher.locationUnited States-
dc.contributor.collegeCollege of Medicine-
dc.contributor.departmentDept. of Laboratory Medicine-
dc.contributor.googleauthorMin Ji Choi-
dc.contributor.googleauthorEun Jeong Won-
dc.contributor.googleauthorJong Hee Shin-
dc.contributor.googleauthorSoo Hyun Kim-
dc.contributor.googleauthorWee-Gyo Lee-
dc.contributor.googleauthorMi-Na Kim-
dc.contributor.googleauthorKyungwon Lee-
dc.contributor.googleauthorMyung Geun Shin-
dc.contributor.googleauthorSoon Pal Suh-
dc.contributor.googleauthorDong Wook Ryang-
dc.contributor.googleauthorYoung Jun Im-
dc.identifier.doi10.1128/AAC.02652-15-
dc.contributor.localIdA02649-
dc.relation.journalcodeJ00189-
dc.identifier.eissn1098-6596-
dc.identifier.pmid27044550-
dc.contributor.alternativeNameLee, Kyung Won-
dc.contributor.affiliatedAuthorLee, Kyung Won-
dc.citation.volume60-
dc.citation.number6-
dc.citation.startPage3653-
dc.citation.endPage3661-
dc.identifier.bibliographicCitationANTIMICROBIAL AGENTS AND CHEMOTHERAPY, Vol.60(6) : 3653-3661, 2016-
dc.date.modified2017-10-24-
dc.identifier.rimsid46885-
dc.type.rimsART-
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Laboratory Medicine (진단검사의학교실) > 1. Journal Papers

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