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dc.contributor.authorLo, Hsiu Jungen_US
dc.contributor.authorTseng, Kuo-Yunen_US
dc.contributor.authorKao, Yeong-Yien_US
dc.contributor.authorTsao, Ming-Yangen_US
dc.contributor.authorLo, Han-Lunen_US
dc.contributor.authorYang, Yun-Liangen_US
dc.date.accessioned2015-07-21T08:28:06Z-
dc.date.available2015-07-21T08:28:06Z-
dc.date.issued2015-06-01en_US
dc.identifier.issn0924-8579en_US
dc.identifier.urihttp://dx.doi.org/10.1016/j.ijantimicag.2015.01.017en_US
dc.identifier.urihttp://hdl.handle.net/11536/124794-
dc.description.abstractThe cph1/cph1 efg1/efg1 double mutant in Candida albicans is defective in filamentous growth and is avirulent in a mouse model. We previously reported that Efg1p but not Cph1p is involved in drug resistance by negatively regulating ERG3 in C. albicans. In the current study, we have found that overexpression of 0411 in Saccharomyces cerevisiae increases susceptibility to the antifungal drug fluconazole. Furthermore, in C. albicans, null mutation of 0411 increased the expression of MDR1 as well as decreased susceptibility to fluconazole and voriconazole but not to amphotericin B. These findings indicate that although Efg1p and Cph1p may have the same effects on virulence, they have opposite effects on drug resistance in C. albicans. (C) 2015 Elsevier B.V. and the International Society of Chemotherapy. All rights reserved.en_US
dc.language.isoen_USen_US
dc.subjectCandida albicansen_US
dc.subjectDrug resistanceen_US
dc.subjectEfflux pumpen_US
dc.subjectVirulence factoren_US
dc.subjectRegulationen_US
dc.titleCph1p negatively regulates MDR1 involved in drug resistance in Candida albicansen_US
dc.typeArticleen_US
dc.identifier.doi10.1016/j.ijantimicag.2015.01.017en_US
dc.identifier.journalINTERNATIONAL JOURNAL OF ANTIMICROBIAL AGENTSen_US
dc.citation.volume45en_US
dc.citation.spage617en_US
dc.citation.epage621en_US
dc.contributor.department生物科技學系zh_TW
dc.contributor.department分子醫學與生物工程研究所zh_TW
dc.contributor.departmentDepartment of Biological Science and Technologyen_US
dc.contributor.departmentInstitute of Molecular Medicine and Bioengineeringen_US
dc.identifier.wosnumberWOS:000354569400009en_US
dc.citation.woscount0en_US
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