Barker Katherine S, Pearson Margaret M, Rogers P David
Department of Pharmacy, College of Pharmacy, University of Tennessee Health Science Center, Memphis, 38163, USA.
J Antimicrob Chemother. 2003 May;51(5):1131-40. doi: 10.1093/jac/dkg217. Epub 2003 Apr 14.
An isolate of S. cerevisiae with reduced susceptibility to fluconazole and itraconazole was developed in the laboratory and used to identify genes that are differentially expressed in association with this phenotype.
S. cerevisiae strain ATCC 9763 was passaged in increasing concentrations of itraconazole. Itraconazole and fluconazole MICs for the initial isolate (9763S) were 2 and 16 mg/L and for the final isolate (9763I) were 16 and > or =64 mg/L, respectively. Duplicate sets of total RNA from 9763S and 9763I were isolated and hybridized to Affymetrix S98 yeast arrays. To validate results, six differentially expressed genes were further examined by RT-PCR.
Of the nearly 6400 open reading frames represented on the array, a total of 116 genes (1.8%) were found to be differentially expressed. Cell wall maintenance genes TIR4 and CCW12, sterol metabolism gene UPC2, small molecule transport genes AUS1 and YHK8, and stress response gene CUP1-1 were expressed at a level at least 2.5-fold higher than the expression level found in 9763S. Eleven energy generation genes, ionic homeostasis genes FRE1, FRE2 and FRE4, and sterol metabolism genes ERG8 and ERG13 were expressed at least 2.5-fold lower than the expression level found in 9763S.
Several genes found to be differentially expressed in this study have been shown previously to be differentially expressed in the fungal response to azole treatment. In addition, the potential role of AUS1 and/or YHK8 as mediators of drug efflux is intriguing and warrants further study.
在实验室中培育出一株对氟康唑和伊曲康唑敏感性降低的酿酒酵母菌株,并用于鉴定与该表型相关的差异表达基因。
将酿酒酵母菌株ATCC 9763在浓度递增的伊曲康唑中传代培养。初始菌株(9763S)对伊曲康唑和氟康唑的最低抑菌浓度(MIC)分别为2mg/L和16mg/L,最终菌株(9763I)对伊曲康唑和氟康唑的MIC分别为16mg/L和≥64mg/L。从9763S和9763I中提取两组重复的总RNA,并与Affymetrix S98酵母基因芯片进行杂交。为验证结果,通过逆转录聚合酶链反应(RT-PCR)进一步检测了6个差异表达基因。
在芯片上代表的近6400个开放阅读框中,共发现116个基因(1.8%)差异表达。细胞壁维持基因TIR4和CCW12、甾醇代谢基因UPC2、小分子转运基因AUS1和YHK8以及应激反应基因CUP1-1的表达水平比9763S中的表达水平至少高2.5倍。11个能量产生基因、离子稳态基因FRE1、FRE2和FRE4以及甾醇代谢基因ERG8和ERG13的表达水平比9763S中的表达水平至少低2.5倍。
本研究中发现的几个差异表达基因先前已被证明在真菌对唑类药物治疗的反应中差异表达。此外,AUS1和/或YHK8作为药物外排介质的潜在作用很有趣,值得进一步研究。