Zeng Yue-bin, Qian Yuan-shu, Ma Lian, Gu Hong-ni
The Second Affiliated Hospital of Shantou University Medical College, Shantou 515041, China.
Chin Med J (Engl). 2007 May 5;120(9):807-13.
Candida albicans is the most frequently seen opportunistic human fungal pathogen. Terbinafine is an allylamine antifungal agent that has been proven to have high clinical efficacy in the therapy of fungal infections, the mechanism of action of terbinafine involves the specific inhibition of fungal squalene epoxidase, resulting in ergosterol deficiency and accumulation of intracellular squalene. We used cDNA microarray analysis technology to monitor global expression profile changes of Candida albicans genes in response to terbinafine treatment, and we anticipated a panoramic view of the responses of Candida albicans cells to the representatives of allylamine antifungal agents at the molecular level in an effort to identify drug class-specific and mechanism-independent changes in gene expression.
Candida albicans strain ATCC 90028 was exposed to either medium alone or terbinafine at a concentration equivalent to the 1/2 minimal inhibitory concentrations (MICs, 4 mg/L) for 90 minutes. RNA was isolated and gene expression profiles were compared to identify the changes in the gene expression profile using a cDNA microarray analysis. Differential expression of 10 select genes detected by cDNA microarray analysis was confirmed by semi-quantitative reverse transcription-polymerase chain reaction (RT-PCR).
A total of 222 genes were found to be responsive to terbinafine, including 121 up-regulated genes and 101 down-regulated genes. These included genes encoding membrane transport proteins belonging to the members of the ATP-binding cassette (ABC) or major facilitator superfamily (MFS; CDR1, AGP2, GAP6, PHO84, HOL3, FCY23, VCX1), genes involved in stress response and detoxification (CDR1, AGP2, HOL3), and gene involved in the ergosterol biosynthesis pathway (ERG12). The results of semi-quantitative RT-PCR were consistent with that of the cDNA microarray analysis.
The up-regulation of the gene encoding the multidrug resistance efflux pump CDR1 may contribute to the terbinafine resistance in Candida albicans. However, the precise roles of other affected genes remain unclear, further studies of these genes and their respective products that play roles in the context of antifungal resistance are warranted.
白色念珠菌是最常见的人类机会性真菌病原体。特比萘芬是一种烯丙胺类抗真菌剂,已被证明在真菌感染治疗中具有较高的临床疗效,其作用机制涉及特异性抑制真菌角鲨烯环氧酶,导致麦角固醇缺乏和细胞内角鲨烯积累。我们使用cDNA微阵列分析技术监测白色念珠菌基因在特比萘芬处理后的整体表达谱变化,期望在分子水平上全景式了解白色念珠菌细胞对烯丙胺类抗真菌剂代表药物的反应,以识别基因表达中药物类别特异性和与作用机制无关的变化。
将白色念珠菌ATCC 90028菌株分别暴露于单独培养基或相当于1/2最小抑菌浓度(MIC,4mg/L)的特比萘芬中90分钟。分离RNA并比较基因表达谱,使用cDNA微阵列分析确定基因表达谱的变化。通过半定量逆转录-聚合酶链反应(RT-PCR)确认cDNA微阵列分析检测到的10个选定基因的差异表达。
共发现222个基因对特比萘芬有反应,包括121个上调基因和101个下调基因。这些基因包括编码属于ATP结合盒(ABC)成员或主要易化子超家族(MFS;CDR1、AGP2、GAP6、PHO84、HOL3、FCY23、VCX1)的膜转运蛋白的基因、参与应激反应和解毒的基因(CDR1、AGP2、HOL3)以及参与麦角固醇生物合成途径的基因(ERG12)。半定量RT-PCR结果与cDNA微阵列分析结果一致。
编码多药耐药外排泵CDR1的基因上调可能导致白色念珠菌对特比萘芬耐药。然而,其他受影响基因的确切作用仍不清楚,有必要进一步研究这些基因及其在抗真菌耐药背景下发挥作用的各自产物。