首页> 外文期刊>Journal of Medical Microbiology: An Official Journal of the Pathological Society of Great Britain and Ireland >Transcriptional regulation of drug-resistance genes in Candida albicans biofilms in response to antifungals
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Transcriptional regulation of drug-resistance genes in Candida albicans biofilms in response to antifungals

机译:白念珠菌生物膜中抗药性基因对抗真菌药物的转录调控

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Biofilm formation is a major virulence attribute of Candida albicans and is directly associated with therapeutic failure. One method by which Candida acquires antifungal resistance is the expression of drug-resistance genes. This study aimed to evaluate the transcriptional regulation of several genes associated with antifungal resistance of C. albicans under planktonic, recently adhered and biofilm growth modes and in C. albicans biofilms in response to antifungal agents. Initially, the antifungal susceptibility of C. albicans cultures in different growth modes was evaluated by standard antifungal susceptibility testing. Next, to assess CDR1, CDR2, MDR1, ERG11, FKS1 and PIL1 expression, RNA was harvested from cells in each growth mode, and from biofilms after drug treatment, and subjected to quantitative real-time RT-PCR (qRT-PCR). Biofilm C. albicans was more resistant to antifungals than recently adhered cells and stationary-phase planktonic cultures. Transcriptional expression of CDR1, CDR2, MDR1, ERG11 and FKS1 was lower in recently adhered C. albicans than in the stationary-phase planktonic cultures. In contrast, PIL1 levels were significantly increased in recently adhered and biofilm modes of growth. The expression of MDR1 in biofilms greatly increased on challenge with amphotericin B but not with the other drugs tested (P&0.01). ERG11 was significantly upregulated by ketoconazole (P&0.01). Caspofungin and amphotericin B significantly upregulated FKS1 expression, whereas they significantly downregulated PIL1 expression (P&0.01). These results indicate that the expression of drug-resistance genes is associated with higher drug resistance of Candida biofilms, and lay a foundation for future large-scale genome-wide expression analysis.
机译:生物膜形成是白色念珠菌的主要毒力属性,与治疗失败直接相关。念珠菌获得抗真菌耐药性的一种方法是耐药基因的表达。这项研究的目的是评估浮游生物,最近粘附的生物膜生长模式和白色念珠菌生物膜对真菌的抗真菌抗性相关的几个基因的转录调控。最初,通过标准的抗真菌药敏试验评估了白色念珠菌培养物在不同生长方式下的抗真菌药敏性。接下来,为了评估CDR1,CDR2,MDR1,ERG11,FKS1和PIL1的表达,从每种生长模式的细胞以及药物处理后的生物膜中收获RNA,并进行实时定量RT-PCR(qRT-PCR)。生物膜白色念珠菌比最近粘附的细胞和固定相浮游培养物对真菌的抵抗力更强。在最近粘附的白色念珠菌中,CDR1,CDR2,MDR1,ERG11和FKS1的转录表达低于固定相浮游培养。相反,在最近粘附的和生物膜生长模式中,PIL1水平显着增加。当用两性霉素B攻击时,生物膜中MDR1的表达大大增加,但用其他测试的药物则没有(P <0.01)。酮康唑显着上调了ERG11(P <0.01)。卡泊芬净和两性霉素B显着上调FKS1表达,而它们显着下调PIL1表达(P <0.01)。这些结果表明,耐药基因的表达与念珠菌生物膜的较高耐药性相关,并为将来大规模基因组范围内的表达分析奠定了基础。

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