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首页> 外文期刊>Molecular Microbiology >Identification and characterization of a Cryptococcus neoformans ATP binding cassette (ABC) transporter-encoding gene, CnAFR1, involved in the resistance to fluconazole.
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Identification and characterization of a Cryptococcus neoformans ATP binding cassette (ABC) transporter-encoding gene, CnAFR1, involved in the resistance to fluconazole.

机译:新型隐球菌ATP结合盒(ABC)转运蛋白编码基因CnAFR1的鉴定和表征,涉及对氟康唑的耐药性。

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Resistance to fluconazole is a possible event during prolonged suppressive drug therapy for cryptococ-cal meningitis, the most frequently encountered life-threatening manifestation of cryptococcosis. The knowledge of this resistance at the molecular level is important for management of cryptococcosis. In order to identify genes involved in azole resistance in Cryptococcus neoformans, a cDNA subtraction library technique was chosen as a strategy. First, a fluconazole-resistant mutant BPY22.17 was obtained from a susceptible clinical isolate BPY22 by in vitro exposure to the drug. Then, a subtractive hybridization procedure was used to compare gene expression between the obtained strains. We identified a cDNA overexpressed in the fluconazole-resistant strain BPY22.17 that was used as a probe to isolate the entire gene in a C. neoformans genomic library. Sequence analysis of this gene identified an ATP Binding Cassette (ABC) transporter-encoding gene called C. neoformans AntiFungal Resistance 1 (CnAFR1). Disruption of CnAFR1 gene in the resistant isolate (BPY22.17) resulted in an enhanced susceptibility of the knock-out mutant cnafr1 against fluconazole, whereas reintroduction of the gene in cnafr1 resulted in restoration of the resistance phenotype, thus confirming that CnAFR1 is involved in fluconazole resistance of C. neoformans. Our findings therefore reveal that an active drug efflux mechanism can be involved in the development of azole resistance in this important human pathogen.
机译:对于隐球菌性脑膜炎(最常遇到的威胁生命的隐球菌病表现),在长期抑制性药物治疗期间,对氟康唑的耐药性可能是事件。在分子水平上对这种抗性的了解对于隐球菌病的管理很重要。为了鉴定新隐球菌中与吡咯抗性有关的基因,选择了cDNA扣除文库技术作为策略。首先,通过体外暴露于药物,从易感的临床分离株BPY22获得了耐氟康唑的突变体BPY22.17。然后,使用减性杂交程序比较获得的菌株之间的基因表达。我们鉴定了在耐氟康唑的菌株BPY22.17中过表达的cDNA,它被用作探针来分离新孢梭菌基因组文库中的整个基因。此基因的序列分析确定了ATP结合盒(ABC)转运蛋白编码基因,称为新孢子虫抗真菌抗性1(CnAFR1)。抗性分离株(BPY22.17)中CnAFR1基因的破坏导致敲除突变体cnafr1对氟康唑的敏感性增强,而cnafr1中基因的重新导入导致抗性表型的恢复,因此证实CnAFR1参与了耐新氟虫对氟康唑的耐药性。因此,我们的发现表明,在这种重要的人类病原体中,积极的药物外流机制可能与吡咯抗性的发展有关。

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