Manchester Academic Health Science Centre, NIHR Translational Research Facility in Respiratory Medicine, University Hospital of South Manchester NHS Foundation Trust, The University of Manchester, Manchester, UK.
FEMS Microbiol Lett. 2012 Jul;332(1):10-9. doi: 10.1111/j.1574-6968.2012.02575.x. Epub 2012 May 21.
Azoles are currently the mainstay of antifungal treatment both in agricultural and in clinical settings. Although the target site of azole action is well studied, the basis of azole resistance and the ultimate mode of action of the drug in fungi are poorly understood. To gain a deeper insight into these aspects of azole action, restriction-mediated plasmid integration (REMI) was used to create azole sensitive and resistant strains of the clinically important fungus Aspergillus fumigatus. Four azole sensitive insertions and four azole-resistant insertions were characterized. Three phenotypes could be re-created in wild-type AF210 by reintegration of rescued plasmid and a further four could be confirmed by complementation of the mutant phenotype with a copy of the wild-type gene predicted to be disrupted by the original insertional event. Six insertions were in genes not previously associated with azole sensitivity or resistance. Two insertions occur in transporter genes that may affect drug efflux, whereas others may affect transcriptional regulation of sterol biosynthesis genes and NADH metabolism in the mitochondrion. Two insertions are in genes of unknown function.
唑类药物目前是农业和临床环境中抗真菌治疗的主要药物。尽管唑类药物作用的靶标位点研究得很好,但唑类耐药的基础以及药物在真菌中的最终作用模式仍知之甚少。为了更深入地了解唑类药物作用的这些方面,使用限制介导的质粒整合(REMI)技术创建了临床上重要的真菌烟曲霉中的唑类敏感和耐药菌株。对四个唑类敏感插入和四个唑类耐药插入进行了表征。通过回收质粒的再整合,可以在野生型 AF210 中重新创建三种表型,并且可以通过用原始插入事件预测破坏的野生型基因的拷贝来互补突变表型来进一步确认另外四种表型。六个插入位于先前与唑类敏感性或耐药性无关的基因中。两个插入发生在可能影响药物外排的转运基因中,而其他插入可能影响固醇生物合成基因的转录调控和线粒体中的 NADH 代谢。两个插入位于功能未知的基因中。