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Characterization of emeA, a norA Homolog and Multidrug Resistance Efflux Pump, in Enterococcus faecalis

机译:粪肠球菌emeA,norA同源和多药耐药性外排泵的特征

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摘要

We hypothesized that multidrug resistance efflux pumps (MDRs) may be contributing to the drug resistance of enterococci. We recently identified potential MDR-encoding genes in the Enterococcus faecalis V583 genome. Among the putative MDRs, we found a gene that encodes a NorA homolog and have characterized this enterococcal MDR in the present study. A mutant from which the enterococcal NorA homolog has been deleted has reduced resistance to several NorA substrates. Complementation of the deletion mutant with the wild-type gene verified the involvement of this enterococcal gene in resistance to ethidium bromide (EtBr) and norfloxacin. Known MDR inhibitors (reserpine, lansoprazole, and verapamil) inhibit the efflux of EtBr and norfloxacin in wild-type strain OG1RF. A fluorescence assay with EtBr allowed us to quantitate the efflux capability of the enterococcal NorA pump. On the basis of these results, we have named this enterococcal gene emeA (enterococcal multidrug resistance efflux).
机译:我们假设多药耐药性外排泵(MDR)可能有助于肠球菌的耐药性。我们最近在粪肠球菌V583基因组中发现了潜在的MDR编码基因。在推定的MDR中,我们发现了一个编码NorA同源物的基因,并在本研究中表征了该肠球菌MDR。删除了肠道球菌NorA同源物的突变体降低了对几种NorA底物的抗性。该缺失突变体与野生型基因的互补证实了该肠球菌基因参与了对溴乙锭(EtBr)和诺氟沙星的抗性。已知的MDR抑制剂(利血平,兰索拉唑和维拉帕米)可抑制EtBr和诺氟沙星在野生型OG1RF菌株中的流出。用EtBr进行的荧光测定使我们能够定量肠球菌NorA泵的流出能力。根据这些结果,我们将该肠球菌基因emeA(肠球菌多药耐药性流出)命名。

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