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Investigation on the effect of known potent S. aureus NorA efflux pump inhibitors on the staphylococcal biofilm formation

机译:研究已知强效 S的效果。金黄色葡萄球菌NorA外排泵抑制剂对葡萄球菌生物膜形成的影响

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The emergence of multidrug resistant microorganisms has triggered the impending need of developing effective antibacterial strategies. Staphylococcus epidermidis and the more virulent S. aureus are able to colonize and form biofilms on implanted medical devices causing clinical acute and chronic infections. The aim of the present work was to assess the effect of NorA efflux pump inhibitors (EPIs) on S. aureus and S. epidermidis biofilm formation by using known synthetic NorA EPIs and thus giving support to the hypothesis that efflux pumps could play an intriguing role in Staphylococcus biofilm formation. In particular, three 2-phenylquinolines (1a–c) and a pyrazolobenzothiazine (2), our previously reported NorA EPIs, at concentrations lower than MIC showed a good ability in reducing biofilm formation in S. aureus (ATCC 29213) and S. epidermidis (ATCC 35984). Then, to assess if biofilm formation inhibitors could be combined with an antibacterial to limit biofilm production, the two best compounds 1c and 2 were tested with ciprofloxacin (CPX) and the results showed an excellent synergistic effect against Staphylococcus strains with a biofilm formation inhibition over 60% at low concentrations. Further, to confirm the involvement of the NorA efflux pump in the biofilm production, NorA EPIs 1c and 2 were tested against a modified S. aureus strain overexpressing the NorA efflux pump (SA-1199B) and results highlighted a strong decrease in biofilm mass. In conclusion, cytotoxicity assays on HeLa and HepG2 cells showed that concentrations useful to inhibit biofilm formation in Staphylococcus strains in combination with CPX were lower than the toxic concentrations for human cells.
机译:多药耐药性微生物的出现触发了开发有效抗菌策略的迫切需求。 表皮葡萄球菌和毒性更强的 S。金黄色葡萄球菌能够在植入的医疗设备上定植并形成生物膜,从而引起临床急性和慢性感染。本工作的目的是评估NorA外排泵抑制剂(EPI)对 S的影响。金黄色 S。通过使用已知的合成NorA EPIs形成表皮生物膜,从而为以下假设提供支持:外排泵可能在葡萄球菌生物膜形成中起着有趣的作用。特别是,我们之前报道过的NorA EPIs,三个2-苯基喹啉(1a–c)和吡唑并苯并噻嗪(2),其浓度低于MIC,显示出良好的减少 S生物膜形成的能力。金黄色(ATCC 29213)和 S。表皮(ATCC 35984)。然后,为了评估生物膜形成抑制剂是否可以与抗菌素联合使用以限制生物膜产生,使用环丙沙星(CPX)对两种最佳化合物1c和2进行了测试,结果显示了对葡萄球菌的优异协同作用在低浓度下,具有生物膜形成抑制作用的菌株超过60%。此外,为确认NorA外排泵参与生物膜生产,针对改良的 S测试了NorA EPI 1c和2。金黄色葡萄球菌过表达NorA外排泵(SA-1199B),其结果表明生物膜质量大大降低。总之,对HeLa和HepG2细胞的细胞毒性试验表明,与CPX联合使用可有效抑制葡萄球菌菌株的生物膜形成的浓度低于对人细胞的毒性浓度。

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