Zimmermann Saskia, Klinger-Strobel Mareike, Bohnert Jürgen A, Wendler Sindy, Rödel Jürgen, Pletz Mathias W, Löffler Bettina, Tuchscherr Lorena
Institute of Medical Microbiology, Jena University Hospital, Jena, Germany.
Center for Sepsis Control and Care, Jena University Hospital, Jena, Germany.
Front Microbiol. 2019 Dec 3;10:2762. doi: 10.3389/fmicb.2019.02762. eCollection 2019.
has acquired resistance to antibiotics since their first use. The protein NorA, an efflux pump belonging to the major facilitator superfamily (MFS), contributes to resistance to fluoroquinolones (e.g., ciprofloxacin), biocides, dyes, quaternary ammonium compounds, and antiseptics. Different compounds have been identified as potential efflux pump inhibitors (EPIs) of NorA that result in increased intracellular concentration of antibiotics, restoring their antibacterial activity and cell susceptibility. However, none of the currently known EPIs have been approved for clinical use, probably due to their toxicity profiles. In the present study, we screened approved drugs for possible efflux pump inhibition. By screening a compound library of approximately 1200 different drugs, we identified nilotinib, a tyrosine kinase inhibitor, as showing the best efflux pump inhibitory activity, with a fractional inhibitory concentration index of 0.1875, indicating synergism with ciprofloxacin, and a minimum effective concentration as low as 0.195 μM. Moreover, at 0.39 μM, nilotinib, in combination with 8 μg/mL of ciprofloxacin, led to a significant reduction in biofilm formation and preformed mature biofilms. This is the first description of an approved drug that can be used as an efflux pump inhibitor and to reduce biofilms formation at clinically achievable concentrations.
自首次使用以来,细菌已对抗生素产生了耐药性。蛋白质NorA是一种属于主要易化子超家族(MFS)的外排泵,它会导致对氟喹诺酮类药物(如环丙沙星)、杀菌剂、染料、季铵化合物和防腐剂产生耐药性。已鉴定出不同的化合物作为NorA的潜在外排泵抑制剂(EPI),这些抑制剂会导致抗生素细胞内浓度增加,恢复其抗菌活性和细胞敏感性。然而,目前已知的EPI均未被批准用于临床,这可能是由于它们的毒性特征。在本研究中,我们筛选了已批准的药物,以寻找可能的外排泵抑制作用。通过筛选一个包含约1200种不同药物的化合物库,我们确定尼洛替尼(一种酪氨酸激酶抑制剂)具有最佳的外排泵抑制活性,其分数抑制浓度指数为0.1875,表明与环丙沙星具有协同作用,最低有效浓度低至0.195μM。此外,在0.39μM时,尼洛替尼与8μg/mL的环丙沙星联合使用,可显著减少生物膜形成和已形成的成熟生物膜。这是首次描述一种已批准的药物,它可以用作外排泵抑制剂,并在临床可达到的浓度下减少生物膜形成。