UMR_MD1, Aix-Marseille Univ, IRBA, TMCD2, Marseille, France.
DISCO beamline, Synchrotron Soleil, Saint-Aubin, France.
Sci Rep. 2017 Aug 29;7(1):9821. doi: 10.1038/s41598-017-08775-4.
Bacterial multidrug resistance is a worrying health issue. In Gram-negative antibacterial research, the challenge is to define the antibiotic permeation across the membranes. Passing through the membrane barrier to reach the inhibitory concentration inside the bacterium is a pivotal step for antibacterial molecules. A spectrofluorimetric methodology has been developed to detect fluoroquinolones in bacterial population and inside individual Gram-negative bacterial cells. In this work, we studied the antibiotic accumulation in cells expressing various levels of efflux pumps. The assays allow us to determine the intracellular concentration of the fluoroquinolones to study the relationships between the level of efflux activity and the antibiotic accumulation, and finally to evaluate the impact of fluoroquinolone structures in this process. This represents the first protocol to identify some structural parameters involved in antibiotic translocation and accumulation, and to illustrate the recently proposed "Structure Intracellular Concentration Activity Relationship" (SICAR) concept.
细菌的多重耐药性是一个令人担忧的健康问题。在革兰氏阴性菌的抗菌研究中,关键是要定义抗生素在膜间的渗透。穿过膜屏障到达细菌内部的抑制浓度是抗菌分子的关键步骤。已经开发出一种荧光光度测定法来检测细菌群体和单个革兰氏阴性菌细胞中的氟喹诺酮类药物。在这项工作中,我们研究了在表达不同水平外排泵的细胞中抗生素的积累。这些测定法使我们能够确定氟喹诺酮类药物在细胞内的浓度,以研究外排活性水平与抗生素积累之间的关系,并最终评估氟喹诺酮类药物结构对此过程的影响。这是第一个确定参与抗生素转运和积累的一些结构参数的方案,并说明了最近提出的“结构-细胞内浓度-活性关系”(SICAR)概念。