Bruhn David F, Scherman Michael S, Liu Jiuyu, Scherbakov Dimitri, Meibohm Bernd, Böttger Erik C, Lenaerts Anne J, Lee Richard E
Department of Chemical Biology and Therapeutics, St. Jude Children's Research Hospital, Memphis, Tennessee, USA.
Mycobacterial Research Laboratories, Department of Microbiology, Colorado State University, Fort Collins, Colorado, USA.
Sci Rep. 2015 Sep 14;5:13985. doi: 10.1038/srep13985.
Spectinamides are new semi-synthetic spectinomycin derivatives with potent anti-tubercular activity. The reported synergism of the precursor spectinomycin with other antibiotics prompted us to examine whether spectinamides sensitize M. tuberculosis to other antibiotics not traditionally used in the treatment of tuberculosis to potentially expand therapeutic options for MDR/XDR Tuberculosis. Whole cell synergy checkerboard screens were performed using the laboratory strain M. tuberculosis H37Rv, lead spectinamide 1599, and a broad panel of 27 antibiotics. In vitro, 1599 synergized with 11 drugs from 6 antibiotic classes. The observed synergy was tested against clinical isolates confirming synergy with Clarithromycin, Doxycycline and Clindamycin, combinations of which were taken forward for in vivo efficacy determination. Co-administration of 1599 and clarithromycin provided additional bacterial killing in a mouse model of acute tuberculosis infection, but not in a chronic infection model. Further studies indicated that mismatched drug exposure profiles likely permitted induction of phenotypic clarithromycin resistance and subsequent loss of synergism. These studies highlight the importance of validating in vitro synergism and the challenge of matching drug exposures to obtain a synergistic outcome in vivo. Results from this study indicate that a 1599 clarithromycin combination is potentially viable, providing the drug exposures can be carefully monitored.
壮观酰胺是具有强效抗结核活性的新型半合成大观霉素衍生物。据报道,前体大观霉素与其他抗生素具有协同作用,这促使我们研究壮观酰胺是否能使结核分枝杆菌对其他传统上不用于治疗结核病的抗生素敏感,从而有可能扩大耐多药/广泛耐药结核病的治疗选择。使用实验室菌株结核分枝杆菌H37Rv、先导壮观酰胺1599和一组27种抗生素进行了全细胞协同棋盘筛选。在体外,1599与来自6类抗生素的11种药物具有协同作用。对临床分离株测试了观察到的协同作用,证实了与克拉霉素、强力霉素和克林霉素的协同作用,并将这些药物的组合用于体内疗效测定。在急性结核感染小鼠模型中,1599与克拉霉素联合给药可增强细菌杀伤作用,但在慢性感染模型中则不然。进一步研究表明,不匹配的药物暴露模式可能会导致表型克拉霉素耐药性的诱导以及随后协同作用的丧失。这些研究强调了验证体外协同作用的重要性以及在体内获得协同结果时匹配药物暴露的挑战。本研究结果表明,1599与克拉霉素的组合可能是可行的,前提是可以仔细监测药物暴露情况。