Chemistry, School of Molecular Sciences, The University of Western Australia, Crawley, WA, 6009, Australia.
School of Biomedical Sciences, The University of Western Australia, Crawley, WA, 6009, Australia.
Sci Rep. 2018 May 2;8(1):6912. doi: 10.1038/s41598-018-25080-w.
The spectrum of activity and mode of action of a novel antibacterial agent, 135C, was investigated using a range of microbiological and genomic approaches. Compound 135C was active against Gram-positive bacteria with MICs for Staphylococcus aureus ranging from 0.12-0.5 μg/ml. It was largely inactive against Gram-negative bacteria. The compound showed bacteriostatic activity in time-kill studies and did not elicit bacterial cell leakage or cell lysis. Checkerboard assays showed no synergy or antagonism when 135C was combined with a range of other antibacterials. Multi-step serial passage of four S. aureus isolates with increasing concentrations of 135C showed that resistance developed rapidly and was stable after drug-free passages. Minor differences in the fitness of 135C-resistant strains and parent wildtypes were evident by growth curves, but 135C-resistant strains did not show cross-resistance to other antibacterial agents. Genomic comparison of resistant and wildtype parent strains showed changes in genes encoding cell wall teichoic acids. 135C shows promising activity against Gram-positive bacteria but is currently limited by the rapid resistance development. Further studies are required to investigate the effects on cell wall teichoic acids and to determine whether the issue of resistance development can be overcome.
我们采用一系列微生物学和基因组学方法研究了新型抗菌药物 135C 的作用方式和作用谱。该化合物对革兰氏阳性菌具有活性,金黄色葡萄球菌的 MIC 值范围为 0.12-0.5μg/ml。它对革兰氏阴性菌的活性较低。时间杀伤研究表明,该化合物具有抑菌活性,不会引起细菌细胞渗漏或裂解。棋盘微量稀释法检测结果显示,135C 与多种其他抗菌药物联合使用时无协同作用或拮抗作用。对四种耐 135C 的金黄色葡萄球菌分离株进行多步连续传代,结果表明耐药性迅速发展,在无药物传代后稳定。生长曲线显示 135C 耐药株和亲本野生型的适应性存在微小差异,但 135C 耐药株对其他抗菌药物没有交叉耐药性。耐药株和野生型亲本株的基因组比较显示,编码细胞壁磷壁酸的基因发生了变化。135C 对革兰氏阳性菌具有良好的活性,但目前受到耐药性快速发展的限制。需要进一步研究细胞壁磷壁酸的影响,并确定是否可以克服耐药性发展的问题。