Key Laboratory of Synthetic and Natural Functional Molecule Chemistry of Ministry of Education, Chemical Biology Innovation Laboratory, College of Chemistry and Materials Science, Northwest University, 1 Xuefu Avenue, Xi'an 710127, PR China.
Key Laboratory of Synthetic and Natural Functional Molecule Chemistry of Ministry of Education, Chemical Biology Innovation Laboratory, College of Chemistry and Materials Science, Northwest University, 1 Xuefu Avenue, Xi'an 710127, PR China.
Bioorg Chem. 2019 Dec;93:103286. doi: 10.1016/j.bioorg.2019.103286. Epub 2019 Sep 16.
Antibiotic-resistant bacteria has become one of the greatest challenges to global human health today. Innovative strategies are needed to identify new therapeutic leads to tackle infections of drug-resistant Gram-negative bacteria. We herein synthesize a series of EB analogues to investigate their antibacterial activities. Select polar functionality at N-terminus of EB exhibited higher activities against multi-drug-resistant Gram-negative pathogens, including E. coli, P. aeruginosa and K. pneumoniae. EB analogue 4g and 4i exhibited potent antibacterial activities against E. coli-ESBL (MIC = 1-4 µg/mL) and E. coli producing NDM-1 (MIC = 4-32 µg/mL), which is superior to the traditional antibiotics (cefazolin, imipenem). Furthermore, the time-kill kinetics studies and the inhibition zone tests indicated that analogue 4i effectively and rapidly cause death of E. coli-ESBL and E. coli-NDM-1. Additionally, accumulation assays and SEM images showed that 4i could permeate bacterial membranes, leading to an irregular cell morphology. Importantly, bacterial resistance for analogue 4i was difficult to induce against E. coli-ESBL. EB analogues here reported low cytotoxicity against L-929 cells and mice model in vivo. We believe that EB analogues with polar functionality could play a pivotal role in the development of novel antibacterial agents in eradicating multi-drug-resistant Gram-negative pathogens infections.
耐药菌已成为当今全球人类健康面临的最大挑战之一。需要创新策略来确定新的治疗方法,以应对耐药革兰氏阴性菌引起的感染。我们在此合成了一系列 EB 类似物,以研究它们的抗菌活性。在 EB 的 N 端引入极性官能团可以显著提高其对多种耐药革兰氏阴性病原体的活性,包括大肠杆菌、铜绿假单胞菌和肺炎克雷伯菌。EB 类似物 4g 和 4i 对产 ESBL 的大肠杆菌(MIC=1-4μg/mL)和产 NDM-1 的大肠杆菌(MIC=4-32μg/mL)具有很强的抗菌活性,优于传统抗生素(头孢唑林、亚胺培南)。此外,时间杀伤动力学研究和抑菌圈试验表明,类似物 4i 能有效、快速地杀死产 ESBL 和产 NDM-1 的大肠杆菌。另外,积累试验和 SEM 图像表明,4i 可以穿透细菌细胞膜,导致细菌形态不规则。重要的是,类似物 4i 对产 ESBL 的大肠杆菌难以诱导耐药性。本文报道的 EB 类似物对 L-929 细胞和小鼠体内模型的细胞毒性较低。我们相信,具有极性官能团的 EB 类似物在开发新型抗菌药物以消除多重耐药革兰氏阴性菌感染方面将发挥关键作用。