Journal of pharmacological sciences · 2018
A quinoline-based FtsZ inhibitor for the study of antimicrobial activity and synergistic effects with β-lactam antibiotics.
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Fang Zhiyuan, Ban Li, Li Yanan, Yuan Wenchang, Liu Zhihua, Liu Ting, Li Xiaomei, Wong Kwok-Yin, Lu Yujing, Sun Ning, Yao Xingang
Аннотация
The antibacterial activity and the synergistic effect with β-lactam antibiotics of a new 1-methylquinolinium iodide derivative were investigated. The experimental results indicate that the compound possesses a strong antibacterial activity against a panel of bacteria including methicillin-resistant Staphylococcus aureus, vancomycin-resistant Enterococcus and NDM-1 Escherichia coli with the MIC values from 0.75 μg/mL to 6 μg/mL. In addition, this compound combined with β-lactam antibiotics shows strong synergistic antimicrobial activities against antibiotic-resistant strains of S. aureus. The results of biochemical studies also reveal that this compound can effectively disrupt GTPase activity, polymerization of FtsZ, and cell division to cause cell death. The compound shows high potential for further development as a new generation of antibacterial agents to fight against the emergence of multidrug-resistant bacteria.
Предметные рубрики MeSH
Anti-Bacterial AgentsBacterial ProteinsCell DivisionCytoskeletal ProteinsDose-Response Relationship, DrugDrug Resistance, BacterialDrug SynergismEscherichia coliGTP PhosphohydrolasesMethicillin-Resistant Staphylococcus aureusPolymerizationQuinolinium CompoundsVancomycin-Resistant Enterococcibeta-Lactamasesbeta-Lactams