Keyhani Shahriar, Alikhani Mohammad Yousef, Doosti-Irani Amin, Shokoohizadeh Leili
Department of Microbiology, Faculty of Medicine, Hamadan University of Medical Sciences, Hamadan, Iran.
Infectious Disease Research Center, Hamadan University of Medical Sciences, Hamadan, Iran.
Iran J Microbiol. 2024 Aug;16(4):552-559. doi: 10.18502/ijm.v16i4.16315.
Today, medicinal plants and their derivatives are considered to reduce the prevalence of antibiotic resistance. The aim of this study was to investigate the effect of essential oil on A efflux pump gene expression and biofilm formation in ciprofloxacin-resistant strains.
A total of 50 clinical strains of resistant to ciprofloxacin were studied. The minimum inhibitory concentration (MIC) of essential oil and its synergistic effect with ciprofloxacin were determined using the microbroth dilution method and the fractional inhibitory concentration (FIC) method. Minimum biofilm inhibition concentration (MBIC) of essential oil was detected. The effect of essential oils on the expression level of the A gene was detected by Real-time PCR.
essential oil showed inhibitory activity against ciprofloxacin-resistant strains of When essential oil was combined with ciprofloxacin, the MIC was reduced 2-4 times. In 28% of the strains, with ciprofloxacin showed a synergistic effect. essential oil reduces the strength of biofilm formation and alters the biofilm phenotype. A significant decrease in A gene expression was observed in all isolates after treatment with essential oil.
Based on the results of this study, it was observed that supplementing essential oil can help reduce ciprofloxacin resistance and inhibit biofilm formation in fluoroquinolone-resistant strains.
如今,药用植物及其衍生物被认为可降低抗生素耐药性的发生率。本研究的目的是调查精油对环丙沙星耐药菌株中A外排泵基因表达及生物膜形成的影响。
共研究了50株对环丙沙星耐药的临床菌株。采用微量肉汤稀释法和分数抑菌浓度(FIC)法测定精油的最低抑菌浓度(MIC)及其与环丙沙星的协同效应。检测精油的最低生物膜抑制浓度(MBIC)。通过实时聚合酶链反应检测精油对A基因表达水平的影响。
精油对环丙沙星耐药菌株显示出抑制活性。当精油与环丙沙星联合使用时,MIC降低了2至4倍。在28%的菌株中,与环丙沙星联合显示出协同效应。精油降低了生物膜形成的强度并改变了生物膜表型。用精油处理后,所有分离株中A基因表达均显著下降。
基于本研究结果,观察到补充精油有助于降低环丙沙星耐药性并抑制氟喹诺酮耐药菌株中的生物膜形成。