Lutfi Lekaa L, Shaldam Moataz A, Shaaban Mona I, Elshaer Soha Lotfy
Department of Microbiology and Immunology, Faculty of Pharmacy, Mansoura University, Mansoura 35516, Egypt.
Department of Microbiology and Immunology, Faculty of Pharmacy, Horus University-Egypt, New Damietta 34518, Egypt.
Microorganisms. 2025 May 27;13(6):1227. doi: 10.3390/microorganisms13061227.
The efflux system is one of the resistance mechanisms that bacteria use to reduce the effectiveness of antibiotics, leading to the development of multidrug resistance. To evaluate other treatment choices, esomeprazole (ESO), omeprazole (OME), pantoprazole (PAN), vitamin D (VD), and vitamin K (VK) were tested for potential efflux pump (EP)-inhibiting activity.
The minimum inhibitory concentrations (MICs) of the tested drugs were determined against ATCC 51503 and PAO1. Quantitative estimation of the EP-inhibiting activity of the tested medications was phenotypically investigated with a semi-automated fluorometric system and genotypically confirmed by real-time polymerase chain reaction (RT-PCR). Data were confirmed through docking study.
ATCC 51503 and PAO1 were positive efflux standard strains. VD and VK revealed an MIC of 625-1250 µg/mL and MIC of 2500-5000 µg/mL, lower than what was detected for PPIs (MIC = 16,000-32,000 µg/mL). Vitamins showed powerful anti-efflux activity with remarkable ethidium bromide accumulation in ATCC 51503 and PAO1. Also, VD and VK significantly lowered the MIC of ciprofloxacin by 64-fold. On the molecular level, OME showed a notable decrease in the relative expression of the efflux-encoding genes and by 91.5% and 99.7% in ATCC 51503 and PAO1, respectively.
This study highlights the anti-efflux activity of ESO, OME, PAN, VD, and VK against the tested Gram-negative strains. Hence, these PPIs and vitamins could be valuable adjuvant treatments to enhance the effectiveness of curing infections caused by MDR strains.
外排系统是细菌用于降低抗生素有效性从而导致多药耐药性产生的耐药机制之一。为评估其他治疗选择,对埃索美拉唑(ESO)、奥美拉唑(OME)、泮托拉唑(PAN)、维生素D(VD)和维生素K(VK)进行了潜在外排泵(EP)抑制活性测试。
测定受试药物对ATCC 51503和PAO1的最低抑菌浓度(MIC)。采用半自动荧光系统对受试药物的EP抑制活性进行表型定量评估,并通过实时聚合酶链反应(RT-PCR)进行基因型确认。数据通过对接研究得到证实。
ATCC 51503和PAO1是阳性外排标准菌株。VD和VK的MIC分别为625 - 1250μg/mL和2500 - 5000μg/mL,低于质子泵抑制剂(PPI)的检测值(MIC = 16,000 - 32,000μg/mL)。维生素在ATCC 51503和PAO1中显示出强大的抗外排活性,溴化乙锭积累显著。此外,VD和VK使环丙沙星的MIC显著降低了64倍。在分子水平上,OME使ATCC 51503和PAO1中编码外排的基因相对表达分别显著降低了91.5%和99.7%。
本研究突出了ESO、OME、PAN、VD和VK对受试革兰氏阴性菌株的抗外排活性。因此,这些PPI和维生素可能是增强治疗多重耐药菌株引起感染有效性的有价值辅助治疗药物。