流出
金黄色葡萄球菌
溴化乙锭
四环素
微生物学
抗生素
红霉素
抗生素耐药性
抗药性
化学
多重耐药
药理学
生物
细菌
生物化学
遗传学
DNA
作者
Ana Carolina Justino de Araújo,Priscilla Ramos Freitas,Cristina Rodrigues dos Santos Barbosa,Débora Feitosa Muniz,Jaime Ribeiro‐Filho,Saulo Relison Tintino,José P. Siqueira-Júnior,José Maria Barbosa‐Filho,Gabriela Ribeiro de Sousa,Henrique Douglas Melo Coutinho
出处
期刊:Current Drug Metabolism
[Bentham Science]
日期:2021-01-05
卷期号:22 (2): 110-113
被引量:5
标识
DOI:10.2174/1389200221999210104204718
摘要
This study aimed to investigate the potential of limonene as an efflux pump (EP) inhibitor in Staphylococcus aureus strains, RN-4220 and IS-58, which carry EPs for erythromycin (MrsA) and tetracycline (TetK), respectively.The evolution of bacterial resistance mechanisms over time has impaired the action of most classes of antibiotics. Staphylococcus aureus is a notable bacterium, with high pathogenic potential and demonstrated resistance to conventional antibiotics. Considering the importance of discovering novel compounds to combat antibiotic resistance, our group previously demonstrated the antibacterial properties of limonene, a compound present in the essential oils of several plant species.This study aimed to investigate the potential of limonene as an efflux pump (EP) inhibitor in Staphylococcus aureus strains RN-4220 and IS-58, which carry EPs for erythromycin (MrsA) and tetracycline (TetK), respectively.The minimum inhibitory concentrations (MIC) of limonene and other efflux pump inhibitors were determined through the broth microdilution method. A reduction in the MIC of ethidium bromide was used as a parameter of EP inhibition.While limonene was not shown to exhibit direct antibacterial effects against EP-carrying strains, in association with ethidium bromide and antibiotics, this compound demonstrated enhanced antibacterial activity, indicating the inhibition of the MrsA and TetK pumps.In conclusion, this pioneering study demonstrated the effectiveness of limonene as an EP inhibitor in S. aureus strains, RN-4220 and IS-58. Nevertheless, further studies are required to characterize the molecular mechanisms associated with limonene-mediated EP inhibition.
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