Laboratório Integrado de Biomoléculas, Departamento de Patologia e Medicina Legal, Universidade Federal do Ceará, Fortaleza, CE, Brazil.
Faculdade de Educação, Ciência e Letras de Iguatu, Universidade Estadual do Ceará, Iguatu, Ceará, Brazil.
Curr Microbiol. 2023 Apr 8;80(5):176. doi: 10.1007/s00284-023-03284-2.
Antimicrobial resistance is a natural phenomenon and is becoming a huge global public health problem, since some microorganisms not respond to the treatment of several classes of antibiotics. The objective of the present study was to evaluate the antibacterial, antibiofilm, and synergistic effect of triterpene 3β,6β,16β-trihydroxyilup-20(29)-ene (CLF1) against Staphylococcus aureus and Staphylococcus epidermidis strains. Bacterial susceptibility to CLF1 was evaluated by minimum inhibitory concentration (MIC) and the minimum bactericidal concentration (MBC) assay. In addition, the effect combined with antibiotics (ampicillin and tetracycline) was verified by the checkerboard method. The biofilms susceptibility was assessed by enumeration of colony-forming units (CFUs) and quantification of total biomass by crystal violet staining. The compound showed bacteriostatic and bactericidal activity against all Staphylococcal strains tested. The synergistic effect with ampicillin was observed only for S. epidermidis strains. Moreover, CLF1 significantly inhibited the biofilm formation and disrupted preformed biofilm of the all strains. Scanning electron microscopy (SEM) images showed changes in the cell morphology and structure of S. aureus ATCC 700698 biofilms (a methicillin-resistant S. aureus strain). Molecular docking simulations showed that CLF1 has a more favorable interaction energy than the antibiotic ampicillin on penicillin-binding protein (PBP) 2a of MRSA, coupled in different regions of the protein. Based on the results obtained, CLF1 proved to be a promising antimicrobial compound against Staphylococcus biofilms.
抗菌耐药性是一种自然现象,正在成为一个巨大的全球公共卫生问题,因为有些微生物对几类抗生素的治疗没有反应。本研究的目的是评估三萜 3β,6β,16β-三羟基齐墩果酸-20(29)-烯(CLF1)对金黄色葡萄球菌和表皮葡萄球菌菌株的抗菌、抗生物膜和协同作用。通过最小抑菌浓度(MIC)和最小杀菌浓度(MBC)测定评估细菌对 CLF1 的敏感性。此外,通过棋盘法验证了与抗生素(氨苄西林和四环素)联合的效果。通过平板计数法(CFUs)评估生物膜的敏感性,并通过结晶紫染色定量总生物量。该化合物对所有测试的葡萄球菌菌株均显示出抑菌和杀菌活性。仅在表皮葡萄球菌菌株中观察到与氨苄西林的协同作用。此外,CLF1 显著抑制了所有菌株的生物膜形成并破坏了已形成的生物膜。扫描电子显微镜(SEM)图像显示金黄色葡萄球菌 ATCC 700698 生物膜(耐甲氧西林金黄色葡萄球菌菌株)的细胞形态和结构发生变化。分子对接模拟表明,CLF1 与抗生素氨苄西林相比,在 MRSA 的青霉素结合蛋白(PBP)2a 上具有更有利的相互作用能,结合在蛋白质的不同区域。根据获得的结果,CLF1 被证明是一种有前途的抗葡萄球菌生物膜的抗菌化合物。