Nazari Mohsen, Taheri Mohammad, Nouri Fatemeh, Bahmanzadeh Maryam, Alikhani Mohammad Yousef
Department of Microbiology, School of Medicine, Hamadan University of Medical Sciences, Hamadan, Iran.
Department of Pharmaceutical Biotechnology, School of Pharmacy, Hamadan University of Medical Sciences, Hamadan, Iran.
Chemotherapy. 2025;70(2):53-64. doi: 10.1159/000542826. Epub 2024 Dec 4.
This study investigates the efficacy of fucoidan combination with antibiotics, against single-species biofilms and mixed-species, individual planktonic, and coculture planktonic conditions of Methicillin-resistant Staphylococcus aureus (MRSA) and Acinetobacter baumannii by time-kill curve analysis.
Fucoidan, a sulfated polysaccharide, was purchased from Sigma-Aldrich, USA. Clinical isolates of MRSA and A. baumannii from diabetic foot ulcers (DFUs) were used, and single-species biofilms and mixed-species biofilms were developed to assess susceptibility to the treatments using MIC, MBC, minimum biofilm inhibitory concentration, minimum biofilm eradication concentration, and time-kill kinetics assays. Cytotoxicity was assessed using MTT assays on human skin fibroblast cells (HSF-PI 16).
The study determined the geometric mean MIC and MBC values for gentamicin, imipenem, and fucoidan in MRSA and A. baumannii cultures, both individually and in co-cultures. The MIC and MBC values were significantly lower under co-culture conditions, indicating enhanced antimicrobial efficacy. Synergy between fucoidan, gentamicin, and imipenem was confirmed through time-kill assays, which showed complete inhibition of bacterial growth and effective biofilm eradication, particularly in mixed-species biofilms. Fucoidan demonstrated low cytotoxicity at optimal concentrations, highlighting their potential as a therapeutic strategy against biofilm-associated infections in DFUs.
The study concludes that fucoidan, in combination with gentamicin and imipenem, effectively disrupts mixed-species biofilms of MRSA and A. baumannii, suggesting fucoidan-based therapies could improve outcomes for DFU patients, warranting further clinical investigation.
本研究通过时间-杀菌曲线分析,研究岩藻依聚糖联合抗生素对耐甲氧西林金黄色葡萄球菌(MRSA)和鲍曼不动杆菌的单菌种生物膜、混合菌种、单个浮游菌及共培养浮游菌状态的疗效。
岩藻依聚糖是一种硫酸化多糖,购自美国西格玛奥德里奇公司。使用从糖尿病足溃疡(DFU)分离出的MRSA和鲍曼不动杆菌临床菌株,构建单菌种生物膜和混合菌种生物膜,通过最低抑菌浓度(MIC)、最低杀菌浓度(MBC)、最低生物膜抑制浓度、最低生物膜根除浓度和时间-杀菌动力学试验评估对治疗的敏感性。使用MTT法对人皮肤成纤维细胞(HSF-PI 16)进行细胞毒性评估。
该研究确定了庆大霉素、亚胺培南和岩藻依聚糖在MRSA和鲍曼不动杆菌单独培养及共培养条件下的几何平均MIC和MBC值。共培养条件下的MIC和MBC值显著更低,表明抗菌效果增强。通过时间-杀菌试验证实了岩藻依聚糖、庆大霉素和亚胺培南之间的协同作用,该试验显示细菌生长完全受到抑制且生物膜被有效根除,尤其是在混合菌种生物膜中。岩藻依聚糖在最佳浓度下显示出低细胞毒性,突出了其作为治疗DFU中生物膜相关感染的治疗策略的潜力。
该研究得出结论,岩藻依聚糖联合庆大霉素和亚胺培南可有效破坏MRSA和鲍曼不动杆菌的混合菌种生物膜,表明基于岩藻依聚糖的疗法可能改善DFU患者的治疗效果,值得进一步的临床研究。