氟苯尼考
微生物学
奥兰诺芬
药理学
化学
医学
抗生素
生物
内科学
类风湿性关节炎
作者
Jianguo Li,Chuanjian Zhang,Liu-Yan Liang,Ting-Yin Lu,Long-Gen Zhong,Wei-Cheng Zhong,Chao-Yan Niu,Jian Sun,Xiao‐Ping Liao,Yu‐Feng Zhou
标识
DOI:10.1093/jambio/lxae299
摘要
Abstract Aims Methicillin-resistant Staphylococcus aureus (MRSA) is an important zoonotic pathogen with multidrug-resistant phenotypes increasingly prevalent in both human and veterinary clinics. This study evaluated the potential of auranofin (AF) as an antibiotic adjuvant to enhance the anti-MRSA activity of florfenicol (FFC) and established a pharmacokinetic/pharmacodynamic (PK/PD) model to compare the efficacy of FFC alone or in combination with AF against MRSA. Methods and results We observed an increased susceptibility and significant synergistic effects of MRSA to FFC in the presence of AF. The combination treatment of FFC and AF significantly inhibited MRSA biofilm formation and decreased the metabolic activity of mature biofilms. Importantly, AF fully restored the efficacy of FFC in both Galleria mellonella larvae and murine models. PK/PD studies demonstrated that the AUC24h/MIC targets required to achieve the bacteriostatic and bactericidal effects were significantly lower with the combination therapy compared to florfenicol monotherapy. Conclusions These results reveal the potential of AF as a novel adjuvant to improve the efficacy of FFC in treating MRSA invasive infections and provide valuable PK/PD insights for designing effective combination therapies.
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