金黄色葡萄球菌
头孢菌素
耐甲氧西林金黄色葡萄球菌
透皮
微生物学
抗菌活性
微球菌科
医学
化学
抗菌剂
药理学
抗生素
生物
细菌
遗传学
作者
Nan Wang,Wei Li,Hui Yu,Wenlin Huang,Yarui Qiao,Qi Wang,Yunfei Wei,Xuming Deng,Li Wang,Minhe Cui,Peng Zhang,Yonglin Zhou
标识
DOI:10.1016/j.bcp.2024.116404
摘要
Methicillin-resistant Staphylococcus aureus (MRSA), a notorious bacterium with high drug resistance and easy recurrence after surgery, has posed significant clinical treatment challenges. In the current scarcity of new antibiotics, the identification of adjuvants to existing antibiotics is a promising approach to combat infections caused by multidrug-resistant Gram-positive bacteria. The in vitro synergy test, which included a MIC assay, time-kill curve, antimicrobial susceptibility testing, and live/dead bacteria staining assay, revealed that laurocapram, a widely used chemical transdermal enhancer, could potentiate the antibacterial activity of cephalosporins against MRSA. In vitro, laurocapram combined with cefixime showed an excellent synergistic activity against MRSA (FICI = 0.28 ± 0.00). In addition, the combination of laurocapram and cefixime may inhibited the formation of MRSA biofilm and caused cell membrane damage. Following that, we discovered that combining laurocapram with cefixime could alleviate the symptoms of mice in the MRSA skin infection model and the MRSA pneumonia model. In conclusion, laurocapram is a promising and low-cost antibacterial adjuvant, providing a new strategy for further exploring the use of lower doses of cephalosporins to combat MRSA infection.
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