Staphylococcus aureus-targeting peptide/surfactant assemblies for antibacterial therapy

被引:6
|
作者
Jiang, Jian [1 ]
Xu, Zhilong [2 ]
Chen, Jie [1 ]
Xu, Ze [1 ]
Huang, Ying [1 ]
Xi, Juqun [1 ,3 ]
Fan, Lei [2 ]
机构
[1] Yangzhou Univ, Inst Translat Med, Sch Med, Dept Pharmacol, Yangzhou 225009, Peoples R China
[2] Yangzhou Univ, Sch Chem & Chem Engn, Yangzhou 225002, Peoples R China
[3] Jiangsu Key Lab Integrated Tradit Chinese & Wester, Yangzhou 225009, Peoples R China
基金
中国国家自然科学基金;
关键词
Cationic trimetric surfactant; -lactamase inhibitor; Antibacterial therapy; LACTAMASE INHIBITOR; NANOPARTICLES; SURFACTANT; RESISTANCE; MECHANISM; ACIDS; SITE;
D O I
10.1016/j.colsurfb.2022.112444
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
To address the challenge from microbial resistance, this work developed a surfactant with 18-carbon single hydrocarbon chain and multi-amine head groups (C18N3). After assembling with Staphylococcus aureus-targeting peptide (CARG), the obtained C18N3/CARG assemblies exhibited excellent antimicrobial activities against Staphylococcus aureus and methicillin-resistant Staphylococcus aureus in vitro and in vivo, in which the targeting peptide CARG bonded specifically to Staphylococcus aureus and C18N3 killed bacteria with a mechanism of membrane disruption. Importantly, C18N3 could also work as a beta-lactamase inhibitor to overcome the bacterial resistance to beta-lactam antibiotics through noncompetitive inhibition. The combination of beta-lactam antibiotic and C18N3/CARG assemblies more effectively suppressed methicillin-resistant Staphylococcus aureus in vitro and in vivo relative to equivalent dose of free antibiotic or C18N3. Thus, the antibacterial platform of antibiotic carrying surfactant assemblies bearing bacteria-targeted peptides, in which C18N3 performed dual function, antibacterial agent and beta-lactamase inhibitor, may help fight against the difficult-to-treat infections.
引用
收藏
页数:10
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