溶葡萄球菌酶
细胞内
微生物学
万古霉素
抗生素
微泡
金黄色葡萄球菌
细胞内寄生虫
耐甲氧西林金黄色葡萄球菌
医学
生物
化学
生物化学
细菌
细胞生物学
小RNA
基因
遗传学
作者
Xiaohong Yang,Beibei Xie,Haibo Peng,Gongming Shi,Sreenivas Banne,Jian Guo,Chenhui Wang,Yun He
标识
DOI:10.1016/j.jconrel.2020.11.045
摘要
Intracellular methicillin-resistant Staphylococcus aureus (MRSA) is extremely difficult to remove by common antibiotics, leading to infection recurrence and resistance. Herein we report a novel exosome-based antibiotic delivery platform for eradicating intracellular MRSA, where mannosylated exosome (MExos) is employed as the drug carrier and preferentially taken up by macrophages, delivering lysostaphin (MExoL) and vancomycin (MExoV) to intracellular pathogens. Combination of MExoL and MExoV eradicated intracellular quiescent MRSA. Moreover, MExos rapidly accumulated in mouse liver and spleen, the target organs of intracellular MRSA, after intravenous (IV) administration. Thus, the MExos antibiotic delivery platform is a promising strategy for combating intracellular infection.
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