孔蛋白
细菌外膜
抗生素
细菌
微生物学
细胞内
胞浆
抗生素耐药性
抗菌剂
革兰氏阴性菌
大肠杆菌
多重耐药
药物输送
小泡
细胞膜
化学
生物
细胞生物学
膜
生物化学
酶
有机化学
基因
遗传学
作者
Meishan Wu,Rachael M. Harrower,Ziang Li,Angela C. Brown
标识
DOI:10.1101/2025.01.08.631972
摘要
The development of novel antimicrobial agents that are effective against Gram-negative bacteria is hindered by the dual membrane cell wall structure of these bacteria. To reach their intracellular targets, most antibiotics must therefore pass through protein channels called porins; however, a common mechanism of acquired resistance is decreased expression of these proteins. Inspired by the ability of outer membrane vesicles (OMVs) to deliver cargo to the bacterial cytosol, we hypothesized that encapsulation of small molecule antibiotics within OMVs would improve the activity of the drugs by facilitating uptake. To test this, we investigated the ability of antibiotic-encapsulated OMVs to inhibit the growth of both Gram-negative and Gram-positive bacteria, including multidrug-resistant clinical isolates. We also demonstrated that this mechanism of delivery does not require porin expression. Together, our results demonstrate the potential of OMVs as novel antibiotic delivery vehicles to treat antibiotic-resistant bacterial infections.
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