细菌
抗生素
革兰氏阴性菌
微生物学
免疫系统
免疫识别
生物
革兰氏阳性菌
药品
克
大肠杆菌
生物化学
药理学
免疫学
遗传学
基因
作者
Rong Sheng Li,Jiahui Liu,Cong Wen,Yaru Shi,Jian Ling,Qiue Cao,Lei Wang,Hu Shi,Cheng Zhi Huang,Na Li
出处
期刊:Science Advances
[American Association for the Advancement of Science (AAAS)]
日期:2023-08-25
卷期号:9 (34)
被引量:12
标识
DOI:10.1126/sciadv.adg9601
摘要
The dearth of antibiotic candidates against Gram-negative bacteria and the rise of antibiotic resistance create a global health concern. The challenge lies in the unique Gram-negative bacterial outer membrane that provides the impermeable barrier for antibiotics and sequesters antigen presentation. We designed a transformable nano-antibiotics (TNA) that can transform from nontoxic nanoparticles to bactericidal nanofibrils with reasonable rigidity (Young's modulus, 21.6 ± 5.9 MPa) after targeting β-barrel assembly machine A (BamA) and lipid polysaccharides (LPSs) of Gram-negative bacteria. After morphological transformation, the TNA can penetrate and damage the bacterial envelope, disrupt electron transport and multiple conserved biosynthetic and metabolic pathways, burst bacterial antigen release from the outer membrane, and subsequently activate the innate and adaptive immunity. TNA kills Gram-negative bacteria in vitro and in vivo with undetectable resistance through multiple bactericidal modes of action. TNA treatment-induced vaccination results in rapid and long-lasting immune responses, protecting against lethal reinfections.
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