生物正交化学
细菌
粪肠球菌
微生物学
抗菌剂
抗生素
革兰氏阳性菌
化学
体外
体内
金黄色葡萄球菌
光热治疗
生物化学
抗生素耐药性
生物
材料科学
点击化学
组合化学
纳米技术
生物技术
遗传学
作者
Tao Feng,Hui Lü,Xiaoting Ye,Chaofan Nie,Jianhong Zhang,Luofeng Yu,Haoyu Jin,Peng Li,Wei Huang
标识
DOI:10.1007/s40843-021-1735-0
摘要
Bacterial infections are grave threats to human health, particularly those caused by the most common Gram-positive bacteria. The massive administration of broad-spectrum antibiotics to treat various bacterial infections has led to the evolution and spread of drug resistance. As a universal antimicrobial technique unapt to induce drug resistance, photothermal therapy (PTT) is attracting extensive attention in recent years. However, its unspecific killing capability and side effects towards adjacent mammalian cells severely impede the practical applications. Herein, we proposed a metabolic engineering strategy to selectively inactivate Gram-positive bacteria by PTT. A bioorthogonal photothermal agent was prepared by the conjugation of IR-780 iodide and dibenzo-cyclooctyne (IR780-DBCO). Upon pre-metabolizing with 3-azido-D-alanine, Gram-positive bacteria rather than Gram-negative ones, such as Staphylococcus aureus and vancomycin-resistant Enterococcus faecalis (VRE), could be specifically tied up by the explosive IR780-DBCO via copper-free click chemistry. Thereafter, they spontaneously detonated under 15 min near-infrared light irradiation and inactivated nearly 100% Gram-positive bacteria in vitro. Moreover, superbug VRE-induced infection was significantly inhibited by this approach in a mouse skin wound model. This metabolic labelling-based photothermal ablation strategy specific to Gram-positive microbes would stimulate the development of precise anti-bacterial candidates for preclinical applications.
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