聚糖
炎症
细菌
生物膜
微生物学
化学
生物
免疫学
糖蛋白
生物化学
遗传学
作者
Yihong Zhang,Wanling Liu,Gen Wei,Quanyi Liu,Guoqiang Shao,Xiang Gu,Xiaomiao Cui,Zijun Zhou,Yuting Wang,Sheng Zhao,Faheem Muhammad,Sirong Li,Tong Li,Yan Du,Hui Wei
出处
期刊:ACS Nano
[American Chemical Society]
日期:2024-03-14
卷期号:18 (12): 9019-9030
被引量:8
标识
DOI:10.1021/acsnano.3c12783
摘要
Urinary tract infections (UTIs), common bacterial infections in communities and medical facilities, are mainly mediated by FimH. The glycan sites of the uromodulin protein play a crucial role in protecting against UTIs by interacting with FimH. A bioinspired approach using glycan-FimH interactions may effectively reduce bacteria through an antiadhesive mechanism, thereby curbing bacterial resistance. However, typical antiadhesive therapy alone fails to address the excessive reactive oxygen species and inflammatory response during UTIs. To bridge this gap, antioxidant nanozymes with antiadhesive ability were developed as nanodecoys to counter bacteria and inflammation. Specifically, ultrasmall dextran-coated ceria (DEC) was engineered to address UTIs, with dextran blocking FimH adhesion and ceria exhibiting anti-inflammatory properties. DECs, metabolizable by the kidneys, reduced bacterial content in the urinary tract, mitigating inflammation and tissue damage. In murine models, DECs successfully treated acute UTIs, repeated infections, and catheter-related UTIs. This dual approach not only highlights the potential of nanozymes for UTIs but also suggests applicability to other FimH-induced infections in the lungs and bowels, marking a significant advancement in nanozyme-based clinical approaches.
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