生物膜
化学
胞外聚合物
抗生素
细菌
细胞毒性
细胞外
生物化学
微生物学
氨基酸
猝灭(荧光)
镧系元素
组合化学
抗菌活性
群体感应
亚胺
药物输送
抗菌剂
抗菌剂
作者
Guangpu Wu,Aimin Jia,Yujin Li,Hui Liu
标识
DOI:10.1021/acs.jafc.6c09171
摘要
Abstract Biofilms are a promising target to combat antibiotic resistance, but D-amino acids require high doses for biofilm inhibition. To overcome this, a novel antibiofilm agent was designed by anchoring D-amino acids onto the pillar[5]arene scaffold via acid-labile imine linkages. Pillar[5]arenes functionalized with D-amino acids showed enhanced antibiofilm activities compared to free D-amino acids, attributed to the localized release of D-amino acids within biofilms. Moreover, synergy was observed when conventional antibiotics ERY and TET were combined with PAY10. Benefiting from biofilm disruption, the combined treatment exposed bacteria to antibiotics, thereby improving MRSA susceptibility. In addition, the pillar[5]arene derivatives exhibited no cytotoxicity at the tested concentrations. Lastly, the expression levels of AgrA and dltD genes in MRSA were downregulated after treatment with PAY10. This revealed that the compound reduced biofilm mass by quenching quorum-sensing signals and repressing the production of extracellular polymeric substances.
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