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纳米银通过抑制FapC淀粉样变性减轻生物膜形成。

Nanosilver Mitigates Biofilm Formation via FapC Amyloidosis Inhibition.

作者信息

Huma Zil-E, Javed Ibrahim, Zhang Zhenzhen, Bilal Hajira, Sun Yunxiang, Hussain Syed Zajif, Davis Thomas P, Otzen Daniel E, Landersdorfer Cornelia B, Ding Feng, Hussain Irshad, Ke Pu Chun

机构信息

ARC Centre of Excellence in Convergent Bio-Nano Science and Technology, Monash Institute of Pharmaceutical Sciences, Monash University, 381 Royal Parade, Parkville, VIC, 3052, Australia.

Department of Chemistry & Chemical Engineering, SBA School of Science & Engineering (SBASSE), Lahore University of Management Science (LUMS), DHA, Lahore, 54792, Pakistan.

出版信息

Small. 2020 May;16(21):e1906674. doi: 10.1002/smll.201906674. Epub 2020 Jan 27.

Abstract

Multidrug resistance of bacteria is a major challenge due to the wide-spread use of antibiotics. While a range of strategies have been developed in recent years, suppression of bacterial activity and virulence via their network of extracellular amyloid has rarely been explored, especially with nanomaterials. Here, silver nanoparticles and nanoclusters (AgNPs and AgNCs) capped with cationic branched polyethylenimine polymer are synthesized, and their antimicrobial potentials are determined at concentrations safe to mammalian cells. Compared with the ultrasmall AgNCs, AgNPs entail stronger binding to suppress the fibrillization of FapC, a major protein constituent of the extracellular amyloid matrix of Pseudomonas aeruginosa. Both types of nanoparticles exhibit concentration-dependent antibiofilm and antimicrobial properties against P. aeruginosa. At concentrations of 1 × 10 m or below, both the bactericidal activity of AgNCs and the antibiofilm capacity of AgNPs are associated with their structure-mediated bio-nano interactions but not ion release. For AgNPs, specifically, their antibiofilm potency correlates with their capacity of FapC fibrillization inhibition, but not with their bactericidal activity. This study demonstrates the antimicrobial potential of safe nanotechnology through the novel route of amyloidosis inhibition.

摘要

由于抗生素的广泛使用,细菌的多重耐药性成为一个重大挑战。尽管近年来已开发出一系列策略,但通过细菌细胞外淀粉样蛋白网络抑制细菌活性和毒力的研究却很少,尤其是使用纳米材料的相关研究。在此,合成了用阳离子支化聚乙烯亚胺聚合物包覆的银纳米颗粒和纳米团簇(AgNPs和AgNCs),并在对哺乳动物细胞安全的浓度下测定了它们的抗菌潜力。与超小的AgNCs相比,AgNPs具有更强的结合能力,可抑制铜绿假单胞菌细胞外淀粉样蛋白基质的主要蛋白质成分FapC的纤维化。两种类型的纳米颗粒均表现出对铜绿假单胞菌的浓度依赖性抗生物膜和抗菌特性。在1×10 m或更低的浓度下,AgNCs的杀菌活性和AgNPs的抗生物膜能力均与其结构介导的生物纳米相互作用有关,而与离子释放无关。具体而言,对于AgNPs,其抗生物膜效力与其抑制FapC纤维化的能力相关,而与其杀菌活性无关。本研究通过抑制淀粉样变性的新途径证明了安全纳米技术的抗菌潜力。

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