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聚(ε-赖氨酸)树枝状大分子作为铜绿假单胞菌群体感应的调节剂

Poly(ε-lysine) dendrons as modulators of quorum sensing in Pseudomonas aeruginosa.

作者信息

Issa Rahaf, Meikle Steve T, James Stuart, Cooper Ian R

机构信息

School of Pharmacy and Biomolecular Sciences, University of Brighton, Huxley Building, Lewes Road, Brighton, BN2 4GJ, UK,

出版信息

J Mater Sci Mater Med. 2015 May;26(5):176. doi: 10.1007/s10856-015-5508-1. Epub 2015 Apr 17.

Abstract

The opportunistic pathogen Pseudomonas aeruginosa is a significant contributor to recalcitrant multi-drug resistant infections. In a vigorous search for alternative therapeutic approaches, the communication system used by this bacterium to synchronise the expression of genes involved in pathogenicity has been identified as a potential target. Poly(ε-lysine) dendrons, composed of three branching generations, were examined herein for their anti-virulence potential and ability to disperse within P. a eruginosa biofilms. These hyperbranched macromolecules reduced attachment and biomass production under different nutrient growth conditions, and at concentrations that were not lethal to planktonic cells (0.2, 0.4 and 0.8 mg/mL). Fluorescent labelling revealed the intracellular localisation and cell-penetrating capacity of the dendron, and showed the rapid uptake and release of unexploited dendron from pre-established P. a eruginosa biofilms. Additionally, the dendron induced complete attenuation of LasA protease, a marker of quorum sensing inactivation, by preventing its accumulation in the external environment. This study thus demonstrates the anti-virulence potential of this class of macromolecules, and could represent a novel therapeutic approach for the treatment of antibiotic-resistant P. a eruginosa infections.

摘要

机会致病菌铜绿假单胞菌是顽固性多重耐药感染的重要成因。在积极寻找替代治疗方法的过程中,这种细菌用于同步致病性相关基因表达的通讯系统已被确定为一个潜在靶点。本文研究了由三代分支组成的聚(ε-赖氨酸)树枝状大分子的抗毒力潜力及其在铜绿假单胞菌生物膜内的分散能力。这些超支化大分子在不同营养生长条件下以及在对浮游细胞无致死性的浓度(0.2、0.4和0.8毫克/毫升)下,降低了细菌的附着和生物量产生。荧光标记揭示了树枝状大分子的细胞内定位和细胞穿透能力,并显示了预先形成的铜绿假单胞菌生物膜对未利用树枝状大分子的快速摄取和释放。此外,树枝状大分子通过阻止群体感应失活标志物LasA蛋白酶在外部环境中的积累,使其完全失活。因此,本研究证明了这类大分子的抗毒力潜力,并可能代表一种治疗耐抗生素铜绿假单胞菌感染的新治疗方法。

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