用氮氧化物功能化抗生素作为一种有效的广谱生物膜根除策略。

Biofilms Pub Date : 2020-07-01 DOI:10.5194/biofilms9-12
Anthony D. Verderosa, K. Fairfull‐Smith, Makrina Totsika
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引用次数: 0

摘要

背景:浮游细菌与表面(生物或非生物)的粘附,以及它们随后聚集成被称为生物膜的多细胞群落的能力,是抗生素治疗失败和多种病原体(如铜绿假单胞菌、大肠杆菌和金黄色葡萄球菌)引起的慢性感染持续存在的主要驱动力;并困扰着全世界的医疗系统。据估计,生物膜参与了人类80%以上的微生物感染,并且通常对传统的抗菌治疗表现出极端的耐药性。因此,迫切需要针对生物膜驻留细胞的新型抗菌剂。在这里,我们介绍了新一代具有强大生物膜根除活性的双作用氮氧化物功能抗生素的开发和评估。方法:利用合成有机化学生产具有靶向生物膜根除能力的新一代氮氧化物功能化抗生素。使用MBECTM装置(一种可重复的高通量静态生物膜形成系统)测试这些化合物的生物膜根除和/或几种细菌的扩散。用一系列稀释的特定测试试剂处理成熟的生物膜,并通过在600nm下的吸收光谱或电镀活细胞计数来量化回收的细菌数量。处理过的生物膜也用活/死(SYTO-9/PI)细菌活力试剂盒染色,并通过荧光和共聚焦激光扫描显微镜进行分析。结果:一氧化二氮功能抗生素对多种医学上重要的病原体表现出强大的生物膜根除活性,包括铜绿假单胞菌、尿路致病性大肠杆菌和金黄色葡萄球菌。在最小生物膜根除浓度(MBEC)测定中,氮氧化物功能化抗生素对金黄色葡萄球菌生物膜的效力是母体抗生素环丙沙星的64倍,对尿路致病性大肠杆菌生物膜的疗效至少是母体抗生素的2倍。结论:目前,抗生素通常对生物膜感染完全无效。一氧化二氮功能化抗生素是一种很有前途的新策略,可以绕过革兰氏阳性和革兰氏阴性生物膜对传统治疗的耐药性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Functionalising antibiotics with nitroxides as an effective broad-spectrum biofilm eradication strategy.

Background:

The adhesion of planktonic bacteria to a surface (biotic or abiotic), and their subsequent ability to aggregate into multicellular communities called biofilms, is a major driving force of failing antibiotic therapy and persistence in chronic infections caused by a variety of pathogens (e.g., Pseudomonas aeruginosa, Escherichia coli, and Staphylococcus aureus) and plaguing healthcare systems worldwide. Biofilms are estimated to be involved in over 80% of all microbial infections in humans, and commonly exhibit extreme resistance to conventional antimicrobial treatments. Consequently, there is an urgent need for novel antimicrobial agents, which target biofilm residing cells. Here, we present the development and evaluation of a new generation of dual-acting nitroxide functionalised antibiotics with potent biofilm eradication activity.

Methodology:

Synthetic organic chemistry was utilised to produce a new generation of nitroxide functionalised antibiotics with targeted biofilm eradication capabilities. These compounds were tested for biofilm eradication and/or dispersal of several bacterial species using the MBECTM device, a reproducible high-throughput static biofilm formation system. Mature biofilms were treated with serial dilutions of the specific test agent(s) and recovered bacterial numbers were quantified by absorbance spectroscopy at 600 nm or plating for viable cell counts. Treated biofilms were also stained with Live/Dead (SYTO-9/PI) bacterial viability kit and analysed by fluorescence and confocal laser scanning microscopy.

Results:

Nitroxide functionalised antibiotics exhibit potent biofilm-eradication activity against a variety of medically important pathogens, including P. aeruginosa, uropathogenic E. coli, and S. aureus. In Minimal Biofilm Eradication Concentration (MBEC) assays nitroxide functionalised antibiotics were 64-fold more potent against S. aureus biofilms, and at least 2-fold more potent against uropathogenic E. coli biofilms than the parent antibiotic ciprofloxacin.

Conclusions:

Currently, antibiotics are often entirely ineffective against biofilm infections. Nitroxide functionalised antibiotics represent a promising new strategy, which could circumvent the resistance of Gram-positive and Gram-negative biofilms to conventional treatments.

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