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细胞外DNA使生物膜酸化并诱导铜绿假单胞菌产生氨基糖苷类耐药性。

Extracellular DNA Acidifies Biofilms and Induces Aminoglycoside Resistance in Pseudomonas aeruginosa.

作者信息

Wilton Mike, Charron-Mazenod Laetitia, Moore Richard, Lewenza Shawn

机构信息

Department of Microbiology, Immunology and Infectious Diseases, Snyder Institute of Chronic Diseases, Cumming School of Medicine, University of Calgary, Calgary, Alberta, Canada.

Department of Microbiology, Immunology and Infectious Diseases, Snyder Institute of Chronic Diseases, Cumming School of Medicine, University of Calgary, Calgary, Alberta, Canada Faculty of Science and Technology, Athabasca University, Athabasca, Alberta, Canada

出版信息

Antimicrob Agents Chemother. 2015 Nov 9;60(1):544-53. doi: 10.1128/AAC.01650-15. Print 2016 Jan.

Abstract

Biofilms consist of surface-adhered bacterial communities encased in an extracellular matrix composed of DNA, exopolysaccharides, and proteins. Extracellular DNA (eDNA) has a structural role in the formation of biofilms, can bind and shield biofilms from aminoglycosides, and induces antimicrobial peptide resistance mechanisms. Here, we provide evidence that eDNA is responsible for the acidification of Pseudomonas aeruginosa planktonic cultures and biofilms. Further, we show that acidic pH and acidification via eDNA constitute a signal that is perceived by P. aeruginosa to induce the expression of genes regulated by the PhoPQ and PmrAB two-component regulatory systems. Planktonic P. aeruginosa cultured in exogenous 0.2% DNA or under acidic conditions demonstrates a 2- to 8-fold increase in aminoglycoside resistance. This resistance phenotype requires the aminoarabinose modification of lipid A and the production of spermidine on the bacterial outer membrane, which likely reduce the entry of aminoglycosides. Interestingly, the additions of the basic amino acid L-arginine and sodium bicarbonate neutralize the pH and restore P. aeruginosa susceptibility to aminoglycosides, even in the presence of eDNA. These data illustrate that the accumulation of eDNA in biofilms and infection sites can acidify the local environment and that acidic pH promotes the P. aeruginosa antibiotic resistance phenotype.

摘要

生物膜由包裹在由DNA、胞外多糖和蛋白质组成的细胞外基质中的表面附着细菌群落构成。细胞外DNA(eDNA)在生物膜形成中具有结构作用,可结合并保护生物膜免受氨基糖苷类药物影响,并诱导抗菌肽耐药机制。在此,我们提供证据表明eDNA导致铜绿假单胞菌浮游培养物和生物膜酸化。此外,我们表明酸性pH值和通过eDNA酸化构成一种信号,铜绿假单胞菌可感知该信号以诱导由PhoPQ和PmrAB双组分调节系统调控的基因表达。在外源0.2% DNA中或在酸性条件下培养的浮游铜绿假单胞菌对氨基糖苷类药物的耐药性增加2至8倍。这种耐药表型需要脂多糖A的氨基阿拉伯糖修饰以及细菌外膜上亚精胺的产生,这可能减少氨基糖苷类药物的进入。有趣的是,添加碱性氨基酸L-精氨酸和碳酸氢钠可中和pH值并恢复铜绿假单胞菌对氨基糖苷类药物的敏感性,即使存在eDNA也是如此。这些数据表明,生物膜和感染部位中eDNA的积累可使局部环境酸化,且酸性pH值促进铜绿假单胞菌的抗生素耐药表型。

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