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Inhibition and Dispersal of Pseudomonas aeruginosa Biofilms by Combination Treatment with Escapin Intermediate Products and Hydrogen Peroxide

机译:氟哌辛中间产物和过氧化氢组合治疗抑制作用铜绿假单胞菌的抑制作用

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摘要

Escapin is an L-amino acid oxidase that acts on lysine to produce hydrogen peroxide (H2O2), ammonia, and equilibrium mixtures of several organic acids collectively called escapin intermediate products (EIP). Previous work showed that the combination of synthetic EIP and H2O2 functions synergistically as an antimicrobial toward diverse planktonic bacteria. We initiated the present study to investigate how the combination of EIP and H2O2 affected bacterial biofilms, using Pseudomonas aeruginosa as a model. Specifically, we examined concentrations of EIP and H2O2 that inhibited biofilm formation or fostered disruption of established biofilms. High-throughput assays of biofilm formation using microtiter plates and crystal violet staining showed a significant effect from pairing EIP and H2O2, resulting in inhibition of biofilm formation relative to biofilm formation in untreated controls or with EIP or H2O2 alone. Similarly, flow cell analysis and confocal laser scanning microscopy revealed that the EIP and H2O2 combination reduced the biomass of established biofilms relative to that of the controls. Area layer analysis of biofilms posttreatment indicated that disruption of biomass occurs down to the substratum. Only nanomolar to micromolar concentrations of EIP and H2O2 were required to impact biofilm formation or disruption, and these concentrations are significantly lower than those causing bactericidal effects on planktonic bacteria. Micromolar concentrations of EIP and H2O2 combined enhanced P. aeruginosa swimming motility compared to the effect of either EIP or H2O2 alone. Collectively, our results suggest that the combination of EIP and H2O2 may affect biofilms by interfering with bacterial attachment and destabilizing the biofilm matrix.
机译:Escapin是一种L-氨基酸氧化酶,其作用于赖氨酸,以产生若干有机酸的过氧化氢(H 2 O 2),氨和平衡混合物,这些有机酸共同称为Escapin中间产物(EIP)。以前的工作表明,合成eIP和H2O2的组合和H2O2功能协同为倾向于多种浮游细菌的抗微生物。我们启动了本研究,以研究EIP和H2O2影响的细菌生物膜的组合如何使用假单胞菌铜绿假单胞菌作为模型。具体地,我们检查了抑制生物膜形成或培养了已建立的生物膜的破坏的EIP和H 2 O 2的浓度。使用微量滴定板和晶体紫色染色的生物膜形成的高通量测定表现出与配对EIP和H 2 O 2的显着影响,导致相对于未处理对照中的生物膜形成或单独用EIP或H 2 O 2的生物膜形成抑制生物膜形成。类似地,流动细胞分析和共聚焦激光扫描显微镜显示EIP和H 2 O 2的组合相对于对照的成立生物膜的生物质。生物膜后疗法的区域层分析表明,生物质的破坏发生在底层。仅需要纳米摩尔对微摩尔浓度的EIP和H 2 O 2,以冲击生物膜形成或破坏,并且这些浓度显着低于导致氏菌菌细菌的杀菌作用的浓度。 EIP和H2O2的微摩尔浓度组合增强的P.铜绿假单胞菌游泳运动与单独的EIP或H2O2的效果相比。统称,我们的结果表明EIP和H 2 O 2的组合可以通过干扰细菌附着和破坏生物膜基质来影响生物膜。

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