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Quorum-Quenching and Matrix-Degrading Enzymes in Multilayer Coatings Synergistically Prevent Bacterial Biofilm Formation on Urinary Catheters

机译:多层涂层中的群体猝灭和基质降解酶协同作用防止尿道上细菌生物膜的形成。

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Bacteria often colonize in-dwelling medical devices and grow as complex biofilm communities of cells embedded in a self-produced extracellular polymeric matrix, which increases their resistance to antibiotics and the host immune system. During biofilm growth, bacterial cells cooperate through specific quorum-sensing (QS) signals. Taking advantage of this mechanism of biofilm formation, we hypothesized that interrupting the communication among bacteria and simultaneously degrading the extracellular matrix would inhibit biofilm growth. To this end, coatings composed of the enzymes acylase and alpha-amylase, able to degrade bacterial QS molecules and polysaccharides, respectively, were built on silicone urinary catheters using a layer-by-layer deposition technique. Multilayer coatings of either acylase or amylase alone suppressed the biofilm formation of corresponding Gram-negative Pseudomonas aeruginosa and Gram-positive Staphylococcus aureus. Further assembly of both enzymes in hybrid nanocoatings resulted in stronger biofilm inhibition as a function of acylase or amylase position in the layers. Hybrid coatings, with the QS-signal-degrading acylase as outermost layer, demonstrated 30% higher antibiofilm efficiency against medically relevant Gram-negative bacteria compared to that of the other assemblies. These nanocoatings significantly reduced the occurrence of single-species (P. aeruginosa) and mixed-species (P. aeruginosa and Escherichia coli) biofilms on silicone catheters under both static and dynamic conditions. Moreover, in an in vivo animal model, the quorum quenching and matrix degrading enzyme assemblies delayed the biofilm growth up to 7 days.
机译:细菌通常定居在居住的医疗设备中,并以复杂的生物膜细胞群的形式生长,这些生物膜群嵌入自生的细胞外聚合物基质中,从而增加了它们对抗生素和宿主免疫系统的抵抗力。在生物膜生长期间,细菌细胞通过特定的群体感应(QS)信号进行协作。利用生物膜形成的这种机制,我们假设中断细菌之间的通讯并同时降解细胞外基质会抑制生物膜的生长。为此,在硅树脂导尿管上使用逐层沉积技术构建了分别由能够降解细菌QS分子和多糖的酶(乙酰化酶和α-淀粉酶)组成的涂层。单独的酰基转移酶或淀粉酶的多层涂层抑制了相应的革兰氏阴性铜绿假单胞菌和革兰氏阳性金黄色葡萄球菌的生物膜形成。杂化纳米涂层中两种酶的进一步组装导致更强的生物膜抑制作用,这取决于层中酰基转移酶或淀粉酶的位置。与其他组件相比,以QS信号降解酰基转移酶为最外层的杂化涂料对医学相关革兰氏阴性细菌的抗生物膜效率提高了30%。这些纳米涂层显着减少了在静态和动态条件下硅导管上单一物种(铜绿假单胞菌)和混合物种(铜绿假单胞菌和大肠杆菌)生物膜的发生。此外,在体内动物模型中,群体猝灭和基质降解酶的组装将生物膜的生长延迟了7天。

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