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壳聚糖纳米粒子上细胞二糖脱氢酶和脱氧核糖核酸酶 I 的共固定化,针对真菌/细菌多微生物生物膜,靶向生物膜基质和微生物。

Co-immobilization of cellobiose dehydrogenase and deoxyribonuclease I on chitosan nanoparticles against fungal/bacterial polymicrobial biofilms targeting both biofilm matrix and microorganisms.

机构信息

Department of Otorhinolaryngology and Head and Neck Surgery, Medical University of Vienna, Vienna, Austria.

Biocatalysis and Biosensing Laboratory, Department of Food Sciences and Technology, BOKU - University of Natural Resources and Life Sciences, 1190 Vienna, Austria.

出版信息

Mater Sci Eng C Mater Biol Appl. 2020 Mar;108:110499. doi: 10.1016/j.msec.2019.110499. Epub 2019 Nov 28.

Abstract

Polymicrobial biofilm related infections have been a major threat in health care. In this study, the co-immobilization of cellobiose dehydrogenase (CDH) and deoxyribonuclease I (DNase) on positively charged chitosan nanoparticles (CSNPs) resulted in a bi-functional nanoparticle (CSNP-DNase-CDH) targeting both biofilm matrix and microorganisms. The in-vitro antibiofilm activities of CSNPs against monomicrobial and polymicrobial biofilms of Candida albicans and Staphylococcus aureus were evaluated. The results showed that CSNPs were able to penetrate across the matrix of biofilms and interfere with embedded microbial cells. CSNP-DNase-CDH exhibited a higher activity than CSNPs loaded with only DNase or CDH for inhibiting monomicrobial and polymicrobial biofilm formation as well as for disrupting pre-formed biofilms. Furthermore, CSNP-DNase-CDH could disrupt the biofilm formation through degradation of eDNA, reduce biofilm thickness, and kill microbial cells on silicone. The bi-functional CSNP is applicable for the protection of medical devices from polymicrobial biofilms or the treatment of device associated infections.

摘要

多微生物生物膜相关感染一直是医疗保健领域的主要威胁。在这项研究中,细胞二糖脱氢酶 (CDH) 和脱氧核糖核酸酶 I (DNase) 共固定在带正电荷的壳聚糖纳米颗粒 (CSNPs) 上,得到了一种针对生物膜基质和微生物的双功能纳米颗粒 (CSNP-DNase-CDH)。评估了 CSNPs 对白色念珠菌和金黄色葡萄球菌单微生物和多微生物生物膜的体外抗生物膜活性。结果表明,CSNPs 能够穿透生物膜基质并干扰嵌入的微生物细胞。CSNP-DNase-CDH 对单微生物和多微生物生物膜形成以及破坏已形成的生物膜的抑制作用均高于仅负载 DNase 或 CDH 的 CSNPs。此外,CSNP-DNase-CDH 可以通过降解 eDNA 来破坏生物膜形成,减少生物膜厚度,并杀死硅酮上的微生物细胞。这种双功能 CSNP 可用于保护医疗器械免受多微生物生物膜的侵害,或用于治疗与器械相关的感染。

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