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脱氧核糖核酸酶和蛋白酶联合处理会干扰多物种口腔生物膜的组成和结构完整性。

Combined DNase and Proteinase Treatment Interferes with Composition and Structural Integrity of Multispecies Oral Biofilms.

作者信息

Karygianni Lamprini, Attin Thomas, Thurnheer Thomas

机构信息

Clinic of Conservative and Preventive Dentistry, Center of Dental Medicine, University of Zurich, 8032 Zurich, Switzerland.

出版信息

J Clin Med. 2020 Apr 1;9(4):983. doi: 10.3390/jcm9040983.

Abstract

Modification of oral biofilms adhering to dental hard tissues could lead to new treatment approaches in cariology and periodontology. In this study the impact of DNase I and/or proteinase K on the formation of a simulated supragingival biofilm was investigated in vitro. Six-species biofilms were grown anaerobically in the presence of DNase I and proteinase K. After 64 h biofilms were either harvested and quantified by culture analysis or proceeded to staining followed by confocal laser scanning microscopy. Microbial cells were stained using DNA-dyes or fluorescent in situ hybridization. Exopolysaccharides, eDNA and exoproteins were stained with Calcofluor, anti-DNA-antibody, and Sypro Ruby, respectively. Overall, results showed that neither DNase I nor proteinase K had an impact on total colony-forming units (CFUs) compared to the control without enzymes. However, DNase I significantly suppressed the growth of , , , and . Proteinase K treatment induced significant increase in and CFUs ( < 0.001), whereas and showed lower CFUs compared to the control. Interestingly, confocal images visualized the biofilm degradation caused by DNase I and proteinase K. Thus, enzymatic treatment should be combined with conventional antimicrobial agents aiming at both bactericidal effectiveness and biofilm dispersal.

摘要

附着于牙齿硬组织的口腔生物膜的改变可能会为龋病学和牙周病学带来新的治疗方法。在本研究中,体外研究了脱氧核糖核酸酶I(DNase I)和/或蛋白酶K对模拟龈上生物膜形成的影响。在存在DNase I和蛋白酶K的情况下,六种细菌的生物膜在厌氧条件下生长。64小时后,生物膜要么被收获并通过培养分析进行定量,要么进行染色,然后进行共聚焦激光扫描显微镜检查。使用DNA染料或荧光原位杂交对微生物细胞进行染色。分别用荧光增白剂、抗DNA抗体和Sypro Ruby对胞外多糖、胞外DNA和胞外蛋白进行染色。总体而言,结果表明,与未添加酶的对照组相比,DNase I和蛋白酶K对总菌落形成单位(CFU)均无影响。然而,DNase I显著抑制了[具体细菌名称1]、[具体细菌名称2]、[具体细菌名称3]、[具体细菌名称4]和[具体细菌名称5]的生长。蛋白酶K处理导致[具体细菌名称6]和[具体细菌名称7]的CFU显著增加(P<0.001),而[具体细菌名称8]和[具体细菌名称9]的CFU与对照组相比更低。有趣的是,共聚焦图像显示了DNase I和蛋白酶K引起的生物膜降解。因此,酶处理应与传统抗菌剂联合使用,以达到杀菌效果和生物膜分散的目的。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4f8f/7231231/022b1c8e5e0b/jcm-09-00983-g001.jpg

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