Large-scale screening identifies enzyme combinations that remove in situ grown oral biofilm

IF 5.9 Q1 MICROBIOLOGY
Signe Maria Nielsen , Karina Kambourakis Johnsen , Lea Benedicte Skov Hansen , Pernille Dukanovic Rikvold , Andreas Møllebjerg , Lorena Gonzalez Palmén , Thomas Durhuus , Sebastian Schlafer , Rikke Louise Meyer
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Abstract

Bacteria in the oral cavity are responsible for the development of dental diseases such as caries and periodontitis, but it is becoming increasingly clear that the oral microbiome also benefits human health. Many oral care products on the market are antimicrobial, killing a large part of the oral microbiome but without removing the disease-causing biofilm. Instead, non-biocidal matrix-degrading enzymes may be used to selectively remove biofilm without harming the overall microbiome.
The challenge of using enzymes to degrade biofilms is to match the narrow specificity of enzymes with the large structural diversity of extracellular polymeric substances that hold the biofilm together. In this study, we therefore perform a large-scale screening of single and multi-enzyme formulations to identify combinations of enzymes that most effectively remove dental biofilm.
We tested >400 different treatment modalities using 44 different enzymes in combinations with up to six enzymes in each formulation, on in vitro biofilms inoculated with human saliva. Mutanase was the only enzyme capable of removing biofilm on its own. Multi-enzyme formulations removed up to 69 % of the biofilm volume, and the most effective formulations all contained mutanase. We shortlisted 10 enzyme formulations to investigate their efficacy against biofilms formed on glass slabs on dental splints worn by 9 different test subjects. Three of the ten formulations removed more than 50 % of the biofilm volume. If optimal enzyme concentration and exposure time can be reached in vivo, these enzyme combinations have potential to be used in novel non-biocidal oral care products for dental biofilm control.
大规模筛选确定可清除原位生长的口腔生物膜的酶组合
口腔中的细菌是导致龋齿和牙周炎等牙科疾病的罪魁祸首,但人们越来越清楚地认识到,口腔微生物群也有益于人类健康。市场上的许多口腔护理产品都具有抗菌作用,能杀死大部分口腔微生物群,但却不能清除致病的生物膜。相反,非杀菌基质降解酶可用于选择性地清除生物膜,而不会损害整个微生物群。使用酶降解生物膜的挑战在于,如何使酶的狭隘特异性与将生物膜固定在一起的胞外聚合物物质的巨大结构多样性相匹配。因此,在这项研究中,我们对单酶和多酶配方进行了大规模筛选,以确定最有效去除牙科生物膜的酶组合。我们使用44种不同的酶组合,每种配方中最多有六种酶,对接种人体唾液的体外生物膜进行了400种不同治疗方式的测试。Mutanase是唯一一种能够单独清除生物膜的酶。多酶制剂可去除多达 69% 的生物膜体积,而最有效的制剂均含有木坦酶。我们筛选出 10 种酶制剂,研究它们对 9 位不同测试对象佩戴的牙夹板上的玻璃板形成的生物膜的功效。在这 10 种配方中,有 3 种能去除 50% 以上的生物膜。如果能在体内达到最佳的酶浓度和暴露时间,这些酶组合就有可能用于新型非杀菌口腔护理产品,以控制牙科生物膜。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Biofilm
Biofilm MICROBIOLOGY-
CiteScore
7.50
自引率
1.50%
发文量
30
审稿时长
57 days
期刊介绍:
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