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哈茨木霉来源的突变酶经突变诱导产生:短期处理以降解成熟变形链球菌生物膜。

Mutanase from Trichoderma harzianum inductively Produced by Mutan: Short-Term Treatment to Degrade Mature Streptococcus mutans Biofilm.

机构信息

Department of Children's Clinic, Ribeirão Preto School of Dentistry, University of São Paulo, Café Avenue s/n, Ribeirão Preto, São Paulo, 14040-904, Brazil.

Department of BioMolecular Sciences, School of Pharmaceutical Sciences of Ribeirão Preto, University of São Paulo, Café Avenue s/n, Ribeirão Preto, São Paulo, 14040-903, Brazil.

出版信息

Curr Microbiol. 2023 Aug 5;80(9):312. doi: 10.1007/s00284-023-03417-7.

DOI:10.1007/s00284-023-03417-7
PMID:37542660
Abstract

This study aimed to evaluate the disruptive effect of fungal mutanase against cariogenic biofilm after short-term treatment. For that, mature Streptococcus mutans biofilms (n = 9) were exposed to active or inactivated enzymes produced by Trichoderma harzianum for 1 min, two times per day. Biofilms were analyzed by amount of matrix water-insoluble polysaccharides, bacterial viability, acidogenicity, and morphology by scanning electron microscopy (SEM). The group treated with active enzymes (AE) had a significantly lower amount of insoluble polysaccharides (893.30 ± 293.69) when compared to the negative control group (NaCl, 2192.59 ± 361.96), yet no significant difference was found when comparing to the positive control group (CHX, 436.82 ± 151.07). Also, there was no significant effect on bacteria metabolism and viability (P-value < 0.05). Data generated by the quantitative analysis were confirmed through scanning electron microscopy images. Thus, fungal mutanase degraded the biofilm after a short-term treatment without interfering with bacterial viability and metabolism. Such findings offer insight to the development of routine oral care products containing this input.

摘要

本研究旨在评估真菌突变酶对致龋生物膜的短期治疗后的破坏作用。为此,将成熟的变形链球菌生物膜(n=9)暴露于哈茨木霉产生的活性或失活酶中,每天两次,每次 1 分钟。通过扫描电子显微镜(SEM)分析基质水不溶性多糖的量、细菌活力、产酸和形态。与阴性对照组(NaCl,2192.59±361.96)相比,用活性酶(AE)处理的组的不溶性多糖量(893.30±293.69)显著降低,但与阳性对照组(CHX,436.82±151.07)相比无显著差异。此外,细菌代谢和活力也没有显著影响(P 值<0.05)。定量分析生成的数据通过扫描电子显微镜图像得到证实。因此,真菌突变酶在短期治疗后降解了生物膜,而不干扰细菌活力和代谢。这些发现为开发含有这种成分的常规口腔护理产品提供了思路。

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Metabolomic Signatures of In Vitro Biofilm Maturation of Streptococcus mutans.变形链球菌体外生物膜成熟的代谢组学特征。
Curr Microbiol. 2022 Feb 7;79(3):86. doi: 10.1007/s00284-022-02778-9.
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Mimicking biofilm formation and development: Recent progress in and biofilm models.模拟生物膜的形成与发展:生物膜模型的最新进展
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Innovative Strategies Toward the Disassembly of the EPS Matrix in Bacterial Biofilms.细菌生物膜中胞外多糖基质分解的创新策略
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Resistance Toward Chlorhexidine in Oral Bacteria - Is There Cause for Concern?口腔细菌对洗必泰的耐药性——是否值得担忧?
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Protocols to Study Dental Caries In Vitro: Microbial Caries Models.体外研究龋齿的实验方案:微生物龋齿模型
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