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有氧-厌氧混合培养条件可诱导体外唾液生物膜产生蛋白水解活性。

Mixed aerobic-anaerobic incubation conditions induce proteolytic activity from in vitro salivary biofilms.

作者信息

Cleaver Leanne M, Moazzez Rebecca, Carpenter Guy H

机构信息

Centre for Host Microbiome Interactions, King's College London Faculty of Dentistry, Oral and Craniofacial Sciences, London, UK.

Centre for Oral, Clinical and Translational Science, King's College London Faculty of Dentistry, Oral and Craniofacial Sciences, London, UK.

出版信息

J Oral Microbiol. 2019 Jul 25;11(1):1643206. doi: 10.1080/20002297.2019.1643206. eCollection 2019.

Abstract

Oral biofilms have not been studied using both metabolome and protein profiling concurrently. Bacteria produce proteases that lead to degradation of functional salivary proteins. The novel protocol described here allows for complete characterisation of  oral biofilms, including proteolytic, metabolic, and microbiome analysis. Biofilms were grown on hydroxyapatite discs from whole mouth saliva, using sterilised saliva as a growth-medium, in different growth environments. Salivary protein degradation was assessed from spent saliva growth-medium using SDS-polyacrylamide gel electrophoresis (SDS-PAGE), and metabolic activity by nuclear magnetic resonance (NMR). Discs were assessed for depth and coverage of biofilms by confocal laser scanning microscopy (CLSM), and biofilms were collected at the end of the experiment for  gene sequence analysis. There was a significant difference in biofilm viability, salivary protein degradation, and metabolites identified between biofilms grown aerobically and biofilms exposed to an anaerobic environment. Bacterial  gene sequencing showed the predominant genus in the 7-day aerobic biofilms was , in aerobic-anaerobic and anaerobic 7-day biofilms , and in aerobic-anaerobic and anaerobic 13-day biofilms . This data suggests new growth requirements and capabilities for analysing salivary biofilms , which can be used to benefit future research into oral bacterial biofilms.

摘要

尚未同时使用代谢组学和蛋白质谱分析来研究口腔生物膜。细菌产生的蛋白酶会导致功能性唾液蛋白降解。本文所述的新方案能够全面表征口腔生物膜,包括蛋白水解、代谢和微生物组分析。生物膜在羟基磷灰石圆盘上由全口唾液生长而成,使用经过消毒的唾液作为生长培养基,置于不同的生长环境中。使用十二烷基硫酸钠 - 聚丙烯酰胺凝胶电泳(SDS - PAGE)从用过的唾液生长培养基中评估唾液蛋白降解情况,并通过核磁共振(NMR)评估代谢活性。通过共聚焦激光扫描显微镜(CLSM)评估圆盘上生物膜的深度和覆盖范围,并在实验结束时收集生物膜用于基因序列分析。在需氧条件下生长的生物膜与暴露于厌氧环境的生物膜之间,生物膜活力、唾液蛋白降解以及鉴定出的代谢物存在显著差异。细菌基因测序表明,7天需氧生物膜中的优势菌属为 ,在需氧 - 厌氧和厌氧7天生物膜中为 ,在需氧 - 厌氧和厌氧13天生物膜中为 。这些数据表明了分析唾液生物膜的新生长需求和能力,可用于推动未来对口腔细菌生物膜的研究。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c78d/6711154/f1d7baddd5e9/ZJOM_A_1643206_F0003_OC.jpg

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