活性龋齿和无龋齿相关变异链球菌代谢重塑的蛋白质组学比较

S. S. Abed, P. Kiranmayi, Venkata R. Kolli
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摘要

简介:龋齿是一种多因素的疾病,主要是由口腔中常见的致龋细菌引起的。龋齿感染通常与产酸细菌变形链球菌有关。如果不及时治疗,蛀牙会导致牙齿脱钙、蛀牙、过敏,甚至牙齿脱落。利用质谱技术进行比较蛋白质组学研究,揭示突变S菌株中与龋齿相关的代谢重塑有利于生物膜的形成和定植。方法:我们进行了差异蛋白质组学分析,以确定与龋齿相关的变形链球菌菌株与健康口腔微生物组中存在的菌株之间蛋白质表达的差异。使用Orbitrap的高性能质谱(MS),已经导致了蛋白质组学在大规模蛋白质分析中的发展。研究人员将5份来自患有龋齿疾病(龋齿活跃)个体的临床标本与来自健康口腔微生物群(无龋齿)的2株分离株进行了比较。消化蛋白质样品,并进行多肽混合物研究。结果和讨论:通过蛋白质组学分析,在两组细菌中发现了3276个表达量相当的蛋白质。其中只有39种蛋白质是组1(没有龋齿的人)特有的,而444种蛋白质是组2特有的。(来自龋齿患者的变形链球菌)。通过PCA分析,对照(无龋)和龋(活跃龋)样本的分组差异有统计学意义。23在S. mutans细菌中发现了显著调节的蛋白(p < 0.05, t检验)。其中23个差异表达蛋白,10个上调,13个下调。通过鉴别不同的多肽和蛋白质,对其进行定量分析,并进行适当的生物信息学分析,可以深入了解变形链球菌在龋齿中形成的生物膜,以及使用各种拮抗剂/纳米颗粒方法作为常规抗生素的替代品进行干预的潜在目标。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Comparative Proteomics in Caries Active and Caries Free Associated S. Mutans Strains for Metabolic Remodeling Favouring Colonization
Introduction: A multifactorial condition, dental caries is primarily brought on by cariogenic bacteria that are frequently present in the mouth. Caries infections are commonly associated with the acid-producing bacteria Streptococcus mutans. If left untreated, dental caries can result in tooth decalcification, cavities, hypersensitivity, and even tooth loss. Comparative proteomics by Mass spectrometry was carried out to reveal caries-associated metabolic remodeling in S mutans isolates favouring biofilm formation and colonization. Methods: We conducted a differential proteomic analysis to determine the differences in protein expression between S.mutans strains linked to dental caries and those present in a healthy oral microbiome. High-performance mass spectrometry (MS) using Orbitrap, has led to the development of proteomics in larger-scale protein analysis. Five clinical specimens from individuals who had caries disease (Caries active) were compared with two isolates from the healthy oral dental microbiota (Caries free). Protein samples were digested, and a peptide mixture investigation was done. Results and Discussion: 3276 proteins that were expressed at comparable amounts in both groups of bacteria and were found by proteomic analysis. Only 39 of these proteins were unique and distinct to group 1 (those without caries), whereas 444 proteins were specific to group 2. (S.mutans from caries patients). Significant differences in the grouping of the control (Caries free) and caries (Caries active) samples were seen through PCA analysis. 23 Significantly regulated proteins in S. mutans bacteria were discovered (p < 0.05, t-test). Among these, 23 differentially expressed proteins, 10 were upregulated, and 13 downregulated. By Identifying differential peptides and proteins, their quantification, and appropriate bioinformatic analysis, there are insights into formation of biofilm by S. mutans in dental caries and potential targets for intervention using various antagonists/ nanoparticle approaches as alternatives to conventional antibiotics.
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