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Optimization and Evaluation of the 30S-S11 rRNA Gene for Taxonomic Profiling of Oral Streptococci

机译:30S-S11 rRNA基因在口腔链球菌分类学分析中的优化与评价

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摘要

The microbiota associated with the initiation and progression of dental caries has yet to be fully characterized. Although much insight has been gained from 16S rRNA hypervariable region DNA sequencing, this approach has several limitations, including poor taxonomic resolution at the species level. Dental caries is a multifactorial disease driven by interactions between the highly complex microbial biofilm community and host factors like diet, oral hygiene habits, and age. The oral streptococci are one of the most dominant members of the plaque biofilm and are implicated in disease but also in maintaining oral health. Current methods used for studying the supragingival plaque community commonly sequence portions of the16S rRNA gene, which often cannot taxonomically resolve members of the streptococcal community past the genus level due to their sequence similarity. The goal of this study was to design and evaluate a more reliable and cost-effective method to identify oral streptococci at the species level by applying a new locus, the 30S-S11 rRNA gene, for high-throughput amplicon sequencing. The study results demonstrate that the newly developed single-copy 30S-S11 gene locus resolved multiple amplicon sequence variants (ASVs) within numerous species, providing much improved taxonomic resolution over 16S rRNA V4. Moreover, the results reveal that different ASVs within a species were found to change in abundance at different stages of caries progression. These findings suggest that strains of a single species may perform distinct roles along a biochemical spectrum associated with health and disease. The improved identification of oral streptococcal species will provide a better understanding of the different ecological roles of oral streptococci and inform the design of novel oral probiotic formulations for prevention and treatment of dental caries. IMPORTANCE The microbiota associated with the initiation and progression of dental caries has yet to be fully characterized. Although much insight has been gained from 16S rRNA hypervariable region DNA sequencing, this approach has several limitations, including poor taxonomic resolution at the species level. This is particularly relevant for oral streptococci, which are abundant members of oral biofilm communities and major players in health and caries disease. Here, we develop a new method for taxonomic profiling of oral streptococci based on the 30S-S11 rRNA gene, which provides much improved resolution over 16S rRNA V4 (resolving 10 as opposed to 2 species). Importantly, 30S-S11 can resolve multiple amplicon sequence variants (ASVs) within species, providing an unprecedented insight into the ecological progression of caries. For example, our findings reveal multiple incidences of different ASVs within a species with contrasting associations with health or disease, a finding that has high relevance toward the informed design of prebiotic and probiotic therapy.
机译:与龋齿的发生和发展相关的微生物群尚未完全表征。尽管从 16S rRNA 高变区 DNA 测序中获得了很多见解,但这种方法存在一些局限性,包括物种水平的分类分辨率较差。龋齿是一种多因素疾病,由高度复杂的微生物生物膜群落与饮食、口腔卫生习惯和年龄等宿主因素之间的相互作用驱动。口腔链球菌是斑块生物膜中最主要的成员之一,与疾病有关,但也与维持口腔健康有关。目前用于研究龈上斑块群落的方法通常对16S rRNA基因的部分进行测序,由于序列相似性,这些基因通常无法从分类学上解析超过属水平的链球菌群落成员。本研究的目的是设计和评估一种更可靠、更具成本效益的方法,通过应用新的位点 30S-S11 rRNA 基因进行高通量扩增子测序,在物种水平上鉴定口腔链球菌。研究结果表明,新开发的单拷贝30S-S11基因位点可解析多个物种内的多个扩增子序列变异(ASV),与16S rRNA V4相比,其分类分辨率大大提高。此外,结果显示,在龋齿进展的不同阶段,物种内不同的ASVs的丰度变化。这些发现表明,单个物种的菌株可能在与健康和疾病相关的生化光谱中发挥不同的作用。改进口腔链球菌物种的鉴定将更好地了解口腔链球菌的不同生态作用,并为设计用于预防和治疗龋齿的新型口服益生菌制剂提供信息。重要性 与龋齿的发生和发展相关的微生物群尚未完全表征。尽管从 16S rRNA 高变区 DNA 测序中获得了很多见解,但这种方法存在一些局限性,包括物种水平的分类分辨率较差。这与口腔链球菌尤其相关,口腔链球菌是口腔生物膜群落的丰富成员,也是健康和龋齿疾病的主要参与者。在这里,我们开发了一种基于 30S-S11 rRNA 基因的口腔链球菌分类分析新方法,该方法比 16S rRNA V4 提高了分辨率(解析 10 个而不是 2 个物种)。重要的是,30S-S11 可以解析物种内的多个扩增子序列变异 (ASV),为龋齿的生态学进展提供前所未有的见解。例如,我们的研究结果揭示了一个物种中不同ASV的多个发病率,这些ASV与健康或疾病有着截然不同的关联,这一发现与益生元和益生菌疗法的知情设计具有高度相关性。

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