Department of Cariology, Academic Centre for Dentistry Amsterdam (ACTA), University of Amsterdam and Free University Amsterdam, the Netherlands.
BMC Microbiol. 2009 Dec 15;9:259. doi: 10.1186/1471-2180-9-259.
BACKGROUND: Most studies examining the commensal human oral microbiome are focused on disease or are limited in methodology. In order to diagnose and treat diseases at an early and reversible stage an in-depth definition of health is indispensible. The aim of this study therefore was to define the healthy oral microbiome using recent advances in sequencing technology (454 pyrosequencing). RESULTS: We sampled and sequenced microbiomes from several intraoral niches (dental surfaces, cheek, hard palate, tongue and saliva) in three healthy individuals. Within an individual oral cavity, we found over 3600 unique sequences, over 500 different OTUs or "species-level" phylotypes (sequences that clustered at 3% genetic difference) and 88 - 104 higher taxa (genus or more inclusive taxon). The predominant taxa belonged to Firmicutes (genus Streptococcus, family Veillonellaceae, genus Granulicatella), Proteobacteria (genus Neisseria, Haemophilus), Actinobacteria (genus Corynebacterium, Rothia, Actinomyces), Bacteroidetes (genus Prevotella, Capnocytophaga, Porphyromonas) and Fusobacteria (genus Fusobacterium).Each individual sample harboured on average 266 "species-level" phylotypes (SD 67; range 123 - 326) with cheek samples being the least diverse and the dental samples from approximal surfaces showing the highest diversity. Principal component analysis discriminated the profiles of the samples originating from shedding surfaces (mucosa of tongue, cheek and palate) from the samples that were obtained from solid surfaces (teeth).There was a large overlap in the higher taxa, "species-level" phylotypes and unique sequences among the three microbiomes: 84% of the higher taxa, 75% of the OTUs and 65% of the unique sequences were present in at least two of the three microbiomes. The three individuals shared 1660 of 6315 unique sequences. These 1660 sequences (the "core microbiome") contributed 66% of the reads. The overlapping OTUs contributed to 94% of the reads, while nearly all reads (99.8%) belonged to the shared higher taxa. CONCLUSIONS: We obtained the first insight into the diversity and uniqueness of individual oral microbiomes at a resolution of next-generation sequencing. We showed that a major proportion of bacterial sequences of unrelated healthy individuals is identical, supporting the concept of a core microbiome at health.
背景:大多数研究人类口腔共生微生物的研究都集中在疾病上,或者在方法上受到限制。为了在早期和可逆转阶段诊断和治疗疾病,深入了解健康是必不可少的。因此,本研究的目的是使用最新的测序技术(454 焦磷酸测序)定义健康的口腔微生物组。
结果:我们从三个健康个体的多个口腔内小生境(牙齿表面、脸颊、硬腭、舌头和唾液)中采样并测序了微生物组。在个体口腔内,我们发现了 3600 多个独特的序列、500 多个不同的 OTU 或“种水平”的分类群(聚类在 3%遗传差异的序列)和 88-104 个高级分类群(属或更包容的分类群)。主要的分类群属于厚壁菌门(链球菌属、韦荣氏球菌科、颗粒杆菌属)、变形菌门(奈瑟菌属、嗜血杆菌属)、放线菌门(棒状杆菌属、罗氏菌属、放线菌属)、拟杆菌门(普雷沃氏菌属、卡他莫拉菌属、卟啉单胞菌属)和梭杆菌门(梭杆菌属)。每个个体样本平均含有 266 个“种水平”的分类群(标准差 67;范围 123-326),脸颊样本的多样性最低,而接近表面的牙齿样本的多样性最高。主成分分析可区分来自脱落表面(舌、颊和腭的黏膜)的样本和来自固体表面(牙齿)的样本的特征。三个微生物组之间的高级分类群、“种水平”的分类群和独特序列有很大的重叠:84%的高级分类群、75%的 OTU 和 65%的独特序列存在于至少两个微生物组中。三个个体共有的 3315 个独特序列中的 1660 个序列(“核心微生物组”)占读段的 66%。重叠的 OTU 贡献了 94%的读段,而几乎所有的读段(99.8%)都属于共享的高级分类群。
结论:我们首次以下一代测序的分辨率深入了解了个体口腔微生物组的多样性和独特性。我们表明,来自无关健康个体的大部分细菌序列是相同的,这支持了健康的核心微生物组的概念。
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