Bach Lydia Luise, Ram Asha, Ijaz Umer Z, Evans Thomas J, Lindström Jan
Institute of Biodiversity, Animal Health and Comparative Medicine, University of Glasgow, Glasgow, United Kingdom.
School of Engineering, University of Glasgow, Glasgow, United Kingdom.
Front Microbiol. 2021 Jan 21;11:573969. doi: 10.3389/fmicb.2020.573969. eCollection 2020.
Our understanding of human microbial communities, in particular in regard to diseases is advancing, yet the basic understanding of the microbiome in healthy subjects over time remains limited. The oropharynx is a key target for colonization by several important human pathogens. To understand how the oropharyngeal microbiome might limit infections, and how intercurrent infections might be associated with its composition, we characterized the oropharyngeal microbiome of 18 healthy adults, sampled weekly over a 40-weeks using culture-independent molecular techniques. We detected nine phyla, 202 genera and 1438 assignments on OTU level, dominated by Firmicutes, Bacteroidetes, and Proteobacteria on phylum level. Individual microbiomes of participants were characterized by levels of high alpha diversity (mean = 204.55 OTUs, sd = 35.64), evenness (19.83, sd = 9.74) and high temporal stability (mean Pearson's correlation between samples of 0.52, sd = 0.060), with greater differences in microbiome community composition between than within individuals. Significant changes in community composition were associated with disease states, suggesting that it is possible to detect specific changes in OTU abundance and community composition during illness. We defined the common core microbiota by varying occurrence and abundance thresholds showing that individual core microbiomes share a substantial number of OTUs across participants, chiefly and . Our results provide insights into the microbial communities that characterize the healthy human oropharynx, community structure and variability, and provide new approaches to define individual and shared cores. The wider implications of this result include the potential for modeling the general dynamics of oropharynx microbiota both in health and in response to antimicrobial treatments or probiotics.
我们对人类微生物群落的理解,尤其是与疾病相关的理解正在不断推进,但对健康受试者微生物组随时间变化的基本认识仍然有限。口咽部是几种重要人类病原体定植的关键靶点。为了了解口咽微生物组如何限制感染,以及并发感染如何与其组成相关联,我们使用非培养分子技术对18名健康成年人的口咽微生物组进行了特征分析,在40周内每周采样一次。我们在OTU水平上检测到9个门、202个属和1438个分类单元,在门水平上以厚壁菌门、拟杆菌门和变形菌门为主。参与者的个体微生物组具有高α多样性水平(平均值 = 204.55个OTU,标准差 = 35.64)、均匀度(19.83,标准差 = 9.74)和高时间稳定性(样本间平均皮尔逊相关性为0.52,标准差 = 0.060),个体间微生物群落组成的差异大于个体内差异。群落组成的显著变化与疾病状态相关,这表明在疾病期间有可能检测到OTU丰度和群落组成的特定变化。我们通过改变出现频率和丰度阈值来定义常见核心微生物群,结果表明个体核心微生物组在参与者之间共享大量OTU,主要是 和 。我们的结果为表征健康人口咽部的微生物群落、群落结构和变异性提供了见解,并为定义个体和共享核心提供了新方法。这一结果的更广泛意义包括对健康状态下以及对抗菌治疗或益生菌反应时口咽微生物群总体动态进行建模的潜力。