Beatty Meabh, Guduric-Fuchs Jasenka, Brown Eoin, Bridgett Stephen, Chakravarthy Usha, Hogg Ruth Esther, Simpson David Arthur
Centre for Experimental Medicine, Queen's University Belfast, Belfast, Northern Ireland, UK.
BMC Genomics. 2014 Oct 25;15(1):933. doi: 10.1186/1471-2164-15-933.
The human microbiome plays a significant role in maintaining normal physiology. Changes in its composition have been associated with bowel disease, metabolic disorders and atherosclerosis. Sequences of microbial origin have been observed within small RNA sequencing data obtained from blood samples. The aim of this study was to characterise the microbiome from which these sequences are derived.
Abundant non-human small RNA sequences were identified in plasma and plasma exosomal samples. Assembly of these short sequences into longer contigs was the pivotal novel step in ascertaining their origin by BLAST searches. Most reads mapped to rRNA sequences. The taxonomic profiles of the microbes detected were very consistent between individuals but distinct from microbiomes reported at other sites. The majority of bacterial reads were from the phylum Proteobacteria, whilst for 5 of 6 individuals over 90% of the more abundant fungal reads were from the phylum Ascomycota; of these over 90% were from the order Hypocreales. Many contigs were from plants, presumably of dietary origin. In addition, extremely abundant small RNAs derived from human Y RNAs were detected.
A characteristic profile of a subset of the human microbiome can be obtained by sequencing small RNAs present in the blood. The source and functions of these molecules remain to be determined, but the specific profiles are likely to reflect health status. The potential to provide biomarkers of diet and for the diagnosis and prognosis of human disease is immense.
人类微生物群落在维持正常生理功能方面发挥着重要作用。其组成的变化与肠道疾病、代谢紊乱和动脉粥样硬化有关。在从血液样本中获得的小RNA测序数据中观察到了微生物来源的序列。本研究的目的是表征这些序列所源自的微生物群。
在血浆和血浆外泌体样本中鉴定出大量非人类小RNA序列。将这些短序列组装成更长的重叠群是通过BLAST搜索确定其来源的关键新步骤。大多数读数映射到rRNA序列。检测到的微生物的分类学图谱在个体之间非常一致,但与其他部位报道的微生物群不同。大多数细菌读数来自变形菌门,而在6个个体中的5个个体中,超过90%的更丰富的真菌读数来自子囊菌门;其中超过90%来自肉座菌目。许多重叠群来自植物,推测是饮食来源。此外,还检测到源自人类Y RNA的极其丰富的小RNA。
通过对血液中存在的小RNA进行测序,可以获得人类微生物群一个子集的特征图谱。这些分子的来源和功能仍有待确定,但特定图谱可能反映健康状况。提供饮食生物标志物以及用于人类疾病诊断和预后的潜力巨大。