微生物群
生物
队列
人体微生物群
医学
计算生物学
遗传学
内科学
作者
Raaj S. Mehta,Galeb Abu-Ali,David A. Drew,Jason Lloyd‐Price,Ayshwarya Subramanian,Paul Lochhead,Amit D. Joshi,Kerry L. Ivey,Hamed Khalili,Gordon Brown,Casey DuLong,Mingyang Song,Long H. Nguyen,Himel Mallick,Eric B. Rimm,Jacques Izard,Curtis Huttenhower,Andrew T. Chan
标识
DOI:10.1038/s41564-017-0096-0
摘要
Characterizing the stability of the gut microbiome is important to exploit it as a therapeutic target and diagnostic biomarker. We metagenomically and metatranscriptomically sequenced the faecal microbiomes of 308 participants in the Health Professionals Follow-Up Study. Participants provided four stool samples—one pair collected 24–72 h apart and a second pair ~6 months later. Within-person taxonomic and functional variation was consistently lower than between-person variation over time. In contrast, metatranscriptomic profiles were comparably variable within and between subjects due to higher within-subject longitudinal variation. Metagenomic instability accounted for ~74% of corresponding metatranscriptomic instability. The rest was probably attributable to sources such as regulation. Among the pathways that were differentially regulated, most were consistently over- or under-transcribed at each time point. Together, these results suggest that a single measurement of the faecal microbiome can provide long-term information regarding organismal composition and functional potential, but repeated or short-term measures may be necessary for dynamic features identified by metatranscriptomics. Metagenomic and metatranscriptomic analyses of stool samples from 308 individuals over time indicate that longitudinal sampling is important for detecting dynamic functional features of the gut microbiome.
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