| Literature DB >> 29335554 |
Raaj S Mehta1,2, Galeb S Abu-Ali3,4, David A Drew1,2, Jason Lloyd-Price3,4, Ayshwarya Subramanian3,4, Paul Lochhead1,2, Amit D Joshi1,2, Kerry L Ivey5,6, Hamed Khalili1,2, Gordon T Brown1,2, Casey DuLong3, Mingyang Song1,2, Long H Nguyen1,2, Himel Mallick3,4, Eric B Rimm5,7, Jacques Izard8, Curtis Huttenhower9,10, Andrew T Chan11,12,13.
Abstract
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.Entities:
Mesh:
Year: 2018 PMID: 29335554 PMCID: PMC6016839 DOI: 10.1038/s41564-017-0096-0
Source DB: PubMed Journal: Nat Microbiol ISSN: 2058-5276 Impact factor: 17.745