Stability of the human faecal microbiome in a cohort of adult men

• Published in: Nature microbiology Vol. 3; no. 3; pp. 347 - 355
• Main Authors: Mehta, Raaj S., Abu-Ali, Galeb S., Drew, David A., Lloyd-Price, Jason, Subramanian, Ayshwarya, Lochhead, Paul, Joshi, Amit D., Ivey, Kerry L., Khalili, Hamed, Brown, Gordon T., DuLong, Casey, Song, Mingyang, Nguyen, Long H., Mallick, Himel, Rimm, Eric B., Izard, Jacques, Huttenhower, Curtis, Chan, Andrew T.
• Format: Journal Article
• Language: English
• Published: London Nature Publishing Group UK 01.03.2018; Nature Publishing Group
• Subjects: 631/326/2565/2134; 631/326/2565/2142; 631/326/2565/855; 631/326/41/2532; 631/337/2019; Adult; Aged; Bacteria - classification; Biomedical and Life Sciences; Cohort Studies; Feces - microbiology; Follow-Up Studies; Gastrointestinal Microbiome; Gene Expression; Gene Expression Profiling; Health Personnel - statistics & numerical data; High-Throughput Nucleotide Sequencing; Humans; Infectious Diseases; Intestinal microflora; Life Sciences; Male; Medical Microbiology; Medical personnel; Metagenomics; Microbiology; Microbiomes; Microbiota; Middle Aged; Parasitology; Prospective Studies; Therapeutic applications; Variation; Virology
• ISSN: 2058-5276; 2058-5276
• DOI: 10.1038/s41564-017-0096-0

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.