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Succession of microbial consortia in the developing infant gut microbiome
Edited by Todd R. Klaenhammer, North Carolina State University, Raleigh, NC, and approved June 24, 2010 (received for review March 2, 2010)

Abstract
The colonization process of the infant gut microbiome has been called chaotic, but this view could reflect insufficient documentation of the factors affecting the microbiome. We performed a 2.5-y case study of the assembly of the human infant gut microbiome, to relate life events to microbiome composition and function. Sixty fecal samples were collected from a healthy infant along with a diary of diet and health status. Analysis of >300,000 16S rRNA genes indicated that the phylogenetic diversity of the microbiome increased gradually over time and that changes in community composition conformed to a smooth temporal gradient. In contrast, major taxonomic groups showed abrupt shifts in abundance corresponding to changes in diet or health. Community assembly was nonrandom: we observed discrete steps of bacterial succession punctuated by life events. Furthermore, analysis of ≈500,000 DNA metagenomic reads from 12 fecal samples revealed that the earliest microbiome was enriched in genes facilitating lactate utilization, and that functional genes involved in plant polysaccharide metabolism were present before the introduction of solid food, priming the infant gut for an adult diet. However, ingestion of table foods caused a sustained increase in the abundance of Bacteroidetes, elevated fecal short chain fatty acid levels, enrichment of genes associated with carbohydrate utilization, vitamin biosynthesis, and xenobiotic degradation, and a more stable community composition, all of which are characteristic of the adult microbiome. This study revealed that seemingly chaotic shifts in the microbiome are associated with life events; however, additional experiments ought to be conducted to assess how different infants respond to similar life events.
Footnotes
- ↵1To whom correspondence should be addressed. E-mail: rel222{at}cornell.edu.
Author contributions: J.E.K., L.T.A., and R.E.L. designed research; J.E.K., N.S., A.D.F., L.T.A., and R.E.L. performed research; J.S. and R.K. contributed new reagents/analytic tools; J.E.K., A.S., J.S., R.K., and R.E.L. analyzed data; and J.E.K., A.S., A.D.F., and R.E.L. wrote the paper.
The authors declare no conflict of interest.
This article is a PNAS Direct Submission.
Data deposition: All 16S rRNA gene and metagenomic sequence data are archived in GenBank (accession no. SRA012472).
This paper results from the Arthur M. Sackler Colloquium of the National Academy of Sciences, “Microbes and Health,” held November 2–3, 2009 at the Arnold and Mabel Beckman Center of the National Academies of Sciences and Engineering in Irvine, CA. The complete program and audio files of most presentations are available on the NAS Web site at http://www.nasonline.org/SACKLER_Microbes_and_Health.
This article contains supporting information online at www.pnas.org/lookup/suppl/doi:10.1073/pnas.1000081107/-/DCSupplemental and http://microbe.calsnet.cornell.edu/leylab/fileshare/ITS_PNAS_SI/.