Robust variation in infant gut microbiome assembly across a spectrum of lifestyles

Author:

Olm Matthew R.1ORCID,Dahan Dylan1,Carter Matthew M.1ORCID,Merrill Bryan D.1ORCID,Yu Feiqiao B.2ORCID,Jain Sunit2ORCID,Meng Xiandong3,Tripathi Surya4,Wastyk Hannah1,Neff Norma2,Holmes Susan15ORCID,Sonnenburg Erica D.1ORCID,Jha Aashish R.6ORCID,Sonnenburg Justin L.12ORCID

Affiliation:

1. Department of Microbiology and Immunology, Stanford University School of Medicine, Stanford, CA, USA.

2. Chan Zuckerberg Biohub, San Francisco, CA, USA.

3. ChEM-H Institute, Stanford University, Stanford, CA 94305, USA.

4. Department of Plant and Microbial Biology, University of California, Berkeley, Berkeley, CA, USA.

5. Department of Statistics, Stanford University, Stanford, CA, USA.

6. Genetic Heritage Group, Program in Biology, New York University Abu Dhabi, Abu Dhabi,United Arab Emirates.

Abstract

Infant microbiome assembly has been intensely studied in infants from industrialized nations, but little is known about this process in nonindustrialized populations. We deeply sequenced infant stool samples from the Hadza hunter-gatherers of Tanzania and analyzed them in a global meta-analysis. Infant microbiomes develop along lifestyle-associated trajectories, with more than 20% of genomes detected in the Hadza infant gut representing novel species. Industrialized infants—even those who are breastfed—have microbiomes characterized by a paucity of Bifidobacterium infantis and gene cassettes involved in human milk utilization. Strains within lifestyle-associated taxonomic groups are shared between mother-infant dyads, consistent with early life inheritance of lifestyle-shaped microbiomes. The population-specific differences in infant microbiome composition and function underscore the importance of studying microbiomes from people outside of wealthy, industrialized nations.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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