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Reconstruction of ancient microbial genomes from the human gut

  • Marsha C Wibowo
  • , Zhen Yang
  • , Maxime Borry
  • , Alexander Hübner
  • , Kun D Huang
  • , Braden T Tierney
  • , Samuel Zimmerman
  • , Francisco Barajas-Olmos
  • , Cecilia Contreras-Cubas
  • , Humberto García-Ortiz
  • , Angélica Martínez-Hernández
  • , Jacob M Luber
  • , Philipp Kirstahler
  • , Tre Blohm
  • , Francis E Smiley
  • , Richard Arnold
  • , Sonia A Ballal
  • , Sünje Johanna Pamp
  • , Julia Russ
  • , Frank Maixner
  • Omar Rota-Stabelli, Nicola Segata, Karl Reinhard, Lorena Orozco, Christina Warinner, Meradeth Snow, Steven LeBlanc, Aleksandar D Kostic
  • Joslin Diabetes Center
  • Max Planck Institute of Geoanthropology
  • University of Trento
  • Instituto Nacional de Medicina Genomica
  • University of Montana
  • Northern Arizona University
  • Boston Children's Hospital
  • University of Nebraska-Lincoln
  • EURAC Research
  • Edmund Mach Foundation
  • Harvard University
  • Pahrump Paiute Tribe
  • Consolidated Group of Tribes and Organizations

Research output: Contribution to journalJournal articleResearchpeer-review

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Abstract

Loss of gut microbial diversity1-6 in industrial populations is associated with chronic diseases7, underscoring the importance of studying our ancestral gut microbiome. However, relatively little is known about the composition of pre-industrial gut microbiomes. Here we performed a large-scale de novo assembly of microbial genomes from palaeofaeces. From eight authenticated human palaeofaeces samples (1,000-2,000 years old) with well-preserved DNA from southwestern USA and Mexico, we reconstructed 498 medium- and high-quality microbial genomes. Among the 181 genomes with the strongest evidence of being ancient and of human gut origin, 39% represent previously undescribed species-level genome bins. Tip dating suggests an approximate diversification timeline for the key human symbiont Methanobrevibacter smithii. In comparison to 789 present-day human gut microbiome samples from eight countries, the palaeofaeces samples are more similar to non-industrialized than industrialized human gut microbiomes. Functional profiling of the palaeofaeces samples reveals a markedly lower abundance of antibiotic-resistance and mucin-degrading genes, as well as enrichment of mobile genetic elements relative to industrial gut microbiomes. This study facilitates the discovery and characterization of previously undescribed gut microorganisms from ancient microbiomes and the investigation of the evolutionary history of the human gut microbiota through genome reconstruction from palaeofaeces.
Original languageEnglish
JournalNature
Volume594
Pages (from-to)234–239
ISSN0028-0836
DOIs
Publication statusPublished - 2021

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

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