Reconstruction of ancient microbial genomes from the human gut

Marsha C. Wibowo(Joslin Diabetes Center), Zhen Yang(Joslin Diabetes Center), Maxime Borry(Max Planck Institute for the Science of Human History), Alexander Hübner(Max Planck Institute for the Science of Human History), Kun D. Huang(Fondazione Edmund Mach), Braden Tierney(Joslin Diabetes Center), Samuel Zimmerman(Joslin Diabetes Center), Francisco Barajas‐Olmos(Secretaria de Salud), Cecilia Contreras-Cubas(Secretaria de Salud), Humberto Garcia‐Ortíz(Secretaria de Salud), Angélica Martínez‐Hernández(Secretaria de Salud), Jacob M. Luber(Joslin Diabetes Center), Philipp Kirstahler(Technical University of Denmark), Tre Blohm(University of Montana), Francis E. Smiley(Northern Arizona University), Richard R. Arnold, Sonia Ballal(Boston Children's Hospital), Sünje Johanna Pamp(Technical University of Denmark), Julia Russ(University of Nebraska–Lincoln), Frank Maixner(Eurac Research), Omar Rota‐Stabelli(Fondazione Edmund Mach), Nicola Segata(University of Trento), Karl J. Reinhard(University of Nebraska–Lincoln), Lorena Orozco(Secretaria de Salud), Christina Warinner(Harvard University), Meradeth Snow(University of Montana), Steven A. LeBlanc(Harvard University), Aleksandar D. Kostic(Joslin Diabetes Center)
Nature
May 12, 2021
Cited by 244Open Access
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Abstract

, 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.


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