Broad diversity of human gut bacteria accessible via a traceable strain deposition system
Thomas C. A. HitchiD, Johannes M. Masson, Charlie PauvertiD, Johanna BoschiD, Selina Nüchtern, Nicole Simone TreicheliD, Marko BalohiD, Soheila Razavi, Afrizal AfrizaliD, Ntana Kousetzi, Andrea M. Aguirre, David WylensekiD, Amy C. CoatesiD, Susan A. V. JenningsiD, Atscharah Panyot, Alina ViehofiD, Matthias A. SchmitziD, Maximilian Stuhrmann, Evelyn C. Deis, Kevin BisdorfiD, Maria Dimitra ChiotelliiD, Artur LissiniD, Isabel SchoberiD, Julius WitteiD, Thorsten CrameriD, , Thomas ClaveliD
Abstract
Numerous bacteria in the human gut microbiome remain unknown and/or have yet to be cultured. While collections of human gut bacteria have been published, few strains have been made publicly available. A major hurdle in making strains publicly available is their deposition to public culture collections. We propose a framework for the bulk-deposition of strains to culture collections, which removes many of the barriers previously identified (www.dsmz.de/bulk-deposit). Using this bulk-deposition system we have created a publicly available collection of human gut isolates. The Human intestinal Bacteria Collection (HiBC) (www.hibc.rwth-aachen.de) contains 340 strains representing 198 species within 29 families and 7 phyla, of which 29 previously unknown species are taxonomically described and named. These included two butyrate-producing species of Faecalibacterium and new dominant species associated with health and inflammatory bowel disease, Ruminococcoides intestinale and Blautia intestinihominis, respectively. Plasmids were prolific within the HiBC isolates, with almost half (46%) of strains containing plasmids, with a maximum of six within a strain. This included a broadly occurring plasmid (pBAC) that exists in three diverse forms across Bacteroidales species. Megaplasmids were identified within two strains, the pMMCAT megaplasmid is globally present within multiple Bacteroidales species. This collection of easily searchable and publicly available gut bacterial isolates will facilitate functional studies of the gut microbiome.
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