The Mouse Intestinal Bacterial Collection (miBC) provides host-specific insight into cultured diversity and functional potential of the gut microbiota

Ilias Lagkouvardos(Leibniz-Institute for Food Systems Biology at the Technical University of Munich), Rüdiger Pukall(Leibniz Institute DSMZ – German Collection of Microorganisms and Cell Cultures), Birte Abt(German Center for Infection Research), Bärbel U. Foesel(German Center for Infection Research), Jan P. Meier‐Kolthoff(Leibniz Institute DSMZ – German Collection of Microorganisms and Cell Cultures), Neeraj Kumar(Leibniz-Institute for Food Systems Biology at the Technical University of Munich), Anne Bresciani(Technical University of Denmark), Inés Martínez(University of Alberta), Sarah Just(Leibniz-Institute for Food Systems Biology at the Technical University of Munich), Caroline Ziegler(Leibniz-Institute for Food Systems Biology at the Technical University of Munich), Sandrine Brugiroux(Ludwig-Maximilians-Universität München), Debora Garzetti(Ludwig-Maximilians-Universität München), Mareike Wenning(Technical University of Munich), Thi Phuong Nam Bui(Wageningen University & Research), Jun Wang(Max Planck Institute for Evolutionary Biology), Floor Hugenholtz(Wageningen University & Research), Caroline M. Plugge(Wageningen University & Research), Daniel A. Peterson(Johns Hopkins University), Mathias W. Hornef(RWTH Aachen University), John F. Baines(Christian-Albrechts-Universität zu Kiel), Hauke Smidt(Wageningen University & Research), Jens Walter(University of Alberta), Karsten Kristiansen(University of Copenhagen), Henrik Bjørn Nielsen(Technical University of Denmark), Dirk Haller(Leibniz-Institute for Food Systems Biology at the Technical University of Munich), Jörg Overmann(German Center for Infection Research), Bärbel Stecher(German Center for Infection Research), Thomas Clavel(Leibniz-Institute for Food Systems Biology at the Technical University of Munich)
Nature Microbiology
August 8, 2016
Cited by 508Open Access
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Abstract

Abstract Intestinal bacteria influence mammalian physiology, but many types of bacteria are still uncharacterized. Moreover, reference strains of mouse gut bacteria are not easily available, although mouse models are extensively used in medical research. These are major limitations for the investigation of intestinal microbiomes and their interactions with diet and host. It is thus important to study in detail the diversity and functions of gut microbiota members, including those colonizing the mouse intestine. To address these issues, we aimed at establishing the Mouse Intestinal Bacterial Collection (miBC), a public repository of bacterial strains and associated genomes from the mouse gut, and studied host-specificity of colonization and sequence-based relevance of the resource. The collection includes several strains representing novel species, genera and even one family. Genomic analyses showed that certain species are specific to the mouse intestine and that a minimal consortium of 18 strains covered 50–75% of the known functional potential of metagenomes. The present work will sustain future research on microbiota–host interactions in health and disease, as it will facilitate targeted colonization and molecular studies. The resource is available at www.dsmz.de/miBC .


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