Extensive personal human gut microbiota culture collections characterized and manipulated in gnotobiotic mice

The proportion of the human gut bacterial community that is recalcitrant to culture remains poorly defined. In this report, we combine high-throughput anaerobic culturing techniques with gnotobiotic animal husbandry and metagenomics to show that the human fecal microbiota consists largely of taxa an...

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Published in:Proceedings of the National Academy of Sciences - PNAS Vol. 108; no. 15; pp. 6252 - 6257
Main Authors: Goodman, Andrew L, Kallstrom, George, Faith, Jeremiah J, Reyes, Alejandro, Moore, Aimee, Dantas, Gautam, Gordon, Jeffrey I
Format: Journal Article
Language:English
Published: United States National Academy of Sciences 12-04-2011
National Acad Sciences
Series:From the Cover
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Summary:The proportion of the human gut bacterial community that is recalcitrant to culture remains poorly defined. In this report, we combine high-throughput anaerobic culturing techniques with gnotobiotic animal husbandry and metagenomics to show that the human fecal microbiota consists largely of taxa and predicted functions that are represented in its readily cultured members. When transplanted into gnotobiotic mice, complete and cultured communities exhibit similar colonization dynamics, biogeographical distribution, and responses to dietary perturbations. Moreover, gnotobiotic mice can be used to shape these personalized culture collections to enrich for taxa suited to specific diets. We also demonstrate that thousands of isolates from a single donor can be clonally archived and taxonomically mapped in multiwell format to create personalized microbiota collections. Retrieving components of a microbiota that have coexisted in single donors who have physiologic or disease phenotypes of interest and reuniting them in various combinations in gnotobiotic mice should facilitate preclinical studies designed to determine the degree to which tractable bacterial taxa are able to transmit donor traits or influence host biology.
Bibliography:http://dx.doi.org/10.1073/pnas.1102938108
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1Present address: Section of Microbial Pathogenesis and Microbial Diversity Institute, Yale University, New Haven, CT 06536.
Author contributions: A.L.G., G.K., J.J.F., G.D., and J.I.G. designed research; A.L.G., G.K., J.J.F., and A.M. performed research; A.R. contributed new reagents/analytic tools; A.L.G., J.J.F., A.R., and J.I.G. analyzed data; and A.L.G. and J.I.G. wrote the paper.
Contributed by Jeffrey I. Gordon, February 24, 2011 (sent for review January 21, 2011)
ISSN:0027-8424
1091-6490
DOI:10.1073/pnas.1102938108