Literature DB >> 21436049

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

Andrew L Goodman1, George Kallstrom, Jeremiah J Faith, Alejandro Reyes, Aimee Moore, Gautam Dantas, Jeffrey I Gordon.   

Abstract

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.

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Year:  2011        PMID: 21436049      PMCID: PMC3076821          DOI: 10.1073/pnas.1102938108

Source DB:  PubMed          Journal:  Proc Natl Acad Sci U S A        ISSN: 0027-8424            Impact factor:   11.205


  10 in total

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Journal:  Nature       Date:  2010-03-04       Impact factor: 49.962

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  10 in total
  286 in total

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3.  Metagenomics and personalized medicine.

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Journal:  J Bacteriol       Date:  2012-06-01       Impact factor: 3.490

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8.  Hierarchical social networks shape gut microbial composition in wild Verreaux's sifaka.

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10.  Engineered Regulatory Systems Modulate Gene Expression of Human Commensals in the Gut.

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