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Series GSE14737 Query DataSets for GSE14737
Status Public on Mar 01, 2009
Title Characterizing a model human gut microbiota composed of members of its two dominant bacterial phyla
Platform organisms Bacteroides thetaiotaomicron; Phocaeicola vulgatus; Parabacteroides distasonis; Methanobrevibacter smithii; Lachnospira eligens; Agathobacter rectalis
Sample organisms Bacteroides thetaiotaomicron; Agathobacter rectalis
Experiment type Expression profiling by array
Summary The adult human gut microbial community is typically dominated by two bacterial phyla (divisions), the Firmicutes and the Bacteroidetes. Little is known about the factors that govern the interactions between their members. Here we examine the niches of representatives of both phyla in vivo. Finished genome sequences were generated from E. rectale and E. eligens, which belong to Clostridium Cluster XIVa, one of the most common gut Firmicute clades. Comparison of these and 25 other gut Firmicutes and Bacteroidetes indicated that the former possess smaller genomes and a disproportionately smaller number of glycan-degrading enzymes. Germ-free mice were then colonized with E. rectale and/or a prominent human gut Bacteroidetes, Bacteroides thetaiotaomicron, followed by whole genome transcriptional profiling of both organisms in their distal gut (cecal) habitat as well as host responses, high resolution proteomic analysis of cecal contents, and biochemical assays of carbohydrate metabolism. B. thetaiotaomicron adapts to E. rectale by upregulating expression of a variety of polysaccharide utilization loci (PULs) encoding numerous glycoside hydrolase gene families, and by signaling the host to produce mucosal glycans that it, but not E. rectale, can access. E. rectale adapts to B. thetaiotaomicron by decreasing production of its glycan-degrading enzymes, increasing expression of selected amino acid and sugar transporters, and facilitating glycolysis by reducing levels of NADH, in part via generation of butyrate from acetate, which in turn is utilized by the gut epithelium. This simplified model of the human gut microbiota illustrates niche specialization and functional redundancy within members of major gut bacterial phyla, and the importance of host glycans as a nutrient foundation that ensures ecosystem stability.
 
Overall design The interactions between E. rectale and B. thetaiotaomicron were characterized by performing whole genome transcriptional profiling of each species after colonization of gnotobiotic mice with each organism alone, or in combination. E. rectale was also profiled during in vitro growth.
 
Contributor(s) Mahowald MA, Rey FE, Seedorf H, Turnbaugh PJ, Gorodn JI
Citation(s) 19321416
Submission date Feb 06, 2009
Last update date Jan 30, 2015
Contact name Federico E Rey
E-mail(s) reyf@wustl.edu
Phone 314-963-0284
Organization name Washington University
Department Pathology
Lab Gordon
Street address 4444 Forest Park Blvd
City St Louis
State/province MO
ZIP/Postal code 63108
Country USA
 
Platforms (1)
GPL7006 [BacEubMsa520350F] Affymetrix Human gut microbiota community GeneChip
Samples (16)
GSM368096 B.thetaiotaomicron_monoassociation_High polysaccharide diet_#1
GSM368097 B.thetaiotaomicron_monoassociation_High polysaccharide diet_#2
GSM368098 B.thetaiotaomicron_monoassociation_High polysaccharide diet_#3
Relations
BioProject PRJNA112197

Download family Format
SOFT formatted family file(s) SOFTHelp
MINiML formatted family file(s) MINiMLHelp
Series Matrix File(s) TXTHelp

Supplementary file Size Download File type/resource
GSE14737_RAW.tar 58.7 Mb (http)(custom) TAR (of CEL)
Processed data included within Sample table

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