Project 2 represents a complementary approach to the one presented in Project 1 for examining genetic diversity in the microbiomes of obese and lean twin pairs. Whereas Project 1 investigates genomic and metabolomic properties of the whole gut microbial community, Project 2focuses on the gene complement of two prominent members of the gut microbiota, offering a genome-anchored view of the microbiome. The fermentative bacterium B. thetatiotaomicron and the methanogenic archaeon M. smithii have been shown in gnotobiotic mouse models to have a synergistic effect on energy harvest from the diet. Project 2 explores the genomic content of populations of these two microbial species obtained from lean and obese monozygotic twins. Our central hypothesis is that the microbiome of obese individuals has a greater capacity for energy harvest: thus, we postulate that there may be an enhancement of energy-acquisition functions in the genomes of these two microbial species obtained from obese individuals. The microbial genome is a dynamic entity, shaped by multiple forces that include gene loss and gain via lateral gene transfer (LGT). One implication of LGT is that no single genome sequence can describe a 'species'. To understand the nature of a microbial species we therefore must focus on the """"""""pan-genome"""""""", the sum of core, vertically inherited genes and the variable, strain-specific genes. Pan-genome size can be vastly larger than the genome of any single isolate, increasing with every isolate sequenced. Wewill determine the extent of variability in the pan-genomes, both in terms of functional gene content and the discovery rate of new genes/isolate, of strains isolated from MZ twin pairs and their mothers and selected based on their core gene phylogenetic (tree-based) relationships. In this Project, we will use a combination of methods including culturing of isolates, comparative genome hybridization, genome amplification and large-scale DNA sequencing. Using data analysis methods outlined in Projects 1 and 3, we will assess the functional consequences of obesity- related pan-genome differences in terms of overall microbial gut metabolism, including inter-species synergisms. In addition, the data generated in Project 2will be used as a starting point for the investigations by the Knightlaboratory in Project 3 to trace the flow of genes in the gut microbiome.

Agency
National Institute of Health (NIH)
Institute
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Type
Research Program Projects (P01)
Project #
5P01DK078669-03
Application #
7905192
Study Section
Special Emphasis Panel (ZDK1)
Project Start
Project End
Budget Start
2009-07-01
Budget End
2010-06-30
Support Year
3
Fiscal Year
2009
Total Cost
$597,541
Indirect Cost
Name
Washington University
Department
Type
DUNS #
068552207
City
Saint Louis
State
MO
Country
United States
Zip Code
63130
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