The long-term objectives of this application are to identify microorganisms as well as human cellular pathways that promote Crohn?s disease, and to develop novel diagnostic tools and therapeutic strategies for this disease. The short-term objectives include the identification of microflora and host expression patterns that are associated with disease activity, and assessment of molecular methods for pathogen identification.
The specific aims are:
Aim 1 : Identify bacterial and archaeal species associated with active Crohn?s disease using broad range ribosomal DNA PCR, laser capture microdissection, and fluorescent in situ hybridization. Tissues with ulcerative colitis, inactive Crohn?s disease, and no apparent disease will serve as some of the controls.
Aim 2 : Quantify differences in relative abundance of bacterial and archaeal species found in Crohn?s disease and controls. An rDNA microarray will be used, as well as a more traditional slot-blot hybridization approach.
Aim 3 : Identify global host gene expression patterns in intestinal tissue and peripheral blood that are associated with Crohn?s disease. Expression patterns will be defined that correlate with disease state and activity, and with bacterial and archaeal microflora profiles. State of the art, high-density human cDNA microarrays, and both unsupervised and supervised pattern recognition algorithms will be used to reveal disease-associated signatures. This combination of approaches offers opportunities for characterizing Crohn?s disease, and for examining the complex interactions of human host and microbial flora during states of health and disease.

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Research Project (R01)
Project #
5R01AI051259-03
Application #
6752044
Study Section
Special Emphasis Panel (ZAI1-GLM-M (J1))
Program Officer
Schmitt, Clare K
Project Start
2002-09-01
Project End
2006-06-30
Budget Start
2004-07-01
Budget End
2005-06-30
Support Year
3
Fiscal Year
2004
Total Cost
$292,500
Indirect Cost
Name
Stanford University
Department
Microbiology/Immun/Virology
Type
Schools of Medicine
DUNS #
009214214
City
Stanford
State
CA
Country
United States
Zip Code
94305
Eckburg, Paul B; Relman, David A (2007) The role of microbes in Crohn's disease. Clin Infect Dis 44:256-62
Bik, Elisabeth M; Eckburg, Paul B; Gill, Steven R et al. (2006) Molecular analysis of the bacterial microbiota in the human stomach. Proc Natl Acad Sci U S A 103:732-7
Palmer, Chana; Bik, Elisabeth M; Eisen, Michael B et al. (2006) Rapid quantitative profiling of complex microbial populations. Nucleic Acids Res 34:e5
Liu, Minghsun; Popper, Stephen J; Rubins, Kathleen H et al. (2006) Early days: genomics and human responses to infection. Curr Opin Microbiol 9:312-9
Gill, Steven R; Pop, Mihai; Deboy, Robert T et al. (2006) Metagenomic analysis of the human distal gut microbiome. Science 312:1355-9
Dethlefsen, Les; Eckburg, Paul B; Bik, Elisabeth M et al. (2006) Assembly of the human intestinal microbiota. Trends Ecol Evol 21:517-23
Eckburg, Paul B; Bik, Elisabeth M; Bernstein, Charles N et al. (2005) Diversity of the human intestinal microbial flora. Science 308:1635-8