The CGIBD Gnotobiotic Animal Core is a highly visible resource that provides CGIBD members with germ-free (sterile) and selectively colonized mice to precisely study host/environmental interactions. This world-class facility has allowed CGIBD members, their trainees and collaborators to perform cutting edge investigations in wild type and genetically engineered gnotobiotic mice in the absence of microbiota (germfree) or colonized with single bacterial species (parent strains and gene deletion/complemented mutants), defined groups of murine or human bacterial species or complex communities of commensal microbiota from human or experimental mice or humans (humanized mice) with dysbiosis to study disease pathogenesis. In the past 4 years, the combined core facilities at UNC-Chapel Hill and North Carolina State University College of Veterinary Medicine have provided 3,479 germ-free or gnotobiotic mice to 19 CGIBD members and 41 external scientists in the U.S. Approximately 70% of these mice have been used by CGIBD members. Our repertoire of gnotobiotic mice has expanded from approximately 6 strains at the last renewal to 29 strains that include wild t3T)e, knockout, transgenic and reporter mice. The Core's specific aims for renewal funding are: 1) provide germ-free (GF) or selectively colonized (gnotobiotic) wild type and mutant mice, their tissues and cells for CGIBD interdisciplinary investigators exploring host/environmental interactions; 2) Derive additional GF genetically engineered mouse strains for CGIBD investigators; 3) Provide technical assistance for CGIBD investigators; and 4) Provide limited gnotobiotic animals and tissues to unfunded new or established investigators with novel hypotheses to generate preliminary data for NIH or foundation grant applications.

Public Health Relevance

The Gnotobiotic Animal Core provides resources for CGIBD members and external investigators to study mechanisms of host/microbial interactions by precisely manipulating the commensal enteric microbiota. Investigators can compare host responses and microbial interactions in mice that are germ free (sterile), monoassociated (single microbial species), colonized with defined groups of bacterial, fungal or viral species or transplanted with of complex groups of microbiota from various phenotypes of mice or humans, for example, control or inflamed hosts. Results of these studies can identify microbial and host elements that mediate host protection, epithelial and immune development, inflammation, infection, neoplasia and recovery from injury.

Agency
National Institute of Health (NIH)
Institute
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Type
Center Core Grants (P30)
Project #
5P30DK034987-34
Application #
9605033
Study Section
Special Emphasis Panel (ZDK1)
Project Start
Project End
2020-03-14
Budget Start
2018-12-01
Budget End
2019-11-30
Support Year
34
Fiscal Year
2019
Total Cost
Indirect Cost
Name
University of North Carolina Chapel Hill
Department
Type
DUNS #
608195277
City
Chapel Hill
State
NC
Country
United States
Zip Code
27599
Carlson, Alexander L; Xia, Kai; Azcarate-Peril, M Andrea et al. (2018) Infant Gut Microbiome Associated With Cognitive Development. Biol Psychiatry 83:148-159
Azcarate-Peril, M Andrea; Butz, Natasha; Cadenas, Maria Belen et al. (2018) An Attenuated Salmonella enterica Serovar Typhimurium Strain and Galacto-Oligosaccharides Accelerate Clearance of Salmonella Infections in Poultry through Modifications to the Gut Microbiome. Appl Environ Microbiol 84:
Evon, D M; Amador, J; Stewart, P et al. (2018) Psychometric properties of the PROMIS short form measures in a U.S. cohort of 961 patients with chronic hepatitis C prescribed direct acting antiviral therapy. Aliment Pharmacol Ther 47:1001-1011
Lee, Mi Kyeong; Carnes, Megan U; Butz, Natasha et al. (2018) Exposures Related to House Dust Microbiota in a U.S. Farming Population. Environ Health Perspect 126:067001
Busch, Evan L; Galanko, Joseph A; Sandler, Robert S et al. (2018) Lifestyle Factors, Colorectal Tumor Methylation, and Survival Among African Americans and European Americans. Sci Rep 8:9470
Jones, Roshonda B; Fodor, Anthony A; Peery, Anne F et al. (2018) An Aberrant Microbiota is not Strongly Associated with Incidental Colonic Diverticulosis. Sci Rep 8:4951
Dellon, Evan S; Selitsky, Sara R; Genta, Robert M et al. (2018) Gene expression-phenotype associations in adults with eosinophilic esophagitis. Dig Liver Dis 50:804-811
Eluri, Swathi; Cross, Raymond K; Martin, Christopher et al. (2018) Inflammatory Bowel Diseases Can Adversely Impact Domains of Sexual Function Such as Satisfaction with Sex Life. Dig Dis Sci 63:1572-1582
Li, Feng; Kakoki, Masao; Smid, Marcela et al. (2018) Causative Effects of Genetically Determined High Maternal/Fetal Endothelin-1 on Preeclampsia-Like Conditions in Mice. Hypertension 71:894-903
Rogala, Allison R; Schoenborn, Alexi A; Fee, Brian E et al. (2018) Environmental factors regulate Paneth cell phenotype and host susceptibility to intestinal inflammation in Irgm1-deficient mice. Dis Model Mech 11:

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