The cotton-top tamarin, which develops a spontaneously occurring colitis, is a valuable animal model for the study of human inflammatory bowel disease. Elucidation of the mechanisms involved in the development of colitis and identification of the contribution of dietary factors and microbiologic agents are important components in the study of the pathogenesis of this disease. Anecdotal information suggests that cotton-top tamarins fed Zu/Preem marmoset diet have a higher incidence of colitis than animals fed Spectrum marmoset diet. The diets differ primarily in cholesterol and water content. The bacterium, Campylobacter jejuni has also been implicated as an etiologic agent in colitis. The objective of this study is to determine if cotton-top tamarins fed the commercially available Zu/Preem marmoset diet have a significantly greater incidence of spontaneously occurring colitis as compared to tamarins which are fed the commercially available Spectrum Marmoset diet, and to ascertain if there is an association between positive Campylobacter jejuni culture and colitis. Baseline physical examination, body weight measurement, colon biopsy, and rectal culture for Campylobacter jejuni were obtained from each animal. Colon biopsies were processed for histologic examination and were graded on a scale of 0 to 3 (0=normal; 1=mild, 2=moderate, 3=severe colitis). All animals with grade 2 or higher colitis were excluded from study. All rectal cultures were negative for Campylobacter jejuni. Ninety-two animals (83 with no colitis and 9 with grade 1 colitis) were randomized into 2 groups by age and sex. One group is fed Zu/Preem marmoset diet and the other group is fed Spectrum marmoset diet. Animals will be monitored at 3 month intervals by physical examination, body weight measurement, colon biopsy, and rectal culture to determine if there is a difference between the two groups in the incidence of colitis or other parameters over time.

Agency
National Institute of Health (NIH)
Institute
National Center for Research Resources (NCRR)
Type
Primate Research Center Grants (P51)
Project #
5P51RR000168-35
Application #
3719039
Study Section
Project Start
Project End
Budget Start
Budget End
Support Year
35
Fiscal Year
1996
Total Cost
Indirect Cost
Name
Harvard University
Department
Type
DUNS #
082359691
City
Boston
State
MA
Country
United States
Zip Code
02115
Shang, L; Smith, A J; Reilly, C S et al. (2018) Vaccine-modified NF-kB and GR signaling in cervicovaginal epithelium correlates with protection. Mucosal Immunol 11:512-522
Sonntag, Kai-Christian; Woo, Tsung-Ung W (2018) Laser microdissection and gene expression profiling in the human postmortem brain. Handb Clin Neurol 150:263-272
Almodovar, Sharilyn; Swanson, Jessica; Giavedoni, Luis D et al. (2018) Lung Vascular Remodeling, Cardiac Hypertrophy, and Inflammatory Cytokines in SHIVnef-Infected Macaques. Viral Immunol 31:206-222
Duke, Angela N; Meng, Zhiqiang; Platt, Donna M et al. (2018) Evidence That Sedative Effects of Benzodiazepines Involve Unexpected GABAA Receptor Subtypes: Quantitative Observation Studies in Rhesus Monkeys. J Pharmacol Exp Ther 366:145-157
Kamberov, Yana G; Guhan, Samantha M; DeMarchis, Alessandra et al. (2018) Comparative evidence for the independent evolution of hair and sweat gland traits in primates. J Hum Evol 125:99-105
Seth, Nitin; Simmons, Heather A; Masood, Farah et al. (2018) Model of Traumatic Spinal Cord Injury for Evaluating Pharmacologic Treatments in Cynomolgus Macaques (Macaca fasicularis). Comp Med 68:63-73
Mauney, Sarah A; Woo, Tsung-Ung W; Sonntag, Kai C (2018) Cell Type-Specific Laser Capture Microdissection for Gene Expression Profiling in the Human Brain. Methods Mol Biol 1723:203-221
Termini, James M; Church, Elizabeth S; Silver, Zachary A et al. (2017) Human Immunodeficiency Virus and Simian Immunodeficiency Virus Maintain High Levels of Infectivity in the Complete Absence of Mucin-Type O-Glycosylation. J Virol 91:
Ma, Qi; Ruan, Hongyu; Peng, Lisheng et al. (2017) Proteasome-independent polyubiquitin linkage regulates synapse scaffolding, efficacy, and plasticity. Proc Natl Acad Sci U S A 114:E8760-E8769
Shang, L; Duan, L; Perkey, K E et al. (2017) Epithelium-innate immune cell axis in mucosal responses to SIV. Mucosal Immunol 10:508-519

Showing the most recent 10 out of 365 publications