This proposal describes a 5-year training program for the development of an independent academic career in Laboratory Medicine and Infectious Diseases. The program will promote the command of genomic and proteomic approaches applied to the study of viral pathogenesis. Kenneth L. Tyler will mentor the P.I.'s scientific development. Dr. Tyler is a recognized leader in the field of viral pathogenesis. As Professor of Neurology, Microbiology, Immunology, and Medicine, he has trained numerous postdoctoral fellows and graduate students. To enhance the training, the program will enlist the expertise of a multidisciplinary board of senior scientists, who will provide scientific and career advice. The University of Colorado provides an ideal setting for training physician-scientists by integrating expertise from diverse resources into customized programs. This environment maximizes the potential for the PI to establish a scientific niche from which a successful academic career can be constructed. ? ? Research will focus on delineating and targeting apoptotic signaling pathways in viral myocarditis. Dr.Tyler's laboratory has used reoviruses to study viral and cellular mechanisms of apoptotic cell death, both in vitro and in well-characterized murine models of viral encephalitis and myocarditis.
Specific aims of this project are (1) to identify the importance of apoptosis as a critical determinant of virus-induced myocarditis, (2) to characterize virus-induced myocarditic signaling pathways in vitro and vivo at the transcriptional and translational levels, and (3) to target critical identified pathways in vivo, as a novel therapeutic strategy for viral myocarditis. Proposed experiments involve detailed analysis of infected murine cardiac myocytes and tissues, using myocarditic and non-myocarditic viruses. Virologic, histologic, immunohistochemical, genomic and proteomic approaches will be employed. Identified pathways will be targeted using specific inhibitors and mice with genetic mutations in pertinent signaling pathways. These studies are designed to identify specific cellular mechanisms of virus-induced apoptosis in the pathogenesis of viral myocarditis. Identification of these pathways is critical for the development of novel therapies for viral myocarditis and other diseases involving apoptotic tissue damage.

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Clinical Investigator Award (CIA) (K08)
Project #
5K08AI052261-06
Application #
7082896
Study Section
Microbiology and Infectious Diseases B Subcommittee (MID)
Program Officer
Cassetti, Cristina
Project Start
2002-09-01
Project End
2010-03-31
Budget Start
2007-04-01
Budget End
2010-03-31
Support Year
6
Fiscal Year
2007
Total Cost
$125,280
Indirect Cost
Name
Children's Research Institute
Department
Type
DUNS #
606977783
City
Washington
State
DC
Country
United States
Zip Code
20010
DeBiasi, Roberta L; Robinson, Bridget A; Leser, J Smith et al. (2010) Critical role for death-receptor mediated apoptotic signaling in viral myocarditis. J Card Fail 16:901-10
Miyamoto, Shelley D; Brown, R D; Robinson, Bridget A et al. (2009) Cardiac cell-specific apoptotic and cytokine responses to reovirus infection: determinants of myocarditic phenotype. J Card Fail 15:529-39
Clarke, P; Debiasi, R L; Goody, R et al. (2005) Mechanisms of reovirus-induced cell death and tissue injury: role of apoptosis and virus-induced perturbation of host-cell signaling and transcription factor activation. Viral Immunol 18:89-115
Clarke, P; Debiasi, R L; Meintzer, S M et al. (2005) Inhibition of NF-kappa B activity and cFLIP expression contribute to viral-induced apoptosis. Apoptosis 10:513-24
DeBiasi, Roberta L; Robinson, Bridget A; Sherry, Barbara et al. (2004) Caspase inhibition protects against reovirus-induced myocardial injury in vitro and in vivo. J Virol 78:11040-50