Human Genes Shaping the Response to Bioterrorism Agents
Collaborating Institution: University of Washington, Seattle, WA
Principal Investigator: Michael Bamshad, Ph.D.
Co-Investigators:
John Kreisel - University of UtahExpected Product: Identification of human genetic disease markers associated with West Nile virus infections.
Introduction:
Emerging pathogens have a unique potential to be weaponized as bioterrorism agents because most humans have no immunity to such infections. The human response to these pathogens varies from aborted infection to overwhelming disease and death. This variation is determined by both environmental factors and host genetic factors (i.e. susceptibility alleles). A significant gap in our knowledge is that most of these genetic factors are unknown. Our goal is to identify alleles influencing susceptibility to severe West Nile virus (WNV) disease using a candidate gene approach. Such alleles must be functionally different than wild-type alleles, and thus likely to have been subject to natural selection—the effects of which can be inferred from the pattern of variation in a gene. Thus, to increase the power of our approach we will first assess patterns of variation in each candidate gene and use these data to 1) find functional alleles, 2) determine which alleles will be most useful in association studies, and 3) identify alleles that influence susceptibility to severe WNV disease in a WNV cohort. To weight the odds of success in our favor, we will analyze genes that have been found in animal models or in vitro to influence WNV disease. Identifying alleles associated with WNV disease will facilitate the development of prognostic tests, vaccines, and therapeutics; and provide insights about how to find susceptibility alleles for other emerging pathogens.