The emergence of epidemic mosquito-borne diseases has led to significant world-wide morbidity and mortality. With the ever-increasing ease of global travel, insect-borne viruses endemic to different geographical regions are now becoming a serious health threat to the American population, as the spread of West Nile has illustrated. Viral pathogens that were once restricted to specific geographic regions are now able to establish persistent infections in previously unexposed populated areas. In addition, changes in global climate zones are creating optimal conditions to establish endemic areas. It is therefore crucial to understand the viral pathogenesis of newly emerging infectious diseases, in order to provide the necessary treatments for unforeseen outbreaks. Whereas infection of the insect host is non-pathogenic, infection of mammals is associated with disease, suggesting that the viruses must use different strategies to move through each host. Little is known about the pathways required for the replication cycles of these viruses in either of their hosts, and less is understood about the innate immune pathways that restrict pathogenesis.

Public Health Relevance

To elucidate the cellular requirements of viral infection, we propose to employ a cell-based high-throughput RNA interference screening assay using viral infection of Drosophila cells with Sindbis virus. The powerful tools available in this model system, including forward genetics and functional genomics, can identify cellular factors and pathways that regulate pathogenesis in a variety of contexts. Observations made in flies can then be compared to the requirements in human cells using small interfering RNA technology. To understand the differences between hosts, our system uniquely situates us to identify novel insights into survival strategies adopted by the pathogens and the host.

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Postdoctoral Individual National Research Service Award (F32)
Project #
5F32AI078666-02
Application #
7779403
Study Section
Special Emphasis Panel (ZRG1-F13-C (20))
Program Officer
Repik, Patricia M
Project Start
2009-03-01
Project End
2010-08-31
Budget Start
2010-03-01
Budget End
2010-08-31
Support Year
2
Fiscal Year
2010
Total Cost
$26,076
Indirect Cost
Name
University of Pennsylvania
Department
Microbiology/Immun/Virology
Type
Schools of Medicine
DUNS #
042250712
City
Philadelphia
State
PA
Country
United States
Zip Code
19104
Rose, Patrick P; Hanna, Sheri L; Spiridigliozzi, Anna et al. (2011) Natural resistance-associated macrophage protein is a cellular receptor for sindbis virus in both insect and mammalian hosts. Cell Host Microbe 10:97-104