DESCRIPTION (provided by applicant): The recent deployment of a bioweapon in an attack on the citizens of the United States has moved bioterrorism from the realm of possible to actual threat. This new realization has brought the need for rapid, high-throughput diagnosis, treatment, and vaccination to the forefront. This application concentrates on development of high-throughput detection of live agents of viral hemorrhagic fever, using the highly lethal SNV (Bunyaviridae: Hantavirus) as the model organism. Furthermore, the technology we will develop under this funding will also be of considerable value as facilitating the advancement of treatments for hantavirus pulmonary syndrome (HPS), the disease associated with SNV. This application will develop reverse genetics technology for hantaviruses with the initial intent of preparation of cellular reporters that produce a green signal when the cells are exposed to live, replication-competent SNV. This development would have considerable potential for expanding the technology to other agents of viral hemorrhagic fever. We have a specific plan to further develop and commercialize the product after the initial development phase funded by this application and will seek further funding to develop basic information on the replication of hantaviruses at the end of the two-year funding cycle.
National Institute of Allergy and Infectious Diseases
CFDA Code
856
DUNS Number
868853094
UEI
F6XLTRUQJEN4
Project Start Date
30-September-2002
Project End Date
31-August-2004
Budget Start Date
30-September-2002
Budget End Date
31-August-2003
Project Funding Information for 2002
Total Funding
$225,000
Direct Costs
$150,000
Indirect Costs
$75,000
Year
Funding IC
FY Total Cost by IC
2002
National Institute of Allergy and Infectious Diseases
$225,000
Year
Funding IC
FY Total Cost by IC
Sub Projects
No Sub Projects information available for 1R21AI053400-01
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Publications are associated with projects, but cannot be identified with any particular year of the project or fiscal year of funding. This is due to the continuous and cumulative nature of knowledge generation across the life of a project and the sometimes long and variable publishing timeline. Similarly, for multi-component projects, publications are associated with the parent core project and not with individual sub-projects.
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No Outcomes available for 1R21AI053400-01
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