The flaviviruses are mosquito-borne viruses that are associated with significant worldwide morbidity and mortality. The dengue viruses (DENV) are members of this group associated with dengue fever, dengue hemorrhagic fever (DHF) and dengue shock syndrome (DSS). These viruses are endemic in most of the tropical and sub-tropical world, and roughly one-third of the Earth's populace lives in areas at risk for dengue transmission. A second member of the flaviviruses. West Nile virus (WNV), is a neurotropic virus;infection can result in encephalitis/meningitis and subsequent long-term neurologic complications or death. Despite this threat, no specific therapy exists for either virus. Treatment is largely supportive, and in the case of DHF and DSS or neuroinvasive WNV, generally requires hospitalization. In this application, we propose to identify and develop small molecule inhibitors of these viruses. We will emphasize the development of molecules that show broad-spectrum activity against multiple flaviviruses, and potentially members of other virus families as well. Initial screening of multiple compound libraries comprising >100,000 compounds will be carried out in collaboration with the Southern Research Institute (SRI). In additional arms of this proposal, the same libraries will be screened for activity against other virus families, including influenza, alphaviruses, and coronaviruses. Therefore, the overall proposal has the potential to identify compounds that are not only active against flaviviruses, but other medically important viruses as well. Multiple techniques will be used to characterize mechanisms of action and targets of antiviral compounds. We will focus on compounds that target one of the following important enzymatic activities of the flavivirus NS5 protein: the RNA-dependent RNA polymerase, which is essential for replication of the viral RNA genome, and the 2'-0-methyltransferase, which is required for the virus to avoid the host innate immune response. Compounds with activities targeting these enzymes will be further developed through the synthesis of structural analogs, analysis of structure activity relationship (SAR), and testing in in vivo (mouse) models of virus infection.

Public Health Relevance

The flaviviruses are associated with significant morbidity, mortality, and economic burden throughout world. Nevertheless, no specific anti-viral therapies for disease associated with these viruses are currently available. This project is designed to identify and develop small molecule anti-viral therapeutics against two medically important flaviviruses-dengue virus and West Nile virus. Furthermore, we will emphasize the development of drugs that show activity against multiple flaviviruses, and possibly other virus families as well.

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Research Program--Cooperative Agreements (U19)
Project #
1U19AI109680-01
Application #
8650366
Study Section
Special Emphasis Panel (ZAI1-LR-M (J1))
Project Start
Project End
Budget Start
2014-03-01
Budget End
2015-02-28
Support Year
1
Fiscal Year
2014
Total Cost
$712,509
Indirect Cost
$27,051
Name
University of Alabama Birmingham
Department
Type
DUNS #
063690705
City
Birmingham
State
AL
Country
United States
Zip Code
35294
Menachery, Vineet D; Yount Jr, Boyd L; Josset, Laurence et al. (2014) Attenuation and restoration of severe acute respiratory syndrome coronavirus mutant lacking 2'-o-methyltransferase activity. J Virol 88:4251-64
Morrison, Thomas E (2014) Reemergence of chikungunya virus. J Virol 88:11644-7