Broad-spectrum, small-molecule inhibitors of bunyaviruses

Information

  • Research Project
  • 7644683
  • ApplicationId
    7644683
  • Core Project Number
    U01AI082108
  • Full Project Number
    1U01AI082108-01
  • Serial Number
    82108
  • FOA Number
    RFA-AI-08-001
  • Sub Project Id
  • Project Start Date
    9/23/2009 - 14 years ago
  • Project End Date
    8/31/2011 - 12 years ago
  • Program Officer Name
    TSENG, CHRISTOPHER K.
  • Budget Start Date
    9/23/2009 - 14 years ago
  • Budget End Date
    8/31/2010 - 13 years ago
  • Fiscal Year
    2009
  • Support Year
    1
  • Suffix
  • Award Notice Date
    9/23/2009 - 14 years ago
Organizations

Broad-spectrum, small-molecule inhibitors of bunyaviruses

DESCRIPTION (provided by applicant): The family Bunyaviridae is comprised of a diverse group of viruses spread across five genera and infecting hosts from both the plant and animal kingdoms. Significant biothreats among these are several human pathogens including Rift Valley fever virus (RVFV), Crimean-Congo hemorrhagic fever virus (CCHF), hantavirus, and La Crosse encephalitis virus (LACV). A broad-spectrum bunyavirus antiviral would have great utility against natural or intentional introduction of these agents into population centers, as well as provide a treatment option in areas where these pathogens are endemic. The goal of the SIGA Bunyavirus product development program described here is to develop a broad-spectrum, small-molecule therapeutic for the treatment and prevention of disease caused by RVFV, a Category A priority pathogen, and LACV, a ategory B pathogen. Using sensitive high-throughput screens developed for both LACV and RVFV, we have identified several candidate compounds (quality hits) with broad-spectrum antiviral properties against these related pathogens from among the 206,000 small molecules in the SIGA chemical compound library. This dual screening strategy has also allowed identification of nontoxic compounds with antiviral activities that extend beyond the family Bunyaviridae against viruses in the Poxviridae, Togaviridae, and Flaviviridae families, presumably by targeting host pathways essential for replication of a diversity of virus families. Lead series will be assessed with respect to mechanism of action, metabolic stability, pharmacokinetic properties, and efficacy in small animal models of bunyavirus disease in an effort to obtain data necessary for the submission of an application for an Investigational New Drug (IND). RELEVANCE (See instructions): To date, there are no specific vaccines or antivirals approved for the treatment of the Category A, B, or C bunyavirus infections in humans.Of note is the presence of four different members of the family Bunyaviridae among the viruses characterized as biothreats to the United States. The development of a broad-spectrum antiviral treatment for bunyavirus infection is the primary goal of the work outlined in this proposal.

IC Name
NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES
  • Activity
    U01
  • Administering IC
    AI
  • Application Type
    1
  • Direct Cost Amount
  • Indirect Cost Amount
  • Total Cost
    1174957
  • Sub Project Total Cost
  • ARRA Funded
    True
  • CFDA Code
    701
  • Ed Inst. Type
  • Funding ICs
    NIAID:1174957\
  • Funding Mechanism
    Research Projects
  • Study Section
    ZAI1
  • Study Section Name
    Special Emphasis Panel
  • Organization Name
    SIGA TECHNOLOGIES, INC.
  • Organization Department
  • Organization DUNS
    932651516
  • Organization City
    CORVALLIS
  • Organization State
    OR
  • Organization Country
    UNITED STATES
  • Organization Zip Code
    97333
  • Organization District
    UNITED STATES