The proposed project will further develop marketable ELISA and lateral-flow immunoassay diagnostics (LFI) in both monoplexed and multiplexed formats for the NIAID category A, BSL-4 filoviruses, and will drive pre-clinical development and validation for these diagnostics. These assays will be used for diagnosis of Ebola virus (EBOV), Sudan virus (SUDV) and Marburg virus (MARV), and will be based on more inexpensive recombinant proteins, rather than reagents that must be produced in high-containment laboratories. We will first scale up production of our existing recombinant filovirus proteins and polyclonal and monoclonal antibodies, in order to meet manufacturing and commercialization requirements. We will next develop second-generation ELISA and LFI prototypes for our existing EBOV, SUDV and MARV antigen detection assays. Third, we will extend the library of available filovirus assays by developing antigen detection tools for the Reston and Bundibugyo viruses. Fourth, we will prepare for commercialization of the assays in both monoplexed multiplexed formats. A multiplexed panel may be ideal for diagnosis as hemorrhagic fevers that are caused by different viruses can present similar symptoms. Antigens from the arenavirus Lassa (LASV), the viral hemorrhagic fever (VHF) most frequently transported out of Africa have already been developed into ELISA and LFI formats by this consortium. Thus, a fifth goal to be accomplished in this project time period is to multiplex LASV antigens with those of the filoviruses in order to develop a broader-scope diagnostic. The resulting multiplexed assays will have utility and marketability for recent travelers who have fallen ill, personnel working in BSL-4 laboratories, in bioterrorism scenarios, and in clinical settings in Africa where these fevers occu naturally. The ultimate goal is to establish a panel of recombinant VHF diagnostics that are easy to use, quick, accurate and cost effective for biodefense and public health purposes. Such diagnostics can be stockpiled to protect civilian and military personnel from viral exposure and release. Viral hemorrhagic fevers are extremely rare in the U.S., but accidental or intentional release could have devastating consequences. Importantly, the simplicity and cost-effectiveness of diagnostics such as these will facilitate the necessary availability of these reagents so that they can be put to immediate use in event of virus exposure or release. Widespread availability of these simple-to-use tests will allow rapid containment of the viruses, and may even serve as a deterrent from using these pathogens as biological weapons.

Public Health Relevance

The potential use of the category A filoviruses as biological weapons, and the emergence of these viruses among humans, wildlife and domesticated animals necessitates development of diagnostics for public health laboratories, hospital-based clinical laboratories, and point-of-care use. The availability of highly sensitive and specific, ye adaptable diagnostics in easy-to-use, inexpensive formats would facilitate usage at any location and would allow more rapid identification of these viruses, differential diagnosis from other causes of similar disease, and provision of appropriate treatments, barriers and ring vaccination protocols to contain the disease.

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Small Business Innovation Research Grants (SBIR) - Phase II (R44)
Project #
2R44AI088843-03A1
Application #
8646651
Study Section
Special Emphasis Panel (ZRG1-IDM-V (12))
Program Officer
Repik, Patricia M
Project Start
2010-04-01
Project End
2017-05-31
Budget Start
2014-06-15
Budget End
2015-05-31
Support Year
3
Fiscal Year
2014
Total Cost
$995,262
Indirect Cost
Name
Corgenix Medical Corporation
Department
Type
DUNS #
619834542
City
Broomfield
State
CO
Country
United States
Zip Code
80020
Schieffelin, John S; Shaffer, Jeffrey G; Goba, Augustine et al. (2014) Clinical illness and outcomes in patients with Ebola in Sierra Leone. N Engl J Med 371:2092-100