SBIR-STTR Award

A New Generation of Anti-viral Vaccines for Aquaculture Using Nanotechnology
Award last edited on: 1/23/2023

Sponsored Program
SBIR
Awarding Agency
DOC : NOAA
Total Award Amount
$247,675
Award Phase
2
Solicitation Topic Code
8.4.6
Principal Investigator
David B Powell

Company Information

ProFISHent Inc

17806 NE 26th Street
Redmond, WA 98052
   (425) 883-9896
   davidp@profishent.com
   www.profishent.com
Location: Single
Congr. District: 01
County: King

Phase I

Contract Number: DG133R-03-CN-0054
Start Date: 00/00/00    Completed: 00/00/00
Phase I year
2003
Phase I Amount
$49,820
This innovative Phase 1 project will test the feasibility of using the science of nanotechnology and emulsion chemistry to produce nanoparticles in a matrix to greatly enhance the immunogenicity of inactivated viruses. This new approach promises to have direct application to the development of potent cost-effective anti-viral vaccines for aquatic animals. These novel formulations should stimulate protective humoral and cellular immune responses by targeting antigen presenting cells. Infectious hematopoietic necrosis virus (IHNV) and infectious salmon anemia virus (ISAV) will be used as model organisms to assess the binding and initial potency of these complex viral carriers. Emphasis will be placed on creating nanoparticles with high affinities to viral particles, followed by a comparison of antibody response kinetics and possible side effects in rainbow trout. Summary of

Anticipated Results:
We expect to initiate the development of a new wave of injectable killed vaccines for fish that elicit strong protective immune responses against intracellular pathogens. The anticipated result of Phase 1 is a highly stable vaccine emulsion system with successful binding of antigens to nano- or microparticles, while maintaining very low side effects in fish. Potent1al commercial applications: Phase 2 & 3 developments of this technology will result in a new generation of aquaculture vaccines that will substantially reduce losses to disease. The lack of adverse effects to biological re-circulation filters is an added benefit. It should be possible to vaccinate and raise a variety of aquatic species previously thought to be too susceptible to diseases

Phase II

Contract Number: DG133R-04-CN-0160
Start Date: 00/00/00    Completed: 00/00/00
Phase II year
2004
Phase II Amount
$197,855
Although companies based outside the U.S. have tested and, in some cases, sold basic anti-viral vaccines to aquaculture producers, practicing veterinarians and virologists have been unimpressed by their extremely limited effectiveness (J. Mullins, pers. comm. 2002; J. Winton, pers. comm. 2004). The consensus is that new approaches are urgently needed to develop viral vaccines that do not rely on DNA technology. ProFishent will apply advances in nanotechnology to the design and construction of efficacious immersion and injection vaccines to prevent mortalities from viruses and, potentially, other intracellular pathogens. Proprietary nanoparticles will be combined with model viruses (ISAV and IHNV) to create potent immunostimulatory complexes. Vaccine prototypes will be optimized and compared to traditional formulations for their ability to stimulate immunity and to protect rainbow trout and Atlantic salmon from laboratory challenges with live pathogens. Fluorescent, antigen-coated particles will also be used to observe the effect of size on uptake and transport by the immune system.

Potential Commercial Applications:
Commercialization of this research in Phase 3 will result in a new platform technology using nontoxic nanoparticle products that will be applicable to both fresh-water and marine aquatic species. The vaccines will be compatible with biological recirculation filter systems. It should be possible to vaccinate and raise a variety of aquatic species previously thought to be too susceptible to pathogens. Unlike DNA vaccines, this family of products will not raise any objections from consumers concerned about genetically modified organisms, nor will it face formidable hurdles by regulatory authorities