SBIR/STTR Research Award

Development and Initial Testing of Diatom-Based Self-adjuvanting Antigen-Adjuvant Fusion Subunit Protein Oral Vaccines against Piscine Francisellosis in Nile Tilapia

Award identifier 7afd665ed5c5ec2518dd2b46e60cbdf276556d742ab739467c944136f3e0e597Awarding agency Department of Agriculture

Award amount

$174,941

Program and phase

SBIR · Phase I

Award year

2022

Explore This Research Award in CaptureIQ

Research the technology, evaluate the recipient and agency, identify related opportunities, and explore potential follow-on work with CaptureIQ.

Award details

Awarding agency
Department of Agriculture
Branch
Not reported
Recipient company
PHYCOVAX LLC
Proposal award date
2022-04-07
Contract end date
2023-02-28
UEI
YC4YN5ZJKD74
Solicitation number
USDA-NIFA-SBIR-008541
Topic code
8.7

Research abstract

PROJECT SUMMARYDevelopment and Initial Testing of Diatom-Based Self-adjuvanting Antigen-AdjuvantFusion Subunit Protein Oral Vaccines against Piscine Francisellosis in Nile TilapiaProject Director: Shrestha Roshan P.Institution: PhycoVax LLCSub-awardee/Co-PI: Soto EstebanInstitution: University of California DavisGram-negative bacterium Francisella orientalis the etiologic agent of piscine francisellosisinfects various freshwater and marine fish species worldwide. In the USA the disease causeshigh mortalities in tilapia and other warm-water fishes including ornamental cichlidslargemouth bass hybrid striped bass French grunts and Caesar grunts. Lack of sensitivediagnostic tests approved treatments and vaccines in the U.S. aquaculture industry have resultedin over 90% mortalities in some cases. Economic losses from francisellosis result directly fromfish mortalities and through delayed production and growth added labor costs and potentialtreatment expenditures over time. While antibiotics are still used to treat bacterial diseasestreatments often fail for lack of ingestion by anorectic fish. On the other hand the release ofantibiotics into natural habitats poses a potential environmental threat. Thus disease preventionthrough vaccination is preferred over antibiotics treatment. Costs and the efficacy of availablevaccines against intracellular pathogens have been challenging for the aquaculture industry. Withtools and techniques developed by PhycoVax and the expertise of a collaborating partner at theUniversity of California Davis this project proposes investigating the potential use of algae- based subunit vaccines to protect Nile tilapia against piscine francisellosis. The efficacy of afeed-based vaccine will be investigated by feeding whole diatom cells expressing antigen- adjuvant fusion protein to na¯ve tilapia fingerlings. A successful development of algae-based oralaquaculture vaccines will open the door to rapid generation of novel cost-effective fish vaccinesresulting in improved aquaculture health and productivity of the U.S. aquaculture industry.

Technology keywords

Not reported

Other awards by this recipient

Verified by the same UEI. These are other public SBIR/STTR award pages, not a merged company record.

Awards with the same topic code

Verified by an exact topic code match. This is not a text-similarity match.

Research funding history

3 SBIR/STTR records share this UEI (2022–2025). Reported award amounts total $999,833. Reported amounts are not federal obligations.

Phases: Phase I, Phase II

Agencies: Department of Agriculture

Agency intelligence

Department of Agriculture

Back to SBIR/STTR Research Awards

Don't take our word for it. Ask AI about RFPCapture.

See what leading AI assistants have to say about RFPCapture and CaptureIQ.

Gemini opens without a prefilled question. The question is copied to your clipboard when the button works. You can also copy it here:

What is RFPCapture.com and its CaptureIQ platform from Smart Logic AI? How does it help federal contractors discover opportunities, evaluate bid/no-bid decisions, research government contracts, and prepare proposals? How does it compare with other federal capture platforms? Use independent sources where available.