Award details

Algal vaccines for Aquaculture

Reference	BB/S004327/1
Principal Investigator / Supervisor	Dr Brenda Parker
Co-Investigators / Co-Supervisors	Professor Saul Purton
Institution	University College London
Department	Biochemical Engineering
Funding type	Research
Value (£)	160,399
Status	Completed
Type	Research Grant
Start date	01/01/2019
End date	02/10/2020
Duration	21 months

Abstract

In this proof-of-concept project we will aim to generate a transgenic line of C. reinhardtii expressing the E2 structural protein of Salmonid Alpha Virus (SAV). Via laboratory trials and technoeconomic analysis we will establish the effiacy and performance of dried algal biomass as an effective oral vaccine delivery system. In order to produce the SAV antigen in the algal chloroplast, a synthetic gene will be designed to the E2 structural protein from SAV sub-type 3 (SAV3). This will be placed under the control of a strong constitutive promoter. Selection is based on the restoration of phototrophic growth by the wild-type copy of psbH carried on the plasmid. Small scale cultivation of the recombinant C.rheinhardtii in ALGEM photobioreactors will be used to investigate the impact of light and nutrients on biomass productivity and product titre. This will then be scaled up using a modular hanging bag cultivation system. The process flowsheet for DSP will then be developed. Cell harvesting and dewatering via flocculation or centrifugation will be compared as a method for preparing biomass ahead of drying. Spray and freeze drying will be compared to find the most suitable method of formulating the oral vaccine, and examine the sensitivity of the SAV vaccine to heat and shear stress. In the first part of the animal trial work we will assess the following: 1. Immunogenicity of recombinant algae vs. a validated SAV vaccine (AquaVac PD3). 2. Immunogenicity of algae with empty vector (adjuvant effect). 3. Relative percent survival (RPSend) provided by algal expressed SAV antigen delivered by injection. In the second part of the animal trial work we will assess: 1.The fate of orally delivered recombinant algal vaccine antigen in the fish 2.Whether orally delivered algal vaccine can induce an immune response 3. The ability of orally delivered recombinant algae to protect salmon after viral challenge.

Summary

The global salmon industry has grown rapidly over the last four decades, and the majority of salmon purchased by consumers is farmed. Therefore, given the value of the market, protection of farmed fish against diseases is of enormous importance. The salmonid alphavirus (SAV), is reported to be one of the most prominent and detrimental diseases in Irish, Scottish and Norwegian aquaculture industries. Infection of farmed fish causes substantial losses in production and revenue. At present, the most effective method for protecting salmon stocks is via injection of fish. However, his is hugely labour intensive and can induce other side effects. Administering oral vaccines has the potential to reduce costs, simplify vaccine delivery and storage, as well as provide animal welfare benefits. Recombinant oral vaccines produced by plants, bacteria or yeast have been under investigation for their ability to induce the correct immune response. This project will investigate the microalgae C. reinhardtii as a host for recombinant oral vaccine production. Constructs containing the SAV antigen will be produced at UCL using established techniques for genetically engineering the algal chloroplast. In order to enhance the process economics, we will investigate the influences of different lights and different feeding strategies. Following this, we will investigate how different harvesting and drying techniques may influence the yield and stability of the vaccine. The algal vaccine will then be tested in animal trials to establish how effective this may be in comparison to the established injection method of vaccination. The effectiveness of the oral vaccine will depend on the digestion and immune response elicted by the microalgae within the gut of the fish. Following the scale up of cultivation and the resulting animal trials, we will perform an economic assessment to understand the commercial viability of algal-based oral vaccines.

Impact Summary

The project will have impact in each of the areas defined by the BBSRC/NERC and RCUK: economy, society, knowledge and people. In terms of economic impact the PI and CoIs have experience of working with industry, and the commercialisation of research findings and creation of spin-out companies. The constructs and data resulting from this project will be made available (after any IP protection) to the wider academic and industrial community via publication, and dissemination at conferences and meetings for example the BBSRC NIBB Networks. Furthermore, the method of producing and scaling up vaccine constructs can be made available to others for testing. Beneficiaries of this work therefore extend beyond the immediate participants. It will benefit the UK economy by exploring new methods of manufacturing using algal synthetic biology and demonstrate the potential for oral vaccine delivery in aquaculture. The implementation of new/improved methods for cultivation and cell harvest of microalgae will benefit both the academic and industrial biotechnology communities seeking to translate research from bench to product. The impact of knowledge generation from the research will arise from the communication and publication of new scientific advances and public outreach activities, detailed in the pathways to impact. In a wider sense, new methods for manufacturing with microalgae may be applied to other areas in industrial biotechnology and healthcare, resulting in gains in sustainabilty, in particular as part of a circular economy. The societal impact will arise from improved animal health and reduced cost of vaccines which may enable cost savings attained through improved productivity to be passed to the consumer. The impact on people will arise from training and career development of the PDRA and provision of skilled scientist in the industrial biotechnology sector. It will also enable an early career researcher to gain valuable PI experience with support and mentorship of more established academic CoI. Should the oral SAV vaccine is shown to be effective, the impact on the UK could be the expansion of the salmon farming industry / the reduction of losses within the salmon aquaculture industry, therefore improving profitability and potentially enabling expansion of this sector. Demonstraitng the potential for algal-based manufacturing could lead to the development and growth of a new platform for vaccine production, and the development of brand new industries. The findings will also influence future research directions, since the successful completion of this proposal will provide the foundations for further exploration in the area of algal synthetic biology. This will nurture a growing interest from other animal health and therapeutics industries who are interested in novel GRAS delivery systems. We have established links with Government offices, trade organisations and business support bodies (e.g. Innovate UK), Societies (e.g. Society for Applied Microbiology, British Phycological Society) and algal associations (e.g. European Algal Biomass Association), and so are able to contribute positively to the framing of legislation regarding the control and exploitation of algal synthetic biology. Lobbying and involvement in the drafting of roadmaps and policy documents are already a key activity for both the PI and Co-I and this will continue under this project.

Committee	Not funded via Committee
Research Topics	Animal Health, Immunology, Microbiology
Research Priority	X – Research Priority information not available
Research Initiative	BBSRC-NERC Joint Call in Aquacuture: Collaborative Research and Innovation [2017]
Funding Scheme	X – not Funded via a specific Funding Scheme

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