Award details

VACCINE. Development of a novel yeast-based oral subunit vaccine against Eimeria spp. in chickens

Reference	BB/P003931/1
Principal Investigator / Supervisor	Professor Damer Blake
Co-Investigators / Co-Supervisors	Professor Fiona Tomley, Professor Dirk Werling
Institution	Royal Veterinary College
Department	Pathology and Pathogen Biology
Funding type	Research
Value (£)	400,104
Status	Completed
Type	Research Grant
Start date	30/12/2016
End date	28/02/2021
Duration	50 months

Abstract

In the work proposed here we will develop Saccharomyces cerevisiae as an oral vaccine vector platform for use with poultry, employing freeze-drying to inactivate and stabilise vaccine formulations. Non-viable yeast cells are not considered as GMOs (EU directive 2001/18/EC) and benefit from Generally Regarded As Safe (GRAS) status. We will build on proof of concept studies with pigs to validate the freeze-drying process, comparing immunity induced in chickens after vaccination with live yeast cultures, bacterial expressed recombinant protein and natural live parasite exposure. Development of a non-GMO vector system with no requirement for a cold chain and which can be included in animal feed would revolutionise poultry vaccination. The yeast system will be developed using three well-established anticoccidial vaccine candidates. Coccidiosis caused by Eimeria parasites remains a major animal health and welfare concern with significant impact on food security and economic productivity. The proteins apical membrane antigen 1 (AMA1), immune mapped protein 1 (IMP1) and microneme protein 3 (MIC3) all show robust anticoccidial vaccine potential against Eimeria tenella, one of the most important species of the genus. To date, these antigens have only been tested individually. Here, we will investigate multiple combinations of these antigens to identify an optimal multi-valent vaccine which can be used in the rational development of equivalent vaccines against other high impact Eimeria species. Major outputs will include understanding of the breadth of immune responses, systemic and local, stimulated by oral yeast-vectored vaccination in different chicken body compartments, indicating the range of pathogens which may be rationally targeted in future applications. Finally, we will use specialised facilities to test in vivo protection stimulated by the optimised vaccine under simulated field conditions, beginning to bridge the gap between tool development and practical use

Summary

Yeast species such as Saccharomyces cerevisiae are useful tools for the high yield production of recombinant proteins and have a Generally Regarded As Safe (GRAS) status. They are capable of performing several complex post-translational modifications that are not achieved in many other expression systems, and are easily grown to very high densities producing large quantities of stable particles. Recently, the idea of using S. cerevisiae as a delivery vehicle for cancer, viral, and bacterial vaccines has been explored, inducing robust humoral and cellular immune responses. In addition to using yeast to produce a vaccine antigen of interest, the yeast cell itself has been shown to have adjuvant-like properties and has the potential to activate both inflammatory and phagocytic receptors expressed on antigen-presenting cells. Our preliminary data demonstrates that freeze-drying recombinant yeast cultures expressing viral protein at their surface renders the recombinant yeast completely non-viable (unpublished). However, the freeze-drying process does not alter conformation of these proteins, as surface expression is equal in live and freeze-dried yeast as quantified by flow cytometry and Western blotting. This has interesting implications in vaccine design as a non-viable S. cerevisiae is not categorised as a genetically modified organism (GMO) and such a killed vaccine would not be subject to GMO regulations. Additionally there would be no need for refrigeration of the freeze-dried yeast, reducing transport and storage costs. Vaccines based upon S. cerevisiae are likely to be particularly valuable against diseases of farmed poultry, where safety, scalability, stability, delivery and cost are crucial. In one example modern poultry production relies on effective control of Eimeria, but current approaches using drugs and live vaccines require improvement. In recent years a panel of coccidial antigens have been identified as vaccine candidates, each individually capable ofinducing up to a 65% reduction in oocyst output. Now, the focus is shifting from antigen discovery to antigen formulation and delivery with yeast being a leading option, especially given the importance of T-cell mediated responses in anticoccidial immunity.

Impact Summary

The work proposed has direct relevance to the Cross-Councils highlight 'novel tools and technologies for vaccinology'. The project falls within BBSRC strategic research priority areas: (1) Animal health (developing strategies to combat disease) (2) Sustainably enhancing agricultural production (improving survival/longevity) and (3) Welfare of managed animals (alleviation of disease). Outputs include establishment of freeze-dried S. cerevisiae as a safe and stable oral vaccine vector for poultry, using the coccidial parasite E. tenella as an example with immediate relevance to poultry production and welfare. Outcomes will assist in increasing UK competitiveness in the global animal production market, improving animal welfare and helping to guarantee a secure supply of safe, healthy food. The following stakeholders will benefit from impact arising from this work. 1. The poultry production industry Chicken production and welfare benefit from many vaccines, but more are urgently required. For many pathogens candidate vaccine antigens have been documented, but progress has been limited by availability of cost-effective strategies for delivery within the tight economic margins inherent to the poultry industry. Validation of freeze-dried S. cerevisiae as a safe, stable vector platform effective when delivered directly to chickens through their diet can revolutionise production, improving economic performance and welfare. Our close relationships with industry representatives can fast track the vector into field use, starting with the anticoccidial vaccine targeted here. Findings will be relevant to vaccines targeting other pathogens in chickens, as well as pigs and ruminants. 2. The animal health industry The UK currently leads the world in the production of live attenuated anticoccidial vaccines but a major limiting factor is the requirement for production in vivo, illustrated by recent production failures and the consequential vaccine shortage. Recombinant anticoccidialvaccines have been sought for more than 30 years. The combination of effective vaccine candidates and a realistic vector system have finally brought such vaccines within reach. The scalability and stability of a yeast-based vaccine would support expansion of vaccination from the minority to the majority of chicken production, improving chicken health. 3. Animal welfare The effective reduction of disease as a result of improved vaccine availability against coccidial and other pathogens supports the Five Freedoms implicit to animal welfare as set out by the Farm Animal Welfare Council. A recombinant anticoccidial vaccine will also reduce the requirement for chicken use in vaccine production. 4. General public and the environment Increased efficiency in poultry production will raise poultry product availability at a lower cost for the consumer, contributing to improved food security. Consequences of improved pathogen control include a reduction in the requirement for chemoprophylaxis, reducing drug consumption, the risk of contamination to the food chain and the environment, and selection for drug resistance. All three investigators are actively engaged in public dissemination of UK research. Students at all levels of education can benefit from the principles established in this work. 5. Skills, knowledge and training The multidisciplinary nature of this project will provide opportunities for broad training to all staff, in addition to other members and students of each host institution, strengthening the research community in the areas of disease control and vaccine development. Broader impact can be achieved using avenues such as the UK Veterinary Vaccines Network. 6. International development Infectious diseases impose serious costs on animal production in developing counties. Translating high quality, innovative, strategic research within UK universities into cheap, efficacious vaccines can improve economic income and alleviate poverty.

Committee	Research Committee A (Animal disease, health and welfare)
Research Topics	Animal Health, Immunology, Microbiology
Research Priority	X – Research Priority information not available
Research Initiative	X - not in an Initiative
Funding Scheme	X – not Funded via a specific Funding Scheme

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