Completed Infection & Immunity Food & Agriculture

Translation of virus like particle foot-and-mouth disease vaccine research to commercial development

In plain English

AI plain-English summary

A cheap, stable vaccine for foot-and-mouth disease—made from hollow protein shells rather than live virus—is moving from the lab toward commercial production. The problem is stark. Foot-and-mouth disease costs the global livestock industry between US$6.5 and $21 billion every year. Current vaccines require growing large quantities of live virus in expensive high-containment facilities, which limits supply and drives up costs. The result is a chronic undersupply of vaccine, particularly in Africa. The researchers have already shown that virus-like particles (VLPs) grown in insect cells can protect cattle against three different serotypes of the virus, and that these particles can be engineered for greater physical stability. If this project succeeds, it will replace a fragile, expensive manufacturing process with one that is cheaper, safer, and faster. New rapid methods will allow the team to design and test stabilised VLPs for multiple viral strains, including newly emerging ones. The goal is to make affordable foot-and-mouth disease vaccines available to livestock farmers in the poorest regions of the world—where the disease currently devastates herds and livelihoods.

View original technical description
Foot-and-mouth disease (FMD) is a highly contagious, acute viral disease of cloven-hoofed, domesticated and wild animals. There are many variants of FMD which cause a global economic impact, estimated at between US$ 6.5 and 21 billion per year. Current vaccines are made of inactivated viruses which are fragile structures that can limit production and result in poor immunity after vaccination. Large quantities of live FMD virus are grown during production in very expensive high containment facilities. Consequently, there is a huge undersupply of vaccine globally, especially in Africa. We have produced virus like particles (VLP) copies of the FMD virus in insect cells, requiring less expensive facilities. We have shown for three serotypes that vaccinating cattle with VLP, with enhanced physical stability, can protect from FMD infection. New rapid methods will be developed to design, express and test physically stabilised VLPs for a wide range of strains, to ensure we can produce vaccines for the current needs and newly emerging viruses. This project will allow optimisation of commercial production methods for VLPs to make the vaccines affordable and available for livestock farmers in the poorest regions of the world.

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Researchers

Bryan Charleston (EPMC Awardee)

Related Research

Grants with similar aims, by meaning.

Improved control of endemic foot-and-mouth disease by development of virus like particle vaccines
Attenuation of FMDV Serotypes/Strains to Develop Stable and Effective Live, Attenuated, Vaccines
The Molecular Biology of FMDV Replication: Towards New Methods of FMDV Disease Control.
Improved vaccine manufacture to control foot-and-mouth disease: Production of recombinant vaccines by design
Improving the quality of FMD vaccines by understanding the correlation of vaccine-induced protection with humoral and cellular immune responses

Original classification

Innovations Project Award

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