Bluetongue virus (BTV), epizootic hemorrhagic disease virus (EHDV), and African horse sickness virus (AHSV) are orbiviruses that present major threats to UK agriculture, causing economically important disease in ruminant livestock, deer and horses.
Transmitted by Culicoides biting midges, numerous BTV strains are circulating in Europe, presenting a high risk to the UK.
This project aims to advance the state-of-the-art molecular diagnostic capabilities within the Non-Vesicular Reference Laboratory (NVRL) at Pirbright to guarantee the timely detection and identification of any circulating orbivirus.
We will develop new molecular diagnostic assays and validate serological tests for BTV antibodies. Our genome sequencing pipeline will enable strain identification and trace viral spread, improving our understanding of genome reassortment and emerging strains.
The project will also improve evidence that cattle imported into the UK from European countries with ongoing BTV circulation have been appropriately vaccinated as required under current import regulations.
Although existing BTV vaccines have worked well in controlled trials, there are concerns that some cattle vaccinated in the field do not show detectable antibodies. This makes it hard to confirm their vaccination status and protection level.
To address this, we will use a combination of serological assays to detect antibodies in vaccinated cattle. Additionally, we will additionally conduct a UK study on cattle vaccinated with BTV-8, monitoring their immune response over a year. By comparing these findings with previous infection studies, we aim to ensure better verification of vaccination and improve our understanding of cattle's immune responses to BTV.
We will also continue to develop new immunological assays to enhance our knowledge of the ruminant immune response to BTV infection and vaccination and critically advance our serological diagnostic capability as well as our ability to improve vaccine research.
Aims, objectives
This project’s overall aim is to further improve prevention and control strategies to BTV and other important orbiviruses, specifically AHSV and EHDV.
Enhance molecular diagnostic capabilities:
- Develop and update molecular diagnostic assays for rapid detection of orbiviruses.
- Implement advanced technologies to respond to emerging strains and new serotypes including BTV-3.
- Validate and apply innovative serological assays for specific BTV antibody detection.
Expand genome sequencing and bioinformatics:
- Utilize full genome sequencing for global strain identification and characterization.
- Trace viral spread and incursion routes for BTV, EHDV, and AHSV.
- Increase bioinformatics capability to study genome reassortment and the emergence of new strains.
Assess and improve vaccination strategies:
- Evaluate immune responses in cattle vaccinated under field conditions.
- Conduct a detailed UK field study on BTV-8 vaccination, monitoring immune response dynamics over a year.
- Compare antibody dynamics in post-import samples with those in the longitudinal vaccination cohort and previous infection studies.
Develop New Immunological Assays:
- Investigate immune responses against BTV VP2 to identify viral targets for neutralizing antibodies.
- Create ELISAs using whole virus particles to detect BTV serotype-specific antibodies.
- Explore the potential for designing a cross-serotype protective BTV vaccine.
Research group
Funding
Collaborators
Centre for Dairy Research, University of Reading