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Northern Ireland’s TB status could be helped by new Actiphage test
Actiphage directly detects and identifies the bacteria responsible for causing TB.

DAERA urged to take all relevant steps to improve current TB testing in Northern Ireland

PBD Biotech, a UK-based diagnostic technology company, has developed a new bovine TB test which could help the TB status in Northern Ireland.

Actiphage, a rapid diagnostic test, directly detects and identifies the bacteria responsible for causing TB infection. This is different from other TB tests which rely on an immune response. Trials of Actiphage have consistently confirmed the test’s ability to detect the bacteria in both milk and blood at less than 10 cells per sample.

Yesterday’s (27 November 2018) Northern Ireland Audit Office Report concluded that all relevant steps to improve the current bovine TB testing regimen in Northern Ireland should be taken by the Department for Agriculture, Environment and Rural Affairs (DAERA).

In October 2018, DAERA met with PBD Biotech to explore how the Actiphage test could be incorporated into their TB eradication programme.

Commenting on yesterday’s Audit Office Report, Dr Berwyn Clarke, PBD Biotech’s chief executive, said: “It is vital that this hidden reservoir of infection is eradicated; otherwise, all other interventions will have very little benefit. And the unreliability of the tests cast doubt on whether TB-free status is genuinely the case.”

Actiphage has already been included in the UK Government’s ‘exceptional private use’ policy for chronic TB breakdowns in England. This development was guided by Actiphage’s field validation during studies performed by farm animal vet, Dick Sibley. Sibly previously helped to clear a dairy herd in Devon that had been infected with TB by integrating Actiphage into a disease management programme.

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Defra shares new Sanitary and Phytosanitary guidance

News Story 1
 Defra has published guidance for the vet sector ahead of a proposed UK-EU Sanitary and Phytosanitary agreement.

The agreement, which will change the movement and trade of animals and related products, could see reductions in checks, paperwork and certification. As well as describing regulatory developments, the advice highlights the importance of animal ID, registration and traceability in disease control and other compliance arrangements.

The guidance can be found here. More detail is expected as negotiations progress. 

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News Shorts
Lords Committee opens Pet Parasite Medication inquiry

The House of Lords Environment and Climate Change Committee will launch its inquiry into Pet Parasite Medication (PPM) on Wednesday (3 June).

Focusing on treatments containing fipronil and imidacloprid, the inquiry will seek to understand distribution pathways and the impacts of PPM use and non-use on biodiversity and human health. It will also cover current regulation, monitoring, and the potential implications for pets and their owners.

The committee will hear evidence from environmental non-governmental organisations and research institutes. The public can follow the proceedings live on Parliament TV or in person in the Palace of Westminster.