Rabbit haemorrhagic disease virus was first identified in China in 1984 and quickly spread to Europe from 1986-88. It is now endemic in most parts of world and is seen in all populations of rabbits (wild, pet and farmed).
The causative agent of viral haemorrhagic disease is a calici virus called rabbit haemorrhagic disease virus.
Rabbit haemorrhagic disease is highly contagious with transmission via oral, nasal or conjunctival routes. Infection most commonly happens through exposure to infected animal, carcass or fomites (food, bedding, water). Mechanical transmission may also be effected by insect vectors. The incubation period (time from initial exposure to onset of clinical signs) is 1-3 days
There are lots of ways your rabbits could pick up the virus:
Food (e.g. hay) or water contaminated by infected wild rabbits.
Birds or insects may bring the virus to your rabbits on their feet or in their droppings, which your rabbits may eat if they graze on the lawn.
The virus may be blown on the wind.
You (or your dog or cat) might accidentally bring the virus home on your feet from infected wild rabbit droppings, and vermin around rabbit hutches might bring it along too. You might pick it up from other peoples’ rabbits, for example at a show or even if another rabbit owner handles your rabbits.
The virus itself if extremely tough and can survive for many months in the environment, and can even resist temperatures of 60 degrees celsius. However, rabbits living indoors (house rabbits) are still at risk from VHD, so they definitely need to be vaccinated with boosters kept up to date.
Disease is subclinical in young rabbits (<8-10 weeks old) but disease is likely to be severe and peracute in naive animals older than this. The severity of disease is caused by widespread haemorrhages and hepatocellular degeneration with diffuse haemorrhages in many organs. Three clinical syndromes exist:
Peracute: death (no clinical signs)
Respiratory signs (dyspnoea, bloody nasal discharge)
Cyanosis of mucous membranes
Death in 12-36h
Death in 1-2 weeks (liver dysfunction)
Diagnosis may be suspected on clinical grounds but can only be confirmed by post mortem examination. Widespread haemorrhages on gross post mortem are highly suggestive.
Control of viral haemorrhagic disease is based on three equally important aspects:
Biosecurity - Maintaining biosecurity involves avoiding introduction of animals into the group and/or implementing stict isolation / quarantine of introductions until proven free of disease, and restricting access of rabbits to external sources of infection - See hygiene below.
Hygiene - Good hygiene is very important in reducing the risk of disease, so keep hutches/cages very clean. Ensure that vermin and wild birds can't get into outdoor hutches or runs. You might need to use weld-mesh with smaller holes! Make sure there is nothing attract to wild mice and rats to your rabbits: sweep up any spilt food and bedding. Don’t pick green foodstuffs from areas where wild rabbits live, and try to stop wild rabbits from getting into your garden. If this is not feasible, make sure it is impossible for wild visitors to have nose-to-nose contact with your pet rabbit.
- Vaccination - To reduce risk of exposure is not sufficient alone to keep out infection and prevent it from continuing to spread. An additional control tool is to ensure animals are immune through vaccination. A combined vaccine against haemorrhagic disease and myxomatosis is available. This product may only be prescribed by your veterinary practitioner from whom advice must be sought.
Vaccination is an important tool in ensuring the success of a control programme. A combined vaccine is available which is indicated for the control of myxomatosis and viral haemorrhagic disease.
Additional information on disease and vaccination is available by clicking here.
For further information on the combined vaccine against myxomatosis and RHD, please click here.
For information on aetiology (Cause of disease) click here.
For information on epidemiology (Factors influencing occurrence of disease) click here.
For information on clinical signs click here.
For information on diagnosis click here.
For information on control click here.