Rabbit haemorrhagic disease
|Rabbit hemorrhagic disease virus|
|CryoEM reconstruction of Rabbit Hemorrhagic Disease Virus (RHDV) capsid. EMDB entry |
|Group:||Group IV ((+)ssRNA)|
|Species:||Rabbit hemorrhagic disease virus|
Rabbit haemorrhagic disease (RHD), also known as rabbit calicivirus disease (RCD) or viral haemorrhagic disease (VHD), is a highly infectious and often fatal disease that affects wild and domestic rabbits of the species Oryctolagus cuniculus. The infectious agent responsible for the disease is rabbit haemorrhagic disease virus (RHDV), or rabbit calicivirus (RCV), genus Lagovirus of the family Caliciviridae. The virus infects only rabbits, and has been used in some countries to control rabbit populations.
- History 1
World geographic distribution 2
- Asia 2.1
- Americas (North and South) 2.2
- Australia 2.3
- New Zealand 2.4
- Europe 2.5
- Transmission 3
- Signs 4
- Diagnosis 5
- Morbidity, mortality, and immunity 6
- Control 7
- Use as biological control agent 8
- See also 9
- References 10
- Further reading 11
- External links 12
RHD first appeared in the Winter of 1983 in Jiangsu Province of the People's Republic of China. It was first isolated and characterized by S.J. Liu et al. in 1984 Scientists cannot pinpoint its exact origins; however, it is believed the disease emerged from a virulent calicivirus spreading asymptomatically in European rabbit populations, particularly in the German Democratic Republic. The Chinese outbreak was spread by the angora rabbit, which had originated in Europe. Fourteen million domesticated rabbits died within nine months in the outbreak.
In 1984 the virus that caused the disease was identified. The virus spread westward and reached Europe in 1988. The virus has since appeared in Mexico, Cuba, Australia, New Zealand and the USA. In 1992, the United Kingdom reported its first case of RHD in domestic show rabbits. By the late 1990s, RHD stretched to forty countries and had become endemic in wild rabbit populations in Europe, Australia, New Zealand and Cuba. In Europe there was a rapid increase in research into RHD, due to the importance of the commercial breeding of rabbits for meat and fur production.
The first reported case in the United States was in Iowa on March 9, 2000. The affected population included Palominos and California Whites. By April 6, 25 of the 27 affected rabbits had died as a result of RHD. In order to contain the disease, the remaining two rabbits were euthanized. No new introductions of rabbits were placed on the farm for two years after the discovery of RHD and August 1999 was the last time rabbits left and/or returned to the farm. The United States experienced other outbreaks of RHD in 2001 (Utah, Illinois, New York) and 2005 (Indiana).
World geographic distribution
Within a few months of RHD being reported in China in 1984, the disease was widely seen in many commercial rabbitries and had reached the Republic of Korea. RHD has also been reported in India and the Middle East.
Americas (North and South)
After outbreaks of RHD in 2000, 2001, and 2005 in domesticated rabbits, the United States has eradicated RHD from its rabbit populations. The native species, cottontails (Sylvilagus floridanus), black-tailed jackrabbits (Lepus californicus) and volcano rabbits (Romerolagus diazzi) seem not to be susceptible to the virus.
In 1991 a strain of the virus, Czech CAPM 351RHDV, was imported to Australia  under strict quarantine conditions to research the safety and usefulness of the virus if it was used as a biological control agent against Australia and New Zealand's rabbit pest problem. Testing of the virus was undertaken on Wardang Island in Spencer Gulf off the coast of the Yorke Peninsula, South Australia. In 1995 the virus escaped quarantine and subsequently killed 10 million rabbits within 8 weeks of its release.
In July 1997, after considering over 800 public submissions, the New Zealand Ministry of Health decided not to allow RHDV to be imported into New Zealand to control rabbit populations. This was backed up in an early August review of the decision by the Director-General of Agriculture. By late August, it was confirmed that RHDV had been deliberately introduced to the Cromwell area of the South Island.
An unsuccessful attempt was made by New Zealand officials to control the spread of the disease. It was, however, being intentionally spread, and several farmers (notably in the Mackenzie Basin area) admitted to processing rabbits that had died from the disease in kitchen blenders for further spreading.
Had the disease been introduced at a better time, there would have been a more effective control of the population. Unfortunately, it was released after breeding had commenced for the season, and rabbits under 2 weeks old at the time of the introduction were immune to the disease. These young rabbits were therefore able to continue to grow and breed back up. Ten years on, rabbit populations (in the Mackenzie Basin in particular) are beginning to reach near pre-plague proportions once again though they have not yet returned to pre RCD levels.
Resistance to RHD in New Zealand rabbits has led to the widespread use of Compound 1080 (Sodium fluoroacetate). Farmers and land managers are having to increase their use of 1080 to protect pastoral land from rabbits and preserve the gains made in recent years through the use of RHD.
RHD is endemic throughout most of Europe. Italy's first case of RHD was recorded in 1986 and Spain's in 1988. France, Belgium (June) and Scandinavia followed in 1990. Within a few years of RHD's first appearance in Europe it had caused the largest mortality in domestic and wild rabbits in Germany, Austria, Spain and Italy. Spain was the worst affected by RHD, which in turn also affected the rabbit-specialized Iberian lynx.
When the United Kingdom's first case of RHD in 1992 was discovered, the disease was transmitted into the wild by domesticated pet rabbits. Sources vary in the number of confirmed cases of RHD; there were 9 known outbreaks in 1994, 32 cases but some sources believe there were as many as 512 cases of RHD in 1995, and around 30 RHD cases in 1996 throughout Scotland, England and Wales.
Transmission of RHD occurs by direct contact with an infected animal and fomites. Rabbits acquire RHD through oral, nasal or conjunctival pathways. Urine, faeces and respiratory secretions may also shed the virus. The virus may also be carried by the wind. Carriers of the virus may remain infectious for up to a month depending on climate conditions; however, the virus has been known to persist for as little as 2 days and as long as 215 days. An infected carcass or hairs from an infected animal may also transmit RHD. Fomites such as clothing, contaminated food, cages, bedding, feeders and water will also harbour the virus. Even though the virus cannot reproduce in other mammals, predators and scavengers such as foxes, ferrets and some birds can excrete the virus through their faeces after ingesting an infected rabbit carcass. Flies, rabbit fleas, and mosquitoes can also spread the virus between rabbits.
Climate appears to play a crucial role in the transmission of RHD. In normal conditions, most outbreaks of RHD occur in winter or spring. High temperatures in late spring and summer will considerably reduce the spread of the virus. RHD will also be more prevalent in dry and semi-dry areas than in areas that are relatively cool and humid.
RHD primarily infects only adult rabbits. In fact, research has shown that rabbits younger than 8 weeks of age are resistant to the virus. The incubation period for the RHD virus is between 1 to 3 days, with death following 1 to 2 days after the infection. There is a wide range of RHD symptoms. Most rabbits will show no signs of external symptoms of RHD.
Symptomatic cases of RHD will display fever, squeals, and often coma leading to death within 12 to 36 hours. In less severe cases, rabbits may display uneasiness, excitement, anorexia, swollen eyelids, paralysis, ocular haemorrhages, and paddling. Convulsions may be seen as well. A fatal bloody discharge from the nose has been exhibited along with blood-stained cage floors, though these symptoms may have occurred after death. Rabbits who have recovered from the less severe symptoms usually develop severe jaundice with weight loss and lethargy. Diarrhoea, constipation and abdominal cramping are then exhibited right before death a few weeks later.
RHD causes rapid development of
- Disease card
- Cooke, B.D. Rabbit Haemorrhagic Disease: Field epidemiology and the management of wild rabbit populations. Common Wealth Scientific and Industrial Research Organisation (CSIRO) Sustainable Ecosystems.
- RCD – Frequently Asked Questions. Rabbit Biocontrol Advisory Group. http://www.maf.govt.ns/mafret/publications/rabbit-biocontrol-advisory-group/rbag0002.htm Retrieved on 2008-02-06.
- Rabbit Calicivirus Disease. Center for Emerging Issues. http://www.aphis.gov/us/ceah/cei/taf/iw_2000_files/domestic/rabbitcal.htm Retrieved on 2008-02-06.
- RHD – A New Rabbit Disease. The British Association For Shooting and Conservation Ltd. http://www.basc.org.uk/media/rabbits.pdf Retrieved on 2008-02-06.
- Rabbit Hemorrhagic. Center for Food Security & Public Health Iowa State University College of Veterinary Medicine. http://www.cfsph.iastate.edu/Factsheets/pdfs/rabbit_hemorrhagic_disease.pdf Retrieved on 2008-02-06.
- Rabbit Viral Haemorrhagic Disease (RVHD). Scottish Natural Heritage. http://www.snh.org/uk/publications/on-line/advisorynotes/31/31.htm Retrieved on 2008-02-06.
- NOAH Compendium of Animal Medicines - Lapinject http://www.noahcompendium.co.uk/CEVA_Animal_Health_Ltd/Lapinject_VHD/-42505.html
- NOAH Compendium of Animal Medicines - Cylap http://www.noahcompendium.co.uk/Fort_Dodge_Animal_Health/Cylap/-44932.html
- Luque, D.; González, J. M.; Gómez-Blanco, J.; Marabini, R.; Chichón, J.; Mena, I.; Angulo, I.; Carrascosa, J. L.; Verdaguer, N.; Trus, B. L.; Bárcena, J.; Castón, J. R. (2012). "Epitope Insertion at the N-Terminal Molecular Switch of the Rabbit Hemorrhagic Disease Virus T=3 Capsid Protein Leads to Larger T=4 Capsids". Journal of Virology 86 (12): 6470–6480.
- "A New Viral Disease of Rabbit". The Merck Veterinary Manual. 2006. Retrieved 2007-06-17.
- Center for Food Security and Public Health
- Cooke, Brian Douglas (2014). "Australia's War Against Rabbits". CSIRO Publishing.
- Strive, Tanja (16 July 2008). "Rabbit Calicivirus Disease (RCD)" (pdf).
- Munro, Robert K.; Williams, Richard T., eds. (1994). Rabbit Haemorrhagic Disease:Issues in Assessment for biological control. Canberra: Bureau of Resource Sciences.
- Williams, David (2009-05-26). "Plan for 1080 drops in MacKenzie Basin". The Press. Retrieved 2009-06-14.
- "Welcome to 1080: The Facts". 1080facts.co.nz. Retrieved 2013-12-05.
- "Iberian Lynx Depends On Rabbits for Survival". Science Daily. 5 July 2011.
- Platt, John R. (12 July 2011). "Deadly Rabbit Disease May Have Doomed Iberian Lynx". Scientific American.
- , National Office of Animal Health rabbit vaccines.
However, it is possible that widespread rabbit deaths might cause predators to prey upon other food sources, such as endangered or rare native species. With proper vaccination plans, the safety of domesticated rabbits should not be a concern.
After the safety of RHD was confirmed by laboratory research, RHD was approved for release as a biological control agent in New Zealand. RHD is safe because it infects rabbits, but not other animals or humans. It is also safe to eat the meat of infected RHD rabbits. Virus mutation is not a concern; many years of research show no evidence that the virus has changed to affect any other species other than European rabbit.
Control measures used against rabbits in New Zealand include poisoning, shooting, ripping, strangulation, garroting, electrocuting, blasting, releasing predators, and fencing.
The estimated combined cost of control and production losses in New Zealand as a result of rabbits is about $23 million annually. This figure is only a small portion of the damage caused by rabbits.
The European rabbit is the second most serious pest in New Zealand. Rabbits compete with livestock for grazing pasture, kill trees, shrubs, and have contributed to the extinction of some native plants. Consequently, rabbits contribute to soil erosion by eliminating the protective vegetation and disturb the soil by burrowing.
Use as biological control agent
There are several vaccines available against VHD in the UK: Cylap, made by Fort Dodge Animal Health; Lapinject made by CEVA Animal Health Ltd; and Anivac, made by Animalcare Ltd. All last 12 months and contain inactivated strains of VHD. A live combination vaccine, Nobivac Myxo-RHD, made by MSD Animal Health, has recently become available. Its active ingredient is a live myxoma-vectored RHD virus strain 009 and it offers a duration of immunity of 1 year against both RHD and myxomatosis.
Because of the highly infectious nature of the disease, strict quarantine is necessary when outbreaks occur. Depopulation, disinfection, surveillance and quarantines are the only way to properly and effectively eradicate the disease. Good disinfectants include 10% sodium hydroxide, 1-2% formalin, 2% One-Stroke Environ, and 10% household bleach. The RHD virus is resistant to ethers or chloroform. Deceased rabbits must be removed immediately and discarded in a safe manner. Surviving rabbits should be quarantined or humanely euthanized. Test rabbits may be used to monitor the virus on vaccinated farms.
Countries that are uninfected by RHD may place restrictions on importation from endemic countries. According to the Merck/Merial Manual For Pet Health, Home Edition, 2007, RHD is a reportable disease in the United States. If a diagnosis is made by a veterinarian, a notification to the "appropriate government authorities" must be made.
Maternal antibodies such as immunoglobulin G (IgG), which are readily transmitted to the young across the placenta, may explain why very young rabbits are resistant to RHD. Some scientists also believe that the immature immune system of a young rabbit cannot produce the number of chemicals needed to initiate clotting in order to kill. Rabbits may develop immunity against other strains of the RHD virus, while others may endure persistent infections. The immunity does not survive through the next generation, leaving open the possibility of further outbreaks in the population.
In the wild, outbreaks in rabbits vary depending on the season, breeding cycles and geographical location. Some areas will see a high morbidity and mortality among its rabbit populations followed by calmer periods.
RHD is extremely hard to locate in the wild since about 75% of rabbits with RHD will die in their burrows underground. Due to this difficulty, the morbidity and mortality estimates for RHD have a broad range. The morbidity rate ranges from 30% to 100% and the mortality rate from 40% to 100%; however, the typical mortality rate is usually around 90%.
Morbidity, mortality, and immunity
Laboratory tests such as reverse transcription polymerase chain reaction (RT-PCR), Western blotting, negative-staining immunoelectron microscopy and ELISAs may be performed on samples from the liver, blood, spleen or other organs.
Rabbits that die from RHD are usually in good outward state. However, the most frequent post-mortem lesions are hepatic necrosis and Enteritis of the small intestine and swollen meninges may also occur.
RHD may be indicated when several animals in the herd die after experiencing a fever and lethargy. Differential diagnosis includes pasteurellosis, myxomatosis, poisoning, heat exhaustion, and E. coli or Clostridium perfringens type E enterotoxemia.