|Group:||Group I (dsDNA)|
|Species:||Suid herpesvirus 1 (SuHV1)|
Aujeszky's disease, usually called pseudorabies in the United States, is a viral disease in swine that has been endemic in most parts of the world. It is caused by Suid herpesvirus 1 (SuHV1). Aujeszky's disease is considered to be the most economically important viral disease of swine in areas where hog cholera has been eradicated. Other mammals, such as humans, cattle, sheep, goats, cats, dogs, and raccoons, are also susceptible. The disease is usually fatal in these animal species bar humans.
Research on SuHV1 in pigs has pioneered animal disease control with genetically modified vaccines. SuHV1 is now used in model studies of basic processes during lytic herpesvirus infection, and for unravelling molecular mechanisms of herpesvirus neurotropism.
In 1902, a Hungarian veterinarian, Aladár Aujeszky, demonstrated a new infectious agent in a dog, ox, and cat, and showed it caused the same disease in swine and rabbits. In the following decades the infection was found in several European countries, especially in cattle, where local intense pruritus is a characteristic symptom. And in the United States a well known disease in cattle called "mad itch" was concluded to be in fact Aujeszky's disease.
The virus is shed in the saliva and nasal secretions of swine infected by the respiratory route. Aerosolization of the virus and transmission by fomites also may occur. The virus may potentially survive for seven hours in humid air, and it may survive on well water for up to seven hours, in green grass, soil, and feces for up to two days, in contaminated feed for up to three days, and in straw bedding for up to four days.
Diagnosis is made mainly by virus isolation in tissue cultures, or through ELISA or PCR tests. Vaccines are available for swine (ATCvet codes: QI09AA01 (WHO) inactivated, QI09AD01 (WHO) live, plus various combinations). The infection has been eradicated in a number of European countries and in the United States, where the domestic swine population in 2004 was declared free of Aujeszky's disease. Here[where?] the infection still remains in feral pig populations.
Respiratory infection is usually asymptomatic in pigs more than 2 months old, but it can cause abortion, high mortality in piglets, and coughing, sneezing, fever, constipation, depression, seizures, ataxia, circling, and excess salivation in piglets and mature pigs. Mortality in piglets less than one month of age is close to 100%, but it is less than 10% in pigs between one and six months of age. Pregnant swine can reabsorb their litters or deliver mummified, stillborn, or weakened piglets. In cattle (see next section), symptoms include intense itching followed by neurological signs and death. In dogs, symptoms include intense itching, jaw and pharyngeal paralysis, howling, and death Any infected secondary host generally only lives two to three days.
Genital infection appears to have been common in a great part of the 20th century in many European countries in swine herds, where boars from boar centres were used for natural service of sows or gilts. This disease manifestation has always been asymptomatic in affected pigs, and presence of the infection on a farm was detected only because of cases in cattle showing pruritus on the hindquarters (vaginal infection, see below).
In susceptible animals other than swine, infection is usually fatal, and the affected animals most often show intense pruritus in a skin area. Pruritus in Aujeszky's disease is considered a phantom sensation, and virus has never been found at the site of pruritus.
Populations of wild boar, or feral hogs (Sus scrofa), in the US commonly contract and spread the virus throughout their range. Mortality is highest in young piglets. Pregnant sows often abort when infected. Otherwise healthy male adults (boars) are typically latent carriers, that is, they harbor and transmit the virus without displaying symptoms or suffering disability.
Swine (both domestic and feral) are usual reservoirs for this virus, though it does affect other species. Aujeszky's disease has been reported in other mammals, including brown bears, and black bears, Florida panthers, raccoons, coyotes, and whitetail deer. In most cases, contact with pigs or pig products was either known or suspected. Outbreaks in farm fur species in Europe (mink and foxes) have been associated with feeding contaminated pig products. Many other species can be experimentally infected. Humans are not potential hosts.
Cattle have been found to be infected either by the respiratory or the vaginal route (iatrogenic cases disregarded). Primary infection of mucous membranes of the upper respiratory tract is associated with head pruritus, while lung infection results in chest pruritus. Vaginal infection of bovines, which regularly show pruritus of the hindquarters, has been found to be associated with a concurrent genital infection in swine on the same premises, and investigations have evidenced that the vaginal infection of cattle had been sexually transmitted by man from genitally infected sows (animal sodomy, zoophilia, bestiallity). Genital infection in swine herds has been closely correlated with the use of boars from boar centres for natural service of sows.
Aujeszky's disease is highly contagious. The infection is commonly considered to be transmitted among swine through nose-to-nose contact, because the virus is mostly present in nasal and oral areas. This notion, however, is contradicted by results from epidemiological studies, according to which the decisive spread within herds occurs by air currents over many meters. Correspondingly, the risk of airborne transmission of highly virulent virus strains from acutely infected herds to other swine herds has been found to be very high. The infection has been found transmitted over distances of many kilometers. Otherwise, the infection is most often transmitted into herds by introduction of acutely or latently infected pigs. Concerning transmission to cattle, see section above.
Although no specific treatment for acute infection with SuHV1 is available, vaccination can alleviate clinical signs in pigs of certain ages. Typically, mass vaccination of all pigs on the farm with a modified live virus vaccine is recommended. Intranasal vaccination of sows and neonatal piglets one to seven days old, followed by intramuscular (IM) vaccination of all other swine on the premises, helps reduce viral shedding and improve survival. The modified live virus replicates at the site of injection and in regional lymph nodes. Vaccine virus is shed in such low levels, mucous transmission to other animals is minimal. In gene-deleted vaccines, the thymidine kinase gene has also been deleted; thus, the virus cannot infect and replicate in neurons. Breeding herds are recommended to be vaccinated quarterly, and finisher pigs should be vaccinated after levels of maternal antibody decrease. Regular vaccination results in excellent control of the disease. Concurrent antibiotic therapy via feed and IM injection is recommended for controlling secondary bacterial pathogens.
Applications in neuroscienceEdit
SuHV1 can be used to analyze neural circuits in the central nervous system (CNS). For this purpose the attenuated (less virulent) Bartha SuHV1 strain is commonly used and is employed as a retrograde and anterograde transneuronal tracer. In the retrograde direction, SuHV1-Bartha is transported to a neuronal cell body via its axon, where it is replicated and dispersed throughout the cytoplasm and the dendritic tree. SuHV1-Bartha released at the synapse is able to cross the synapse to infect the axon terminals of synaptically connected neurons, thereby propagating the virus; however, the extent to which non-synaptic transneuronal transport may also occur is uncertain. Using temporal studies and/or genetically engineered strains of SuHV1-Bartha, second, third, and higher order neurons may be identified in the neural network of interest.
- Fenner, Frank J.; Gibbs, E. Paul J.; Murphy, Frederick A.; Rott, Rudolph; Studdert, Michael J.; White, David O. (1993). Veterinary Virology (2nd ed.). Academic Press, Inc. ISBN 0-12-253056-X.
- Pedro-Pons, Agustín (1968). Patología y Clínica Médicas. 6 (3rd ed.). Barcelona: Salvat. p. 714. ISBN 84-345-1106-1.
- Michigan Animal News
- Mettenleiter (2008). "Molecular Biology of Animal Herpesviruses". Animal Viruses: Molecular Biology. Caister Academic Press. ISBN 978-1-904455-22-6.
- Sandri-Goldin RM (editor). (2006). Alpha Herpesviruses: Molecular and Cellular Biology. Caister Academic Press. ISBN 978-1-904455-09-7.
- Pomeranz L, Reynolds A, Hengartner C (2005). "Molecular Biology of Pseudorabies Virus: Impact on Neurovirology and Veterinary Medicine". Microbiol Mol Biol Rev. 69 (3): 462–500. PMC . PMID 16148307. doi:10.1128/MMBR.69.3.462-500.2005.
- "Pseudorabies: Introduction". The Merck Veterinary Manual. 2006. Retrieved 2007-03-31.
- Pensaert M, Labarque G, Favoreel H, Nauwynck H (2004). "Aujeszky's disease vaccination and differentiation of vaccinated from infected pigs". Dev Biol (Basel). 119: 243–54. PMID 15742635.
- Amass, S.F. (2006). "Exotic Diseases: Are you Prepared? Are you Ready?". Proceedings of the North American Veterinary Conference. Retrieved 2007-03-31.
- Carter, G.R.; Flores, E.F.; Wise, we all love pigs D.J. (2006). "Herpesviridae". A Concise Review of Veterinary Virology. Retrieved 2006-06-04.
- Bitsch, Viggo (2015). Principal epidemiological features of Aujeszky's disease in swine and cattle. ISBN 978-87-994685-1-5. http://suhv1epidemiology.blogspot.com/
- Bitsch, Viggo (2015)
- Berryman Institute: Managing Wild Pigs
- Finnish Food Safety Authority Evira: Aujeszkyn tauti (AD, pseudorabies) (Finnish)
- Bartha A (1961). "Experimental reduction of virulence of Aujesky's disease virus". Magyar Allatorvosok Lapja. 16: 42–45.
- Koyuncu OO, Perlman DH, Enquist LW (Jan 16, 2013). "Efficient retrograde transport of pseudorabies virus within neurons requires local protein synthesis in axons". Cell Host Microbe. 13 (1): 54–66. PMC . PMID 23332155. doi:10.1016/j.chom.2012.10.021.
- Kratchmarov R, Taylor MP, Enquist LW (2013). "Role of us9 phosphorylation in axonal sorting and anterograde transport of pseudorabies virus". PLOS ONE. 8 (3): e58776. PMC . PMID 23527020. doi:10.1371/journal.pone.0058776.