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RESEARCH ARTICLE

Arbovirus infections of animals: congenital deformities, encephalitis, sudden death and blindness

Peter D Kirkland
+ Author Affiliations
- Author Affiliations

Virology Laboratory, Elizabeth Macarthur Agriculture Institute, Menangle, NSW 2568, Australia
Postal address: PMB 4008, Narellan, NSW 2567, Australia
Tel: +61 2 4640 6331
Fax: +61 2 4640 6429
Email: peter.kirkland@dpi.nsw.gov.au

Microbiology Australia 39(2) 103-105 https://doi.org/10.1071/MA18030
Published: 18 April 2018

Viruses from five different taxonomic families have been shown to be the cause of disease outbreaks in either domesticated or wild animals. These include viruses spread by both mosquitoes and biting midges from the genus Culicoides, especially C. brevitarsis. A number of arboviruses also present significant impediments to the international movement of live animals, semen and embryos.


Alphaviruses

Ross River virus is intermittently incriminated as a cause of fever, lethargy and arthralgia in horses. However, there are few cases supported by convincing laboratory confirmation.


Flaviviruses

Infection of dogs, chickens and horses with Murray Valley encephalitis virus (MVEV) and West Nile Virus (WNV) occurs intermittently in regions where there are large mosquito populations. However, disease is rare and has only been reported in horses. In 2011 there was an outbreak of neurological disease in horses in southern Australia1, with MVE identified in five horses that died in Victoria2. A few MVE cases were also confirmed in NSW and SA. Otherwise there have only been a few sporadic cases confirmed3,4 with anecdotal reports of others5.

Concurrent with the MVE cases in 2011 in NSW there was an extensive outbreak of encephalitis in horses due to WNV, with approximately 1100 cases observed and a case fatality rate of 11% (A.J. Read et al., unpubl. data). A number of cases were also observed in SA and Victoria. This large outbreak had a number of unusual features. This was the first epidemic of equine neurological disease due to WNV in Australia. Unlike the 1999 outbreak in the USA, no cases were observed in birds. The NSW 2011 outbreak was due to a variant strain of WNV of Australian origin6. The geographic distribution was also unusual. While there were cases throughout the Riverina Region (where the first outbreak of MVE had occurred in people), cases were distributed throughout the Central and Northern Tablelands (extending from Forbes to Narrabri), with a large number of cases in the Hunter Valley, the Sydney Basin and Illawarra region. WNV had never been detected on the eastern side of the Great Divide previously.


Orbiviruses

The Orbivirus genus of the family Reoviridae contains a large spectrum of viruses that cause disease in livestock and wildlife. Most are transmitted by biting midges but some are spread by mosquitoes and ticks. Viruses belonging to the bluetongue serogroup (BTV) have an extremely high profile globally, either as a cause of disease, mainly in sheep, or through international trade restrictions. Of the 29 serotypes, 12 have been detected in Australia. Most are detected intermittently in the far north of Australia, although serotypes 1 and 21 are widespread along the east coast from Cape York south to the Hunter Valley region, with occasional movement onto the NSW south coast as the distribution of their vector, Culicoides brevitarsis, fluctuates.

In northern Australia incursions of novel genotypes of BTV have been detected, with nucleic acid sequencing indicating that these have been introduced by long distance dispersal of vectors from South-East Asia.

Australia has not experienced the severe outbreaks with large scale mortalities as have occurred in Africa, the Mediterranean basin and the USA. Experimental infection studies in sheep have shown that some of the serotypes of BTV found in Australia are asymptomatic while others can produce moderately severe disease. The absence of disease in Australia is largely due to the lack of overlap between the distribution of C. brevitarsis and sheep flocks. The presence of BTVs is the greatest impediment to the export of live animals, semen and embryos from ruminant and camelid species. Consequently, because the principal vector has well defined geographical limits determined by seasonal influences, animal health authorities in Australia have established a ‘bluetongue free zone’ to support the export of ruminants and germplasm. The National Arbovirus Monitoring Program7 (NAMP), based on systematic sampling of sentinel cattle and vectors, underpins this zoning strategy.

Viruses belonging to the epizootic haemorrhagic disease of deer (EHDV) group, which are closely related to BTVs, are also widespread in Australia and mainly infect cattle and deer. Disease has never been observed in Australia.

Between 1994 and 1996 an unusual epidemic was observed in kangaroos, characterised by varying degrees of blindness. The epidemic commenced in western NSW in summer 1994, spread south and west into Vic and SA, and, after interruptions to transmission during winter and spring, eventually reached southern WA in 1996. Disease affected mostly western grey kangaroos, but eastern grey and red kangaroos and even euros were involved. Blindness was shown to be due to chorioretinitis and mild encephalitis8. The disease was successfully reproduced after the inoculation of eastern and western grey kangaroos with isolates of Wallal virus9. The vector was not proven but this virus has been isolated from several Culicoides species.

A syndrome of sudden death almost always without any prior signs, has occurred on several occasions in captive populations of Tammar wallabies, held mainly in research institutions in eastern NSW and southern Qld. The first outbreak in 1998 decimated research populations in the Sydney region with more than 230 animals affected10. The gross pathology was very similar to severe acute bluetongue where vascular damage results in extensive congestion and haemorrhage. Eubenangee virus, a close relative of BTV, was isolated from these animals. However, the vector involved remains unclear.

In the Northern Territory between 1999 and 2004, a similar syndrome of acute death in northern black wallaroos was associated with infection with a Wallal group virus, blindness in agile wallabies with a Eubenangee group virus and death in red kangaroos with a Wongorr group virus (L. Melville et al., unpubl. obs.).

Finally, the equine population is not spared from infections with orbiviruses. In Australia, Elsey virus is a mosquito-borne orbivirus that has been associated with encephalitis in several horses in the NT and Qld11.


Bunyaviruses

The Bunyaviruses (Family Peribunyaviridae, genus Orthobunyavirus) comprise the largest group of vector-borne viruses with members transmitted by mosquitoes, biting midges, sandflies and ticks. Akabane virus is the most prominent to infect animals in Australia and was the cause of a large outbreak of congenital deformities in calves in 1974, with approximately 8000 cases in NSW. Outbreaks occur at intervals of about 15–20 years. Climatic variations have a profound impact on the distribution of the principal midge vector, C. brevitarsis, either as an outcome of higher rainfall and mild winters resulting in greater dispersal of midges and virus, or temporary reductions in population immunity in times of drought as a result of restricted midge and virus distribution12. The major epidemics have been mostly confirmed in regions of NSW that adjoin the endemic North and Central Coast regions13. The impact of the virus is greatest in cattle due to their long (9 month) gestation but sheep and goats can also suffer losses. The type of defect depends on the stage of gestation at which the dam was infected14. In cattle infected late in gestation calves can be born with encephalitis. Infection in the fifth and sixth months of gestation results in arthrogryposis and scoliosis, with the severity and incidence of abnormalities greater in earlier stages of pregnancy. The most severe defects follow infection in the third and fourth months of gestation and affected calves are born with hydranencephaly. The most severe cases have almost complete destruction of the cerebral hemispheres although the brain stem and cerebellum are generally unaffected. When cattle are infected at the most susceptible stages of gestation, up to 50% of calves can be born with defects15. In small ruminants, with a much shorter pregnancy, severe hydranencephaly and arthrogryposis occur concurrently and animals are usually still born16.

Aino virus has been associated with an outbreak of congenital defects reported about 40 years ago17, but no further outbreaks have occurred.


Rhabdoviruses

Also known as ‘Three Day Sickness’ by farmers due to the spectacular acute but transient illness, bovine ephemeral fever (BEF) virus (Family Rhabdoviridae, genus Ephemerovirus) had attracted attention because of the large scale epidemics that had spread from Northern Australia through most of NSW and sometimes into Vic. and SA between 1930–197018. BEFV only infects cattle and buffalo, causing a severe but short febrile disease, often associated with recumbency, locomotor difficulties, shifting lameness and difficulties in swallowing19 – signs similar to rabies in cattle. There is a high morbidity but generally low mortality and the majority of animals recover rapidly (typically in about three days, hence the colloquial name). In the endemic coastal regions of NSW north of Sydney and in Qld and the NT, infection is restricted to younger animals born since the last occasion that the virus was spread20. Beyond the endemic areas, cattle of all ages are affected21.

The disease can have a severe impact in dairy herds because there is almost complete cessation of milk production in infected cows22. In beef herds, the decline in milk availability can severely impact on calf health and growth. The severe fever often induces a temporary infertility in males that lasts for several months but can be permanent. Although the epidemiological patterns and association of outbreaks with high rainfall suggest a mosquito vector, there remains a dearth of supporting evidence. There is some evidence to incriminate Culex annulirostris as the most likely vector23,24.



References

[1]  Roche, S.E. et al. (2013) Descriptive overview of the 2011 epidemic of arboviral disease in horses in Australia. Aust. Vet. J. 91, 5–13.
Descriptive overview of the 2011 epidemic of arboviral disease in horses in Australia.Crossref | GoogleScholarGoogle Scholar | 1:STN:280:DC%2BC3szjtV2iug%3D%3D&md5=e1774fa0784be87e42569282ddef8e1eCAS |

[2]  Mann, R.A. et al. (2013) Molecular characterization and phylogenetic analysis of Murray Valley encephalitis virus and West Nile virus (Kunjin subtype) from an arbovirus disease outbreak in horses in Victoria, Australia, in 2011. J. Vet. Diagn. Invest. 25, 35–44.
Molecular characterization and phylogenetic analysis of Murray Valley encephalitis virus and West Nile virus (Kunjin subtype) from an arbovirus disease outbreak in horses in Victoria, Australia, in 2011.Crossref | GoogleScholarGoogle Scholar |

[3]  Barton, A.J. et al. (2015) A case of Murray Valley encephalitis in a 2-year-old Australian Stock Horse in south-east Queensland. Aust. Vet. J. 93, 53–57.
A case of Murray Valley encephalitis in a 2-year-old Australian Stock Horse in south-east Queensland.Crossref | GoogleScholarGoogle Scholar | 1:STN:280:DC%2BC2Mrot1GksQ%3D%3D&md5=a041c903dad8c6cd8088bf975ff26dfdCAS |

[4]  Gordon, A.N. et al. (2012) Confirmed case of encephalitis caused by Murray Valley encephalitis virus infection in a horse. J. Vet. Diagn. Invest. 24, 431–436.
Confirmed case of encephalitis caused by Murray Valley encephalitis virus infection in a horse.Crossref | GoogleScholarGoogle Scholar |

[5]  Gard, G.P. et al. (1977) Association of Australian arboviruses with nervous disease in horses. Aust. Vet. J. 53, 61–66.
Association of Australian arboviruses with nervous disease in horses.Crossref | GoogleScholarGoogle Scholar | 1:STN:280:DyaE2s7otFagsQ%3D%3D&md5=eb749e04228c3ae44fbfc8e3c32479c5CAS |

[6]  Frost, M.J. et al. (2012) Characterization of virulent West Nile Virus Kunjin Strain, Australia, 2011. Emerg. Infect. Dis. 18, 792–800.
Characterization of virulent West Nile Virus Kunjin Strain, Australia, 2011.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BC38XptVahtb0%3D&md5=effdc4f9201c14e8bf27cc7ab7de075fCAS |

[7]  Animal Health Australia (2018) National arbovirus monitoring program. https://www.animalhealthaustralia.com.au/what-we-do/disease-surveillance/national-arbovirus-/monitoring-program (accessed 25 February 2018).

[8]  Hooper, P.T. et al. (1999) Epidemic of blindness in kangaroos – evidence of a viral aetiology. Aust. Vet. J. 77, 529–536.
Epidemic of blindness in kangaroos – evidence of a viral aetiology.Crossref | GoogleScholarGoogle Scholar | 1:STN:280:DyaK1MvisVWrtQ%3D%3D&md5=2dd7ecd9184e86226dde6a10884da235CAS |

[9]  Reddacliff, L. et al. (1999) Experimental reproduction of viral chorioretinitis in kangaroos. Aust. Vet. J. 77, 522–528.
Experimental reproduction of viral chorioretinitis in kangaroos.Crossref | GoogleScholarGoogle Scholar | 1:STN:280:DyaK1MvisVWrtA%3D%3D&md5=b72009637a6538ff191fd6f4aa1e9b93CAS |

[10]  Rose, K.A. et al. (2012) Epizootics of sudden death in tammar wallabies (Macropus eugenii) associated with orbivirus infection. Aust. Vet. J. 90, 505–509.
Epizootics of sudden death in tammar wallabies (Macropus eugenii) associated with orbivirus infection.Crossref | GoogleScholarGoogle Scholar | 1:STN:280:DC%2BC3s7mslOitA%3D%3D&md5=86dd4473ed2919e1b429698c084864c1CAS |

[11]  Attoui, H. et al. (2009) Peruvian horse sickness virus and Yunnan orbivirus, isolated from vertebrates and mosquitoes in Peru and Australia. Virology 394, 298–310.
Peruvian horse sickness virus and Yunnan orbivirus, isolated from vertebrates and mosquitoes in Peru and Australia.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD1MXhsVajtLrK&md5=64ae11be8a65ac3e42419a658aa6dabdCAS |

[12]  Kirkland, P.D. et al. (1983) An impending epidemic of bovine congenital abnormalities. Aust. Vet. J. 60, 221–223.
| 1:STN:280:DyaL2c%2Flt1aruw%3D%3D&md5=a0ef4eb1948dc48e6c5d2709d97fe869CAS |

[13]  Shepherd, N.C. et al. (1978) Congenital bovine epizootic arthrogryposis and hydranencephaly. Aust. Vet. J. 54, 171–177.
Congenital bovine epizootic arthrogryposis and hydranencephaly.Crossref | GoogleScholarGoogle Scholar | 1:STN:280:DyaE1c3ls1Gksw%3D%3D&md5=3e508ae572fdb12929d2aad52944eb91CAS |

[14]  Kirkland, P.D. et al. (1988) The development of Akabane virus induced congenital abnormalities in cattle. Vet. Rec. 122, 582–586.
| 1:STN:280:DyaL1czit1OltQ%3D%3D&md5=cdccc4a02c17c4942a388918093a5279CAS |

[15]  Jagoe, S. et al. (1993) An outbreak of Akabane virus induced abnormalities in calves following agistment in an endemic region. Aust. Vet. J. 70, 56–58.
An outbreak of Akabane virus induced abnormalities in calves following agistment in an endemic region.Crossref | GoogleScholarGoogle Scholar | 1:STN:280:DyaK3s3gslCkuw%3D%3D&md5=e02fbf0f8f054a3c38947760e5e928b9CAS |

[16]  Kirkland, P.D. (2015) Akabane virus infection. Rev. Sci. Tech. Off. Int. Epiz. 34, 403–410.
Akabane virus infection.Crossref | GoogleScholarGoogle Scholar | 1:STN:280:DC%2BC28vlt1GltQ%3D%3D&md5=a6161272475c9361cbbf441e9a8698a2CAS |

[17]  Coverdale, O.R. et al. (1978) Congenital abnormalities in calves associated with Akabane virus and Aino virus Aust. Vet. J. 54, 151–152.
Congenital abnormalities in calves associated with Akabane virus and Aino virusCrossref | GoogleScholarGoogle Scholar | 1:STN:280:DyaE1c3ls1GltA%3D%3D&md5=995bed4242c146635146dddb52eacd9aCAS |

[18]  St George, T.D. et al. (1977) The epizootiology of bovine ephemeral fever in Australia and Papua-New Guinea. Aust. Vet. J. 53, 17–28.
The epizootiology of bovine ephemeral fever in Australia and Papua-New Guinea.Crossref | GoogleScholarGoogle Scholar |

[19]  St George, T.D. et al. (1989) Bovine ephemeral fever. In The Arboviruses: Epidemiology and Ecology. Vol. II. (Monath, T.P. ed.) pp. 71–86. Florida: CRC Press.

[20]  Uren, M.F. et al. (1987) Epidemiology of Bovine Ephemeral Fever in Australia 1981–1985. Aust. J. Biol. Sci. 40, 125–136.
| 1:STN:280:DyaL1c%2FitlOitg%3D%3D&md5=7c3fe785b25c61b7e1f75db060133322CAS |

[21]  Finlaison, D.S. et al. (2010) An epizootic of bovine ephemeral fever in New South Wales in 2008 due to long distance dispersal of vectors. Aust. Vet. J. 88, 301–306.
An epizootic of bovine ephemeral fever in New South Wales in 2008 due to long distance dispersal of vectors.Crossref | GoogleScholarGoogle Scholar | 1:STN:280:DC%2BC3cnns1Wntw%3D%3D&md5=4739a9b5f756c07a7f0f33fee375c870CAS |

[22]  Davis, S.S. et al. (1984) The effect of bovine ephemeral fever on milk production. Aust. Vet. J. 61, 128–129.
The effect of bovine ephemeral fever on milk production.Crossref | GoogleScholarGoogle Scholar | 1:STN:280:DyaL2c3ls1emtA%3D%3D&md5=7c0baa54ff6c64725cc4c9616f74a9b4CAS |

[23]  Standfast, H.A. et al. (1976) The isolation of ephemeral fever from mosquitoes in Australia. Aust. Vet. J. 52, 242.
The isolation of ephemeral fever from mosquitoes in Australia.Crossref | GoogleScholarGoogle Scholar |

[24]  Finlaison, D.S. et al. (2014) Application of a real time polymerase chain reaction assay to the diagnosis of bovine ephemeral fever during an outbreak in New South Wales and northern Victoria in 2010. Aust. Vet. J. 92, 24–27.
Application of a real time polymerase chain reaction assay to the diagnosis of bovine ephemeral fever during an outbreak in New South Wales and northern Victoria in 2010.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BC2cXhs1ygsbs%3D&md5=a27109603aaf61a71170a3bb32567c5eCAS |


Biography

Dr Peter Kirkland is the Head of the Virology Laboratory at the state government Elizabeth Macarthur Agriculture Institute at Menangle NSW. Dr Kirkland has had a long career in diagnostic and research projects in animal health. He has been instrumental in the identification of several new viruses, including Menangle virus that was transmitted from flying foxes to pigs, a novel pestivirus that was responsible for a major disease outbreak in pigs and viruses that have caused blindness and sudden deaths in macropods. In 2007 he led the EMAI team during the diagnosis and response to the equine influenza outbreak and in 2011 the investigation of the large West Nile virus outbreak in horses in NSW. His research interests include vector borne viruses and the development and evaluation of rapid diagnostic assays for viral diseases of animals.