Bluetongue Virus

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Description

Bluetongue is an infectious, noncontagious arthropodborne viral disease primarily of domestic and wild ruminants. Infection with bluetongue virus is common worldwide but is usually subclinical or mild in most infected ruminants. Bluetongue is almost exclusively a disease of sheep, particularly the fine-wool and mutton breeds, although white-tailed deer ( Odocoileus virginianus ), and pronghorn ( Antilocapra americana ) and desert bighorn sheep ( Ovis canadensis ) may develop severe clinical disease in North America.

Aetiology

Bluetongue virus is the type-species of the genus Orbivirus in the family Reoviridae. There are 24 serotypes worldwide, although not all serotypes exist in any one geographic area, eg, only 5 serotypes (2, 10, 11, 13, and 17) have been reported in the USA. Distribution throughout the world parallels the spatial and temporal distribution of vector species of Culicoides biting midges, which are the only significant natural transmitters of the virus. Of more than 1,400 Culicoides species worldwide, fewer than 20 are actual or possible vectors of bluetongue virus. Continued cycling of the virus among competent Culicoides vectors and susceptible ruminants is critical to viral ecology. In the USA, the principal biologic vector is C variipennis sonorensis , which limits distribution of the virus to southern and western regions. In Australia the principal vector is C brevitarsis , while in Africa, Europe, and the Middle East it is C imicola . In each geographic region, secondary vector species may attain local importance. Vectors become infected with bluetongue virus by imbibing blood from infected vertebrates; transovarial transmission has not been reported. High affinity of the virus to blood cells, especially the sequestering of viral particles in invaginations of RBC membranes, contributes to prolonged viremia in the presence of neutralizing antibody. The extended viremia in cattle (up to 9 wk), and the host preference of most vector species of Culicoides for cattle, provides a mechanism for year-round transmission in domestic ruminants. Mechanical transmission by other bloodsucking insects is of minor significance. Bluetongue virus is not contagious, and concentrations in secretions and excretions are minimal, making oral or aerosol transmission unlikely. However, semen from viremic bulls can serve as a source of infection for cows through natural service or artificial insemination. Embryo transfer is regarded as safe, provided that donors are not viremic and an appropriate washing procedure for embryos is used. Accidental infection has been reported in dogs in the USA following administration of a modified live virus vaccine that was contaminated with the virus. Serologic evidence of infection with bluetongue virus has been found in large carnivores in Africa, perhaps as a result of ingesting virus-infected viscera.

Hosts

  • Ruminants, including sheep, cattle, deer, goats, and camelids

Pathogenesis

  • Transfer occurs through blood from viremic animals via biting midges (Culicoides spp.)
  • Replication in haematopoietic and endothelial cells of blood vessels
  • Clinical signs vary between species, with sheep most severely affected
    • Pyrexia
    • Ocular and nasal discharge
    • Drooling from mouth uclers
    • Swelling of the mouth, head and neck
    • Lameness
    • Subdural hemorrhages
    • Inflammation of the coronary band
  • Cattle as the main reservoir
  • A blue tongue is rarely seen as as a clinical sign of infection
  • Resulting loss of condition, reduction in wool an meat production, which can be followed by death

Diagnosis

  • Clinical signs can be confirmed through the lab:
    • RT-PCR to detect viral RNA
    • ELISA serology for Ab and rising Ab titres

Clinical Signs

Laboratory Tests

Pathology

Complete loss of integrity of epithelium. Uncommon.

  • Characteristic of Bluetongue Virus,
  • Epithelium lost and haemorrhage produces blue / black discoloration of the tongue, hence the name.



  • Grossly:
    • Infarctions -> necrosis
    • Haemorrhage
  • Histologically:
    • Necrosis -> calcification or regeneration (depends on age of lesion)

Treatment

  • BTV is NOTIFIABLE
  • Vigilance in recognizing clinical signs
  • Restriction of movement:
    • Protection Zone: 100km radius around infected premises, movement within zone allowed but not in or out
      • Vaccination within PZ using appropriate serotype is encouraged but still voluntary
    • Surveillance Zone: 50km radius beyond PZ
  • Vector control: ectoparasiticides, etc.

Links

References