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Antigenicity
- RNA virus closely related to Classical Swine Fever and Border Disease Virus
- 2 Serological Types
- BVDV-1 is traditional, existing as two biotypes
- BVDV-1nc: noncytopathogenic
- BVDV-1c: cytopathogenic
- BVDV-2 is an emerging hemorrhagic virus
- BVDV-1 is traditional, existing as two biotypes
Hosts
- Cattle
Pathogenesis
BVDV-1c
- Infects cattle regardless of age
- Usually mild: diarrhoea with recovery in 10 dyas
- Immunosuppression can lead to secondary infection
BVDV-2nc
- Transient thrombocytopenia and leukopenia over 2 weeks
- Hemorrhages
- Secondary infection
- Death
BVDV-1nc
- Transplacental infection of naive heifers
- Outcome depends on age of fetus at contraction
- 0-110 days: abortion or persistently infected (PI) calves born
- 110-220 days: congenital damage with noticeable CNS and musculoskeletal lesions
- 220 days to term: active immunity developed
Mucosal Disease
- Mucosal disease is caused by a superinfection of PI animals with a second homologous cytopathic biotype (eg BVDV-1nc followed by BVDV-1c)
- Infection typically occurs between 6-18 months of age but is variable
- Superinfection will quickly spread horizontally among PI animals
- Invariable fatal
- Characterized by oral and enteric erosions, particularly overlying Peyer's patches, and ulceration of the feet
- Animals can show anorexia, depression and/or diarrhoea for 2-5 days before death
- Vaccination can lead to iatrogenic infection in undiagnosed PI calves
Epidemiology
- A major concern is that it can be confused with FMD (especially as it often occurs with clinical signs of salivation and depression)
- Virus is widespread: 60-70% exposure by 4 years of age
- Often may sweep through a whole colony of young stock causing profuse diarrhoea (perhaps febrile) for a few days and then recover
- Due to primary exposure to cytopathic strain of virus
- PI cows:
- 100% vertical transmission to offspring
- Are infected with BVDV-1nc and NEVER BVDV-1c
- Are often antibody-negative (though they can show low levels of Ab to heterologous virus)
- Show a wide range of clinical signs:
- Severe congenital damage (ataxia)
- Poor body condition
- Increased susceptibility to enteric and respiratory disease
- Act as the herd reservoir of BVDV
- Can ONLY be identified by blood testing
- Transfer via semen, direct contact with acutely infected animals, or vertical from dam to offspring
- Transfer can be iatrogenic: repeated use of needles and gloves, etc.
Diagnosis
- Traditional test: virus isolation followed by serology on infected cells
- ELISA for virus antigen in animals with persistent viremia (will show up 3-8 days post-infection)
- PI calves often appear virus negative as a result of receiving neutralizing Ab in colostrum: can be countered by RT-PCR
- Paired serum samples from cows with acute BVDV
- Herd sampling by ELISA for antibody on bulk milk
Control
- No known treatment to reverse persistent infection or to cure mucosal disease
- BUT, without exposure to BVDV, the whole herd is at risk as there is no developed immunity
- Vaccination of dams before pregnancy will prevent PI calves being born
- Beta-propiolactone inactivated vaccine
- Combine with screening for antigen and removal of PI animals