BVDV Flashcards

1
Q

Classifications and diseases (3)

A

Pestiviruses: BVDV – cattle: BVD/mucosal disease
Flaviviridae family: BDV – sheep: border disease
Pestivirus genus: CSFV – pigs: classical swine fever

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2
Q

Two geneotypes

Two biotypes

A

Genotypes:
BVDV 1: classical form of disease
BVDV 2: severe acute BVD (haemorrhagic syndrome)

Biotypes:
non-cytopathic: BVD
noncytopathic followed by cytopathic: mucosal disease

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3
Q

BVDV

Herd level (7)
Individuals (2)
A

Herd level:

  • decreased fertility
  • abortion
  • congenital defects
  • stunted calves
  • immunosuppression
  • (diarrhoea) – transient
  • Transplacental transmission – PI which sheds virus

Individuals:

  • mucosal disease MD
  • persistently infected PI – sheds virus through every orifice/skin
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4
Q

BVD PI (3)

A

NCP affects when pregnant and crosses placenta and before immune system starts to work and thinks part of self – Persistently infected. The first third of gestation when calf is immunotolerant.

important reservoir of virus

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5
Q

Initial BVD infection (5)

Clinical presentation (4)

A
  • high morbidity, low mortality
  • mild fever, inappetance and mild diarrhoea
  • reduced milk yield in dairy cows
  • rapid recovery within a few days (2-3 days)
  • production of virus neutralising antibodies so become immune

Clinical presentation
• reduced fertility, EED (early embryonic death), abortion
• persistently infected calves - excrete the virus & may develop Mucosal Disease
• birth of calves with congenital defects –cerebellar hyperplasia – ataxic, intension tremor, shaking, nystagmus
• rarely acute haemorrhagic enteritis ± death

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6
Q

Mucosal disease (4)

  • acquirement (4)
  • age
  • outcome (3)
A
  • infrequent consequence of BVDV infection : fatal disease (acute/chronic)
  • develops only in PI animals [infected NCP BVDV in utero]
  • requires presence of NCP and antigenically related CP virus
  • Mechanisms - mutation of NCP virus in PI animal, or superinfection of PI animal by CP virus (encountered de novo in the environment)
  • 6months-2 years
  • invariably fatal
  • acute cases die within 1 - 2 weeks
  • chronic cases may live for 2 months or more
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7
Q

Mucosal Disease Epidemiology

3 different circumstances of infection

A

Non-immun pregnant cow:

  • day 0- 120: abortion/ foetal stunting
  • day 120-240: congenital defects/abortion/foetal stunting
  • day 240-280: (calving) abortion/foetal stunting
  • Immune pregnant cow or heifer (seropositive for BVDV having encountered the virus previously) (colostral antibody to BVDV) - Infection during pregnancy will not affect the foetus
  • Persistently infected cow or heifer (specific immunotolerance to BVD virus) (no colostral antibody to BVDV) - Persistently infected (PI) calf (or abortion).
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8
Q

MD clinical findings

  • subjective (7)
  • objective (6)
A

Subjective:
• depression
• reduced appetite / anorexia
• salivation - wetting of hair around the mouth
• profuse, homogeneous, watery diarrhoea
• lacrimation ± crusting around the eyes
• mucopurulent nasal discharge ± crusting around the nose
• loss of body condition - can be severe if chronic

Objective:
• ulcers - all parts of the oropharynx and extending onto the muzzle
• dry, cracked and inflamed rhinarium
• oral pain - resent mouth being opened
• oral flare / flush - reddening of oral mucous membranes
• ulcers in the interdigital cleft
• ± dermatitis - scabs and skin crusts - heels, perineal region and between the hind legs

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9
Q

MD Dx (4)

A
  • clinical signs
  • serology – BVD antibody negative, BVD virus positive indicating persistent infection (theoretically test twice; reality don’t – welfare issue so euth.)
  • virus isolation
  • post mortem
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10
Q

MD DDx (8)

A
  • Foot-and-Mouth Disease - notifiable
  • Bluetongue - notifiable
  • Bovine Viral Diarrhoea (BVD) / Mucosal Disease
  • Malignant Catarrhal Fever
  • Bovine Papular Stomatitis (BPS)
  • Calf Diphtheria
  • Actinobacillosis - Wooden Tongue
  • Actinomycosis - Lumpy Jaw
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11
Q

MD Pathology (5)

A
  • microvesicles in the stratified squamous epithelia causing ulcers
  • lesions throughout the alimentary tract
  • transverse arrangement of ulcers on the palate
  • longitudinal oesophageal ulcers
  • depletion of gut-associated lymphoid tissue (GALT) ± underlying lymph nodes
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12
Q

BVDV control

A
  1. Find PIs and remove:
    Identify persistently infected animals (Ag +ve : AB –ve)
    Establish exposure (Ag –ve : AB +ve)
  2. Protect against infection (Vaccine, Isolation / biosecurity)
  3. Monitor disease status: Screen tests (blood / milk)
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13
Q

BVDV Testing

  • types (4)
  • issues with blood sampling (5)
A
  • Bulk milk testing in dairy herds (ELISA and PCR; 300 cow limit?)
  • Individual animal blood samples (Beef & dairy) (ELISA and PCR)
  • Ear notch samples (calves) PCR
  • Test bulls and herd replacements

Blood sampling:
• Not <1 mo age – do ear tages
• Screen tests – at least 5 from each management group (9-18mo – any colostrum AB should have weaned) look for antibody
• Remember colostral ab can confuse – so don’t do anything until 9 months
• Remember seroconversion may be occurring – animal AB positive it has seroconverted already (not common)
• Does not distinguish between current, historic or vaccine exposure (unless repeated screens are done)

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