CS: Underperformance and Infectious Dz Flashcards

1
Q

Measures of beef performance?

A
  • daily live weight gain (0.8kg/d, 1kg/d when weaning?)
  • % in calf (>95%)
  • more qualitative d/t block calving cf. dairy
  • live calfs /no. cows put to bull (aim >95%, slightly cows cf. heifers)
  • muscle: fat ration for grading carcasse
  • involuntary culls
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2
Q

Measures dairy performance?

A
  • calving interval (aim 365 or 400d ish)
  • growth rate (0.7kg/d)
  • milk yield (~7,500l/cow/year average)
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3
Q

Diseases affecting performance?

A
> biggest 
- mastitis
- lameness 
> also
- lepto
- IBR
- BVD
- Neospora
- Salmonella
- Campy
- Endometritis
- TB 
- E. Coli 
- Johnes (^ prevalence) 
- SARA
- Fatty liver/pregnany toxaemia
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4
Q

Assessnig presence endemic dz

A
  • Bulk milk tank sampling (Brucellosis serology also, mastitis cell count, low fat for SARA)
  • CMT
  • observation (lameness etc.)
  • intradermal (eg. TB)
    > check different age groups (if + serology only present older cows likely historic infection rather than active)
    -
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5
Q

How can disease be avoided?

A
  • vax and isolate new stock
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6
Q

How do different Johnes tests differ in sense and spec?

A
  • milk higher sensitivity as threshold for + outcome lowered (cf blood)
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7
Q

Effects of Neospora caninum ?

A
> losses d/t
- v post weaning weight
- v milk yield
- premature culling
- ABORTION 
> signs
- often none
- early embreyonic death (if infected
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8
Q

How is neospora caninum transmitted?

A
  • vertical and horizontal
    > vertical
  • parasite migration during pregnancy to foetus from PI dams
  • will affect several generations and successive pregnancies
    > horizontal
  • dogs IH, cows ingest oocysts from feaces
  • CAN BECOME pi
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9
Q

Dx neospora caninum?

A
  • histopath on aborted foetuses
  • serology of dam or calf (if calf + assume dam also +, but PI animals Ab levels fluctuate so can get false -ves: Better test needed if trying to eradicate dz or maintain free herd
  • PCR/IHC to differentiate from other protozoa on histo
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10
Q

Is there a vax for neospora? Control/prevention?

A
  • not currently
  • cull infected cattle
  • breed seronegative stock
  • consider embryo transfer for infected stock high genetic merit
  • dogs away from farm
  • biosecurity at calving, dispose of placentas and aborted material
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11
Q

Clinical effects of BVDV

A
  • infertility (abortions/stillbirths/mummification)
  • birth defects (weak sickly calves, neuro signs)
  • ill thrift and stunted growth
  • poor condition
  • IMMUNOCOMPROMISE -> 2* infection; esp scours and pneumonia
  • v milk yield
  • mucosal dz if cytopathic form mutates (6-18mo)
    • Better groups list **
  • Naïve, non-pregnant, immunocompetent: no CS in 70-90%
  • Acute: fever, lethargy, anorexic, ocular discharge, nasal discharge, oral lesions, diarrhoea, reduced milk yield
  • Chronic: mucosal disease.
  • In-utero infection: abortions, congenital defects (cerebellar hypoplasia) weak, small calves, unthrifty PI calves.
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12
Q

Tests for IDing presence BVDV?

A
  • Ab ELISA to see exposure of herd (bulk milk or bloods)

- PIs Antigen/viral RNA/virus isolation hunt: bulk milk or young stock bloods or ear notch 2 samples 3wks apart

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13
Q

How can BVD potentially be eradicated on farm?

A
  • eradicate PI reservoir
  • vax all breeding females to prevent new PIs born (killed vax so 2 jabs needed, ensure well before 1st service eg. yearlings)
  • booster each service
  • with active infection may need to vax other stages +- dam few weeks before calving to ^ colostrol abs
  • continue bloodm onitoring 12mo after last PI identified
  • purchase animals from BVDV free herds or quarantine 1m and blood test
  • isolate cows bought in calf until parturition then screen calves PI (trojan mother poss with variable ab titre but no active infection despite PI calf)
  • prevent contact with neighbouring farms using double perimeter fence
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14
Q

What can interfere with testing calves?

A
  • MDA

- blood sample pre-colostrum or >4mo

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15
Q

How else may BVDV be spread

A

semen

  • PI bulls
  • check semen before AI (not allowed to sell AI semen from BVD+ bulls but if DIY be careful)
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16
Q

Diseases affected performance by type of pathogen

A

> Bacteria: Mastitis (S Aureus), TB, Johne’s, metritis, leptospirosis, pneumonia in calves (growth stunt)
Prions: BSE
Viruses: BVDV, Rotavirus, FMDV, BTV, IBR(not so common but nasty outbreaks),
Protozoa: Coccidia, Neospora (causes abortions)
Parasites: Ostertagia (affects growth of young stock), Fluke (affects young and older animals)
Metabolic: SARA, ketosis, milk fever, hypomagnesia

17
Q

Which diseases have greatest economic impact on farm?

A
  • IBR
  • Lepto
  • BVD
18
Q

overview of IBR

A
  • causes range of dz
  • very infectious
  • life-long latency ni trigem ganglia
  • recrudescence poss
19
Q

Most common linical signs of IBR

A

> Rhinotracheitis

  • Most common disease caused by a BoHV-1 infection
  • Can also cause reproductive (infectious pustular balanoposthitis/infectious pustular vulvovaginitis) , nervous (typucally calves
20
Q

Is viraemia detectable with IBR?

A

No - virus excreted from mucosal surfaces

21
Q

Dx IBR?

A
>Serology
Ab detected 2-6 weeks post infection
Highest during early clinical signs
- isolate seronegatvies and breed, snatch calves from sero+ and test 
>Virus neutralisation – collect 1 sample then 2nd 4w later
ELISA
DIVA vaccines available
Virus isolation
Nasal / vaginal swabs
Sperm sample
Tissue sample – dead / aborted animals
Needs to be collected during acute disease – as latent
>Bulk milk tank 
Serology
PCR
22
Q

Biosecurity associated with protecting a herd from IBR

A

> Buying in infected animals is the most common source of infection
- Buy from disease free herds
- Quaratine & test new animals before mixing into herd
Remove seropositive animals
Vaccines (DIVA)
- just preweaning can alleviate all clinical forms of IBR
- MLV IM (feedlot cattle, can cause abortion)
- MLV intranasal (can be used in outbreaks, does not cause abortions or interfere with passive immunity), inactivated, killed
4-6 months old
Biosecurity
Foot baths for staff
Gloves when handling infected cows
Prevent proximity of infected and non-infected animals
Oronasal spread
Indirect spread
Contaminated semen
Embryo transfer
Humans
Contaminated materials
Airborne transmission

23
Q

Eradicating IBR

A
> No direct tx
Isolate
NSAIDs
> Carrier cattle should be identified and culled
> Vaccination
DIVA
In non-infected animals
Bi-annually – Spring & Autumn
24
Q

Is the ab ELISA for IBR sensitive? specific?

A

Very sensitive? I think - check this, presentation not clear
- + animals must be classified as exposied