LA Diagnostics and Vaccines Flashcards
What are the sample options on farm and when are these relevant?
- bulk milk sample or split bulk tank test : any contagious disease
- young stock check : BVD, if Ab+ then a carrier (if PI then will not have AB)
- individual cows: TB or any eradication programme
Diagnostic options for identifying pathogen presence/exposure/disease?
- antibody ELISA (with DIVA vax)
- cell mediated response (g-INF test, skin test for TB)
- pathogen ELISA or PCR (IBR)
- pathogen culture
- slaughterhouse
- PM
What can you infer about a disease if older cows are AB+ but younger cows are AB-?
- previous exposure to pathogen
- active spreading nt likely or all cows would be affected
- or different timing of a vax schedule
What pots should be used for serology samples?
- serum pots (clots)
- RED or PLAIN
What pots should be used for PCR and Ag ELISA samples?
- heparinised
- GREEN or PURPLE
What pots should be used for serology and PCR on milk?
Tube iwth preservative : DONT DIP IN BULK TANK! Contamination poss.
What pots should be used for culture of milk?
Sterile pot without preservative
What should be checked with the lab when interpretting test results?
- sensitivty
- specificity
- NPV
- PPV (predicting values)
IS the johnes test sensitive?
- not very
- milk more sensitive than blood ?
What are the 2 types of prevalence of a disease that can be reported?
- individual prevalence
- herd prevalence
What 2 types of testing can be used to identify disease in a herd? Which is more sensitive/specific?
- Parallel (v spec, ^ sense)
- Series (^ spec, v sense) = confirmation testing. eg. skin test followed by g-IFN test for TB
What is the sense/spec of IBR testing?
Good
- generally good for viral, less good for bacterial
What 3 reasons may we be testing a herd?
- testing for presence/prevalence (random samples)
- testing ot eradicate (must test all individuals)
- testing for abscnece ( eg. FMD so contagious that only few samples needed to prove not likely present)
How sense/spec is the TB test?
- 99.9% spec
- 80% sense
> parallel testing so spec v and sesne^ ??
Give an eg of a disease you would want to eradicate? monitor? Tx? Vaccinate against the disease?
- eradicate FMD
- monitor BVDV
- tx Leptospriosis to v excretion (zoonotic)
- vax for
> pathogen or toxin (eg. clostridium)
> DIVA for dz
What must be remembered when thinking about treating a dz?
no point treating unless you can manage it at point of entry
- GI worms, liver luke, claf scours, bTB, lepto, IBR
- No vaccine for bad management!
Outline concepts of disease management and which diseases are relevant to each
- housing, hygiene, ventilation
- colostrum management
- all in all out concept (poultry)
- stocking density (resp disease, environmental mastitis)
- rotational grazing (GI worms)
- Water trough management (IBR)
How can poor disease management be identified from hx or records?
- dry cow tube use
- mastitis cow tube use
- preventative tx with Halocur (Crypto scouring calf tx)
- use of vax
> always look at disease, farm management etc. before jumping to a quick fix
Which diseases can cross react tests and vaccines?
- TB test and Johnes vax
How can vax be sued as part of disease management?
- v pathogen load (lepto)
- protect herd from reintroduction (BVD/IBR)
- improve efficacy of current practice (rota/corona) eg . colostrum
> typically raise herd immunity -> v pathogen load -> v infected animals -> infection dies out -> eradication
Which type of infections are vaccines more effective for?
- viral good
- bacterial less good
How can vax interfere with testing? How can this be overcome?
- most common testing based on serology
- vaccines -> immune response
- consider MDA
> create sentinel groups that are not vaccinatede - if these test + for disese then it is naturally occouring in the herd
- if consistently testing -ve may be able to stop vaccinating at some point
What are DIVA vax?
- differentiating infected from vaccinated animals
- sensivity/specificity of the differentiating test
> available for IBR, AI, FMD, bTB in development
How do differing types of vaccine impact the response?
- live: immunity v spread after inoculation
- attenuated live: local immunity developee
- deadL immunity response depends on adjuvant used
- subunit vax eg. FMD AG presenting alfalfa (genetically modified)
- toxin based for clostridial disease
- boosters
How long shuld a vaccine be used after opening?
within 24hours
- always check farm fridge