6.2.2: Mastitis Flashcards
A cow that presents with clinical mastitis in the first 30 days of lactation is considered to have mastitis of a lactation or dry period origin?
First 30 days after calving = dry period origin
A cow that presents with clinical mastitis at over 30 days of lactation is considered to have mastitis of a lactation or dry period origin?
Over 30 days into lactation = lactation origin
What key questions are essential to forming a mastitis control plan for a herd?
- Is it dry period origin or lactation period origin?
- Is it environmental or contagious?
How do you differentiate between a mastitis that is caused by contagious vs environmental pathogens?
- Use the bulk milk somatic cell count (BMSCC)
- Over 300,000 cells/ml = likely to be a contagious pathogen
- Consider subclinical infections/persistency; contagious pathogens are well-adapted to persist in the udder
- Seasonality can be a good indicator of environmental rather than contagious and can still be observed in cows housed all year round
What 2 categories of data are necessary to monitor mastitis at a herd level?
- Somatic cell count - usually readily available
- Clinical mastitis data - relies on farmer detection and record-keeping
True/false: the majority of mastitis cases that present in the 1st month after calving are due to infections picked up in the dry period.
True
* This is useful at a herd level.
* It does not necessarily hold true for every individual cow.
How do we monitor SCC across the dry period? What does this tell us?
- Record SCC in last milking before drying, and in first milking after calving
- Compare 2 figures
- High –> low = we cured this :)
- High –> high = we did not cure OR we cured and then got another infection.
- Low –> high = picked up an infection
- Low –> Low = we prevented a new infection
This is about monitoring across the dry period.
A and B
A - Reason: new IMI prevented
B - Treatment outcome: Success :)
This is about SCC monitoring across the dry period.
C and D
C - Reason: New IMI acquired.
D - Treatment outcome: Failure :(
E and F
E - Reason: existing IMI cured and new IMI prevented
F - Treatment outcome: Success :)
G and H
G - Reason: Existing IMI not cured OR existing IMI cured and new IMI acquired
H - Treatment outcome: Failure :(
What does this graph show us?
- Spikes = when cow is most likely to pick up new infection (NOT the same as when mastitis is detected)
- High risk times: start of dry period, towards end of dry period (lactogenesis and approach to calving) into start of lactation
- Low risk times: middle of dry period. Risk tapers down as lactation continues.
How can we detect mastitis?
- Clinical exam/foremilking - for clots/consistency/colour of milk
- Conductivity - changes with inflammation. Fitted in some parlours.
- California Milk Test - crude but detects elevation in SCC (subclinical mastitis)
- Individual cow somatic cell counts (ICSCC) - useful for detecting subclinically affected cows
Characteristics of contagious pathogens (mastitis)
- Adapted to the mammary gland
- Can cause persistent infection and hard to get rid of
- Spread between the cows at milking
- Less common than environmental mastitis
- e.g. Staph aureus, Strep agalactiae, Strep dysgalactiae, Mycoplasma spp
Characteristics of environmental pathogens (mastitis)
- Opportunistic invaders from the cow’s environment
- Examples: S, uberis, Staph species other than Staph aureus, Coliforms such as E. coli , and Klebsiella, Pseudomonas, Proteus, Serratia species, Gram +ve bacilli, yeast, Prototheca
- Environmental mastitis is more common than contagious mastitis in the UK