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Mastitis: Intramammary Infection IMI. Clinical Mastitis - Animal healthswellingheatrednesspaindisturbed function. Mastitis. Physical appearance - color, flakes, clots, etcpH - normal 6.5 increase to 7 Cellularity - increase in SCCChloride - increase Cl-Catalase - tissue damage - O2 release.
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3. Mastitis
8. Milk Cultures Infection level in herd
Type of infections
Source of infections
Control and Prevention
9. Milk Cultures Infection level in herd
Type of infections
Source of infections
Control and Prevention
Treatment
10. Milk Cultures
12. Mastitis: Intramammary Infection IMI
13. Contagious Mastitis Definition: Caused by pathogens passed from cow to cow at milking via hands, inflations, wash rags and other vectors
14. Contagious Mastitis
15. Contagious Pathogens
17. Strep ag MastitisStreptococcus agalactiae Lives only in infected quarters
Spread from cow to cow(milking, hands, common cloth)
Subclinical
High SCC and Reduced production
Treatment:
Lactation 60 - 95% (75%)
Dry off 80 - 98%
18. Strep ag SusceptibleLaboratory Testing
19. Strep ag Susceptible Herd Treatment - NY
20. Approved IMM Drug List Amoxi-Mast- Rx
Masti-Clear - OTC
Dariclox- Rx
Gallimycin-36 - OTC
Hetacin K- Rx
Pirsue- Rx
ToDAY (Cefa-lak)- OTC
21. Strep ag Mastitis Control & Prevention:
pre & post milking teat dipping
separate paper towel
milk infected cows last
dry cow treat all cows
screen replacements (home & purchase animals)
CMT, culture milk or culture bulk tank milk
know the history of the purchase herd
22. Strep ag Mastitis
25. Lives in infected quarters & infected skin
injured teat ends (mechanical, chemical, weather)
Spread from cow to cow(milking, hands, common cloth)
Nonclinical with high SCC & reduce production
Clinical (mild to severe) with repeated flare-ups
Treatment:
Lactation 15% (10 – 60)
Dry off 50% (40 – 70)
Can become “chronic”, long standing infections Staph MastitisStaphylococcus aureus
26. Staph Mastitis Control & Prevention:
pre & post milking teat dipping
separate paper towel
milk infected cows last
dry cow treat all cows
cull cows with long standing infections (chronic)
screen replacements (home & purchase animals)
27. Treatment of S.aureus IMIAntibiotics
28. Staphylococci MastitisStaph intermedius, Staph hyicus, Staph chromogenes
29. Staphylococci MastitisStaph intermedius, Staph hyicus, Staph chromogenes
30. Mastitis in HeifersCoagulase-Negative Staphylococci Lactating cows: highest prevalence of CNS during lactation occurs at calving
CNS are part of normal skin flora
Many infections are transient
Estimates of infection prevalence for heifers at calving 2-20% of quarters
31. Mycoplasma MastitisMycoplasma bovis Lives in infected quarters, respiratory & reproductive tract
Spread from cow to cow (milking, nasal & vaginal discharge)
Subclinical; high SCC and reduce production
Clinical; multiple quarters (mild to severe)
mulitple quarters, sandy texture & tannish-color milk
joint infections- swollen & lame
Treatment: none
nonresponsive to antibiotic treatment
32. Culturing Mycoplasma
33. Mycoplasma Mastitis Control & Prevention:
pre & post milking teat dipping
milk infected cows last
cull infected cows or segregate infected cows
culture replacements (home & purchase animals)
culture bulk tanks or know herd history
34. Mycoplasma bovis- when to be concerned
35. Mycoplasma bovis- when to be concerned
36. Environmental Mastitis
38. ColiformsE. coliKlebsiellae sp Etiology: fecal organisms
poor hygiene (not cow to cow)
higher incidence in hot summer (July-Aug)
bedding (Klebsiella with wood products
Clinical mastitis
Acute/toxic (15% will be severe & life threating)
rarely chronic (Klebsiella more common)
39. ColiformsE. coliKlebsiellae sp Treatment: supportive
fluids (IV & oral)
NSAID (ei, Banimine-flunixin meglumine, etc)
antibiotic therapy of little value
Control & Prevention
Clean & dry bedding
inorganic - sand
maintained and monitored
J-5 vaccination in dry period (3x)
40. Acute Coliform Mastitis Therapy Antimcrobials will NOT replace a competent immune system!
selenium-vitamin E
concurrent metabolic disease
core-antigen vaccines
Shock is the primary concern
Correction of tissue perfusion deficits
41. Supportive Fluids 40 to 60 L of isotonic saline
OR
2 L of 7.5% saline (hypertonic)
Hypocalcemia is most consistent serum chemistry change
42. ColiformsE. coliKlebsiellae sp Treatment: supportive
fluids (IV & oral)
NSAID
antibiotic therapy of little value
Control & Prevention
Clean & dry bedding
inorganic - sand
maintained and monitored
J-5 vaccination in dry period (3x)
45. Streptococcus MastitisStr. uberis, enterococci, Str. dysgalactiae Etiology: fecal organisms, rumen, genitalia
poor hygiene (not cow to cow)
higher incidence late dry period
any time during lactation
Clinical mastitis
mild (<15% will be clinical )
usually short duration, can become chronic (ave 45 days)
Treatment
Lactation 15-85% (78% , Wilson, 1993)
Dry off >75%
46. Streptococcus sp susceptibility93 isolates
47. Efficacy for Gram-Positive Pathogens
48. Antimicrobials and mild mastitis No antimicrobial use increased SCC, prevalence of Strep uberis
49. Streptococcus MastitisStr. uberis, enterococci, Str. dysgalactiae Control & Prevention
premilking sanitation - Teat Dipping
clean & dry: housing & bedding
dry cows management
close up & maternity pens
clean dry bedding
51. Serratia spp Etiology: common soil & plant inhabit
poor hygiene & wet areas
resistant in chlorhexidine gluconate teat dips
greater incidence from dry period
Clinical mastitis
mild
chronic lasting several lactations
nonresponsive to therapy
Control
check teat dip & environmental sanitation
E. coli J5 vaccine to reduce incidence & severity
52. Pseudomonas spp Etiology: water & wet bedding
poor hygiene & wet areas
resistant in chlorhexidine gluconate teat dips
low level iodine in drop hoses
contaminated water system (hot water heaters)
Clinical mastitis
chronic infection
nonresponsive to therapy
Control
check teat dip & environmental sanitation
sand bedding
E. coli J5 vaccine to reduce incidence & severity
53. Corynebacterium bovis (differ from Arcanbacterium pyogenes)
54. Corynebacterium (Arcanbacterium pyogenes)
55. Yeast/Nocardia(Opportunistic pathogen)
56. These pie charts show the culture result of the clinical cases for the two dairies from September 2002 to June 2003. Both herd had similar levels of clinical cases where no pathogens were isolated from the milk. 53% for the denDulk dairy and 55% for Green Meadows. This is similar to that shown in the last presentation by Dr. Hess. Coliform infections were isolated 22% of the cases for den Dulk and 14% for Green Meadow’s dairies. Gram-positive pathogens of Streptococcal and Staphylococcal bacteria was isolated 22% and 19%, respectively. Staph aureus infection accounted for the higher Gram-positive pathogens in the denDulk herd.These pie charts show the culture result of the clinical cases for the two dairies from September 2002 to June 2003. Both herd had similar levels of clinical cases where no pathogens were isolated from the milk. 53% for the denDulk dairy and 55% for Green Meadows. This is similar to that shown in the last presentation by Dr. Hess. Coliform infections were isolated 22% of the cases for den Dulk and 14% for Green Meadow’s dairies. Gram-positive pathogens of Streptococcal and Staphylococcal bacteria was isolated 22% and 19%, respectively. Staph aureus infection accounted for the higher Gram-positive pathogens in the denDulk herd.
57. This decision tree was used on the dairy to determine the type of treatment for clinical mastitis. No antibiotic were used before examining the culture results.
At the time that the clinical episode occurred:
Cows without fever were separated and monitored.
Cows with a fever were given an anti-inflammatory and fluids if needed.
Follow culture examination on the following day, the treated protocols basically divided the cows into two categories: 1)Gram-positive pathogens which received antibiotic treatment, or 2) Gram-negative pathogens or “no growth on culture” that did NOT receive antibiotic treatment.
This decision tree was used on the dairy to determine the type of treatment for clinical mastitis. No antibiotic were used before examining the culture results.
At the time that the clinical episode occurred:
Cows without fever were separated and monitored.
Cows with a fever were given an anti-inflammatory and fluids if needed.
Follow culture examination on the following day, the treated protocols basically divided the cows into two categories: 1)Gram-positive pathogens which received antibiotic treatment, or 2) Gram-negative pathogens or “no growth on culture” that did NOT receive antibiotic treatment.