59. Mastitis diagnosis and treatment in cattle Flashcards

1
Q

Mastitis?

A

The mastitis

  • Definition – mostly caused by microorganisms and rarely due to other cause
  • Inflammatory response
  • The infection

o Mostly through the teat canal (ascending)

o Mechanically through the skin of the udder through blood and lymphatic spreading (viruses)

• Economic impact of mastitis

o Direct cost

§ Discarded milk

§ Medicine and veterinary costs

o Indirect costs

§ Decreased milk price

§ Milk production decreases in the remaining lactation due to elevated SCC

§ Separation of the animal require labour

§ Cost of replacement heifers

§ Culling

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2
Q

Classification of mammary gland infections based on pathological changes?

A

Classification of mammary gland infections based on pathological changes

  1. Galactophoritis – gland cistern and teat cistern infection
  2. Parenchymal mastitis – minor cistern and ductus infection
  3. Interstitial mastitis – inflammation in the alveoli and the interstitial tissue between the lobules
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3
Q

Clinical forms of mastitis?

A

Clinical forms of mastitis

• Clinical mastitis: 20%

o Per acute

§ Abnormal milk

§ Abnormal mammary gland

§ Sick cow (elevation in clinical baseline values, shock exitus)

o Acute

§ Abnormal milk

§ Abnormal mammary gland

o Manifest by inflammation changes in the tissue such as redness, heat, pain and swelling

o Subacute

§ Abnormal milk only

§ Manifest by clots, flakes, and or changes in the colour and consistency of the milk secretion

o Chronic

§ Chronic form with fibrosis, nodules and/or abscessation in the mammary gland

• Subclinical mastitis: 80%

o Presence of inflammation with normal appearing mammary gland and visibly normal milk

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4
Q

Diagnosis of clinical and subclinical mastitis?

A

Diagnosis of clinical and subclinical mastitis

• Clinical mastitis

o Alterations in the milk + clinical signs of the animal

§ After milking the 1st strips, we preform test milking

§ During this we observe the mammary gland

§ In case of positivity separated milking + treatment

• Subclinical mastitis

o Somatic cell count (SCC)

§ Leukocytes mean 80% of the somatic cells in uninfected quarters and 99% in uninfected

quarters

o Milk lactose concentration decrease

§ In damaged tissue, the secretory cells are unable to lactose biosynthesis

o Milk lactate dehydrogenase (LDH) concentration increase

§ Due to cell damage LDH is released into the milk (secretory cells + leucocytes)

o Milk N-acetyl-b-D-glucosamidase (NAGase) -increase

§ Due to epithelial cell damage exerts from cell lysosomes

o Acute phase proteins (haptoglobin, milk amyloid A)

§ Due to increased permeability, they cross the blood-milk barrier and occur in milk

o Electrical conductivity (EC) of the milk increase

§ Sodium chloride increase, potassium decreases

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5
Q

Subclinical mastitis direct and indirect?

A

Subclinical mastitis: somatic cell count determination

• Direct

o Microscopic determination

o Automated electronic cell counters (flow cytometry)

o Portable counters (DeLaval, Porta SCC)

• Indirect

o California milk test (CMT)

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6
Q

Evaluation of CMT?

A
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7
Q

Additional tools in diagnostic of intramammary infections?

A

Additional tools in diagnostic of intramammary infections

  • Bacteriological culture sampling
  • PCR sampling
  • The sampling

o At the level of the quarter

o At the level of the cow

o At the of the herd

• Selection criteria

o Clinically affected animals before the

therapy

o At the time of drying off

o After calving

o Animals with high SCC

• Bacteriological culture sampling

o Easy culturing (! mycoplasma spp!)

• Bulk tank microbiology

o Raw milk quality testing

o IMI link: S.aureas, strep agalactiae and mycoplasma spp.

o Other pathogens: not only from the cow

o Standard plate count – SPC (bactoscan, flow cytometry)

o Target numbers of bulk tank microbiology

  • On farm culturing method
  • Classical laboratory culturing
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8
Q

Sampling for microbiological culture sampling?

A

Sampling guide for microbiological culture sampling
0. Clan hand or glove
1. Cleaning and drying of the teat
2. Predisposing and towel cleaning
3. Milking 1st 4-6 strings
4. Cleaning the teat end with alcohol on a towel
5. Keeping the tube in 45 degrees on string is milked into the tube
6. Identification of the tube
7. Freezer (coliform!!)
8. Cooling bag, lab, transport
• Staph Aureus- at the end of milking

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9
Q

PCR?

A

PCR – polymerase chain reaction

  • Advantage within 4 hours
  • Multiplex PCR and real time PCR assays
  • Not able to distinguish between dead and alive organisms
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10
Q

Pharmacological therapy of mastitis?

A

Pharmacological therapy of mastitis

• Cases occurring in early lactation

o The immunity of the cow is impaired

o There are fewer circulating neutrophils, harder to get

into the udder

o Bacteria easier causing a septicaemia

• Answer if the immune system

o Release of immature neutrophils from BM

o Less effective phagocytosis

o EC release of ROS (reactive oxygen species)

o Much more tissue damage

o Endotoxins are free in tissue to cause more inflammation

o Maybe toxic shock

• Normal cow

o Phagocytosis

o Internal killing by ROS

o Endotoxins protected

• Periparturient cow

o No successful phagocytosis

o External killing by ROS

o Endotoxins are free in tissue

• Because all of these in the periparturient period toxic mastitis is more common Mastitis Acuta Gravis

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11
Q

Antibiotic treatment?

A

Antibiotic treatment

  • 1st steps when choosing AB
  • Lactating cow vs. Dry cow
  • How many administrations?
  • Further medical therapy
  • Initiation of treatment as early as EC change
  • Faster and more complete recurrence than self-cure
  • Decrease the chance of remission
  • Crease milk yield drop
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12
Q

How to choose AB?

A

How to choose AB?

  1. Sensitivity
  2. Bactericidal or bacteriostatic
  3. Withdrawal period
  4. Price

• Intramammary treatment

o The conus is partially inserted into the teat canal

o Close the end of the teat and massage up to the direction of the udder

o Post dip all 4 teats

o Record treatment

• AB treatment

o Local treatment (IMM)

o Parenteral treatment (IM)

o Combination (IMM+IM)

o Aggressive treatment

§ Longer duration

§ Higher dose

  • For parenteral treatment only those AB, which reach sufficient concentration in the alveoli
  • If no cure at 2 days, do we need to change treatment?
  • If at day 4 still no progression towards cure

o Change AB

o Preferably on the basis of bacteriology and sensitivity

o Never treat longer than 7 days

o High likelihood of a yeast – check for it

o Cull or dry off quarte

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13
Q

Effectiveness of treatment?

A

Effectiveness of treatment

  • Bacteriological elimination à <400,000 SCC ↓
  • Up to 4-6 weeks
  • No cure: subclinical mastitis (SCC remains high)
  • Clinical cure rate
  • It is normal for cured cows to still have clots at day 4 or 5
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14
Q

General guidelines of AB usage?

A

General guidelines

• AB usage should involve veterinary guidance and extra label use should be avoided when on label use is a

possibility

• AB should only be used when there is a reasonable likelihood that a bacterial infection that is sensitive to the

proposed AB is present

  • Narrow spectrum AB that are less critical for treating human illness should be used as 1st choice
  • Antibiotics should be sued for as short a

duration as possible

  • No treatment, culling
  • Low cure rate
  • Beta lactamase positivity ↓↓↓
  • In vitro susceptibility ≠ cure
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15
Q

Aditional treatments and vaccination?

A

Additional treatments

  • More milking events, oxytocin
  • Fluid therapy
  • Anti-inflammatory drugs (meloxicam, metamizole)
  • Glucose IV
  • Non-AB treatment

o Relative low number of scientific evidence

o Disinfectants

o Bacterial culture

Vaccination

  • Staph aureus
  • E.coli
  • Contra versional results
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