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ABCDMycoplasmal pneumonia•Chronic infection of ciliated epithelium
•Increased cost• Interventions, fixed cost
•Reduce revenue• Reduced growth rate (# sold)• Cull/substandard pigs (price penalty)• Mortality
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ABCDWhat is “success”?
• Final customer…the pig• Welfare & well being
• Producer• Biology financial
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ABCDStudy designs
• Random, blinded evaluations• block by source, sex, weight, etc
• Four weeks from vaccination to challenge
• Four week monitoring period
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ABCDImmunity
• Passive Immunity• Protects from challenge• May interact with active immunization
• Active Immunity• Level/duration of protection
Thacker,et al 2000; BIVI 2000
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ABCDCellular Immunity
• Dr. E Thacker• Various levels of cellular immune
response
• Sensitized via vaccination
• All vaccines protected lungs
Swine Health & Production
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ABCDCMI Relationship
• CMI = Cell mediated immunity
• Peripheral lymphocytes
• Association with growth rate?• Higher CMI level at challenge• Higher ADG
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ABCDClinical study
• Higher CMI responses associated with• Higher Average Daily Gain
• Reduced Lung lesions
• Replication of results
Roof, AASV 2001
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ABCDCombination control
• Application of vaccines & therapeutics
• “Complimentary” strategies?
• Sources of active immunity• Immunization• Field organism exposure
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ABCDNatural exposure
• Slow onset in continuous production systems• Low level introduction/late spread
• Aerosol spread & dose
• Alone or complicated disease
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ABCDLinkage
• Several methods to develop immunity
• Prior to vaccines…• Strategic medications one week per
month
• Study case
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ABCDProphylaxis & Metaphylaxis• Established clinical disease
• “Peri” outbreak• Little or no overt clinical disease• Exposure has occurred• “Incubation” period
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ABCDMetaphylaxis
• Metaphylaxis: e.g. Strategic-Dosing
• natural exposure allows infection and incubation immediately prior to short-term medication to shut down the incubation process prior to expression of disease and associated negative biologic and economic consequences
• Exposure may aid development of protective long-term active immunity against endemic diseases
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ABCDMetaphylaxis
• Limited duration of therapeutic medication:
• Advantages• limits cost• organism/antibiotic exposure time• development of resistance
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ABCD
• Inability to exclude infection • Disease outbreaks later in production
• SEW/18-week wall, etc• Lawsonia/PPE
• Vaccines not available or only partially effective• APP• Streptococcus• Compliance failure
Potential for Metaphylactic Strategic-Dosing
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ABCDPotential
• Change in epidemiology• Timing of vaccination prior to exposure• Newly diagnosed disease
• Multiple disease challenges require broad spectrum intervention tool
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ABCDCase study
• Commercial 3-site production system in Midwest
• Consistent history of decreased performance 8-12 weeks post-placement in finisher (18-22 weeks of age)
ADGF/GADFI
• Inconsistent diagnostic findings
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ABCDDesign
• 2 animals per pen were serially bled every two weeks
• Serology was initially performed on placement and closeout samples to screen for M. hyo, PRRS, SIV, TGE, Salmonella and Lawsonia activity
• Additional serology was performed on bi-weekly samples for pathogens shown to be active in finishing based on screening serology
Swine Health & Production, 2000
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ABCDTherapeutic options• Treatment 1: Denagard +Aureomycin
pulsed 5 times (2, 4, 7, 10, and 13 weeks post-placement) and Aureomycin 100g/t given weeks 3, 5, 6, 8, 9, 11, and 12 [“Continuous”]
• Treatment 2: Denagard(35 g/t) + Aureomycin(10 mg/lb BW) pulsed 5 times (2, 4, 7, 10, and 13 weeks post-placement) [“Pulse”]
• Treatment 3: Non-medicated Controls
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ABCDOutcomes
• Consistently observed performance did not occur during any 2-week interval
• Perhaps because 2/3 of the animals in the barn/airspace were on systemic antibiotics which infection pressure
• However both med strategies significantly improved overall survivability and performance
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ABCDImpact on Mycoplasma
MYCOPLASMA serology
0
0.05
0.1
0.15
0.2
0.25
0.3
0.35
0.4
0.45
0.5
0 2 4 6 8 10 12 14 16
Week
Tw
ee
n 2
0 O
D
Continuous Med Mhyo
Pulse Med Mhyo
Control Mhyo
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ABCDImmunology
• Both strategic and continuous medication strategies significantly improved ADFI, ADG, F/G and survivability while being cost-effective
• There were no significant performance differences between strategic and continuous medication strategies
• Strategic medication permitted natural Mycoplasma exposure and immune response (seroconversion) as w/ NMC’s while improving/protecting growth performance
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ABCDImplications
• Therapeutic use of medications or biologics
• Goals of model• Growth• Lungs
• Defined vs. natural exposure• Immunity
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ABCDEnd consumers
• The pig• Reduced clinical disease• Maintenance of therapeutic application &
use• Welfare
• Consumer• Reduced medication use
• Residue, resistance• More efficient resource use
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ABCDSummary thoughts
• Immunologic advantages in Mycoplasma control• Single point application• Defined investment• Limited residue/resistance
• Limitations• Incomplete control...