Posted by Dr. Steve Dudley on June 29 2009 13:49
- These two diseases have been the most economically important diseases recently.
- Prevention and control strategies have been an area of focus in herd health.
- We have come a long way in our understanding of these pathogens, but there is still much to learn and accomplish.
- Porcine Reproductive and Respiratory Syndrome Virus
- PRRS is the disease..... PRRSV is the virus
- Several Other Names
- SAMS
- SMD
- SIRS
- Blue Ear
- Lelystad
- Most economically important disease of swine
- $650 Million Annually
- Has dictated large amount of production System design.
PRRSV: The Basics
- Family of viruses known as Arteriviruses
- Much heterogeneity in the genome
- RNA viruses have errors in transcription
- Strains vary markedly in virulence
- European and U.S. strains genetically distinct, although thy arose around the same time.
- No Protective epitopes have really been identified
- Replicates within the white blood cells in the lungs (PAMS)
PRRSV Testing
- Polymerase Chain Reaction (PCR)
- Detects virus. Very sensitive. Beware of false +
- Enzyme Linked Immunosorbent Assay (ELISA)
- Detect antibody. Passive, Active.
- Sequential testing. False + and False -
- Restriction Fragment Length Polymorphism (RFLP)
- Characterizes virus groups. Poor test
- Viral Sequencing
- Small portion of genome looked at. Dendograms
- Value?
Biosecurity
- Biosecurity is probably the most important factor that producers can control to minimize the impact of PRRSV in their system
- Down-time for personnel
- Ante-rooms
- Shower-in-shower-out facilities
- Cleaning/Disinfecting facilities
- All-in-all-out pig movement
- Screens/netting/rodent control
- Air filters
- Danish Entry
PRRSV Treatment Considerations
- Antibiotic therapy
- Macrolide Class will concentrate in PAMs and provide some anti-inflammatory action. Ex=Pulmotil and Draxxin
- Treat other infections based on Culture/Sensitivity
- Vaccination
- Protect those not yet exposed
- Activate Cellular Mediated Immunity. Decreases replication and shedding.
- Anti-inflammatory Drugs
- Interferon
PRRSV: Immunologic Control
- Vaccines
- Modified Live Commercial products (ATP/ResPRRS)
- Killed vaccines (clinic/autogenous)
- Subunit vaccines (MJ PRRSV)
- Natural Exposure
- Serum Therapy
- Incoming gilts
- Whole herd
- Mid-gestation
PRRSV Research: What's new?
- Transmission of PRRSV via aerosal.
- Length of viral shedding in infected animals.
- MLV use during disease outbreaks
- New Highly pathogenic strain characterized
PRRSV: Aerosol Transmission
- This route has always been suspected, but was very difficult to prove.
- University of Minnesota has been looking into this method very intently.
- Trial at UM was designed as follows:
- 4 barns: 1 infected, and 1 low biosecurity, 1 medium biosecurity, and 1 high biosecurity 120 m from infected
- Repeated trial 26 times in 2 week incriments
Aerosol results
- Low level of biosecurity (no intervention) resulted in a high rate of infection.
- Medium level of biosecurity: showering but no air filters= 8/26 infected.
- High level: showering and air filters resulted in no infection.
- The best times for infection were cool/cold days, with mild prevailing winds, high humidity, and low UV index.
Length of PRRSV shedding
- Study at ISU inc3luded 109 pigs infected with PRRSV at 3 weeks of age.
- Results from the trial included:
- Peak viremia was between 7 and 21 DPI
- Most pigs cleared the virus by day 42
- Occasional positive animals (2-7%) through 154 DPI. Intermittently shedding.
- Lymphoid tissues remained positive through 202 DPI.
- The virus persisted in the population longer than previously thought.
- Virus likely sequesters in lymphoid tissues, and reappears during times of immune-stress
- These results make us re-think
- Isolation times
- Purchasing animals from previously positive herds
- What it takes for a herd to consistently produce negative iso-weans.
New Use for PRRSV MLV?
- UM study looked for alternative ways to use the MLV products already on the market in G/F pigs.
- Vaccine administered at 1 week after PRRSV infection. Some pigs were then infected with a different highly pathogenic strain 98 days afte the first infection.
- The objective was to study the therapeutic effects of vaccine intervention and prevention of re-infection.
- Vaccine did not produce sterilizing immunity.
- Vaccination did not prevent re-infection
- Vaccine did reduce viral shedding.
- Vaccination was able to decrease the clinical impact of disease.
- The success of this intervention would likely vary depending on the strain of PRRSV that your pigs are challenged with.