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22/05/2006 lintjeshof 1 PCV2 and PRRS in relation to PMWS, secondary infections and management factors F. Dirven (Lintjeshof NL)

PCV2 and PRRS in relation to PMWS, secondary infections ... · PDF filePMWS, secondary infections and management factors F. Dirven ... (pac man) are destroyed ... parvo 26, 30 weeks

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Page 1: PCV2 and PRRS in relation to PMWS, secondary infections ... · PDF filePMWS, secondary infections and management factors F. Dirven ... (pac man) are destroyed ... parvo 26, 30 weeks

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PCV2 and PRRS in relation to PMWS, secondary infections

and management factors

F. Dirven (Lintjeshof NL)

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orcineorcineregardingregarding thethe pigpig

ircoirco--CircularCircular ((typetype of of genomegenome))

VV

22

PP

CC

irusirus

TypTyp

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• Clinical symptoms first described in Canada (1991) and

France (1996)

• Wasting of pigs especially 1-2 weeks post weaning (often

without any other symptoms like coughing or diarrhoes …)

• Sometimes already symptoms in suckling pigs (sneezing,

wasting)

• Somtimes abortions in sows in all stages of pregnancy (West

et al., 1999; Allan et al., AASP 2000)

Porcine Circovirus Typ 2 (PCV2)

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• Also pcv2 virus in healthy herds (SPF), virus has become endemic ( Antibodies in all herds)

• Mutation of the virus from symptomless to pathogene.

• Suspension of mammalian proteins from pig diets (due to BSE)

• Increase of mycotoxins in pig diets (multifactorial)

• Higher production (30 piglets/sow/year) and concentration of pig production

• „Mistake for PRRS symptoms“

• Genetic change (pietrain strains??)

Theories, why PCV2 Symptoms did occur so „late“(since about 1998) although the virus is already

circulating in pig populations since decades

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Pathogenesis (PCV2) experimental

• Oronasaal infection seronegative SPF gilt (DURING GESTATION)

viraemia

virusreplication in embryo

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PATHOGENESIS

INFECTION PCV2

55-75 DAYS GESTATION

UP 75 DAYSGESTATION

POSTNATALPIGLETS

MUMMYFICATIONSTILL BIRTHS

GESTATION GOES ON

VIRUS POS.PIGLETS

NOT GROSSLY AFFECTED

* LYMPHOIEDDEPLETION

* MONOCYTE INFILTRATION

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Lymphoïd depletion in lymphnodes due to PCV2

- Lnn. are producing cells for the immunesystem- Decreased production lymphocytes (defense cells)- Macrophages (pac man) are destroyed (monocyte

infiltration), a decrease up to 30%- Immune system (defense system) is weakened and

sometimes unable to challenge new sec. infections- At this stage pcv2 is not yet developing disease, the

piglet is infected with pcv2 virus without symptoms ( only enlarged lnn. and dark tear traces)

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Pathogenesis (pcv2) in field conditions

Important role by cofactors• Cofactors stimulate immunesystem of a piglet

infected with pcv2• Pcv2 replication and pcv2 infiltration in lnn• Pcv2 responsible or lymphodepletion in lnn which

indicates immunosupression

• Secundairy infections PMWS

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immunityimmuno stimulation

pathologic pmws in lnn

secundary bact . infections clinical symptoms of PMWS

immunosupression

lymphodepletion

pcv2 replication

immunosystem piglet with pcv2

cofactors

virus ( prrs, ppv and auy)other stress factors

toxines

INTRUTERINE I

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PMWS

SSyndromyndrom

MMultisystemicultisystemic

WWastingasting

PPostweaningostweaning

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Co-factors

• Viruses as prrs and ppv (often together)

• Vaccination ; every irrelevant immunogen (adjuvant) can give immunostimulation

• Stress factors: mixing, overcrowding and feed changes

• Mycotoxins• Other bacteria.

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PCV2 – Potentiation of clinical symptoms dueto coinfektion with PRRSV

G1G1 99 ------ 00 <1<1

Harms et al., AASP 2000

GroupGroup NN InfectionInfectionMortalMortal..

(%)(%)clinicclinic((scalescale))

G4G4 1717 PRRSV+PCV2PRRSV+PCV2 5959 1212

G3G3 1313 PRRSVPRRSV 00 99

G2G2 1919 PCV2PCV2 3232 <1<1

(Infection of 3 weeks old CD/CD pigs)

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Immunstimulation may induce PMWS

Kyriakis et al., J Comp Pathol. Januar 2002

M.hyoM.hyo NaClNaCl--SolSol..M.hyoM.hyo

NaClNaCl--SolSol.. BaypamuneBaypamuneBaypamuneBaypamune

NaClNaCl--SolSol.. NaClNaCl--SolSol..NaClNaCl--SolSol..

Day 7Day 7 Day 42Day 42GroupGroup

11

22

33

InjectionsInjections at at dayday of liveof liveDay 28Day 28

ControlledControlled fieldfield studystudy withwith 3 3 groupsgroups (28 (28 pigletspiglets eacheach) in a ) in a farmfarm withwith PMWS PMWS symptomssymptoms

PMWSPMWS--SymptomsSymptoms in :in :42,9% of M.hyo 42,9% of M.hyo vaccinatedvaccinated groupgroup,,50% of 50% of BaypamuneBaypamune injectedinjected groupgroup and and onlyonly 10,7% of 10,7% of NaClNaCl--injectedinjected groupgroup !!

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PMWSPMWS: a : a complexcomplex withwith manymany facesfaces !!!!

PRRS Circo

Strepto-

coccus

Unfavour-able vaccine

gramme Management Stress

APP

Postweaning-Multisystemic-Wasting-Syndrom

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Circo

Strepto-

kokken

Ungünstige Impfpro-gramme Management Stress

APP

Postweaning-Multisystemic-Wasting-Syndrom

PMWSPMWS afterafter controlcontrol of PRRSVof PRRSV

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Circo

Strepto-

kokken

Management Stress

APP

PMWSPMWS afterafter contolcontol of PRRSV and of PRRSV and optimizationoptimization of of managementmanagement

Postweaning-Multisystemic-Wasting-Syndrom

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Circo

Postweaning-Multisystemic-Wasting-Syndrom

PCV2PCV2 afterafter controlcontrol of PRRSV, of PRRSV, otherother infectionsinfectionsand and optimizationoptimization of of managementmanagement

PCV2 PCV2 allonealloneusuallyusually doesdoesnotnot induceinduce

clinicalclinicalsymptomssymptoms

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PMWS

First in Canada (1991), now almost worldwide.Responsible for many economical losses.Netherlands first symptoms in 1997.

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CLINICAL SIGNS

• From weaning until 40 kg bodyweight .• Sneezing, coughing and pneumonia.• Fever, lowered daily intake.• Paleness ( stomach ulceration )• Wasting up to 10 %.• Lowered uniformity.• Combination with PDNS.

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PDNS

S S yndromyndrom

D D ermatitisermatitis undund

N N ephropathieephropathie

P P orcineorcine

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PDNS• High conc. pcv2 antibodies• persistant immunostimulation (viruses,stress,

mycotoxines etc.)

• production (auto)immunecomplexes• Obstruction smaller bloodvessels (skin, kidneys)• No therapy (sometimes in early stage cortico’s)

• Losses up to 5 % ( all ages )

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Pathologic Findings (PMWS)

• Enlarged inguinal lymph nodes• Gastric ulceration• Enlarged kidneys (pdns)• Interstitial pneumonia• Bronchopneumonia

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Technical data

• Mortality up to 25-30 %• Daily gain lowered - after weaning

- in fattening period• Higher feed conversion

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Epidemiological

• All types of farms are dealing with pmws ( also SPF herds )

• Only reproductive part is not affected• 100 % prevalence of pcv2 antibodies• Influence of management factors• Frequently in combination with PRRS

Page 25: PCV2 and PRRS in relation to PMWS, secondary infections ... · PDF filePMWS, secondary infections and management factors F. Dirven ... (pac man) are destroyed ... parvo 26, 30 weeks

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Secondary infections

• M. Hyopneumoniae: vaccination (double shot) relapses

vaccination in pmws context

• APP : Type 2 and 9.

• Haemophilus parasuis: frequently involved

• Pasteurella / bordetella : sneezing/ coughing

• Streptococcus : different types

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Prevention and control

Reduce the economical losses by• Reducing infection pressure ( sec. inf.)• Increase the immune status ( increase of

passive and active immunity )• Vaccination sows during gestation with

pcv2 vaccin

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Vaccination• Serotherapy ( difficult and risky)

• New safe vaccin (sow vaccination)• Maternal PCV antibodies (by sow vaccination) are

protecting for PMWS (challenge at 3 weeks age gives less clinicalpmws signs)

• Maternal antibodies present until 4 weeks in a piglet• High pcv2 antibodies after several piglet vaccinations (min.

4 weeks old) gave also protection against PMWS, butimmunity only after 25 days

• Conlusion: Vaccination of piglets after 4 weeks of age is tolate (antibody production only 25 days later), herdvaccination is more economic en efficious

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Passive immunity by piglets

• Bodyweight at birth: sow feeding schedulefeed composition ( vitamins, minerals etc.)co infections ( prrs, ppv ,infl.)

• Colostral immunity : piglet and sow

• Lactation of the sow : geneticallyduration

• Weight at weaning : 5 – 7 kg bodyweight

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Active immunity of pigletAfter weaning passive immunity turns to active immunity

• Feed intake• Feed composition• Housing• Stress factors• Genetics• Vaccinations

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Reducing infection pressure in general

• Strict biosecurity, no animals or semen from outside unless

quarantine

• Hygiene, cleaning and disinfect every room , sterile instruments

• Cross fostering only strictly necessarily in first days

• All in all out systems• Separation or euthanasia ( sick animals to hospital

room)

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Reducing infection pressure specific

• Which infections are present? ( prrs, m.hyo, influenza, app, h. parasuis, pasteurella etc.)

• Primairy and secundairy infections• How to reduce these infections?

(Starting up management measures, strategic antibiotic therapy, vaccination programs)

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Control of PMWS

Strictly carrying out of• Management programs• Vaccination programs • Antibiotic therapy

Monitoring

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Management factors

Hygiene Lower stock density Removal to hospital room

Biosecurity No (re) mixing Extra vitamins

Climate control Small groups Appropriate vaccination program

One site herds Feeding systems/schedule

rodents

All in all out Cross fostering

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Vaccination program exampledisease gilt sow pigletsauy 12,16 and 26 weeks Every 4 months 12 weeks

ery 12, 16 weeks lactation

parvo 26, 30 weeks lactationprrs 18 weeks Every 4 months 2 weeksm. hyo 17 weeks 1, 3 weeksapp 17 weeks Every 3 months 6, 10 weeksinfluenza Comb auy Combination auy Combination auye. coli 3 weeks before

farrowingpcv gestation

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Monitoring

• Rapid reaction on new pathogens or reinfections

• Measurement tool for effect of vaccinations ( seroconversions)

• Health status• Eradication of certain diseases

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Depop and repop

• Only when severe economical losses due to PMWS

• Not in swine dense areas• No animals or semen from outside (spf)• Partial depop- repop.

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Conclusions• PCV2 and PRRS are responsible for lymphodepletion. It

opens “the door” to sec. infections by immunosuppression.• Also other cofactors give immunosupression (stress,

vaccinations)• The complex pcv2 - prrs- cofactors - sec. infections is

called PMWS• Prevention by reducing secondary Infection pressure and

increasing immunity• Control by management - vaccination programs and

strategic antibiotic therapies• New PCV2 vaccine is launched in a few country’s• Total repop is very risky and expensive, partial depop is

perhaps an option• Monitoring is important

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Thank you for you’re attention

Dr. F. Dirven