Respiratory disease in pigs Flashcards

1
Q

Why are respiratory diseases such a major problem to the pig industry?

A

Animal welfare
Performance & production
Mortality
Meat quality

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2
Q

How does respiratory disease impact production in pigs?

A

Morbidity and mortality.
Treatment/veterinary costs/need for vaccination.
Reduced growth rates/increased days to slaughter.
Reduced FCE (energy into immune system).
Variation in supply – growth rates, back fat.
Penalties at abattoir – slow line, increased trimming.
Assurance schemes/market (multiplier).
Environmental impact- more food, slurry, antibiotics.

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3
Q

What pathogens are involved in respiratory disease of pigs?

A

-Bacterial/mycoplasmal
-Viral
-Parasitic
Secondary bacterial infection of lung tissue already compromised by primary pathogens frequently occurs.
Often more than one agent involved.
Often highly contagious.
Spread by direct or aerosol contact.
Or indirect via birds and vehicles.

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4
Q

What defence mechanisms in the pig are present against respiratory infection?

A
Nasal chambers
- Turbinates create turbulence. 
- Changing airway diameters alter speed
Mucociliary apparatus.
Cough reflex.
Pulmonary alveolar macrophages.
Neutrophil invasion.
Antibody production (airway IgA, alveolar IgG).
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5
Q

Respiratory disease in pigs is multifactorial…

A

Environment
Management
Breed and age
Exposure to pathogens

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6
Q

What clinical signs are seen in pig respiratory disease?

A
Coughing (often 1st thing noticed). 
Dyspnoea +/- hyperpnoea.
Snuffling sounds (nasal obstruction).
Heart failure and cor pulmonale (severe/chronic).
Pleurisy.
Anorexia.
Ocular discharge.
Sudden death.
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7
Q

How would you diagnose respiratory disease in pigs?

A

History and CE/observation may provide tentative diagnosis.
Clinical examination often limited.
-Brief auscultation may be possible and increased lung sounds may be evident:
-Wheezing – narrowed airways
-Bubbling sounds – blocking of bronchioles
-Squeaking sounds – pleuritic
-Harsh rubbing sounds – pleurisy
This must be confirmed with lab tests/PME.
Abattoir surveillance data may indicate current diseases.
Remember mixed infections!

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8
Q

What sort of respiratory diseases do you see in pre-weaned pigs?

A
Progressive atrophic rhinitis.
Bordetella bronchisepticum.
Inclusion body rhinitis (pig CMV).
PRRSv (reproductive and respiratory syndrome virus).
Enzootic pneumonia (Mycoplasma sp).
Glassers disease (Haemophilus parasuis).
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9
Q

What sort of respiratory diseases do you see in weaners, growers and fatteners?

A
Bordetella bronchiseptica
Glassers disease
Actinobacillus pleuropneumonia
Pasteurella multocida
Mycoplasma hyopneumonia (EP) / hyorrhinis
PRRSV
Porcine respiratory coronavirus (PRCV)
Influenza
PMWS?/PCVAD
(Aujeszky’s disease (pig herpesvirus 1))
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10
Q

What are some examples of significant respiratory disease in non-immune adult pigs?

A
Glassers disease
Actinobacillus pleuropneumoniae
Pasteurellosis
Enzootic pneumonia
PRRSV
Influenza
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11
Q

What is progressive atrophic rhinitis?

A

Toxigenic Pasteurella multocida in association with Bordetella bronchiseptica.
Colonisation of nasal mucosa by B.b with production of cytotoxin – allowing P.m to invade.
PM damages osteoblasts with osteolytic toxin and enhances osteoclast activity.
CS usually seen at 3-9 wks age – sneezing, nasal discharge/h+, facial deformity - later.
Reduced growth rates and increased risk of pneumonia.

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12
Q

How to diagnose progressive atrophic rhinitis?

A

Causal organisms can be cultured from nasal swabs, serology for B. bronchiseptica.
PME – Section snout at level of 2nd premolar – damage to turbinates assessed on 0 (no damage) -5 (severe) scale

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13
Q

How to treat and control progressive atrophic rhinitis?

A

Antibiotics may help if early
Vacc: sows 2-6wks before farrowing
Control: Depop-repop with AR-free stock, strategic medication if CS, screening herds with ELISA for B. bronchiseptica

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14
Q

Bordetella bronchisepticum in pigs…

A

Found in most pig populations.
Generally mild, self-limiting rhinitis (non-progressing).
Therefore, clinically and economically of little importance.
Only a problem when in combination with toxigenic Pasteurella multocida.

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15
Q

What is inclusion body rhinitis in pigs?

A

Porcine Cytomegalovirus (herpesvirus)
>90% UK herds affected
Transmission pig-pig or aerosol
Mostly young pigs but outbreak in naive herd may affect all ages
CS: sneezing, serous nasal discharge and brown ocular discharge, high morbidity, low mortality.

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16
Q

How to diagnose and control inclusion body rhinitis in pigs?

A

Diagnosis: ELISA, inclusion bodies from nasal swabs.
Control: Maintain closed herd, protect suckling pigs from exposure.

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17
Q

What is PRRS?

A

PRRS virus – Arterivirus.
Virus replicates in and destroys macrophages and endothelial cells →vasculitis.
Mixed infections with other resp pathogens very common.
Clinical signs – weaned pigs, mild coughing, sneezing, tachypnoea, innapetence, increased mortality.

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18
Q

How to treat PRRS?

A

In-feed/water antibiotics to cover period at risk – to reduce 2o bacterial infections (usually 6-8 wks).

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19
Q

How to control PRRS?

A

Early weaning off-site to break cycle, review pig flow, consider partial dep-pop of 1st and 2nd stage housing, vaccination @ weaning and breeding stock.
- Vaccination:
Modified live (avoid in pregnant)
Killed (breeders)
Use in breeders and growers.
- Stabilise infection:
Expose gilts / vaccinate prior to breeding.
Stream grower pigs in separate airspaces.
- Eradication:
Stabilise sow/gilt infection and then depopulate all exc sows. Wean off-site to rest buildings for period.
- Depop-repop:
Infection transmits up to 3km.
Purchase uninfected stock and quarantine / test at isolation.
Purchase uninfected semen.

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20
Q

What is enzootic pneumonia?

A

30-80% pigs have lesions at slaughter.
Mostly caused by Mycoplasma hyopneumoniae with frequent superimposed infection, esp. Pasteurella multocida.
Spread pig-pig mostly, also aerosol and wind (2 miles).
Multifactorial – housing, temperature, humidity, mixing different ages/sources, overcrowding, continuous throughput systems.
Immunity short-lived, no colostral transfer.

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21
Q

What is the typical clinical picture of M.hyopneumoniae (that causes enzootic pneumonia)?

A

Weaned pigs
↑coughing – non-productive, worsened by exercise
↓FCE - <14%
Variance in growth - 17% reduction in DLWG
2º infection

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22
Q

How to diagnose M.hyopneumoniae (enzootic pneumonia)?

A
Herd history
Clinical signs
Lung lesions at slaughter/PME
Culture (difficult) /PCR
Histology
Serology
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23
Q

How to treat M.hyopneumoniae (enzootic pneumonia)?

A

Acute cases may respond to antibiotics but only if early.

Strategic dosing of growing pigs may be necessary on some farms.

24
Q

Control of M.hyopneumoniae (enzootic pneumonia)…

A
Improve environment &amp; management...
-ventilation, groupings, husbandry. 
All-in, all-out management of growers. 
De-pop, re-pop infected herd. 
Partial de-pop and tx – original breeding stock retained and treated (10d), all other pigs removed
Medicated early weaning (removed at 5d)
Vaccination (1 and 3wks).
25
Q

What is Glässer’s Disease?

A

Haemophilus parasuis – found in the nasal cavity of many pigs
Usually a 2ry invader but can also be a primary pathogen (so usually relies on other pathogens to take effect first).
Associated with polyserositis, arthritis and meningitis. Resp. signs usually in weaners - 4 months of age as piglets have colostral immunity
CS: acute onset pyrexia, cough, dyspnoea, lameness, swollen joints, CNS signs.

26
Q

How to diagnose Glässer’s Disease?

A

History, cs, PCR, ELISA, PME

27
Q

How to treat and control Glässer’s Disease?

A

Tx: Antibiotic injections to sick pigs, in-feed/water Abs to contacts. Early tx essential.

Control: Avoid stress, strategic medication at times of high risk, Vaccination <10 wks of age

28
Q

What is APP?

A

Actinobacilus pleuropneumoniae.
12 capsular subtypes but cross reactions occur
Produces toxins that kill macrophages and neutrophils
Explosive outbreaks of pneumonia with high morbidity and mortality – to - seroconversion with few clinical signs
CS: sudden onset, sudden deaths, pyrexia, dyspnoea (jerky), coughing, blood-stained foamy mucus from mouth and nose.

29
Q

How to diagnose APP?

A

ELISA, culture from nasal swabs/lung tissue, PCR, PME- fibrinous pleuritis and firm lung infarcts.

30
Q

How to treat and control APP?

A

Tx: Parenteral Abs, Isolation, NSAIDs.

Control: Closed herd, eradicate with de-pop, re-pop, wean piglets at 10d and move to separate unit.

31
Q

What is pasteurellosis?

A

Pasteurella multocida –important as secondary invaders – EP, AR, APP
Can also act as a primary pathogen – resulting in pneumonic pasteurellosis or pasteurella septicaemia
CS: mostly sporadic dz of 10-20wk old growers, pyrexia, dyspnoea, open-mouth breathing, coughing, sudden death.

32
Q

How to treat and control Pasteurellosis?

A

Tx: Parenteral Abs.

Control: improve management, segregated early weaning.

33
Q

What is Aujesky’s disease?

A

Pseudorabies.
Swine herpesvirus type 1 (SHV1)
Notifiable and not present in UK (present in NI until 2012).
Clinical presentation is age and strain specific:
- <4 wks: neurological, mortality <100%.
- 4 wks – 5 months: neurological + pneumonia, mortality <15%
- Adult: few clinical signs
–Abortion and mummification
–URT coughing
–Rare neurological signs
Slaughter policy in UK, targeted vaccination in NI, Ireland, Spain.

34
Q

What is swine influenza?

A

Influenza A virus, orthomyxovirus
Direct pig-pig transmission, also airborne
Mostly young pigs but rapid involvement of up to 100% pigs
CS: Pyrexia, lethargic, prostrate, skin erythema, anorexia, severe cough sneezing, dyspnoea, conjunctivitis, pregnant sows may abort
Recovery equally rapid (5 days).

35
Q

How to diagnose swine influenza?

A

ELISA, PCR, PME – severe congestion of upper resp. tract, enlarged LNs, necrotising bronchiolitis.

36
Q

How to treat and control swine influenza?

A

Tx: Abs to prevent 2o bacterial infection.

Control: Closed herd.

37
Q

What is PRCV?

A

Porcine respiratory coronavirus.
May be subclinical, usually mild disease.
PME: Interstitial pneumonia, hyperplasia of bronchial epithelium, virus in macrophages
The exact role of the virus is unknown but it is thought to predispose to other respiratory diseases

38
Q

What are the clinical signs of PRCV?

A
Coughing:
- In growers and finishers (endemic).
- Across all age groups (epizootic)
Absence of other causes:
- Occasional pasteurellosis.
Not usually a significant problem but:
- Contributes to multifactorial pneumonia.
- Indicates biosecurity issue on high health herd.
39
Q

What is PMWS?

A
PCV-2 associated disease – respiratory component is very important. 
Immunosuppressive.
90% UK pigs seropositive.
Involved in many disease syndromes.
Can cause respiratory signs in growers.
40
Q

What are some examples of parasites found in pigs?

A

Metastrongylus:

  • Relatively uncommon
  • Earth worm as intermediate host
  • Most likely in outdoor units
  • Worms found in lungs 20-24d after the pig consumes the egg containing L1
  • Coughing and dyspnoea in piglets or growers.

Ascaris suum:
- Milk spot liver most common symptom but coughing may be observed due to migrating larvae 1 wk after infestation.

41
Q

What is PRDC?

A

Porcine Respiratory Disease Complex.
PRDC results from a combination of infectious agents and environmental stressors.
Results in reduced performance, increased medication costs and increased mortality.
Typically 30-70% of pigs will be affected, with a mortality rate of 4-6 %.
Usually seen in pigs 14-20wks old.
CS: Lethargy, anorexia, fever, nasal discharge, ocular discharge, coughing, laboured breathing, purple discolouration of skin, especially of ear-tips – variable CS, depending on pathogens involved and baseline level of immunity.

42
Q

What agents are involved in PRDC?

A
Viral agents often involved include:
PRRS*
Coronavirus
Swine Influenza virus
Circovirus (PCV2)*
The bacterial agents often involved, which may act alone or together, are primarily:
Mycoplasma hyopneumoniae*
Haemophilus parasuis
Streptococcus suis
Bordetella bronchiseptica
Actinobacillus suis
Actinobacillus pleuropneumoniae

*Considered most important.

43
Q

What is the epidemiology of PRDC?

A

A new-born pig receives colostral protection from its mother – dependent upon her immunity.
This immunity will decline over time, with young pigs becoming susceptible to challenge.
As they become exposed, infection follows the usual pattern of colonisation, replication, excretion and immune development.
Disease may occur following replication and excretion phases and duration will depend upon the level of replication and the agents involved.
In the typical continual production system of, say, weekly farrowings, older pigs are a source of infection for younger pigs, maintaining a cycle of infection
However, it should also be realised that this source of infection is also relevant to the breeding herd. A trickle of challenge to immune sows will maintain their immunity and help maximise colostral protection
Conversely excessive challenge may override their immunity, rendering them a source of infection for their own and other litters.

44
Q

How would you diagnose PRDC?

A
  • Detailed clinical history, including age of onset, morbidity and mortality estimates, response to treatment, and the most current vaccination status of the sows and pigs.
  • On-farm/laboratory post-mortem examination of affected pigs with appropriate diagnostic sampling.
  • Cross-sectional blood sampling of the herd to establish epidemiological pictures of suspected pathogens.
  • Use of abattoir data for slaughter pigs to indicate levels of lung consolidation and pleurisy and the involvement of other pathogens (e.g. Actinobacillus pleuropneumonieae- Acpp) (BPHS).
45
Q

How can PRDC be controlled?

A

Medication and vaccination are fundamental to the long-term control of PRDC but are no substitute for sound management principles.
- Even the best and most extensive programmes will not overcome extreme disease where pig-flow and management have not been corrected.
Vaccines should only be used with full diagnostic knowledge, including targeting the timing of vaccination. Vaccines againstMycoplasmaand PCV2 are probably the most widely used vaccines in young piglets, but strategies are also needed to identify additional pathogens for which vaccine can be introduced.

46
Q

How can PRDC be controlled?

A

Medication and vaccination are fundamental to the long-term control of PRDC but are no substitute for sound management principles.
- Even the best and most extensive programmes will not overcome extreme disease where pig-flow and management have not been corrected.
Vaccines should only be used with full diagnostic knowledge, including targeting the timing of vaccination. Vaccines againstMycoplasmaand PCV2 are probably the most widely used vaccines in young piglets, but strategies are also needed to identify additional pathogens for which vaccine can be introduced.

47
Q

What medication is administered for PRDC?

A
  • Where bacterial involvement is identified, strategic medication can be used to supplement vaccination programmes.
  • Prophylactic or metaphylactic use may be appropriate where the timing of disease is readily identifiable.
  • Parenteral or oral medication (via water or in feed) can be appropriate. In high disease-level situations, where bacteria play a significant role, long-term suppressant medication – usually via the feed – is still widely used.
  • However, in such situations a full herd analysis with attention to pig-flow and management and preventative vaccination should be made in order to reduce such dependency on antibiotic use.
48
Q

What is the gold standard for trying to control the respiratory diseases involved in PRDC?

A

All-in-all-out.

  • The first rule of control must be separation of age groups by building or room and application of hygiene controls between occupations by the use of ‘all-in-all-out’ (AIAO) principles.
  • Washing, disinfecting, drying and resting are fundamental requirements.
  • To achieve AIAO production, the pig-flow through the buildings must be established and maintained.
49
Q

PRDC - Buildings…

A

Match production to suit building provision, identifying bottlenecks
Where necessary alter buildings (by divisions, new buildings, etc.)
Consider what the correct stocking rates are for the buildings.
Ensure buildings are adequately ventilated – to remove polluted air and excess heat without draughts or over-ventilation.

50
Q

PRDC - Production…

A

Review productivity in light of building availability and, where appropriate, consider batch production, i.e. produce a larger number of pigs less often to enable filling and emptying of buildings.
Ensure evenness of production from the breeding herd. This will avoid overstocking or under-stocking and will reduce the temptation to mix ages.
Avoid back-mixing slow-growing pigs to younger groups. If thinning is necessary, forward mixing of the best pigs in a group is less hazardous.

51
Q

PRDC - Sick pigs

A

Deal with sick pigs correctly. Not only is the sick pig a welfare concern in its own right, it is a threat to healthy pigs.
Therefore:
Hospitalise sick pigs.
Never return recovered pigs to the mainstream system, especially by mixing with younger groups.
Hospital pens should be clean and cleanable, isolated but well attended by stockmen. Washing hands and changing boots/overalls after attending hospitals should be standard.

52
Q

PRDC - Partial depopulation

A

It may be appropriate to apply partial depopulation strategies in which older infected animals are removed from the farm, creating a break in production
Such actions should be combined with attention to disease control in the younger pigs to prevent the situation rapidly repeating itself once re-stocking has taken place. This may in itself involve an increase in vaccine use in sows or piglets, or the administration of medication to sows and/or piglets, either to eliminate or severely suppress specific pathogens.
The actual programme needed will depend on each farm situation but any potential depopulation should allow refurbishment, alteration and review of accommodation with respect to pig-flow and building quality.

53
Q

PRDC - Full depopulation…

A

In the extreme case, full herd depopulation may be appropriate, particularly where major rebuilding is needed and disease levels are unsustainable
Herd depopulation and repopulation requires meticulous advance planning to minimise loss of production whilst achieving the necessary cleaning
A minimum unoccupied period is needed (generally 6 weeks), with thorough cleaning and disinfection, aided by timing the programme such that the empty period is in mid-summer – June provides the highest intensity of sunlight which aids cleaning and drying.

54
Q

PRDC - Biosecurity…

A

To limit the spread and occurrence of disease
To improve overall herd health
To increase the growth and efficiency of the herd
-Airborne eg windborne spread from neighbouring unit
-Mechanical eg vehicles, machinery and equipment
-People, footwear and clothing
-Birds, rats, mice, insects and other animals
(domestic, farm and wildlife)
-Contaminated feed, water, semen, bedding etc.

55
Q

What is the British Pig Health Scheme?

A

Voluntary scheme run by AHDB pork
Team of specialist Pig Vets who visit abattoirs and examine 50 pigs from each slap mark killed that day
They record Enzootic Pneumonia like lesions, Pleuropneumonia (APP-like lesions), Viral Pneumonia, Pleurisy, Pericarditis, Peritonitis, Pyaemia, Milk spot, Abscesses, Liver Scarring, Papular Dermatitis (Mange-like lesions) and Tail Bites
This helps to monitor overall health, and can give an early identification of emerging disease problems or outbreaks.

56
Q

What is the British Pig Health Scheme?

A

Voluntary scheme run by AHDB pork.
Team of specialist Pig Vets who visit abattoirs and examine 50 pigs from each slap mark killed that day.
They record Enzootic Pneumonia like lesions, Pleuropneumonia (APP-like lesions), Viral Pneumonia, Pleurisy, Pericarditis, Peritonitis, Pyaemia, Milk spot, Abscesses, Liver Scarring, Papular Dermatitis (Mange-like lesions) and Tail Bites.
This helps to monitor overall health, and can give an early identification of emerging disease problems or outbreaks.