Pigs: a step-by-step guide to sampling and post-mortem

Page last updated: Thursday, 26 March 2020 - 6:29pm

Please note: This content may be out of date and is currently under review.

The Department of Primary Industries and Regional Development has created a sampling and post-mortem guide to assist veterinarians investigating pig disease. 

You can download a PDF copy from the Documents link on this page, or WA veterinarians can request a laminated hard copy by emailing livestockbiosecurity@dpird.wa.gov.au. 

A guide to sampling and post-mortem of pigs

Equipment required:

  • standard post-mortem kit including boning and skinning knives, scissors, scalpel blades, forceps
  • large shears or pruning secateurs to cut through ribs and jaw, bone saw
  • shears or small axe and hammer for brain removal
  • dry swabs, swabs in media (viral transport media, Amies media/charcoal), specimen jars for individual
  • fresh samples, 10% formalin, large containers for pooled formalin fixed samples
  • personal protection equipment – overalls, gloves, mask, eye protection
  • laboratory submission forms, permanent markers.

Sampling guidelines:

  • The base sample list is not exhaustive – consider submitting any other samples that may be useful (i.e. feed, water etc) and any lesions or abnormalities.
  • Fresh and fixed samples of any discrete lesions should also be submitted.
  • Consider sampling cohort animals (i.e. blood, faeces, swabs).
  • Complete a submission form to submit with samples. Tape to the outside of the esky/box of samples. Submissions forms and detailed packaging instructions are available on agric.wa.gov.au.
  • Consider sending photographs or videos to the DPIRD laboratory at DDLS@dpird.wa.gov.au .

Contact the DPIRD laboratory on (08) 9368 3351 prior to submission if you suspect a reportable, zoonotic or exotic disease.

Base sample list – pigs

Ante-mortem samples

Post-mortem samples

 
Fresh
Fixed

Blood:

  • Lithium heparin
  • Clotted
  • EDTA (+ smears)


Faeces


Swabs of discharges etc

Spleen
Lymph nodes
Tonsil
Ileum
Brain (swab or small section of cortex)
Liver
Lung
Kidney
Stomach contents
Faeces
Brain
(submitted whole)
Kidney
Liver
Lung
Spleen
Lymph nodes
Tonsil
Stomach
Small and large intestine
Ileum
Heart
Skeletal muscle
  • Chill bloods;
    consider spinning and separating serum and
    clot for transport.
  • Do not send sharps.
  • For swabs use the
    appropriate media
    then chill:
    • Amies or charcoal
      for bacteria
    • viral transport media for viruses and PCR
    • dry swabs (as a last resort) +/- a small drop of
      sterile saline for PCR.
  • Special media (e.g. Mycoplasma media) available on request.

Collect a 3x3cm piece of tissue and 
store in a sterile
container / sample pot.


Refrigerate or chill – DO NOT freeze.

Pool tissues into 10% neutral
buffered formalin
at a ratio of
10 parts formalin
to 1 part tissue.


Keep at room
temperature.


Seal containers and package well to
avoid spills.

 

 

Pig post-mortem procedure

1. Examine the animal for skin lesions, lesions on the eyes or ears, discharges from any orifice, evidence of diarrhoea, swollen joints or traumatic injuries (i.e. tail bite injuries).

Sample skin lesions by collecting pieces of affected skin into a sterile container and into formalin. Swab discharges or collect a fresh sample of the exudate/fluid.

Eyes and ears can be submitted whole in formalin for histopathology if they are abnormal.

2. In cases of lameness or joint swelling, open and sample the affected joints and a selection of major joints (i.e. hip joints, carpal joints, tarsus, stifle, elbow).

Incise through the skin with a knife. Incise the joint capsule with a sterile scalpel and collect a sterile swab of joint fluid into Amies. Consider submitting the joint whole or a sample of joint capsule in formalin.

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3. Position the pig right side down. Reflect both limbs and skin the flank. Examine the musculature and hip joint. Sample hindlimb skeletal muscle into formalin. Samples submitted in formalin should be <1cm thick.

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4. Open the abdomen and reflect the abdominal wall towards you; take care not to perforate the intestines. Look for peritoneal exudate; if present, sample into a sterile sample pot or swab into Amies media.

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5. Use shears to remove the rib cage by cutting along the bottom and top of the ribs. Trim away the diaphragm and muscle to expose the thoracic cavity.

6. Examine the organs in-situ. Record any abnormalities by writing a description and taking photographs. Collect any pleural or pericardial exudate into a sterile container or swab into Amies media.

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7. Skin underneath the neck and chin. Use shears to cut through the mandibular symphysis and split the lower jaw.

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8. Roll the head dorsally, split the lower jaw apart. Grasp and pull the tongue backwards while cutting the soft tissues along both mandibles.

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9. Examine the oral cavity. If there are oral lesions present (i.e. vesicles, ulcers) collect a sample into formalin, swabs into Amies, and swabs or epithelial tags into viral transport media or a sterile container. Vesicular fluid can be aspirated and placed in a plain blood tube.

10. Sample the tonsils. The tonsils are the pitted, textured area of the soft palate outlined below. Using scissors, remove the tonsils. Place half into formalin and half into a sterile container.

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11. Grasp the tongue and pull it caudally. Cut the hyoid bones, dissect along the trachea and oesophagus into the chest and remove the thoracic viscera all together. You will need to cut through the oesophagus, aorta and caudal vena cava where they pass through the diaphragm.

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12. Examine the trachea, oesophagus, bronchial lymph nodes, lungs, pericardium and heart. Open the trachea and main stem bronchi.

Bread slice the lungs to ensure lesions deep in the lung are not missed.

13. Collect thin sections (no greater than 1cm thick) of lung, trachea, bronchial lymph node, oesophagus and any lesions into formalin. Collect a 3cm cube of fresh lung into a sterile container. If bronchial lymph nodes are enlarged or obvious, collect a fresh sample into a sterile container.

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14. Examine the pericardium and heart. Cut through the ventricles (see below). Collect a ‘T-shaped’ section of heart which includes left and right ventricular free wall and interventricular septum and add this to the formalin pot. The tissue should be <1cm thick.

Open the left and right ventricles and incise up into the atria and great vessels. Examine the heart valves. Sample any lesions into a sterile jar and into formalin and swab any exudates into Amies.

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15. In the abdomen, examine the spleen. Collect a 3cm cube of spleen into a sterile container and a thin section (<1cm) into formalin.

16. Cut the diaphragm away from the body wall. Grasp the mesenteric root and pull the viscera caudally, lifting the intestines and liver out of the abdomen and cutting the mesentery. The kidneys and urogenital tract should remain in the abdomen. Leaving the colon as the last point of attachment, incise the colon as far caudally as possible and collect a faecal sample.

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17. Dissect the liver from the intestines. Examine and bread slice the organ. Collect a 3x3cm fresh sample of liver into a sterile container and a <1cm thick section into formalin.

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18. Spread out the intestine by cutting through the mesenteric root. Identify the ileum, caecum and ileocaecal junction (below).

19. Collect a 5cm long section of ileum and place half into formalin and half into a sterile container. Collect an ileocaecal lymph node (see below) into both formalin and a sterile container.

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20. Examine the remaining sections of the intestinal tract. Open the stomach and examine the mucosa. Collect a sample of stomach contents into a sterile container and a piece of stomach into formalin.

21. Examine the small and large intestine. Open sections of all areas of the intestinal tract and examine the mucosa, especially in cases of diarrhoea. If there are abnormal contents or areas of mucosa target these areas; collect fresh intestinal contents or swabs in Amies.

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Collect short segments of duodenum, jejunum, caecum and colon. Take care not to scrape the mucosal surface of pieces of tissue placed into formalin.

22. Remove both kidneys, cut in half lengthways and examine the cortex, medulla and pelvis. Collect a 3x3cm piece of kidney into a sterile container. Collect a thin piece of kidney which includes cortex, medulla and pelvis into formalin.

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23. Examine the bladder. If there is evidence of urogenital disease, collect a sample of bladder into formalin and a urine sample into a sterile container.

24. Examine the urogenital tract (ovaries and uterus or testes). Bread slice these tissues. Collect fresh and fixed samples if required.

25. Remove the brain. Saw or split the head sagittally in a large pig or remove the calavarium with shears in a small pig. See the Brain removal guides on the DPIRD website for guidance. Collect a sample of fresh brain into a sterile container. A small piece of cortex (olfactory lobe or occipital cortex) is sufficient. Alternatively, collect a meningeal swab. The rest of the brain should be submitted whole in formalin.

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26. If there is a history of neurological signs, consider collecting additional samples such as spinal cord and peripheral nerve.

27. All samples should be labelled clearly. Samples should be submitted as described in the sampling guidelines with a completed submission form.

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Contact the lab on (08) 9368 3351 prior to submission if you suspect a zoonotic, reportable or exotic disease.

For other livestock veterinary bench guides, see our Sampling and post-mortem guides webpage.

Contact information

Livestock Biosecurity