The index herd with PMWS in Sweden: presence of serum amyloid A, circovirus 2 viral load and antibody levels in healthy and PMWS-affected pigs

• Published in: Acta veterinaria scandinavica 2009-03, Vol.51 (13), p.13-13, Article 13
• Main Authors: Wallgren, Per, Brunborg, Inger Marit, Blomqvist, Gunilla, Bergström, Gunnar, Wikström, Frida, Allan, Gordon, Fossum, Caroline, Jonassen, Christine Monceyron
• Format: Article
• Language: English
• Subjects: Animal and Dairy Science; Animal models in research; Animals; Antibodies; Antibodies, Viral - blood; Circoviridae Infections - epidemiology; Circoviridae Infections - immunology; Circoviridae Infections - veterinary; Circoviridae Infections - virology; Circovirus - immunology; Disease Outbreaks - veterinary; DNA, Viral - blood; Glycoproteins; Husdjursvetenskap; Immune response; Male; Measurement; Physiological aspects; Porcine Postweaning Multisystemic Wasting Syndrome - blood; Porcine Postweaning Multisystemic Wasting Syndrome - epidemiology; Porcine Postweaning Multisystemic Wasting Syndrome - immunology; Porcine Postweaning Multisystemic Wasting Syndrome - virology; Serum Amyloid A Protein - metabolism; Sweden - epidemiology; Swine; Veterinary Science; Veterinärmedicin; Viral antibodies; Viremia; Wasting syndrome
• ISSN: 1751-0147; 0044-605X; 1751-0147
• DOI: 10.1186/1751-0147-51-13

Postweaning Multisystemic Wasting Syndrome (PMWS) is an emerging disease in pigs of multifactorial origin, but associated to porcine circovirus type 2 (PCV2) infection. PMWS was first diagnosed in Sweden at a progeny test station that received pigs aged five weeks from 19 different nucleus herds on the day after weaning. The objective of this study was to examine, for the first time in an index outbreak of PMWS, the relationship between PCV2 virus, antibodies to PCV2 and serum amyloid a (SAA) in sequentially collected serum samples from pigs with and without signs of PMWS. Forty pigs of the last batch that entered the station at a mean age of 37.5 days were monitored for signs of PMWS during the first 55 days after arrival. Serum was collected on six occasions and analysed for presence of PCV2 DNA and antibodies to PCV2, as well as for levels of SAA. Four of the pigs (10%) were concluded to have developed PMWS, with necropsy confirmation in three of them. These pigs displayed low levels of maternal antibodies to PCV2, more than 107 PCV2 viral DNA copies per ml serum and failed to mount a serological response to the virus. Starting between day 23 and 34 after arrival, an increase in PCV2 viral load was seen in all pigs, but PCV2 did not induce any SAA-response. Pigs that remained healthy seroconverted to PCV2 as the viral load was increased, regardless of initially having low or high levels of PCV2-antibodies. In this index case of PMWS in Sweden, pigs affected by PMWS were not able to mount a relevant serum antibody response which contributed to the disease progression. The maximal PCV2 virus load was significantly higher and was also detected at an earlier stage in PMWS-affected pigs than in healthy pigs. However, a viral load above 107 PCV2 DNA copies per ml serum was also recorded in 18 out of 34 pigs without any clinical signs of PMWS, suggesting that these pigs were able to initiate a protective immune response to PCV2.