Display options
Share it on

Porcine Health Manag. 2018 Feb 01;4:2. doi: 10.1186/s40813-018-0079-4. eCollection 2018.

Comparison of serum pools and oral fluid samples for detection of porcine circovirus type 2 by quantitative real-time PCR in finisher pigs.

Porcine health management

Gitte Blach Nielsen, Jens Peter Nielsen, John Haugegaard, Sanne Christiansen Leth, Lars E Larsen, Charlotte Sonne Kristensen, Ken Steen Pedersen, Helle Stege, Charlotte K Hjulsager, Hans Houe

Affiliations

  1. MSD Animal Health Nordic, Havneholmen 25, 1561 Copenhagen V, Denmark.
  2. 2Department of Veterinary and Animal Sciences, University of Copenhagen, Grønnegårdsvej 2+8, 1870 Frederiksberg C, Denmark.
  3. Porcus Veterinary Pig Practice, Ørbækvej 276, 5220 Odense, SØ Denmark.
  4. National Veterinary Institute, Henrik Dams Allé, Bygning 205B, 2800 Kgs. Lyngby, Denmark.
  5. SEGES Pig Research Centre, Vinkelvej 11, 8620 Kjellerup, Denmark.
  6. Ø-vet A/S, Køberupvej 33, 4700 Næstved, Denmark.

PMID: 29435356 PMCID: PMC5793352 DOI: 10.1186/s40813-018-0079-4

Abstract

BACKGROUND: Porcine circovirus type 2 (PCV2) diagnostics in live pigs often involves pooled serum and/or oral fluid samples for group-level determination of viral load by quantitative real-time polymerase chain reaction (qPCR). The purpose of the study was to compare the PCV2 viral load determined by qPCR of paired samples at the pen level of pools of sera (SP) from 4 to 5 pigs and the collective oral fluid (OF) from around 30 pigs corresponding to one rope put in the same pen. Pigs in pens of 2 finishing herds were sampled by cross-sectional (Herd 1) and cross-sectional with follow-up (Herd 2) study designs. In Herd 1, 50 sample pairs consisting of SP from 4 to 5 pigs and OF from around 23 pigs were collected. In Herd 2, 65 sample pairs consisting of 4 (SP) and around 30 (OF) pigs were collected 4 times at 3-week intervals.

RESULTS: A higher proportion of PCV2-positive pens (86% vs. 80% and 100% vs. 91%) and higher viral loads (mean difference: 2.10 and 1.83 log(10) PCV2 copies per ml) were found in OF versus SP in both herds. The OF cut-off value corresponding to a positive SP (>3 log(10) PCV2 copies per ml) was estimated to 6.5 and 7.36 log(10) PCV2 copies per ml for Herds 1 and 2, respectively. Significant correlations between SP and OF results were found in Herd 1 (rho = 0.69) and the first sampling in Herd 2 (rho = 0.39), but not for the subsequent consecutive 3 samplings in Herd 2.

CONCLUSIONS: The proportion and viral loads of PCV2 positive pens were higher in collective OF (including up to 30 pigs) compared to SP (including 4-5 pigs) of the same pens. Also, OF seemed to detect the PCV2 infection earlier with OF values just below 6.5 (Herd 1) and 7.36 (Herd 2) log(10) being associated with a negative SP for the same pen. Nevertheless, a statistically significant correlation between SP and OF could not be found for all sampling time points, probably due to a high within-pen variation in individual pig viral load becoming very evident in SP of only four or five pigs. Consequently, the results imply that OF is well suited for detecting presence of PCV2 but less so for determining the specific viral load of pigs in a pen.

Keywords: Diagnostics; Finishers; Oral fluid; Pooling; Porcine circovirus type 2; Serum

Conflict of interest statement

Permission to conduct the field trial in Herd 2 was received from the Danish Health and Medicines Authority (License no. 2014022507) and a written consent was obtained from the herd owner.Not applicab

References

  1. J Vet Diagn Invest. 2011 Mar;23(2):233-40 - PubMed
  2. Vaccine. 2009 Dec 9;27(52):7313-21 - PubMed
  3. PLoS One. 2015 Oct 02;10(10):e0139586 - PubMed
  4. Prev Vet Med. 2017 Jun 1;141:14-21 - PubMed
  5. Transbound Emerg Dis. 2011 Apr;58(2):121-7 - PubMed
  6. Vet J. 2011 Jan;187(1):23-32 - PubMed
  7. Vet Microbiol. 2011 Apr 21;149(1-2):225-9 - PubMed
  8. PCR Methods Appl. 1994 Jun;3(6):365-8 - PubMed
  9. J Vet Diagn Invest. 2011 Mar;23(2):248-53 - PubMed
  10. Vet Microbiol. 2008 Dec 10;132(3-4):260-73 - PubMed
  11. Vet Res. 2010 May-Jun;41(3):31 - PubMed
  12. Vet Microbiol. 2014 Dec 5;174(3-4):296-301 - PubMed
  13. Prev Vet Med. 2011 Mar 1;98(4):250-8 - PubMed
  14. Prev Vet Med. 2000 May 30;45(1-2):83-106 - PubMed
  15. J Appl Microbiol. 2012 Nov;113(5):1014-26 - PubMed
  16. Clin Vaccine Immunol. 2011 Nov;18(11):1865-71 - PubMed
  17. Anim Health Res Rev. 2010 Dec;11(2):217-34 - PubMed
  18. Vaccine. 2009 Jun 19;27(30):4031-7 - PubMed
  19. J Vet Diagn Invest. 2008 May;20(3):274-82 - PubMed
  20. Virus Res. 2012 Mar;164(1-2):78-89 - PubMed
  21. Vaccine. 2008 Jun 25;26(27-28):3443-51 - PubMed
  22. J Virol Methods. 2004 Apr;117(1):75-80 - PubMed
  23. N Engl J Med. 1978 Oct 26;299(17):926-30 - PubMed
  24. J Vet Diagn Invest. 2015 Mar;27(2):140-9 - PubMed
  25. J Vet Diagn Invest. 2008 Mar;20(2):156-63 - PubMed
  26. Vet Microbiol. 2011 Apr 21;149(1-2):91-8 - PubMed
  27. Vet Microbiol. 2009 Mar 30;135(3-4):272-82 - PubMed
  28. Vet J. 2012 Jul;193(1):180-4 - PubMed
  29. J Virol Methods. 2004 Dec 15;122(2):171-8 - PubMed
  30. Vet Microbiol. 2009 Jan 1;133(1-2):172-8 - PubMed
  31. Prev Vet Med. 2012 May 1;104(3-4):292-300 - PubMed
  32. Vet Microbiol. 2005 Dec 20;111(3-4):223-9 - PubMed
  33. Prev Vet Med. 2003 May 15;58(3-4):171-8 - PubMed
  34. Virus Res. 2012 Mar;164(1-2):10-9 - PubMed
  35. Vet Microbiol. 2012 Dec 28;161(1-2):229-34 - PubMed
  36. Vet Res. 2016 Dec 3;47(1):121 - PubMed

Publication Types