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Title: You can pool faecal samples from individual pigs to test for Porcine Circovirus Type 2 and Lawsonia intracellularis using real-time PCRs
Type: Conference abstract for conferenceConference abstract for conference
Participant(s):
Forfatter:  Holyoake, Patricia K.
Department of Primary Industries, Australia

Author:  Hjulsager, Charlotte Kristiane (Cwisno: 39095)
Technical University of Denmark
Email:

Author:  Larsen, Lars Erik (Cwisno: 39284)
Technical University of Denmark
Email:

Forfatter:  Pedersen, Ken S.
University of Copenhagen

Forfatter:  Johansen, Markku
Pig Research Centre, Denmark

Forfatter:  Stege, Helle
University of Copenhagen

Forfatter:  Moore, Karen
Department of Primary Industries, Australia

Author:  Ståhl, Marie (Cwisno: 45700)
Technical University of Denmark
Email:

Author:  Angen, Øystein (Cwisno: 39395)
Technical University of Denmark

Forfatter:  Nielsen, Jens Peter
University of Copenhagen
Abstract: Introduction Real-time PCR tests have been developed to detect and quantify Porcine Circovirus type 2 (PCV2) and Lawsonia intracellularis in pigs’ faeces. Pooling of individual faecal samples is often used to reduce the costs of diagnostic testing. The objective of this study was to evaluate any change in the test sensitivity of PCV2 and L. intracellularis real-time PCR when individual faecal samples were pooled. Materials and Methods Forty eight faecal samples were collected from the rectum of individual pigs (>10 weeks) from four farms. Faecal samples were classified as diarrhoea +/- based on subjective assessment of consistency. Three individual samples were combined to make 16 pooled samples (8 diarrhoea; 8 non-diarrhoea). Individual and pooled samples were tested using real-time PCR tests specific for PCV2 and L. intracellularis. A positive result in any of the three individual samples was deemed “group positive”. Changes in test sensitivity after combining the three individual samples were evaluated. Results The sensitivity and specificity of the pooled faecal samples for L. intracellularis were 86.4% and 100%, respectively. The sensitivity and specificity of the pooled faecal samples for PCV2 were 97% and 100%, respectively. Conclusions These preliminary results suggest that three individual faecal samples may be pooled for PCV2 or L. intracellularis testing using real-time PCR with minimal loss of sensitivity. Under the conditions of this study, the sensitivity of pooling was reduced when quantities of L. intracellularis or PCV2 in individual samples were low.
Published:
File(s):
Presented at: 4th European Symposium of Porcine Health Management, Bruges
See the publication in DTU Orbit See the publication in DTU Orbit

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