کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
5800346 | 1555355 | 2014 | 6 صفحه PDF | دانلود رایگان |

- The AUC of PCV2 load during the production period was used as infection indicator.
- Three pig subpopulations with different serum PCV2 loads and ADWG were identified.
- ADWG in PCV2-SD affected pig farms is modulated by serum PCV2 load.
- The higher the PCV2 load, the lower the ADWG from weaning to slaughter age.
Porcine circovirus type 2 (PCV2) is a ubiquitous virus that mainly affects nursery and fattening pigs causing systemic disease (PCV2-SD) or subclinical infection. A characteristic sign in both presentations is reduction of average daily weight gain (ADWG). The present study aimed to assess the relationship between PCV2 load in serum and ADWG from 3 (weaning) to 21 weeks of age (slaughter) (ADWG 3-21). Thus, three different boar lines were used to inseminate sows from two PCV2-SD affected farms. One or two pigs per sow were selected (60, 61 and 51 piglets from Pietrain, Pietrain Ã Large White and Duroc Ã Large White boar lines, respectively). Pigs were bled at 3, 9, 15 and 21 weeks of age and weighted at 3 and 21 weeks. Area under the curve of the viral load at all sampling times (AUCqPCR 3-21) was calculated for each animal according to standard and real time quantitative PCR results; this variable was categorized as “negative or low” (<104.3 PCV2 genome copies/ml of serum), “medium” (â¥104.3 to â¤105.3) and “high” (>105.3). Data regarding sex, PCV2 antibody titre at weaning and sow parity was also collected. A generalized linear model was performed, obtaining that paternal genetic line and AUCqPCR 3-21 were related to ADWG 3-21. ADWG 3-21 (mean ± typical error) for “negative or low”, “medium” and “high” AUCqPCR 3-21 was 672 ± 9, 650 ± 12 and 603 ± 16 g/day, respectively, showing significant differences among them. This study describes different ADWG performances in 3 pig populations that suffered from different degrees of PCV2 viraemia.
Journal: Veterinary Microbiology - Volume 174, Issues 3â4, 5 December 2014, Pages 296-301