Detection of PRRSV circulation in herds without clinical signs of PRRS: Comparison of five age groups to assess the preferred age group and sample size

摘要

A cross-sectional study was conducted to find the most effective diagnostic approach to detect circulation of porcine reproductive and respiratory syndrome virus (PRRSV). The study was performed in 10 Dutch swine herds, with sows and fattening pigs or breeding stock. Herds did not experience clinical signs of PRRS during the last 6 months before sampling, but a PRRSV infection was confirmed at most 2 years before sampling. Blood samples were collected from 5 age groups: sows during early and late gestation, weaners at 9 weeks of age, fatteners or breeding stock at 16 and 22 weeks of age. For each category, 20 serum samples were examined; in total 100 serum samples per herd. Samples were analysed for PRRSV antibodies with ELISA (n = 1002), and rt-PCR when ELISA S/P-ratios were above 1.5 (n = 307) or below 0.4 (n = 187; random selection from each age group). A logistic regression analysis was used to obtain factors associated with the probability of virus detection in a pig (PCR positive test result). Herd, ELISA-result, and age group were included as explanatory variables. Variables remained in the model when statistically significant. ELISA results showed that none of the herds could be considered to be free of PRRSV infection. Mean PRRSV seroprevalence in unvaccinated animals varied between 18% and 82%, and mean PRRS-virus prevalence varied between 0% and 41%. In only one of the 10 herds, no PRRS-virus could be detected. The odds of finding PRRS-virus in blood samples were 8.6 (95% CI, 5.3-13.9) in pigs of 9 weeks of age and 4.6 (95% CI, 3.0-7.0) in pigs of 16 weeks of age, compared with fatteners of 22 weeks of age. This result indicates that 9- to 16-week-old pigs are the preferred age group to detect PRRS-virus, in herds without clinical signs of PRRS. We concluded that PRRS-virus circulation could be detected in 8 out of 9 of the study-herds, with a relatively low number of blood samples. Testing 12 blood samples in both rt-PCR and ELISA, with 6 samples in pigs 9 weeks of age and 6 samples in pigs 16 weeks of age, will lead to a cost-efficient first evaluation of the PRRSV infection-status in herds without clinical signs of PRRS