Abstract

BackgroundDefining shedding and exposure status for PRRSV is essential in herd stabilisation protocols and weaning-age pigs is a key subpopulation. Oral fluid (OF) sampling is a welfare-friendly and cost saving promising alternative to blood sampling. The first objective of our study was to compare the rate of detection of PRRSV-1 in individual serum sample, individual OF sample, litter-based OF sample, collected the day before weaning. The second objective was to evaluate the interest of pooling samples.ResultsThe study was performed on a 210-sows, PRRSV-1 exposed, with confirmed shedding, non-vaccinated against PRRSV, herd. 80 litters were sampled and 26 were viropositive and therefore included. The rate of detection of PRRSV-1 with RT-qrtPCR in blood samples, iOF and cOF was 67, 23 and 77%, respectively. The Ct values from RT-qrtPCR on collective OF were statistically lower if the serum of the piglet of the litter was positive. The lower the Cycle threshold (Ct) value of RT-qrtPCR on collective OF, the higher the probability that the serum sampled in the same litter was positive. Ability to detect PRRSV RNA after pooling was 67% for sera and 58% for cOF.ConclusionsThe rate of detection of PRRSV-1 was about the same in cOF and blood samples. Virus sequencing, if required, should be performed on individual serum samples. The smaller the Ct of a cOF sample from a litter, the greater the likelihood that the serum sample from a piglet of that litter is positive.A cost-effective and representative sampling protocol to monitor sow herds stabilisation of a sow batch could be: to collect both cOF and one serum sample per litter; to perform firstly RT-qrtPCR on pooled cOF; in case of negative results to consider the batch negative; in case of positive results in a unvaccinated herd or a killed vaccine vaccinated one to consider the batch positive; in case of positive result in a herd vaccinated with a modified live vaccine serum samples of litters with positive cOF should be tested for sequencing (selecting the litters with the lowest Ct for cOF).

Highlights

  • IntroductionDefining shedding and exposure status for PRRS virus (PRRSV) is essential in herd stabilisation protocols and weaning-age pigs is a key subpopulation

  • Defining shedding and exposure status for Porcine Reproductive and Respiratory Syndrome (PRRS) virus (PRRSV) is essential in herd stabilisation protocols and weaning-age pigs is a key subpopulation

  • Porcine Reproductive and Respiratory Syndrome (PRRS) is caused by a virus of the Arteriviridae family known as PRRS virus (PRRSV) and has become enzootic in most pig production areas [1]

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Summary

Introduction

Defining shedding and exposure status for PRRSV is essential in herd stabilisation protocols and weaning-age pigs is a key subpopulation. Porcine Reproductive and Respiratory Syndrome (PRRS) is caused by a virus of the Arteriviridae family known as PRRS virus (PRRSV) and has become enzootic in most pig production areas [1]. It has a dramatic impact on the health and welfare of pigs, making it the number one enemy of the swine industry worldwide. In the USA, production losses due to the disease were estimated to reach US$ 560 million per year [2]. PRRSV strains can be genetically differentiated into PRRSV-1 (mainly predominant in European countries) and PRRSV-2 (mainly predominant in North America and Asia) [4, 5]. In France, only closely-related PRRSV-1 strains have been isolated until now [6, 7]

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