Abstract

Pooled samples are used in veterinary and human medicine as a cost-effective approach to monitor disease prevalence. Nonetheless, there is limited information on the effect of pooling on test performance, and research is required to determine the appropriate number of samples which can be pooled. Therefore, this study aimed to evaluate the use of pooled serum samples as a herd-level surveillance tool for infectious production-limiting diseases: bovine viral diarrhoea (BVD), infectious bovine rhinotracheitis (IBR), enzootic bovine leukosis (EBL) and Neospora caninum (NC), by investigating the maximum number of samples one can pool to identify one positive animal, using commercial antibody-detection ELISAs. Four positive field standards (PFS), one for each disease, were prepared by pooling highly positive herd-level samples diagnosed using commercially available ELISA tests. These PFS were used to simulate 18 pooled samples ranging from undiluted PFS to a dilution representing 1 positive in 1,000 animals using phosphate-buffered saline as diluent. A 1:10 dilution of the PFS resulted in positive results for IBR, BVD and EBL. Moreover, for IBR and BVD, results were still positive at 1:100 and 1:30 dilutions, respectively. However, for NC, a lower dilution (8:10) was required for a seropositive result. This study indicates that, at herd-level, the use of pooled serum is a useful strategy for monitoring infectious diseases (BVD, IBR and EBL) but not NC, using readily available diagnostic assays.

Highlights

  • Sample pooling is a method used in human and veterinary medicine to obtain disease information in a cost-effective way, where individual results are not required and the diagnostic method is labour intensive

  • PCR tests were used to estimate the presence of bovine viral diarrhoea virus (BVD) in serum pools of 30 animals at auction markets (Smith et al 2008) and pooled calf ear notch samples were used as a rapid method to detect BVD-positive animals (Kennedy et al 2006)

  • This study aimed to evaluate the influence of dilution when pooling bovine serum samples on the ability to assess the BVD, infectious bovine rhinotracheitis (IBR), enzootic bovine leukosis (EBL) and Neospora caninum (NC) herd prevalence using commercially available antibody-detection enzyme-linked immunosorbent assay (ELISA)

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Summary

Introduction

Sample pooling is a method used in human and veterinary medicine to obtain disease information in a cost-effective way, where individual results are not required and the diagnostic method is labour intensive. The use of sample pooling has been reported for molecular and immune-based diagnostic methods. PCR tests were used to estimate the presence of bovine viral diarrhoea virus (BVD) in serum pools of 30 animals at auction markets (Smith et al 2008) and pooled calf ear notch samples were used as a rapid method to detect BVD-positive animals (Kennedy et al 2006). Pooled faeces and bulk milk samples have been used to detect the presence of Salmonella spp. in calves (Singer et al 2006) and Staphylococcus aureus in cows with mastitis (Ronco et al 2018). An Australian study evaluated the use of pooled serum for the identification of BVD and demonstrated that a single high antibody-positive individual could give a positive result in pools of up to 128 animals, while

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