Abstract

BackgroundHost genetics has been shown to play a role in porcine reproductive and respiratory syndrome (PRRS), which is the most economically important disease in the swine industry. A region on Sus scrofa chromosome (SSC) 4 has been previously reported to have a strong association with serum viremia and weight gain in pigs experimentally infected with the PRRS virus (PRRSV). The objective here was to identify haplotypes associated with the favorable phenotype, investigate additional genomic regions associated with host response to PRRSV, and to determine the predictive ability of genomic estimated breeding values (GEBV) based on the SSC4 region and based on the rest of the genome. Phenotypic data and 60 K SNP genotypes from eight trials of ~200 pigs from different commercial crosses were used to address these objectives.ResultsAcross the eight trials, heritability estimates were 0.44 and 0.29 for viral load (VL, area under the curve of log-transformed serum viremia from 0 to 21 days post infection) and weight gain to 42 days post infection (WG), respectively. Genomic regions associated with VL were identified on chromosomes 4, X, and 1. Genomic regions associated with WG were identified on chromosomes 4, 5, and 7. Apart from the SSC4 region, the regions associated with these two traits each explained less than 3% of the genetic variance. Due to the strong linkage disequilibrium in the SSC4 region, only 19 unique haplotypes were identified across all populations, of which four were associated with the favorable phenotype. Through cross-validation, accuracies of EBV based on the SSC4 region were high (0.55), while the rest of the genome had little predictive ability across populations (0.09).ConclusionsTraits associated with response to PRRSV infection in growing pigs are largely controlled by genomic regions with relatively small effects, with the exception of SSC4. Accuracies of EBV based on the SSC4 region were high compared to the rest of the genome. These results show that selection for the SSC4 region could potentially reduce the effects of PRRS in growing pigs, ultimately reducing the economic impact of this disease.

Highlights

  • Host genetics has been shown to play a role in porcine reproductive and respiratory syndrome (PRRS), which is the most economically important disease in the swine industry

  • The objectives of the current study were to (1) reestimate genetic parameters for host response to experimental PRRS virus (PRRSV) infection in growing pigs by including three additional, unrelated populations, (2) investigate additional genomic regions associated with weight gain and viremia in response to PRRSV challenge, (3) determine if there is a smaller informative haplotype block within the ~1 Mb region on SSC4 associated with host response to PRRSV infection, (4) determine which haplotypes within the SSC4 region are associated with the favorable effects of the quantitative trait locus (QTL) for viremia and weight gain, and (5) investigate accuracies of genomic estimated breeding values (GEBV) for host response to PRRS based on the SSC4 region and the rest of the genome, by using cross-validation

  • These results show that the effect of this region was present in six unrelated populations from five different breeding companies

Read more

Summary

Introduction

Host genetics has been shown to play a role in porcine reproductive and respiratory syndrome (PRRS), which is the most economically important disease in the swine industry. A region on Sus scrofa chromosome (SSC) 4 has been previously reported to have a strong association with serum viremia and weight gain in pigs experimentally infected with the PRRS virus (PRRSV). For decades the swine industry has been battling the economically important disease of porcine reproductive and respiratory syndrome (PRRS), caused by the PRRS virus (PRRSV) but success has been limited. A quantitative trait locus (QTL) was identified on Sus scrofa (SSC) 4 that explains a considerable amount of the total genetic variance for serum viremia and weight gain of weaned piglets following experimental infection [2]. The addition of three trials to the data analyzed in Boddicker et al [3] has potentially increased the power in order to find these, likely smaller, effects

Objectives
Results
Conclusion
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call