Abstract

BackgroundGenetic improvement for disease resilience is anticipated to be a practical method to improve efficiency and profitability of the pig industry, as resilient pigs maintain a relatively undepressed level of performance in the face of infection. However, multiple biological functions are known to be involved in disease resilience and this complexity means that the genetic architecture of disease resilience remains largely unknown. Here, we conducted genome-wide association studies (GWAS) of 465,910 autosomal SNPs for complete blood count (CBC) traits that are important in an animal’s disease response. The aim was to identify the genetic control of disease resilience.ResultsUnivariate and multivariate single-step GWAS were performed on 15 CBC traits measured from the blood samples of 2743 crossbred (Landrace × Yorkshire) barrows drawn at 2-weeks before, and at 2 and 6-weeks after exposure to a polymicrobial infectious challenge. Overall, at a genome-wise false discovery rate of 0.05, five genomic regions located on Sus scrofa chromosome (SSC) 2, SSC4, SSC9, SSC10, and SSC12, were significantly associated with white blood cell traits in response to the polymicrobial challenge, and nine genomic regions on multiple chromosomes (SSC1, SSC4, SSC5, SSC6, SSC8, SSC9, SSC11, SSC12, SSC17) were significantly associated with red blood cell and platelet traits collected before and after exposure to the challenge. By functional enrichment analyses using Ingenuity Pathway Analysis (IPA) and literature review of previous CBC studies, candidate genes located nearby significant single-nucleotide polymorphisms were found to be involved in immune response, hematopoiesis, red blood cell morphology, and platelet aggregation.ConclusionsThis study helps to improve our understanding of the genetic basis of CBC traits collected before and after exposure to a polymicrobial infectious challenge and provides a step forward to improve disease resilience.

Highlights

  • Genetic improvement for disease resilience is anticipated to be a practical method to improve efficiency and profitability of the pig industry, as resilient pigs maintain a relatively undepressed level of performance in the face of infection

  • Significant genetic correlations were found for several complete blood count (CBC) traits collected after exposure to the challenge with the economically important production traits of grow-tofinish growth rate (GFGR) and treatment rate (TR) in response to the polymicrobial challenge (− 0.82 ± 0.47 to 0.89 ± 0.26) [10], which may further indicate the potential of developing those CBC traits as indicator traits of disease resilience

  • In addition to the genetic correlations with resilience already reported for these data by Bai et al [10], we found significant genetic correlations for platelet concentration in Blood 3 collected at 2-weeks after exposure to a polymicrobial infectious challenge with GFGR (0.40 ± 0.22) and TR (− 0.46 ± 0.26), and for the change of monocyte concentration from Blood 1 to Blood 3 (MONOΔ13) collected at 2-weeks before and 2-weeks after exposure to the challenge with GFGR (0.63 ± 0.21)

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Summary

Introduction

Genetic improvement for disease resilience is anticipated to be a practical method to improve efficiency and profitability of the pig industry, as resilient pigs maintain a relatively undepressed level of performance in the face of infection. Disease resilience is a complex trait composed of multiple biological functions, such as growth, health, nutrient status, and other dynamic elements, including the efficiency of immune response and the rate of recovery from infection [5]. Significant genetic correlations (either positive or negative) were found for several CBC traits collected after exposure to the challenge with the economically important production traits of grow-tofinish growth rate (GFGR) and treatment rate (TR) in response to the polymicrobial challenge (− 0.82 ± 0.47 to 0.89 ± 0.26) [10], which may further indicate the potential of developing those CBC traits as indicator traits of disease resilience. This allows multivariate models to be used for joint analyses of these genetically correlated traits, which provides the potential to improve statistical power and explore pleiotropy [11,12,13,14]

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