Abstract

BackgroundIt is unclear whether improving feed efficiency by selection for low residual feed intake (RFI) compromises pigs’ immunocompetence. Here, we aimed at investigating whether pig lines divergently selected for RFI had different inflammatory responses to lipopolysaccharide (LPS) exposure, regarding to clinical presentations and transcriptomic changes in peripheral blood cells.ResultsLPS injection induced acute systemic inflammation in both the low-RFI and high-RFI line (n = 8 per line). At 4 h post injection (hpi), the low-RFI line had a significantly lower (p = 0.0075) mean rectal temperature compared to the high-RFI line. However, no significant differences in complete blood count or levels of several plasma cytokines were detected between the two lines. Profiling blood transcriptomes at 0, 2, 6, and 24 hpi by RNA-sequencing revealed that LPS induced dramatic transcriptional changes, with 6296 genes differentially expressed at at least one time point post injection relative to baseline in at least one line (n = 4 per line) (|log2(fold change)| ≥ log2(1.2); q < 0.05). Furthermore, applying the same cutoffs, we detected 334 genes differentially expressed between the two lines at at least one time point, including 33 genes differentially expressed between the two lines at baseline. But no significant line-by-time interaction effects were detected. Genes involved in protein translation, defense response, immune response, and signaling were enriched in different co-expression clusters of genes responsive to LPS stimulation. The two lines were largely similar in their peripheral blood transcriptomic responses to LPS stimulation at the pathway level, although the low-RFI line had a slightly lower level of inflammatory response than the high-RFI line from 2 to 6 hpi and a slightly higher level of inflammatory response than the high-RFI line at 24 hpi.ConclusionsThe pig lines divergently selected for RFI had a largely similar response to LPS stimulation. However, the low-RFI line had a relatively lower-level, but longer-lasting, inflammatory response compared to the high-RFI line. Our results suggest selection for feed efficient pigs does not significantly compromise a pig’s acute systemic inflammatory response to LPS, although slight differences in intensity and duration may occur.

Highlights

  • It is unclear whether improving feed efficiency by selection for low residual feed intake (RFI) compromises pigs’ immunocompetence

  • Results of Gene set enrichment analysis (GSEA) based on gene sets derived from Kyoto Encyclopedia of Genes and Genomes (KEGG) pathways were largely consistent with those of GSEA based on gene sets derived from Gene ontology (GO) terms, but provided information on the fine differences between the two lines in terms of the dynamics of their inflammatory responses to LPS (Fig. 9)

  • Expression levels of genes associated with antigen processing and presentation, ribosome biogenesis, DNA repair and homologous recombination, RNA transport, cell adhesion, and the Fanconi anemia pathway were lower in the low-RFI animals than in the high-RFI animals, especially at 24 hpi

Read more

Summary

Introduction

It is unclear whether improving feed efficiency by selection for low residual feed intake (RFI) compromises pigs’ immunocompetence. Compared to high-RFI pigs, pigs selected for low RFI have reduced feed intake, but similar rate of growth [2,3,4] This difference occurs likely because the low-RFI pigs are more efficient in allocating resources for production and maintenance [5]. Based on resource allocation theory [5], selection for high feed efficiency is expected to compromise the animal’s capacity to handle immune stimulation, such as the response that occurs during infectious diseases [8]. This has been confirmed in studies on chickens and beef cattle, where selection for increased feed efficiency negatively affected their immune system [9]

Objectives
Methods
Results
Discussion
Conclusion
Full Text
Paper version not known

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