Immune-related miRNA-mRNA regulation network in the livers of DHAV-3-infected ducklings

Fengyao Wu1,2, Fengying Lu1,2, Xin Fan1,3

  • 1Institute of Veterinary Medicine, Jiangsu Academy of Agricultural Sciences, Nanjing, Jiangsu Province, China.

BMC Genomics
|February 6, 2020
PubMed
Abstract

Insights

Duck hepatitis A virus type 3 (DHAV-3) infection disrupts duckling immunity by altering miRNA and mRNA expression. This study reveals key immune pathways and regulatory networks involved in DHAV-3 pathogenesis.

Area of Science:

  • Veterinary Virology
  • Molecular Biology
  • Immunology

Background:

  • Duck hepatitis A virus type 3 (DHAV-3) poses a significant threat to the duck industry.
  • The molecular mechanisms of DHAV-3 infection in ducklings are not well understood.
  • Understanding host-pathogen interactions is crucial for disease control.

Purpose of the Study:

  • To investigate the genetic regulatory network of miRNA-mRNA interactions in DHAV-3 infected ducklings.
  • To identify signaling pathways affected by DHAV-3 infection.
  • To elucidate the role of miRNAs in the host immune response to DHAV-3.

Main Methods:

  • Global miRNA and mRNA expression profiling using high-throughput sequencing on duckling liver tissues.
  • Construction of miRNA-mRNA networks based on differentially expressed molecules.
  • Bioinformatic analysis of enriched signaling pathways and potential miRNA regulators.

Main Results:

  • Identified 156 differentially expressed miRNAs (DEMs) and 7717 differentially expressed genes (DEGs).
  • Constructed a network of 19,606 negatively correlated miRNA-mRNA pairs.
  • Enriched immune-related pathways including cytokine-cytokine receptor interaction, apoptosis, and Toll-like receptor signaling. Identified specific miRNAs (e.g., apl-miR-32-5p) as potential regulators and found host miRNAs targeting DHAV-3 genome.

Conclusions:

  • This is the first integrated miRNA-mRNA analysis in DHAV-3 infected ducklings.
  • MiRNAs play critical roles in regulating immune response genes during DHAV-3 infection.
  • Revealed an immune-related miRNA-mRNA regulatory network, enhancing understanding of DHAV-3 pathogenesis and host-virus interactions.