The Cellular and Viral circRNAs Induced by Fowl Adenovirus Serotype 4 Infection

Xiao-Na Liu1, Xiao-Ran Guo1, Ying Han1

  • 1College of Veterinary Medicine, Hebei Agricultural University, Baoding, China.

Insights

Fowl adenovirus serotype 4 (FAdV-4) infection alters cellular circular RNAs (circRNAs) and produces viral circRNAs. Some viral circRNAs enhance FAdV-4 replication, offering insights into host-virus interactions and disease mechanisms.

Area of Science:

  • Virology
  • Molecular Biology
  • Bioinformatics

Background:

  • Circular RNAs (circRNAs) are crucial in biological processes and are affected by viral infections.
  • Hydropericardium-hepatitis syndrome (HHS), caused by fowl adenovirus serotype 4 (FAdV-4), devastates the poultry industry.
  • Understanding circRNA dynamics during FAdV-4 infection is vital for disease control.

Purpose of the Study:

  • To investigate the expression and characteristics of cellular and viral circRNAs during FAdV-4 infection in leghorn male hepatoma (LMH) cells.
  • To determine the role of identified circRNAs in FAdV-4 replication and host-virus interactions.

Main Methods:

  • Transcriptome analysis of FAdV-4-infected LMH cells.
  • Bioinformatic analysis to identify and characterize differentially expressed cellular and viral circRNAs.
  • Gene Ontology (GO) and KEGG pathway enrichment analysis.
  • Validation of circRNA expression using semiquantitative RT-PCR and sequencing.
  • Competing endogenous RNA (ceRNA) network analysis.

Main Results:

  • 19,154 cellular circRNAs identified, with 135 differentially expressed (DE) in FAdV-4 infected cells.
  • DE cellular circRNAs are involved in various biological processes.
  • 2,014 viral circRNAs identified, with 10 verified.
  • Seven viral circRNAs potentially generated via alternative splicing were located in FAdV-4 proteins.
  • Viral circRNA expression correlates with viral replication efficiency; some promote FAdV-4 replication.
  • ceRNA analysis suggests circRNAs modulate host or viral genes via microRNAs (miRNAs).

Conclusions:

  • FAdV-4 infection induces significant changes in cellular circRNA expression and produces novel viral circRNAs.
  • Specific viral circRNAs play a role in promoting FAdV-4 replication.
  • These findings provide novel insights into FAdV-4 pathogenesis and host-virus interactions, potentially aiding in developing control strategies.

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