Gene expression profile and long non-coding RNA analysis, using RNA-Seq, in chicken embryonic fibroblast cells infected by avian leukosis virus J

Arch Virol. 2018 Mar;163(3):639-647. doi: 10.1007/s00705-017-3659-8. Epub 2017 Dec 2.

Abstract

Avian leukosis virus J (ALVJ) infection induces hematopoietic malignancy in myeloid leukemia and hemangioma in chickens. However, little is known about the mechanisms underpinning the unique pathogenesis of ALVJ. In this study, we investigated the gene expression profiles of ALVJ-infected chicken cells and performed a comprehensive analysis of the long non-coding RNAs (lncRNAs) in CEF cells using RNA-Seq. As a result, 36 differentially expressed lncRNAs and 91 genes (FC > 2 and q-values < 0.05) were identified. Bioinformatics analysis revealed that these differentially expressed genes are involved in the innate immune response. Target prediction analysis revealed that these lncRNAs may act in cis or trans and affect the expression of genes which are involved in the anti-viral innate immune responses. Toll-like receptor, RIG-I receptor, NOD-like receptor and JAK-STAT signaling pathways were enriched. Notably, the induced expression of innate immunity genes, including B2M, DHX58, IFI27L2, IFIH1, IRF10, ISG12(2), MX, OAS*A, RSAD2, STAT1, TLR3, IL4I1, and IRF1 (FC > 2 and correlation > 0.95), were highly correlated with the upregulation of several lncRNAs, including MG066618, MG066617, MG066601, MG066629, MG066609 and MG066616. These findings identify the expression profile of lncRNAs in chicken CEF cells infected by ALVJ virus and provide new insights into the molecular mechanisms of ALVJ infection.

MeSH terms

  • Animals
  • Avian Leukosis Virus / genetics*
  • Avian Leukosis Virus / growth & development
  • Avian Leukosis Virus / immunology
  • Cell Line
  • Chick Embryo
  • Computational Biology
  • DEAD Box Protein 58 / genetics
  • DEAD Box Protein 58 / immunology
  • Fibroblasts / immunology
  • Fibroblasts / virology*
  • Gene Expression Profiling
  • Gene Expression Regulation
  • Host-Pathogen Interactions*
  • Immunity, Innate
  • Janus Kinase 1 / genetics
  • Janus Kinase 1 / immunology
  • NLR Proteins / genetics
  • NLR Proteins / immunology
  • RNA, Long Noncoding / genetics*
  • RNA, Long Noncoding / immunology
  • STAT Transcription Factors / genetics
  • STAT Transcription Factors / immunology
  • Sequence Analysis, RNA
  • Signal Transduction
  • Toll-Like Receptors / genetics
  • Toll-Like Receptors / immunology
  • Transcriptome / immunology*

Substances

  • NLR Proteins
  • RNA, Long Noncoding
  • STAT Transcription Factors
  • Toll-Like Receptors
  • Janus Kinase 1
  • DEAD Box Protein 58