Transcriptome Analysis Reveals the Neuro-Immune Interactions in Duck Tembusu Virus-Infected Brain

Int J Mol Sci. 2020 Mar 31;21(7):2402. doi: 10.3390/ijms21072402.

Abstract

The duck Tembusu virus (DTMUV) is a mosquito-borne flavivirus. It causes severe symptoms of egg-drop, as well as neurological symptoms and brain damage in ducks. However, the specific molecular mechanisms of DTMUV-induced neurovirulence and host responses in the brain remain obscure. To better understand the host-pathogen and neuro-immune interactions of DTMUV infection, we conducted high-throughput RNA-sequencing to reveal the transcriptome profiles of DTMUV-infected duck brain. Totals of 117, 212, and 150 differentially expressed genes (DEGs) were identified at 12, 24, and 48 h post infection (hpi). Gene ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) enrichment analyses uncovered genes and pathways related to the nervous system and immune responses in duck brain. Neuro-related genes, including WNT3A, GATA3, and CHRNA6, were found to be significantly downregulated. RIG-I-like receptors (DHX58, IFIH1) and Toll-like receptors (TLR2 and TLR3) were activated, inducing the expression of 22 interferon stimulated genes (ISGs) and antigen-processing and -presenting genes (TAP1 and TAP2) in the brain. Our research provides comprehensive information for the molecular mechanisms of neuro-immune and host-pathogen interactions of DTMUV.

Keywords: DTMUV; Transcriptome analysis; brain; host–pathogen interaction; molecular mechanism; neuro-immune interaction.

MeSH terms

  • ATP Binding Cassette Transporter, Subfamily B, Member 2 / genetics
  • ATP Binding Cassette Transporter, Subfamily B, Member 2 / metabolism
  • ATP Binding Cassette Transporter, Subfamily B, Member 3 / genetics
  • Animals
  • Brain / immunology
  • Brain / metabolism*
  • Brain / pathology
  • Brain / virology
  • Ducks / genetics
  • Ducks / immunology
  • Flavivirus / immunology*
  • Flavivirus / pathogenicity
  • Flavivirus Infections / immunology*
  • Flavivirus Infections / metabolism
  • Flavivirus Infections / pathology
  • Flavivirus Infections / veterinary*
  • GATA3 Transcription Factor / genetics
  • GATA3 Transcription Factor / metabolism
  • Gene Expression Profiling / veterinary*
  • Host-Pathogen Interactions / genetics*
  • Host-Pathogen Interactions / immunology
  • Host-Pathogen Interactions / physiology*
  • Interferons / metabolism
  • Neuroimmunomodulation / genetics*
  • Neuroimmunomodulation / immunology
  • Receptors, Nicotinic / genetics
  • Receptors, Nicotinic / metabolism
  • Receptors, Retinoic Acid / genetics
  • Receptors, Retinoic Acid / metabolism
  • Toll-Like Receptors / genetics
  • Toll-Like Receptors / metabolism
  • Transcriptome
  • Wnt3A Protein / genetics
  • Wnt3A Protein / metabolism

Substances

  • ATP Binding Cassette Transporter, Subfamily B, Member 2
  • ATP Binding Cassette Transporter, Subfamily B, Member 3
  • GATA3 Transcription Factor
  • Receptors, Nicotinic
  • Receptors, Retinoic Acid
  • Toll-Like Receptors
  • Wnt3A Protein
  • Interferons

Supplementary concepts

  • Tembusu virus