MicroRNA-23b Promotes Avian Leukosis Virus Subgroup J (ALV-J) Replication by Targeting IRF1

Sci Rep. 2015 May 18:5:10294. doi: 10.1038/srep10294.

Abstract

Avian leukosis virus subgroup J (ALV-J) can cause several different leukemia-like proliferative diseases in the hemopoietic system of chickens. Here, we investigated the transcriptome profiles and miRNA expression profiles of ALV-J-infected and uninfected chicken spleens to identify the genes and miRNAs related to ALV-J invasion. In total, 252 genes and 167 miRNAs were differentially expressed in ALV-J-infected spleens compared to control uninfected spleens. miR-23b expression was up-regulated in ALV-J-infected spleens compared with the control spleens, and transcriptome analysis revealed that the expression of interferon regulatory factor 1 (IRF1) was down-regulated in ALV-J-infected spleens compared to uninfected spleens. A dual-luciferase reporter assay showed that IRF1 was a direct target of miR-23b. miR-23b overexpression significantly (P = 0.0022) decreased IRF1 mRNA levels and repressed IRF1-3'-UTR reporter activity. In vitro experiments revealed that miR-23b overexpression strengthened ALV-J replication, whereas miR-23b loss of function inhibited ALV-J replication. IRF1 overexpression inhibited ALV-J replication, and IRF1 knockdown enhanced ALV-J replication. Moreover, IRF1 overexpression significantly (P = 0.0014) increased IFN-β expression. In conclusion, these results suggested that miR-23b may play an important role in ALV-J replication by targeting IRF1.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • 3' Untranslated Regions
  • Animals
  • Avian Leukosis / genetics*
  • Avian Leukosis / virology*
  • Avian Leukosis Virus / classification
  • Avian Leukosis Virus / isolation & purification
  • Avian Leukosis Virus / physiology*
  • Chickens*
  • Gene Expression Profiling
  • Gene Expression Regulation
  • Gene Regulatory Networks
  • High-Throughput Nucleotide Sequencing
  • Interferon Regulatory Factor-1 / genetics*
  • MicroRNAs / genetics*
  • RNA Interference*
  • RNA, Messenger / genetics
  • Reproducibility of Results
  • Transcriptome
  • Virus Replication*

Substances

  • 3' Untranslated Regions
  • Interferon Regulatory Factor-1
  • MicroRNAs
  • RNA, Messenger