Regulation of Avian Leukosis Virus Subgroup J Replication by Wnt/β-Catenin Signaling Pathway

Viruses. 2021 Sep 30;13(10):1968. doi: 10.3390/v13101968.

Abstract

Wnt/β-catenin signaling is a highly conserved pathway related to a variety of biological processes in different cells. The regulation of replication of various viruses by Wnt/β-catenin signaling pathway has been reported. However, the interaction between the Wnt/β-catenin pathway and avian leukosis virus is unknown. In the present study, we investigated the effect of modulating the Wnt/β-catenin pathway during avian leukosis virus subgroup J (ALV-J) infection. The activation of the Wnt/β-catenin pathway by GSK-3 inhibitor increased ALV-J mRNA, viral protein expression, and virus production in CEF cells. This increase was suppressed by iCRT14, one of the specific inhibitors of the Wnt/β-catenin signaling pathway. Moreover, treatment with iCRT14 reduced virus titer and viral gene expression significantly in CEF and LMH cells in a dose-dependent manner. Inhibition Wnt/β-catenin signaling pathway by knockdown of β-catenin reduced virus proliferation in CEF cells also. Collectively, these results suggested that the status of Wnt/β-catenin signaling pathway modulated ALV-J replication. These studies extend our understanding of the role of Wnt/β-catenin signaling pathway in ALV-J replication and make a new contribution to understanding the virus-host interactions of avian leukosis virus.

Keywords: GSK-3 inhibitor; Wnt/β-catenin signal pathway; avian leukosis virus subgroup J; iCRT14; virus replication.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Avian Leukosis / virology
  • Avian Leukosis Virus / metabolism*
  • Cell Line
  • Chick Embryo
  • Chickens / virology
  • China
  • Gene Expression / genetics
  • Gene Expression Regulation, Viral / genetics
  • Glycogen Synthase Kinase 3 / metabolism
  • Poultry Diseases / virology
  • Pyridines / pharmacology
  • Pyrroles / pharmacology
  • RNA, Messenger
  • Thiazolidinediones / pharmacology
  • Virus Replication / physiology*
  • Wnt Signaling Pathway / physiology*

Substances

  • Pyridines
  • Pyrroles
  • RNA, Messenger
  • Thiazolidinediones
  • iCRT14
  • Glycogen Synthase Kinase 3