Myxoma virus selectively disrupts type I interferon signaling in primary human fibroblasts by blocking the activation of the Janus kinase Tyk2

Fuan Wang, John W. Barrett, Qing Shao, Xiujuan Gao, Gregory A. Dekaban, Douglas McFadden

Research output: Contribution to journalArticle

13 Citations (Scopus)

Abstract

Poxviruses currently are known to disrupt Jak-STAT signal transduction induced by interferon (IFN) through two distinct mechanisms: (1) secreted poxviral IFN decoy receptors that prevent the initiation of IFN signaling from type I or II receptors at the cell surface; and (2) poxviral phosphatase that dephosphorylates STAT1 intracellularly. Here, we report a novel mechanism by which poxviruses can inhibit Jak-STAT signaling in response to type I IFN. Myxoma virus (MV) is a highly species-restricted member of the poxvirus family that infects only rabbits under the natural setting. Interestingly, primary human fibroblasts support a permissive MV infection that is only partially sensitive to the antiviral state induced by type I IFN. In this study we show that when type I IFN is added to primary human fibroblasts following MV infection, the tyrosine phosphorylation of the Janus kinase Tyk2 is specifically blocked, thereby preventing the subsequent activation of downstream STAT1 and STAT2. In stark contrast, type II IFN-induced activation of Jak1, Jak2 and STAT1 remains largely unaffected in MV-infected human fibroblasts. Unlike the de-activation of STAT1 by the poxvirus phosphatase, which is delivered into the cell by the input virions, the Tyk2 inhibition by MV infection requires new viral gene expression. Thus, our study documents a previously unrecognized immune evasion mechanism exploited by a poxvirus to selectively disrupt the type I IFN-Jak-STAT signaling cascade.

Original languageEnglish (US)
Pages (from-to)136-146
Number of pages11
JournalVirology
Volume387
Issue number1
DOIs
StatePublished - Apr 25 2009
Externally publishedYes

Fingerprint

Myxoma virus
Poxviridae
Janus Kinases
Interferon Type I
Fibroblasts
Virus Diseases
Phosphoric Monoester Hydrolases
Interferon-gamma
Interferon Receptors
Immune Evasion
Viral Genes
Cell Surface Receptors
Virion
Interferons
Antiviral Agents
Tyrosine
Signal Transduction
Phosphorylation
Rabbits
Gene Expression

Keywords

  • Antiviral
  • Immune evasion
  • Jak
  • Poxvirus
  • STAT1

ASJC Scopus subject areas

  • Virology

Cite this

Myxoma virus selectively disrupts type I interferon signaling in primary human fibroblasts by blocking the activation of the Janus kinase Tyk2. / Wang, Fuan; Barrett, John W.; Shao, Qing; Gao, Xiujuan; Dekaban, Gregory A.; McFadden, Douglas.

In: Virology, Vol. 387, No. 1, 25.04.2009, p. 136-146.

Research output: Contribution to journalArticle

Wang, Fuan ; Barrett, John W. ; Shao, Qing ; Gao, Xiujuan ; Dekaban, Gregory A. ; McFadden, Douglas. / Myxoma virus selectively disrupts type I interferon signaling in primary human fibroblasts by blocking the activation of the Janus kinase Tyk2. In: Virology. 2009 ; Vol. 387, No. 1. pp. 136-146.
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