Variation in interferon sensitivity and induction between Usutu and West Nile (lineages 1 and 2) viruses

Virology. 2015 Nov:485:189-98. doi: 10.1016/j.virol.2015.07.015. Epub 2015 Aug 14.

Abstract

Given the pivotal role of monocyte-derived dendritic cells (DCs) in determining the magnitude of the antiviral innate immune response, we sought to determine whether Usutu virus (USUV) and West Nile virus (WNV) lineages (L)1 and L2 can infect DCs and affect the rate of type I interferon (IFN) activation. The sensitivity of these viruses to types I and III IFNs was also compared. We found that USUV can infect DCs, induce higher antiviral activities, IFN alpha subtypes and the IFN stimulated gene (ISG)15 pathway, and is more sensitive to types I and III IFNs than WNVs. In contrast, we confirmed that IFN alpha/beta subtypes were more effective against WNV L2 than WNV L1. However, the replication kinetics, induction of IFN alpha subtypes and ISGs in DCs and the sensitivity to IFN lambda 1-3 did not differ between WNV L1 and L2.

Keywords: IFN; Interferon; Monocyte-derived dendritic cells; USUV; Usutu virus; WNV; West Nile virus.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adaptor Proteins, Signal Transducing
  • Cell Differentiation
  • Cytokines / genetics
  • Cytokines / immunology
  • Dendritic Cells / drug effects*
  • Dendritic Cells / immunology
  • Dendritic Cells / virology
  • Encephalitis Viruses, Japanese / drug effects*
  • Encephalitis Viruses, Japanese / genetics
  • Encephalitis Viruses, Japanese / immunology
  • Gene Expression Regulation
  • Host-Pathogen Interactions
  • Humans
  • Interferon-alpha / classification
  • Interferon-alpha / genetics
  • Interferon-alpha / immunology
  • Interferon-alpha / pharmacology*
  • Interferon-beta / classification
  • Interferon-beta / genetics
  • Interferon-beta / immunology
  • Interferon-beta / pharmacology*
  • Intracellular Signaling Peptides and Proteins / genetics
  • Intracellular Signaling Peptides and Proteins / immunology
  • Lipopolysaccharides / pharmacology
  • Monocytes / cytology
  • Primary Cell Culture
  • RNA-Binding Proteins
  • Signal Transduction
  • Species Specificity
  • Transcription Factors / genetics
  • Transcription Factors / immunology
  • Ubiquitins / genetics
  • Ubiquitins / immunology
  • Viral Load / drug effects
  • Viral Load / immunology
  • Virus Replication / drug effects
  • Virus Replication / immunology
  • West Nile virus / drug effects*
  • West Nile virus / genetics
  • West Nile virus / immunology

Substances

  • Adaptor Proteins, Signal Transducing
  • Cytokines
  • HERC5 protein, human
  • IFIT1 protein, human
  • Interferon-alpha
  • Intracellular Signaling Peptides and Proteins
  • Lipopolysaccharides
  • RNA-Binding Proteins
  • Transcription Factors
  • Ubiquitins
  • ISG15 protein, human
  • Interferon-beta