S1PR1 expression correlates with inflammatory responses to Newcastle disease virus infection

Infect Genet Evol. 2016 Jan:37:37-42. doi: 10.1016/j.meegid.2015.10.021. Epub 2015 Oct 24.

Abstract

Newcastle disease virus (NDV) is the causative agent of Newcastle disease, which is characterized by inflammatory pathological changes in the organs of chickens. The inflammatory response to this disease has not been well characterized. Previous reports showed that the sphingosine-1-phosphate-1 receptor (S1PR1), a G protein-coupled receptor, is important to the activation of inflammatory responses. To understand better the viral pathogenesis and host inflammatory response, we analyzed S1PR1 expression during NDV infection. We observed a direct correlation between chicken embryo fibroblast (CEF) cellular inflammatory responses and S1PR1 expression. Virulent NDV-infected CEF cells also had elevated levels of pro-inflammatory cytokines (IL-1β, IL-6 and IL-18). When S1PR1 was inhibited by using the specific antagonist W146, pro-inflammatory cytokine production declined. Overexpression of S1PR1 resulted in increased virus-induced IL-1β production. S1PR1 expression levels did not impact significantly NDV replication. These findings highlight the important role of S1PR1 in inflammatory responses in NDV infection.

Keywords: Cytokines; Inflammatory response; Newcastle disease virus (NDV); S1PR1.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Anilides / pharmacology
  • Animals
  • Cells, Cultured
  • Chick Embryo
  • Cytokines / genetics*
  • Cytokines / metabolism
  • Fibroblasts / cytology
  • Fibroblasts / immunology
  • Fibroblasts / virology
  • Newcastle Disease / genetics
  • Newcastle Disease / immunology*
  • Newcastle Disease / virology
  • Newcastle disease virus / pathogenicity
  • Organophosphonates / pharmacology
  • Poultry Diseases / genetics
  • Poultry Diseases / immunology
  • Poultry Diseases / virology*
  • Receptors, Lysosphingolipid / genetics*
  • Receptors, Lysosphingolipid / metabolism
  • Up-Regulation

Substances

  • 3-amino-4-(3-hexylphenylamino)-4-oxobutylphosphonic acid
  • Anilides
  • Cytokines
  • Organophosphonates
  • Receptors, Lysosphingolipid