Vaccinia virus-encoded cytokine receptor binds and neutralizes chicken interferon-gamma

Virology. 1998 Sep 1;248(2):231-40. doi: 10.1006/viro.1998.9278.

Abstract

To counteract the host immune response, poxviruses have evolved secreted factors that bind cytokines and thereby neutralize their biological activities. The vaccinia virus B8R gene encodes a protein that neutralizes interferon-gamma (IFN-gamma) from several mammals including man, cow, rat, and rabbit but not mice. We now report that the activity of the B8R gene product is not restricted to cytokines of mammals: it also efficiently neutralized chicken IFN-gamma. B8R blocked chicken IFN-gamma-mediated induction of guanylate binding protein RNA in the chicken fibroblast cell line CEC-32 and secretion of nitric oxide in HD-11 cells. Radiolabeled baculovirus-expressed B8R efficiently bound to immobilized recombinant chicken IFN-gamma. Scatchard analysis revealed a binding constant of chicken IFN-gamma to B8R of approximately 0.5 nM. A mutant form of chicken IFN-gamma which lacks the 18 C-terminal amino acids and which has lost more than 99% of its biological activity was able to block the IFN-gamma-neutralizing effect of B8R. Binding studies showed that the mutant protein bound radiolabeled B8R only about threefold less well than wild-type chicken IFN-gamma but failed to compete with wild-type chicken IFN-gamma for binding to the cellular receptor. These results suggest that the extreme C terminus of chicken IFN-gamma is crucial for binding to its cellular receptor but less important for recognition by the viral cytokine receptor.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cell Line
  • Chickens
  • GTP-Binding Proteins / metabolism
  • Gene Deletion
  • Humans
  • Interferon-gamma / antagonists & inhibitors
  • Interferon-gamma / metabolism*
  • Mice
  • Nitric Oxide / metabolism
  • Rabbits
  • Rats
  • Receptors, Cytokine / metabolism*
  • Vaccinia virus / metabolism*

Substances

  • Receptors, Cytokine
  • Nitric Oxide
  • Interferon-gamma
  • GTP-Binding Proteins