Monoclonal antibody routinely used to identify avirulent strains of Newcastle disease virus binds to an epitope at the carboxy terminus of the hemagglutinin-neuraminidase protein and recognizes individual mesogenic and velogenic strains

J Clin Microbiol. 2005 Aug;43(8):4229-33. doi: 10.1128/JCM.43.8.4229-4233.2005.

Abstract

Newcastle disease virus (NDV) strains are classified as having high (velogenic), intermediate (mesogenic), or low (lentogenic) pathogenesis and virulence in chickens. Recent studies have established that the hemagglutinin-neuraminidase (HN) protein plays an important role in viral tropism and virulence. A monoclonal antibody (AVS-I) has previously been shown to be specific for lentogenic strains of NDV (Srinivasappa et al., Avian Dis. 30:562-567, 1986) and is routinely used to identify these strains. We have used competition antibody binding assays with a previously characterized panel of monoclonal antibodies, binding to chimeric HN proteins, and the characterization of an escape mutant to localize the binding site of AVS-I to the extreme carboxy terminus of the protein. In addition, we have shown that AVS-I does recognize at least one mesogenic strain and one velogenic strain of the virus, calling into question the potential of this antibody as a diagnostic reagent for avirulent NDV strains.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Antibodies, Monoclonal / immunology*
  • Binding Sites, Antibody
  • Epitopes
  • HN Protein / chemistry
  • HN Protein / immunology*
  • HN Protein / toxicity
  • Hemagglutination Inhibition Tests
  • Neutralization Tests
  • Newcastle disease virus / immunology
  • Newcastle disease virus / isolation & purification*
  • Newcastle disease virus / pathogenicity
  • Protein Conformation
  • Structure-Activity Relationship
  • Virulence

Substances

  • Antibodies, Monoclonal
  • Epitopes
  • HN Protein