Diagnostic methods for African horsesickness virus using monoclonal antibodies to structural and non-structural proteins

Vet Microbiol. 1992 Nov;33(1-4):143-53. doi: 10.1016/0378-1135(92)90042-r.

Abstract

A panel of 32 hybridoma cell lines secreting monoclonal antibodies (MAbs) reactive with African horsesickness virus serotype 4 (AHSV-4) has been developed. Four of the MAbs recognized the major core antigen VP7, twenty recognized the outer capsid protein VP2 and eight reacted with the non-structural protein NS1. With the VP7-specific MAbs a rapid and sensitive double antibody sandwich immunoassay has been developed to detect viral antigen in infected Vero cells and in spleen tissue from AHSV-infected horses. The sensitivity of the assay is 10 ng viral antigen per 100 microliters. The NS1-specific MAbs allowed visualization by immunofluorescence of tubule-like structures in the cytoplasm of infected Vero cells. This can be very useful as a confirmatory diagnostic procedure. The antigenic map of the outer capsid VP2 protein with MAbs is also reported.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • African Horse Sickness / diagnosis*
  • African Horse Sickness Virus / immunology*
  • African Horse Sickness Virus / isolation & purification
  • Animals
  • Antibodies, Monoclonal* / biosynthesis
  • Antibodies, Monoclonal* / immunology
  • Antigens, Viral / immunology*
  • Binding, Competitive
  • Blotting, Western
  • Capsid / immunology
  • Enzyme-Linked Immunosorbent Assay
  • Fluorescent Antibody Technique
  • Horses
  • Hybridomas
  • Mice
  • Neutralization Tests
  • Precipitin Tests
  • Vero Cells
  • Viral Proteins / immunology*

Substances

  • Antibodies, Monoclonal
  • Antigens, Viral
  • Viral Proteins