More Information
A simple and rapid immunoperoxidase test for the identification of equine herpesvirus-1
Authors: Motha MXJ, Chote KJPublication: New Zealand Veterinary Journal, Volume 46, Issue 2, pp 80, Apr 1998
Publisher: Taylor and Francis
Animal type: Horse, Livestock
Subject Terms: Diagnostic procedures, Viral, Disease/defect, Infectious disease
Article class: Correspondence
Abstract: Equine herpesvirus 1 (EHV1) is an alphaherpesvirus which is a major cause of abortion in mares and it is of a considerable economic importance worldwide (Crabb and Studdert, 1996). EHV-1 has been isolated in New Zealand from cases of abortion and perinatal mortalities (Hutton and Durham, 1997; Horner, 1989). Recently, a herpesvirus was isolated from a lung sample from an aborted foetus and this virus was identified as EHV1 by the immunoperoxidase technique with the use of a monoclonal antibody specific for EHV1. The lung tissue from the aborted foetus was processed and inoculated on to equine foetal kidney and RK13 cell cultures. Early signs of a cytopathic effect (CPE) in the form of three to five foci were observed in the RK13 cell cultures 2 days after inoculation. The CPE was characterised by focal rounding and aggregation of cells suggestive of a herpesvirus CPE. The cells were washed once with 0.15 M sodium chloride solution and fixed immediately using 20% acetone solution for 5 minutes. The cell sheet was dried for 2 hours at 37ºC and stained by the immunoperoxidase technique (Meyling, 1984). For the staining, two monoclonal antibodies were used on duplicate cell cultures showing CPE. The first monoclonal antibody was
Access to the full text of this article is available to members of:
- SciQuest - Complimentary Subscription
Login
Otherwise:
Register for an account