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Clinical and Diagnostic Laboratory Immunology, November 2000, p. 940-944, Vol. 7, No. 6
Graduate Program in Microbiology, Instituto
de Ciências Biomédicas, Universidade de São
Paulo,1 and Fundação de Amparo
à Pesquisa do Estado de São Paulo,2
São Paulo, and Departamento de Patologia
Veterinária, Faculdade de Ciências Agrárias e
Veterinárias, Universidade Estadual Paulista, 14870-000,
Jaboticabal,3 São Paulo, Brazil
Received 22 May 2000/Returned for modification 19 July
2000/Accepted 24 August 2000
A liquid phase blocking ELISA (LPB-ELISA) was adapted for the
detection and quantification of antibodies to Newcastle disease virus.
Sera from vaccinated and unvaccinated commercial flocks of ostriches
(Struthio camelus) and rheas (Rhea americana)
were tested. The purified and nonpurified virus used as the antigen and
the capture and detector antibodies were prepared and standardized for
this purpose. The hemagglutination-inhibition (HI) test was regarded as
the reference method. The cutoff point for the LPB-ELISA was determined
by a two-graph receiver operating characteristic analysis. The
LPB-ELISA titers regressed significantly (P < 0.0001) on the HI titers with a high correlation coefficient
(r = 0.875). The two tests showed good agreement
(
1071-412X/00/$04.00+0
Copyright © 2000, American Society for Microbiology. All rights reserved.
Detection and Quantification of Antibodies to Newcastle Disease
Virus in Ostrich and Rhea Sera Using a Liquid Phase Blocking
Enzyme-Linked Immunosorbent Assay
= 0.82; P < 0.0001), relative sensitivity
(90.91%) and specificity (91.18%), and accuracy (91.02%), suggesting
that they are interchangeable.
*
Corresponding author. Mailing address: Laboratório de
Virologia e Imunologia, Departamento de Patologia Veterinária,
Faculdade de Ciências Agrárias e Veterinárias, Universidade
Estadual Paulista (UNESP), Via de Acesso Prof. Paulo Donato Castellane,
Km 05, 14870-000, Jaboticabal, São Paulo, Brazil. Phone:
55-16-3232500, ext. 225. Fax: 55-16-3224275. E-mail:
aramisap{at}asbyte.com.br.
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