COMPARISON OF THE REACTIVITIES OF BACULOVIRUS-EXPRESSED RECOMBINANT NORWALK VIRUS CAPSID ANTIGEN WITH THOSE OF THE NATIVE NORWALK VIRUS-ANTIGEN IN SEROLOGIC ASSAYS AND SOME EPIDEMIOLOGIC OBSERVATIONS

Citation
Ky. Green et al., COMPARISON OF THE REACTIVITIES OF BACULOVIRUS-EXPRESSED RECOMBINANT NORWALK VIRUS CAPSID ANTIGEN WITH THOSE OF THE NATIVE NORWALK VIRUS-ANTIGEN IN SEROLOGIC ASSAYS AND SOME EPIDEMIOLOGIC OBSERVATIONS, Journal of clinical microbiology, 31(8), 1993, pp. 2185-2191
Citations number
30
Categorie Soggetti
Microbiology
ISSN journal
00951137
Volume
31
Issue
8
Year of publication
1993
Pages
2185 - 2191
Database
ISI
SICI code
0095-1137(1993)31:8<2185:COTROB>2.0.ZU;2-E
Abstract
Since the discovery of the Norwalk virus (NV) by immune electron micro scopy (IEM) in 1972, serologic studies with this virus have relied on particle-positive fecal material from infected volunteers as the sourc e of antigen because it has not been possible to propagate this virus in cell culture. However, the recent cloning of the W (strain 8FIIa) g enome and expression of the capsid protein in a baculovirus system to form ''virus-like particles'' has provided a consistent source of anti gen (designated rNV). The purpose of the present study was to compare the antigenicities of these rW particles with those of native W antige n derived from human fecal material by using well-characterized sera o btained from earlier studies. In IEM studies, the rNV antigen reacted with NV-specific antibodies in a manner similar to that observed previ ously when particle-positive fecal material was used as antigen. In ad dition, a direct enzyme-linked immunosorbent assay, in which the rW an tigen was used as antigen, proved efficient and specific for the detec tion of serologic responses to W compared with the previously establis hed techniques of IEM and blocking antibody immunoassays in which part icle-positive fecal material was used as the antigen. The availability of an unlimited source of antigen will enable serologic studies that will greatly increase our understanding of the epidemiology of W and i ts role in human enteric illness.