J Gen Virol Try IJSEM Online
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


J Gen Virol 65 (1984), 197-201; DOI 10.1099/0022-1317-65-1-197
© 1984 Society for General Microbiology

This Article
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via CrossRef
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Ferguson, M.
Right arrow Articles by Schild, G. C.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Ferguson, M.
Right arrow Articles by Schild, G. C.
Agricola
Right arrow Articles by Ferguson, M.
Right arrow Articles by Schild, G. C.

Neutralization Epitopes on Poliovirus Type 3 Particles: an Analysis Using Monoclonal Antibodies

Morag Ferguson, P. D. Minor, D. I. Magrath, Qui Yi-Hua{dagger}, M. Spitz and G. C. Schild

National Institute for Biological Standards and Control, Holly Hill, Hampstead, London NW3 6RB, U.K.

Monoclonal antibodies to poliovirus type 3 secreted by 51 hybridoma cell clones have been characterized in terms of (i) virus-neutralizing properties, (ii) reactivity in antigen-blocking tests with infectious, 155S (‘D’ antigen) and empty 80S (‘C’ antigen) poliovirus particles and (iii) reactivity in immunoblot tests with the isolated protein components of the poliovirus capsid. The antibodies could be separated into three groups on the basis of their reactivities with ‘D’ and ‘C’ antigens. All antibodies that reacted with both ‘D’ and ‘C’ antigen had potent neutralizing activity. Only a proportion of antibodies that reacted uniquely with ‘D’ antigen possessed neutralizing activity. Unexpectedly, one of 24 ‘C’ antigen-specific antibodies inhibited virus growth. None of the antibodies that possessed virus-neutralizing activity reacted with isolated poliovirus capsid proteins, although the majority of these have been shown in previous studies to be specific for VP1 on intact virus particles. These findings suggest that antigenic determinants involved in virus neutralization do not survive the denaturing conditions required for the isolation of poliovirus capsid proteins and consequently are likely to be specified by the structural conformation of VP1 rather than by amino acid sequence alone. However, several of the antibodies which bound uniquely to ‘C’ antigen reacted in immunoblot tests, five with VP1 and one with VP3. Some of these antibodies also possessed heterotypic reactivity with the corresponding capsid proteins separated from other poliovirus types.

Keywords: poliovirus type 3, monoclonal Abs, neutralization, immunoblot

{dagger} Present address: National Vaccine and Serum Institute, Beijing, China.

Received 22 July 1983; accepted 10 October 1983.





HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
INT J SYST EVOL MICROBIOL MICROBIOLOGY J GEN VIROL
J MED MICROBIOL ALL SGM JOURNALS
Copyright © 1984 by the Society for General Microbiology.