Fusion proteins with multiple copies of the major antigenic determinant of foot-and-mouth disease virus protect both the natural host and laboratory animals

1 Medical Biological Laboratory TNO, P.O. Box 45, 2280 AA Rijswijk, The Netherlands and 2 Wellcome Biotechnology Limited, Ash Road, Pirbright, Woking, Surrey, GU24 0NQ, U.K. Proteins consisting of one, two or four copies of the amino acid sequence 137 to 162, which contains the major immunogenic sit...

Full description

Saved in:
Bibliographic Details
Published in:Journal of general virology Vol. 68; no. 12; pp. 3137 - 3143
Main Authors: Broekhuijsen, M.P, Rijn, J.M.M. van, Blom, A.J.M, Pouwels, P.H, Enger-Valk, B.E, Brown, F, Francis, M.J
Format: Journal Article
Language:English
Published: Reading Soc General Microbiol 01-12-1987
Society for General Microbiology
Subjects:
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
Description
Summary:1 Medical Biological Laboratory TNO, P.O. Box 45, 2280 AA Rijswijk, The Netherlands and 2 Wellcome Biotechnology Limited, Ash Road, Pirbright, Woking, Surrey, GU24 0NQ, U.K. Proteins consisting of one, two or four copies of the amino acid sequence 137 to 162, which contains the major immunogenic site of VP1 of foot-and-mouth disease virus, attached to the N-terminus of -galactosidase have been expressed in Escherichia coli cells. In guinea-pigs the protein containing one copy (P71) of the viral determinant elicited only low levels of neutralizing antibody whereas protective levels were elicited by the proteins containing two (P72) or four (P74) copies of the determinant. Single inoculations of the P72 and P74 proteins containing as little as 2 µg or 0.8 µg of peptide respectively were sufficient to protect all the animals against challenge infection. Moreover, the equivalent of 40 µg of peptide in P74 protected pigs against challenge infection after one inoculation. Keywords: foot-and-mouth disease virus, fusion protein, immunogenic peptide Received 22 July 1987; accepted 20 August 1987.
Bibliography:ObjectType-Article-2
SourceType-Scholarly Journals-1
ObjectType-Feature-1
content type line 23
ObjectType-Article-1
ObjectType-Feature-2
ISSN:0022-1317
1465-2099
DOI:10.1099/0022-1317-68-12-3137