Previous Article | Next Article ![]()
Journal of Clinical Microbiology, April 2000, p. 1397-1403, Vol. 38, No. 4
Rabies Centre of Expertise, Animal Diseases
Research Institute, Canadian Food Inspection Agency, Nepean,
Ontario, Canada, K2H 8P9
Received 30 July 1999/Returned for modification 1 December
1999/Accepted 4 January 2000
A recombinant rabies virus phosphoprotein fusion product (GST-P)
was used to generate a series of monoclonal antibodies (MAbs) with anti-P reactivity. Competitive binding assays classified 27 of
these MAbs into four groups (I to IV), and 24 of them were deemed to
recognize linear epitopes, as judged by their reaction in immunoblots.
The linear epitope recognized in each case was mapped by using two
series of N- and C-terminally deleted recombinant phosphoproteins.
Assessment of the reactivities of representative MAbs to a
variety of lyssavirus isolates by an indirect fluorescent antibody
test indicated that group I MAbs, which recognized a highly conserved
N-terminal epitope, were broadly cross-reactive with all lyssaviruses
assayed, while group III MAbs, which reacted with a site overlapping
that of group I MAbs, exhibited variable reactivities and
group IV MAbs reacted with most isolates of genotypes 1, 6, and 7 only.
In contrast, group II MAbs, which recognized an epitope located
within a highly divergent central portion of the protein, were
exquisitely strain specific. These anti-P MAbs are potentially useful
tools for lyssavirus identification and discrimination.
0095-1137/00/$04.00+0
A Panel of Monoclonal Antibodies Targeting the Rabies Virus
Phosphoprotein Identifies a Highly Variable Epitope of Value for
Sensitive Strain Discrimination
*
Corresponding author. Mailing address: Rabies Centre of
Expertise, Animal Diseases Research Institute, Canadian Food Inspection Agency, 3851 Fallowfield Rd., Nepean, Ontario K2H 8P9, Canada. Phone:
(613) 228-6698. Fax: (613) 228-6669. E-mail:
nadindaviss{at}em.agr.ca.
This article has been cited by other articles:
Copyright © 2009 by the American Society for Microbiology. For an alternate route to Journals.ASM.org, visit: http://intl-journals.asm.org | More Info»