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Clinical and Diagnostic Laboratory Immunology, May 1999, p. 341-344, Vol. 6, No. 3
Department of Diagnostic
Medicine-Pathobiology, College of Veterinary Medicine, Manhattan,
Kansas 66506
Received 16 November 1998/Returned for modification 5 January
1999/Accepted 6 February 1999
This is the first report of the production of monoclonal antibodies
against elk coronavirus. The nucleoprotein gene of elk coronavirus was
amplified by PCR and was cloned and expressed in a prokaryotic
expression vector. Recombinant nucleocapsid protein was used to
immunize mice for the production of hybridomas. Twelve hybridomas that
produced monoclonal antibodies against the nucleocapsid protein of elk
coronavirus were selected by an indirect fluorescent-antibody test, an
enzyme-linked immunosorbent assay, and a Western blot assay. Ten of the
monoclonal antibodies were of the immunoglobulin G1 (IgG1) isotype, one
was IgG2a, and one was IgM. All had kappa light chains. By
immunohistochemistry four monoclonal antibodies detected bovine
coronavirus and elk coronavirus in formalin-fixed intestinal tissues.
Antinucleoprotein monoclonal antibodies were found to be better at
ruminant coronavirus detection than the anti-spike protein monoclonal
antibodies. Because nucleoprotein is a more abundant antigen than spike
protein in infected cells, this was not an unexpected finding.
1071-412X/99/$04.00+0
Copyright © 1999, American Society for Microbiology. All rights reserved.
Production, Characterization, and Uses of
Monoclonal Antibodies against Recombinant Nucleoprotein of
Elk Coronavirus
*
Corresponding author: Sanjay Kapil, Department of
Diagnostic Medicine-Pathobiology, 1800 Denison Ave., College of
Veterinary Medicine, Manhattan, KS 66506. Phone: (785) 532-4457. Fax:
(785) 532-4481. E-mail: kapil{at}vet.ksu.edu.
This is contribution no. 99-169-J from the Kansas Agricultural
Experiment Station.
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