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Journal of Clinical Microbiology, December 1999, p. 3952-3956, Vol. 37, No. 12
Department of Virology,
Received 20 April 1999/Returned for modification 5 July
1999/Accepted 16 August 1999
The major capsid protein VP2 of human parvovirus B19, when studied
in a denatured form exhibiting linear epitopes, is recognized exclusively by immunoglobulin G (IgG) antibodies of patients with acute
or recent B19 infection. By contrast, conformational epitopes of VP2
are recognized both by IgG of the acute phase and by IgG of past
immunity. In order to localize the VP2 linear epitope(s) specific for
acute-phase IgG, the entire B19 capsid protein sequence was mapped by
peptide scanning using well-characterized acute-phase and control sera.
A unique heptapeptide epitope showing strong and selective reactivity
with the acute-phase IgG was detected and characterized. By using this
linear epitope (VP2 amino acids 344 to 350) and virus-like particles
exhibiting conformational VP2 epitopes, an innovative approach,
second-generation epitope-typing enzyme immunoassay, was set up for
improved diagnosis of primary infections by human parvovirus B19.
0095-1137/99/$04.00+0
Copyright © 1999, American Society for Microbiology. All rights reserved.
Acute-Phase-Specific Heptapeptide Epitope for
Diagnosis of Parvovirus B19 Infection
*
Corresponding author. Mailing address: Haartman
Institute and HUCH Diagnostic, Department of Virology, P.O. Box 21 (Haartmaninkatu 3), FIN-00014 University of Helsinki, Finland. Phone:
358-50-5249 086. Fax: 358-9-1912 6491. E-mail:
klaus.hedman{at}helsinki.fi.
Journal of Clinical Microbiology, December 1999, p. 3952-3956, Vol. 37, No. 12
0095-1137/99/$04.00+0
Copyright © 1999, American Society for Microbiology. All rights reserved.
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