J Virol, May 1998, p. 4541-4545, Vol. 72, No. 5
Boehringer Mannheim GmbH, R&D Infectious
Diseases, 82377 Penzberg, Germany
Received 10 November 1997/Accepted 3 February 1998
In order to elucidate the structure and morphology of hepatitis G
virus (HGV), a recently isolated flavivirus, we generated a panel of
eight monoclonal antibodies (MAbs) against the putative second envelope
protein (E2) following DNA immunization. The MAbs were shown to be
specific for four different epitopes on recombinant E2. MAb Mc6 was the
only antibody able to detect the linear epitope LTGGFYEPL. In addition,
Mc6 was able to immunoprecipitate viral particles in human blood
samples as detected by reverse transcription-PCR amplification
of HGV RNA. This precipitation could be competed by addition of
saturating amounts of the linear peptide or abolished by addition of
Nonidet P-40. We conclude that, albeit lacking the N-terminal sequence
of a functional core protein, HGV builds classical viral
particles displaying E2 envelope protein on their outer surfaces.
0022-538X/98/$04.00+0
Copyright © 1998, American Society for Microbiology. All rights reserved.
Identification of Hepatitis G Virus Particles in
Human Serum by E2-Specific Monoclonal Antibodies Generated by
DNA Immunization
*
Corresponding author. Mailing address: Boehringer
Mannheim GmbH, R&D Infectious Diseases, Nonnenwaldstr. 2, D-82377
Penzberg, Germany. Phone: (49 8856) 60-3509. Fax: (49 8856)
60-3129. E-mail: ALFRED_ENGEL{at}BMG.BOEHRINGER-MANNHEIM.COM.
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