Previous Article | Next Article ![]()
J Virol, July 1998, p. 6218-6222, Vol. 72, No. 7
Laboratory of Hepatitis Viruses, Division of
Viral Products, Center for Biologics Evaluation and Research, Food
and Drug Administration, Bethesda, Maryland 20892
Received 20 January 1998/Accepted 30 March 1998
Monoclonal antibody (MAb) 190/4 blocks binding of hepatitis A virus
(HAV) to the HAV cellular receptor 1 (havcr-1) and protects African
green monkey kidney (AGMK) clone GL37 cells (GL37 cells) against HAV
infection. BS-C-1 and CV-1 cells, two widely used AGMK cell lines, did
not react with MAb 190/4 but expressed havcr-1, as judged by Western
blot analysis. The cDNA coding for havcr-1 was amplified from BS-C-1
and CV-1 total cellular RNA by reverse transcription-PCR. Alignment of
the amino acid sequences inferred from the cDNA nucleotide sequences
showed that BS-C-1 and CV-1 havcr-1 differed from GL37 havcr-1 by
having two substitutions in the Cys-rich region, N48H and K108Q, and 10 to 11 additional substitutions plus the insertion of 18 to 22 amino
acids in the mucin-like region. Studies with chimeras of GL37 havcr-1
and BS-C-1 havcr-1 showed that the K108Q substitution was responsible
for the lack of reaction of MAb 190/4 with BS-C-1 and CV-1 cells. Binding studies indicated that HAV bound to dog cell transfectants expressing the BS-C-1 havcr-1 as well as the GL37/BS-C-1 havcr-1 chimeras. These results indicate that antigenic variants of havcr-1 are
expressed in AGMK cells and that binding of HAV to these havcr-1 variants tolerates changes in protective epitope 190/4.
0022-538X/98/$04.00+0
Copyright © 1998, American Society for Microbiology. All rights reserved.
Polymorphisms of the Hepatitis A Virus Cellular
Receptor 1 in African Green Monkey Kidney Cells Result in Antigenic
Variants That Do Not React with Protective Monoclonal
Antibody 190/4
*
Corresponding author. Mailing address: Division of
Viral Products, CBER-FDA, 8800 Rockville Pike, Bldg. 29A-NIH, Room
1D10, HFM-448, Bethesda, MD 20892. Phone: (301) 827-1870. Fax: (301) 480-5326. E-mail: gk{at}helix.nih.gov.
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»