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Journal of Clinical Microbiology, April 2001, p. 1449-1455, Vol. 39, No. 4
0095-1137/01/$04.00+0   DOI: 10.1128/JCM.39.4.1449-1455.2001
Copyright © 2001, American Society for Microbiology. All rights reserved.

Definition of a Divergent Epitope That Allows Differential Detection of Early Protein p41 from Human Herpesvirus 6 Variants A and B

Yunhe Xu,1,2 Annika Linde,1,2 Helena Dahl,1,2 and Gosta Winberg1,2,*

Department of Virology, Swedish Institute for Infectious Disease Control, 171 82 Solna,1 and Karolinska Institute, Microbiology and Tumor Biology Center, 171 77 Stockholm,2 Sweden

Received 1 December 2000/Returned for modification 4 January 2001/Accepted 29 January 2001

The human herpesvirus 6 (HHV-6) early protein, p41, encoded by the U27 gene has been detected in oligodendrocytes of multiple sclerosis (MS) patients by using a monoclonal antibody (MAb to p41/38). We here report the antigenic epitope of HHV-6 p41 recognized by this MAb. First, we established that the MAb to p41/38 recognizes a nuclear antigen in HHV-6A strain GS-infected cells but not in HHV-6B strain Z29-infected cells. Secondly, we compared the reactivity of the MAb to p41/38 to that of another p41-specific MAb (MAb to p41) on immunoblots with purified p41-glutathione S-transferase fusion protein from strains GS and Z29 and GS- and Z29-infected-cell lysates. The two MAbs were tested in an enzyme-linked immunosorbent assay against a panel of synthetic peptides covering the amino acid substitutions between the GS- and Z29-derived p41 proteins, as determined by DNA sequencing of our cloned isolates of the U27 gene. The MAb to p41/38 reacted specifically with a peptide comprising p41 residues 321 to 340 from strain GS. The critical residue in this peptide was serine 328, as the substitution S328N in the Z29 strain rendered the corresponding peptide nonreactive. The p41 S328 marker was present in three of three HHV-6A strains, while four of four sequenced p41 genes from HHV-6B strains had N328. Our findings are of value for the interpretation of previous findings of p41 expression in brains of MS patients and may allow a more detailed analysis of the role of HHV-6 variants in other disorders.


* Corresponding author. Mailing address: Karolinska Institute, MTC, P.O. Box 280, Nobels Vag 16, SE-17177 Stockholm, Sweden. Phone: 468 457 2610 or 468 728 6249. Fax: 468 31 9470 or 468 337272. E-mail: Gosta.Winberg{at}mtc.ki.se.


Journal of Clinical Microbiology, April 2001, p. 1449-1455, Vol. 39, No. 4
0095-1137/01/$04.00+0   DOI: 10.1128/JCM.39.4.1449-1455.2001
Copyright © 2001, American Society for Microbiology. All rights reserved.



This article has been cited by other articles:

  • Tuke, P W, Hawke, S, Griffiths, P D, Clark, D A (2004). Distribution and quantification of human herpesvirus 6 in multiple sclerosis and control brains. Mult Scler 10: 355-359 [Abstract]  
  • Alvarez-Lafuente, R., Martin-Estefania, C., de las Heras, V., Castrillo, C., Picazo, J. J., Varela de Seijas, E., Gonzalez, R. A. (2002). Active Human Herpesvirus 6 Infection in Patients With Multiple Sclerosis. Arch Neurol 59: 929-933 [Abstract] [Full Text]