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Infection and Immunity, September 1998, p. 4073-4079, Vol. 66, No. 9
0019-9567/98/$04.00+0
Copyright © 1998, American Society for Microbiology. All rights reserved.
The Dominant Epitope of Borrelia garinii Outer Surface
Protein C Recognized by Sera from Patients with Neuroborreliosis
Has a Surface-Exposed Conserved Structural Motif
Marianne J.
Mathiesen,1
Arne
Holm,2
Michael
Christiansen,1
Jens
Blom,3
Klaus
Hansen,1
Søren
Østergaard,2,
and
Michael
Theisen1,*
Department of Clinical
Biochemistry1 and
Department of
Molecular Cell Biology,3 Statens Serum
Institut, and
Department of Chemistry, Royal Veterinary and
Agricultural University,2 Copenhagen, Denmark
Received 4 March 1998/Returned for modification 8 April
1998/Accepted 27 May 1998
Epitope mapping of outer surface protein C (OspC) by using sera
from patients with neuroborreliosis led to the identification of one
single major immunodominant epitope within the C-terminal 10 amino acid
residues. Peptide binding studies and alanine replacement scanning of
the C-terminal decapeptide, PVVAESPKKP, revealed a critical role for
the PKKP sequence and its terminal carboxyl group for the binding of
immunoglobulin M (IgM) antibodies from patients with Lyme borreliosis.
Electron microscopy of antibody-labeled spirochetes indicated that the
C-terminal region is exposed on the surface of the spirochete. Based on
homology to proteins of known function, this region most probably
adopts a polyproline II-like helix, which is found in surface-exposed
structures involved in protein-protein interactions. This structural
motif is highly conserved in Borrelia species causing Lyme
borreliosis and subjected to purifying selection. We suggest that the
abundance of the C-terminal region of OspC on the surface of B. burgdorferi allows a multimeric high-avidity
interaction between the spirochete and surface Igs on B cells.
The resulting cross-linking of surface Igs on B cells may induce a
T-cell-independent B-cell activation without IgM-to-IgG switching, thus
explaining the lack of IgG antibodies to OspC in neuroborreliosis.
*
Corresponding author. Mailing address: Department of
Clinical Biochemistry, Statens Serum Institut, Artillerivej 5, DK-2300 Copenhagen S, Denmark. Phone: (45) 32683779. Fax: (45) 32683228. E-mail: mth{at}ssi.dk.
Present address: Novo Research Institute, Bagsværd, Denmark.
Infection and Immunity, September 1998, p. 4073-4079, Vol. 66, No. 9
0019-9567/98/$04.00+0
Copyright © 1998, American Society for Microbiology. All rights reserved.
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