Doubly Branched Hexasaccharide Epitope on the Cell Wall Polysaccharide of Group A Streptococci Recognized by Human and Rabbit Antisera
Autor: | Milan S. Blake, John Kim, Francis Michon, Samuel L. Moore, B. Mario Pinto, France-Isabelle Auzanneau, Blair D. Johnston, Margaret A. Johnson |
---|---|
Rok vydání: | 2005 |
Předmět: |
Glycoconjugate
Molecular Sequence Data Immunology Microbiology Group A Epitope Antigen Cell Wall Carbohydrate Conformation Animals Humans Trisaccharide Antiserum chemistry.chemical_classification biology Immunodominant Epitopes Immune Sera Polysaccharides Bacterial Bacterial polysaccharide Antibodies Bacterial Infectious Diseases Carbohydrate Sequence chemistry Polyclonal antibodies Microbial Immunity and Vaccines biology.protein Parasitology Rabbits Glycoconjugates Haptens |
Zdroj: | Infection and Immunity. 73:6383-6389 |
ISSN: | 1098-5522 0019-9567 |
DOI: | 10.1128/iai.73.10.6383-6389.2005 |
Popis: | A number of epitope specificities associated with the cell wall polysaccharide antigen of group A streptococci were identified in a polyclonal rabbit antiserum induced in rabbits by whole group A streptococci and in polyclonal convalescent human antisera from children that had recovered from streptococcal A infections. The identification was achieved by using a series of synthetic oligosaccharides, glycoconjugates, and bacterial polysaccharide inhibitors to inhibit the binding of the group A helical polysaccharide to the polyclonal antisera. The exclusively dominant epitope expressed in the convalescent human antisera was the doubly branched extended helical hexasaccharide with the structure α-l-Rhap(1→2)[β-d-GlcpNAc(1→3)]α-l-Rhap(1→3)α-l-Rhap(1→2)[β-d-GlcpNAc(1→3)]α-l-Rhap. The hexasaccharide epitope also bound with the highest immunoreactivity to the rabbit antiserum. In contrast, the human antisera did not show significant binding to the singly branched pentasaccharide with the structure α-l-Rhap(1→2)α-l-Rhap(1→3)α-l-Rhap(1→2)[β-d-GlcpNAc(1→3)]α-l-Rhapor the branched trisaccharide α-l-Rhap(1→2)[β-d-GlcpNAc(1→3)]α-l-Rhap, although both these haptens bound significantly to the same rabbit antiserum, albeit with less immunoreactivity than the hexasaccharide. Inhibition studies using streptococcal group A and B rabbit antisera and the inhibitors indicated above also suggested that the group A carbohydrate, unlike the group B streptococcal polysaccharide, does not contain the disaccharide α-l-Rhap(1→2)α-l-Rhapmotif at its nonreducing chain terminus, stressing the importance of mapping the determinant specificities of these two important streptococcal subcapsular group polysaccharides to fully understand the serological relationships between group A and group B streptococci. |
Databáze: | OpenAIRE |
Externí odkaz: |