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Streptococcal Receptor Polysaccharides: Recognition Molecules for Oral Biofilm Formation

BACKGROUND: Strains of viridans group streptococci that initiate colonization of the human tooth surface typically coaggregate with each other and with Actinomyces naeslundii, another member of the developing biofilm community. These interactions generally involve adhesin-mediated recognition of str...

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Autores principales: Yoshida, Yasuo, Palmer, Robert J, Yang, Jinghua, Kolenbrander, Paul E, Cisar, John O
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2006
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2147599/
https://www.ncbi.nlm.nih.gov/pubmed/16934113
http://dx.doi.org/10.1186/1472-6831-6-S1-S12
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author Yoshida, Yasuo
Palmer, Robert J
Yang, Jinghua
Kolenbrander, Paul E
Cisar, John O
author_facet Yoshida, Yasuo
Palmer, Robert J
Yang, Jinghua
Kolenbrander, Paul E
Cisar, John O
author_sort Yoshida, Yasuo
collection PubMed
description BACKGROUND: Strains of viridans group streptococci that initiate colonization of the human tooth surface typically coaggregate with each other and with Actinomyces naeslundii, another member of the developing biofilm community. These interactions generally involve adhesin-mediated recognition of streptococcal receptor polysaccharides (RPS). The objective of our studies is to understand the role of these polysaccharides in oral biofilm development. METHODS: Different structural types of RPS have been characterized by their reactions with specific antibodies and lectin-like adhesins. Streptococcal gene clusters for RPS biosynthesis were identified, sequenced, characterized and compared. RPS-producing bacteria were detected in biofilm samples using specific antibodies and gene probes. RESULTS: Six different types of RPS have been identified from representative viridans group streptococci that coaggregate with A. naeslundii. Each type is composed of a different hexa- or heptasaccharide repeating unit, the structures of which contain host-like motifs, either GalNAcβ1-3Gal or Galβ1-3GalNAc. These motifs account for RPS-mediated recognition, whereas other features of these polysaccharides are more closely associated with RPS antigenicity. The RPS-dependent interaction of S. oralis with A. naeslundii promotes growth of these bacteria and biofilm formation in flowing saliva. Type specific differences in RPS production have been noted among the resident streptococcal floras of different individuals, raising the possibility of RPS-based differences in the composition of oral biofilm communities. CONCLUSION: The structural, functional and molecular properties of streptococcal RPS support a recognition role of these cell surface molecules in oral biofilm formation.
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spelling pubmed-21475992007-12-20 Streptococcal Receptor Polysaccharides: Recognition Molecules for Oral Biofilm Formation Yoshida, Yasuo Palmer, Robert J Yang, Jinghua Kolenbrander, Paul E Cisar, John O BMC Oral Health Proceedings BACKGROUND: Strains of viridans group streptococci that initiate colonization of the human tooth surface typically coaggregate with each other and with Actinomyces naeslundii, another member of the developing biofilm community. These interactions generally involve adhesin-mediated recognition of streptococcal receptor polysaccharides (RPS). The objective of our studies is to understand the role of these polysaccharides in oral biofilm development. METHODS: Different structural types of RPS have been characterized by their reactions with specific antibodies and lectin-like adhesins. Streptococcal gene clusters for RPS biosynthesis were identified, sequenced, characterized and compared. RPS-producing bacteria were detected in biofilm samples using specific antibodies and gene probes. RESULTS: Six different types of RPS have been identified from representative viridans group streptococci that coaggregate with A. naeslundii. Each type is composed of a different hexa- or heptasaccharide repeating unit, the structures of which contain host-like motifs, either GalNAcβ1-3Gal or Galβ1-3GalNAc. These motifs account for RPS-mediated recognition, whereas other features of these polysaccharides are more closely associated with RPS antigenicity. The RPS-dependent interaction of S. oralis with A. naeslundii promotes growth of these bacteria and biofilm formation in flowing saliva. Type specific differences in RPS production have been noted among the resident streptococcal floras of different individuals, raising the possibility of RPS-based differences in the composition of oral biofilm communities. CONCLUSION: The structural, functional and molecular properties of streptococcal RPS support a recognition role of these cell surface molecules in oral biofilm formation. BioMed Central 2006-06-15 /pmc/articles/PMC2147599/ /pubmed/16934113 http://dx.doi.org/10.1186/1472-6831-6-S1-S12 Text en Copyright © 2006 Yoshida et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an open access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Proceedings
Yoshida, Yasuo
Palmer, Robert J
Yang, Jinghua
Kolenbrander, Paul E
Cisar, John O
Streptococcal Receptor Polysaccharides: Recognition Molecules for Oral Biofilm Formation
title Streptococcal Receptor Polysaccharides: Recognition Molecules for Oral Biofilm Formation
title_full Streptococcal Receptor Polysaccharides: Recognition Molecules for Oral Biofilm Formation
title_fullStr Streptococcal Receptor Polysaccharides: Recognition Molecules for Oral Biofilm Formation
title_full_unstemmed Streptococcal Receptor Polysaccharides: Recognition Molecules for Oral Biofilm Formation
title_short Streptococcal Receptor Polysaccharides: Recognition Molecules for Oral Biofilm Formation
title_sort streptococcal receptor polysaccharides: recognition molecules for oral biofilm formation
topic Proceedings
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2147599/
https://www.ncbi.nlm.nih.gov/pubmed/16934113
http://dx.doi.org/10.1186/1472-6831-6-S1-S12
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