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Role of O-Acetylation in the Immunogenicity of Bacterial Polysaccharide Vaccines

The incidence of infectious diseases caused by several bacterial pathogens such as Haemophilus influenzae type b, Streptococcus pneumoniae, and Neisseria meningitidis, has been dramatically reduced over the last 25 years through the use of glycoconjugate vaccines. The structures of the bacterial cap...

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Autores principales: Berti, Francesco, De Ricco, Riccardo, Rappuoli, Rino
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6100563/
https://www.ncbi.nlm.nih.gov/pubmed/29865239
http://dx.doi.org/10.3390/molecules23061340
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author Berti, Francesco
De Ricco, Riccardo
Rappuoli, Rino
author_facet Berti, Francesco
De Ricco, Riccardo
Rappuoli, Rino
author_sort Berti, Francesco
collection PubMed
description The incidence of infectious diseases caused by several bacterial pathogens such as Haemophilus influenzae type b, Streptococcus pneumoniae, and Neisseria meningitidis, has been dramatically reduced over the last 25 years through the use of glycoconjugate vaccines. The structures of the bacterial capsular polysaccharide (CPS) antigens, extracted and purified from microbial cultures and obtained with very high purity, show that many of them are decorated by O-acetyl groups. While these groups are often considered important for the structural identity of the polysaccharides, they play a major role in the functional immune response to some vaccines such as meningococcal serogroup A and Salmonella typhi Vi, but do not seem to be important for many others, such as meningococcal serogroups C, W, Y, and type III Group B Streptococcus. This review discusses the O-acetylation status of CPSs and its role in the immunological responses of these antigens.
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spelling pubmed-61005632018-11-13 Role of O-Acetylation in the Immunogenicity of Bacterial Polysaccharide Vaccines Berti, Francesco De Ricco, Riccardo Rappuoli, Rino Molecules Review The incidence of infectious diseases caused by several bacterial pathogens such as Haemophilus influenzae type b, Streptococcus pneumoniae, and Neisseria meningitidis, has been dramatically reduced over the last 25 years through the use of glycoconjugate vaccines. The structures of the bacterial capsular polysaccharide (CPS) antigens, extracted and purified from microbial cultures and obtained with very high purity, show that many of them are decorated by O-acetyl groups. While these groups are often considered important for the structural identity of the polysaccharides, they play a major role in the functional immune response to some vaccines such as meningococcal serogroup A and Salmonella typhi Vi, but do not seem to be important for many others, such as meningococcal serogroups C, W, Y, and type III Group B Streptococcus. This review discusses the O-acetylation status of CPSs and its role in the immunological responses of these antigens. MDPI 2018-06-02 /pmc/articles/PMC6100563/ /pubmed/29865239 http://dx.doi.org/10.3390/molecules23061340 Text en © 2018 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Berti, Francesco
De Ricco, Riccardo
Rappuoli, Rino
Role of O-Acetylation in the Immunogenicity of Bacterial Polysaccharide Vaccines
title Role of O-Acetylation in the Immunogenicity of Bacterial Polysaccharide Vaccines
title_full Role of O-Acetylation in the Immunogenicity of Bacterial Polysaccharide Vaccines
title_fullStr Role of O-Acetylation in the Immunogenicity of Bacterial Polysaccharide Vaccines
title_full_unstemmed Role of O-Acetylation in the Immunogenicity of Bacterial Polysaccharide Vaccines
title_short Role of O-Acetylation in the Immunogenicity of Bacterial Polysaccharide Vaccines
title_sort role of o-acetylation in the immunogenicity of bacterial polysaccharide vaccines
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6100563/
https://www.ncbi.nlm.nih.gov/pubmed/29865239
http://dx.doi.org/10.3390/molecules23061340
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