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Exploitation of bacterial N-linked glycosylation to develop a novel recombinant glycoconjugate vaccine against Francisella tularensis
Glycoconjugate-based vaccines have proved to be effective at producing long-lasting protection against numerous pathogens. Here, we describe the application of bacterial protein glycan coupling technology (PGCT) to generate a novel recombinant glycoconjugate vaccine. We demonstrate the conjugation o...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3866875/ https://www.ncbi.nlm.nih.gov/pubmed/23697804 http://dx.doi.org/10.1098/rsob.130002 |
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author | Cuccui, Jon Thomas, Rebecca M. Moule, Madeleine G. D'Elia, Riccardo V. Laws, Thomas R. Mills, Dominic C. Williamson, Diane Atkins, Timothy P. Prior, Joann L. Wren, Brendan W. |
author_facet | Cuccui, Jon Thomas, Rebecca M. Moule, Madeleine G. D'Elia, Riccardo V. Laws, Thomas R. Mills, Dominic C. Williamson, Diane Atkins, Timothy P. Prior, Joann L. Wren, Brendan W. |
author_sort | Cuccui, Jon |
collection | PubMed |
description | Glycoconjugate-based vaccines have proved to be effective at producing long-lasting protection against numerous pathogens. Here, we describe the application of bacterial protein glycan coupling technology (PGCT) to generate a novel recombinant glycoconjugate vaccine. We demonstrate the conjugation of the Francisella tularensis O-antigen to the Pseudomonas aeruginosa carrier protein exotoxin A using the Campylobacter jejuni PglB oligosaccharyltransferase. The resultant recombinant F. tularensis glycoconjugate vaccine is expressed in Escherichia coli where yields of 3 mg l(−1) of culture were routinely produced in a single-step purification process. Vaccination of BALB/c mice with the purified glycoconjugate boosted IgG levels and significantly increased the time to death upon subsequent challenge with F. tularensis subsp. holarctica. PGCT allows different polysaccharide and protein combinations to be produced recombinantly and could be easily applicable for the production of diverse glycoconjugate vaccines. |
format | Online Article Text |
id | pubmed-3866875 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | The Royal Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-38668752014-01-03 Exploitation of bacterial N-linked glycosylation to develop a novel recombinant glycoconjugate vaccine against Francisella tularensis Cuccui, Jon Thomas, Rebecca M. Moule, Madeleine G. D'Elia, Riccardo V. Laws, Thomas R. Mills, Dominic C. Williamson, Diane Atkins, Timothy P. Prior, Joann L. Wren, Brendan W. Open Biol Research Glycoconjugate-based vaccines have proved to be effective at producing long-lasting protection against numerous pathogens. Here, we describe the application of bacterial protein glycan coupling technology (PGCT) to generate a novel recombinant glycoconjugate vaccine. We demonstrate the conjugation of the Francisella tularensis O-antigen to the Pseudomonas aeruginosa carrier protein exotoxin A using the Campylobacter jejuni PglB oligosaccharyltransferase. The resultant recombinant F. tularensis glycoconjugate vaccine is expressed in Escherichia coli where yields of 3 mg l(−1) of culture were routinely produced in a single-step purification process. Vaccination of BALB/c mice with the purified glycoconjugate boosted IgG levels and significantly increased the time to death upon subsequent challenge with F. tularensis subsp. holarctica. PGCT allows different polysaccharide and protein combinations to be produced recombinantly and could be easily applicable for the production of diverse glycoconjugate vaccines. The Royal Society 2013-05 /pmc/articles/PMC3866875/ /pubmed/23697804 http://dx.doi.org/10.1098/rsob.130002 Text en http://creativecommons.org/licenses/by/3.0/ © 2013 The Authors. Published by the Royal Society under the terms of the Creative Commons Attribution License http://creativecommons.org/licenses/by/3.0/, which permits unrestricted use, provided the original author and source are credited. |
spellingShingle | Research Cuccui, Jon Thomas, Rebecca M. Moule, Madeleine G. D'Elia, Riccardo V. Laws, Thomas R. Mills, Dominic C. Williamson, Diane Atkins, Timothy P. Prior, Joann L. Wren, Brendan W. Exploitation of bacterial N-linked glycosylation to develop a novel recombinant glycoconjugate vaccine against Francisella tularensis |
title | Exploitation of bacterial N-linked glycosylation to develop a novel recombinant glycoconjugate vaccine against Francisella tularensis |
title_full | Exploitation of bacterial N-linked glycosylation to develop a novel recombinant glycoconjugate vaccine against Francisella tularensis |
title_fullStr | Exploitation of bacterial N-linked glycosylation to develop a novel recombinant glycoconjugate vaccine against Francisella tularensis |
title_full_unstemmed | Exploitation of bacterial N-linked glycosylation to develop a novel recombinant glycoconjugate vaccine against Francisella tularensis |
title_short | Exploitation of bacterial N-linked glycosylation to develop a novel recombinant glycoconjugate vaccine against Francisella tularensis |
title_sort | exploitation of bacterial n-linked glycosylation to develop a novel recombinant glycoconjugate vaccine against francisella tularensis |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3866875/ https://www.ncbi.nlm.nih.gov/pubmed/23697804 http://dx.doi.org/10.1098/rsob.130002 |
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