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Recombinant Plants Provide a New Approach to the Production of Bacterial Polysaccharide for Vaccines
Bacterial polysaccharides have numerous clinical or industrial uses. Recombinant plants could offer the possibility of producing bacterial polysaccharides on a large scale and free of contaminating bacterial toxins and antigens. We investigated the feasibility of this proposal by cloning and express...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3912152/ https://www.ncbi.nlm.nih.gov/pubmed/24498433 http://dx.doi.org/10.1371/journal.pone.0088144 |
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author | Smith, Claire M. Fry, Stephen C. Gough, Kevin C. Patel, Alexandra J. F. Glenn, Sarah Goldrick, Marie Roberts, Ian S. Whitelam, Garry C. Andrew, Peter W. |
author_facet | Smith, Claire M. Fry, Stephen C. Gough, Kevin C. Patel, Alexandra J. F. Glenn, Sarah Goldrick, Marie Roberts, Ian S. Whitelam, Garry C. Andrew, Peter W. |
author_sort | Smith, Claire M. |
collection | PubMed |
description | Bacterial polysaccharides have numerous clinical or industrial uses. Recombinant plants could offer the possibility of producing bacterial polysaccharides on a large scale and free of contaminating bacterial toxins and antigens. We investigated the feasibility of this proposal by cloning and expressing the gene for the type 3 synthase (cps3S) of Streptococcus pneumoniae in Nicotinia tabacum, using the pCambia2301 vector and Agrobacterium tumefaciens-mediated gene transfer. In planta the recombinant synthase polymerised plant-derived UDP-glucose and UDP-glucuronic acid to form type 3 polysaccharide. Expression of the cps3S gene was detected by RT-PCR and production of the pneumococcal polysaccharide was detected in tobacco leaf extracts by double immunodiffusion, Western blotting and high-voltage paper electrophoresis. Because it is used a component of anti-pneumococcal vaccines, the immunogenicity of the plant-derived type 3 polysaccharide was tested. Mice immunised with extracts from recombinant plants were protected from challenge with a lethal dose of pneumococci in a model of pneumonia and the immunised mice had significantly elevated levels of serum anti-pneumococcal polysaccharide antibodies. This study provides the proof of the principle that bacterial polysaccharide can be successfully synthesised in plants and that these recombinant polysaccharides could be used as vaccines to protect against life-threatening infections. |
format | Online Article Text |
id | pubmed-3912152 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-39121522014-02-04 Recombinant Plants Provide a New Approach to the Production of Bacterial Polysaccharide for Vaccines Smith, Claire M. Fry, Stephen C. Gough, Kevin C. Patel, Alexandra J. F. Glenn, Sarah Goldrick, Marie Roberts, Ian S. Whitelam, Garry C. Andrew, Peter W. PLoS One Research Article Bacterial polysaccharides have numerous clinical or industrial uses. Recombinant plants could offer the possibility of producing bacterial polysaccharides on a large scale and free of contaminating bacterial toxins and antigens. We investigated the feasibility of this proposal by cloning and expressing the gene for the type 3 synthase (cps3S) of Streptococcus pneumoniae in Nicotinia tabacum, using the pCambia2301 vector and Agrobacterium tumefaciens-mediated gene transfer. In planta the recombinant synthase polymerised plant-derived UDP-glucose and UDP-glucuronic acid to form type 3 polysaccharide. Expression of the cps3S gene was detected by RT-PCR and production of the pneumococcal polysaccharide was detected in tobacco leaf extracts by double immunodiffusion, Western blotting and high-voltage paper electrophoresis. Because it is used a component of anti-pneumococcal vaccines, the immunogenicity of the plant-derived type 3 polysaccharide was tested. Mice immunised with extracts from recombinant plants were protected from challenge with a lethal dose of pneumococci in a model of pneumonia and the immunised mice had significantly elevated levels of serum anti-pneumococcal polysaccharide antibodies. This study provides the proof of the principle that bacterial polysaccharide can be successfully synthesised in plants and that these recombinant polysaccharides could be used as vaccines to protect against life-threatening infections. Public Library of Science 2014-02-03 /pmc/articles/PMC3912152/ /pubmed/24498433 http://dx.doi.org/10.1371/journal.pone.0088144 Text en © 2014 Smith et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Smith, Claire M. Fry, Stephen C. Gough, Kevin C. Patel, Alexandra J. F. Glenn, Sarah Goldrick, Marie Roberts, Ian S. Whitelam, Garry C. Andrew, Peter W. Recombinant Plants Provide a New Approach to the Production of Bacterial Polysaccharide for Vaccines |
title | Recombinant Plants Provide a New Approach to the Production of Bacterial Polysaccharide for Vaccines |
title_full | Recombinant Plants Provide a New Approach to the Production of Bacterial Polysaccharide for Vaccines |
title_fullStr | Recombinant Plants Provide a New Approach to the Production of Bacterial Polysaccharide for Vaccines |
title_full_unstemmed | Recombinant Plants Provide a New Approach to the Production of Bacterial Polysaccharide for Vaccines |
title_short | Recombinant Plants Provide a New Approach to the Production of Bacterial Polysaccharide for Vaccines |
title_sort | recombinant plants provide a new approach to the production of bacterial polysaccharide for vaccines |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3912152/ https://www.ncbi.nlm.nih.gov/pubmed/24498433 http://dx.doi.org/10.1371/journal.pone.0088144 |
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