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Improved delivery of the OVA-CD4 peptide to T helper cells by polymeric surface display on Salmonella
BACKGROUND: Autotransporter proteins represent a treasure trove for molecular engineers who modify Gram-negative bacteria for the export or secretion of foreign proteins across two membrane barriers. A particularly promising direction is the development of autotransporters as antigen display or secr...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4055283/ https://www.ncbi.nlm.nih.gov/pubmed/24898796 http://dx.doi.org/10.1186/1475-2859-13-80 |
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author | Zhang, Junjie De Masi, Leon John, Beena Chen, Wenxin Schifferli, Dieter M |
author_facet | Zhang, Junjie De Masi, Leon John, Beena Chen, Wenxin Schifferli, Dieter M |
author_sort | Zhang, Junjie |
collection | PubMed |
description | BACKGROUND: Autotransporter proteins represent a treasure trove for molecular engineers who modify Gram-negative bacteria for the export or secretion of foreign proteins across two membrane barriers. A particularly promising direction is the development of autotransporters as antigen display or secretion systems. Immunologists have been using ovalbumin as a reporter antigen for years and have developed sophisticated tools to detect specific T cells that respond to ovalbumin. Although ovalbumin-expressing bacteria are being used to trace T cell responses to colonizing or invading pathogens, current constructs for ovalbumin presentation have not been optimized. RESULTS: The activation of T helper cells in response to ovalbumin was improved by displaying the OVA-CD4 reporter epitope as a multimer on the surface of Salmonella and fused to the autotransporter MisL. Expression was optimized by including tandem in vivo promoters and two post-segregational killing systems for plasmid stabilization. CONCLUSIONS: The use of an autotransporter protein to present relevant epitope repeats on the surface of bacteria, combined with additional techniques favoring stable and efficient in vivo transcription, optimizes antigen presentation to T cells. The technique of multimeric epitope surface display should also benefit the development of new Salmonella or other enterobacterial vaccines. |
format | Online Article Text |
id | pubmed-4055283 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-40552832014-06-13 Improved delivery of the OVA-CD4 peptide to T helper cells by polymeric surface display on Salmonella Zhang, Junjie De Masi, Leon John, Beena Chen, Wenxin Schifferli, Dieter M Microb Cell Fact Research BACKGROUND: Autotransporter proteins represent a treasure trove for molecular engineers who modify Gram-negative bacteria for the export or secretion of foreign proteins across two membrane barriers. A particularly promising direction is the development of autotransporters as antigen display or secretion systems. Immunologists have been using ovalbumin as a reporter antigen for years and have developed sophisticated tools to detect specific T cells that respond to ovalbumin. Although ovalbumin-expressing bacteria are being used to trace T cell responses to colonizing or invading pathogens, current constructs for ovalbumin presentation have not been optimized. RESULTS: The activation of T helper cells in response to ovalbumin was improved by displaying the OVA-CD4 reporter epitope as a multimer on the surface of Salmonella and fused to the autotransporter MisL. Expression was optimized by including tandem in vivo promoters and two post-segregational killing systems for plasmid stabilization. CONCLUSIONS: The use of an autotransporter protein to present relevant epitope repeats on the surface of bacteria, combined with additional techniques favoring stable and efficient in vivo transcription, optimizes antigen presentation to T cells. The technique of multimeric epitope surface display should also benefit the development of new Salmonella or other enterobacterial vaccines. BioMed Central 2014-06-04 /pmc/articles/PMC4055283/ /pubmed/24898796 http://dx.doi.org/10.1186/1475-2859-13-80 Text en Copyright © 2014 Zhang 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 credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Zhang, Junjie De Masi, Leon John, Beena Chen, Wenxin Schifferli, Dieter M Improved delivery of the OVA-CD4 peptide to T helper cells by polymeric surface display on Salmonella |
title | Improved delivery of the OVA-CD4 peptide to T helper cells by polymeric surface display on Salmonella |
title_full | Improved delivery of the OVA-CD4 peptide to T helper cells by polymeric surface display on Salmonella |
title_fullStr | Improved delivery of the OVA-CD4 peptide to T helper cells by polymeric surface display on Salmonella |
title_full_unstemmed | Improved delivery of the OVA-CD4 peptide to T helper cells by polymeric surface display on Salmonella |
title_short | Improved delivery of the OVA-CD4 peptide to T helper cells by polymeric surface display on Salmonella |
title_sort | improved delivery of the ova-cd4 peptide to t helper cells by polymeric surface display on salmonella |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4055283/ https://www.ncbi.nlm.nih.gov/pubmed/24898796 http://dx.doi.org/10.1186/1475-2859-13-80 |
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