Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: Zhang, Junjie, De Masi, Leon, John, Beena, Chen, Wenxin, Schifferli, Dieter M
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
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
_version_ 1782320635994701824
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
work_keys_str_mv AT zhangjunjie improveddeliveryoftheovacd4peptidetothelpercellsbypolymericsurfacedisplayonsalmonella
AT demasileon improveddeliveryoftheovacd4peptidetothelpercellsbypolymericsurfacedisplayonsalmonella
AT johnbeena improveddeliveryoftheovacd4peptidetothelpercellsbypolymericsurfacedisplayonsalmonella
AT chenwenxin improveddeliveryoftheovacd4peptidetothelpercellsbypolymericsurfacedisplayonsalmonella
AT schifferlidieterm improveddeliveryoftheovacd4peptidetothelpercellsbypolymericsurfacedisplayonsalmonella