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A quorum sensing-based in vivo expression system and its application in multivalent bacterial vaccine
BACKGROUND: Delivery of antigens by live bacterial carriers can elicit effective humoral and cellular responses and may be an attractive strategy for live bacterial vaccine production through introduction of a vector that expresses an exogenous protective antigen. To overcome the instability and met...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4372277/ https://www.ncbi.nlm.nih.gov/pubmed/25888727 http://dx.doi.org/10.1186/s12934-015-0213-9 |
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author | Chu, Teng Ni, Chunshan Zhang, Lingzhi Wang, Qiyao Xiao, Jingfan Zhang, Yuanxing Liu, Qin |
author_facet | Chu, Teng Ni, Chunshan Zhang, Lingzhi Wang, Qiyao Xiao, Jingfan Zhang, Yuanxing Liu, Qin |
author_sort | Chu, Teng |
collection | PubMed |
description | BACKGROUND: Delivery of antigens by live bacterial carriers can elicit effective humoral and cellular responses and may be an attractive strategy for live bacterial vaccine production through introduction of a vector that expresses an exogenous protective antigen. To overcome the instability and metabolic burden associated with plasmid introduction, alternative strategies, such as the use of in vivo-inducible promoters, have been proposed. However, screening an ideal in vivo-activated promoter with high efficiency and low leak expression in a particular strain poses great challenges to many researchers. RESULTS: In this work, we constructed an in vivo antigen-expressing vector suitable for Edwardsiella tarda, an enteric Gram-negative invasive intracellular pathogen of both animals and humans. By combining quorum sensing genes from Vibrio fischeri with iron uptake regulons, a synthetic binary regulation system (ironQS) for E. tarda was designed. In vitro expression assay demonstrated that the ironQS system is only initiated in the absence of Fe(2+) in the medium when the cell density reaches its threshold. The ironQS system was further confirmed in vivo to present an in vivo-triggered and cell density-dependent expression pattern in larvae and adult zebrafish. A recombinant E. tarda vector vaccine candidate WED(ironQS-G) was established by introducing gapA34, which encodes the protective antigen glyceraldehyde-3-phosphate dehydrogenase (GAPDH) from the fish pathogen Aeromonas hydrophila LSA34 into ironQS system, and the immune protection afforded by this vaccine was assessed in turbot (Scophtalmus maximus). Most of the vaccinated fish survived under the challenge with A. hydrophila LSA34 (RPS = 67.0%) or E. tarda EIB202 (RPS = 72.3%). CONCLUSIONS: Quorum sensing system has been extensively used in various gene structures in synthetic biology as a well-functioning and population-dependent gene circuit. In this work, the in vivo expression system, ironQS, maintained the high expression efficiency of the quorum sensing circuit and achieved excellent expression regulation of the Fur box. The ironQS system has great potential in applications requiring in vivo protein expression, such as vector vaccines. Considering its high compatibility, ironQS system could function as a universal expression platform for a variety of bacterial hosts. |
format | Online Article Text |
id | pubmed-4372277 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-43722772015-03-25 A quorum sensing-based in vivo expression system and its application in multivalent bacterial vaccine Chu, Teng Ni, Chunshan Zhang, Lingzhi Wang, Qiyao Xiao, Jingfan Zhang, Yuanxing Liu, Qin Microb Cell Fact Research BACKGROUND: Delivery of antigens by live bacterial carriers can elicit effective humoral and cellular responses and may be an attractive strategy for live bacterial vaccine production through introduction of a vector that expresses an exogenous protective antigen. To overcome the instability and metabolic burden associated with plasmid introduction, alternative strategies, such as the use of in vivo-inducible promoters, have been proposed. However, screening an ideal in vivo-activated promoter with high efficiency and low leak expression in a particular strain poses great challenges to many researchers. RESULTS: In this work, we constructed an in vivo antigen-expressing vector suitable for Edwardsiella tarda, an enteric Gram-negative invasive intracellular pathogen of both animals and humans. By combining quorum sensing genes from Vibrio fischeri with iron uptake regulons, a synthetic binary regulation system (ironQS) for E. tarda was designed. In vitro expression assay demonstrated that the ironQS system is only initiated in the absence of Fe(2+) in the medium when the cell density reaches its threshold. The ironQS system was further confirmed in vivo to present an in vivo-triggered and cell density-dependent expression pattern in larvae and adult zebrafish. A recombinant E. tarda vector vaccine candidate WED(ironQS-G) was established by introducing gapA34, which encodes the protective antigen glyceraldehyde-3-phosphate dehydrogenase (GAPDH) from the fish pathogen Aeromonas hydrophila LSA34 into ironQS system, and the immune protection afforded by this vaccine was assessed in turbot (Scophtalmus maximus). Most of the vaccinated fish survived under the challenge with A. hydrophila LSA34 (RPS = 67.0%) or E. tarda EIB202 (RPS = 72.3%). CONCLUSIONS: Quorum sensing system has been extensively used in various gene structures in synthetic biology as a well-functioning and population-dependent gene circuit. In this work, the in vivo expression system, ironQS, maintained the high expression efficiency of the quorum sensing circuit and achieved excellent expression regulation of the Fur box. The ironQS system has great potential in applications requiring in vivo protein expression, such as vector vaccines. Considering its high compatibility, ironQS system could function as a universal expression platform for a variety of bacterial hosts. BioMed Central 2015-03-18 /pmc/articles/PMC4372277/ /pubmed/25888727 http://dx.doi.org/10.1186/s12934-015-0213-9 Text en © Chu et al.; licensee BioMed Central. 2015 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), 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 Chu, Teng Ni, Chunshan Zhang, Lingzhi Wang, Qiyao Xiao, Jingfan Zhang, Yuanxing Liu, Qin A quorum sensing-based in vivo expression system and its application in multivalent bacterial vaccine |
title | A quorum sensing-based in vivo expression system and its application in multivalent bacterial vaccine |
title_full | A quorum sensing-based in vivo expression system and its application in multivalent bacterial vaccine |
title_fullStr | A quorum sensing-based in vivo expression system and its application in multivalent bacterial vaccine |
title_full_unstemmed | A quorum sensing-based in vivo expression system and its application in multivalent bacterial vaccine |
title_short | A quorum sensing-based in vivo expression system and its application in multivalent bacterial vaccine |
title_sort | quorum sensing-based in vivo expression system and its application in multivalent bacterial vaccine |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4372277/ https://www.ncbi.nlm.nih.gov/pubmed/25888727 http://dx.doi.org/10.1186/s12934-015-0213-9 |
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