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An autotransporter display platform for the development of multivalent recombinant bacterial vector vaccines
Stockholm University, Faculty of Science, Department of Biochemistry and Biophysics. Xbrane Bioscience AB, Sweden.
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2014 (English)In: Microbial Cell Factories, ISSN 1475-2859, E-ISSN 1475-2859, Vol. 13, -162 p.Article in journal (Refereed) Published
Abstract [en]

Background: The Autotransporter pathway, ubiquitous in Gram-negative bacteria, allows the efficient secretion of large passenger proteins via a relatively simple mechanism. Capitalizing on its crystal structure, we have engineered the Escherichia coli autotransporter Hemoglobin protease (Hbp) into a versatile platform for secretion and surface display of multiple heterologous proteins in one carrier molecule. Results: As proof-of-concept, we demonstrate efficient secretion and high-density display of the sizeable Mycobacterium tuberculosis antigens ESAT6, Ag85B and Rv2660c in E. coli simultaneously. Furthermore, we show stable multivalent display of these antigens in an attenuated Salmonella Typhimurium strain upon chromosomal integration. To emphasize the versatility of the Hbp platform, we also demonstrate efficient expression of multiple sizeable antigenic fragments from Chlamydia trachomatis and the influenza A virus at the Salmonella cell surface. Conclusions: The successful efficient cell surface display of multiple antigens from various pathogenic organisms highlights the potential of Hbp as a universal platform for the development of multivalent recombinant bacterial vector vaccines.

Place, publisher, year, edition, pages
2014. Vol. 13, -162 p.
Keyword [en]
Antigen delivery, Recombinant live vaccine, Surface display, Autotransporter, Multivalent
National Category
Biological Sciences
Identifiers
URN: urn:nbn:se:su:diva-114273DOI: 10.1186/s12934-014-0162-8ISI: 000348547000001OAI: oai:DiVA.org:su-114273DiVA: diva2:799048
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AuthorCount:13;

Available from: 2015-03-28 Created: 2015-02-25 Last updated: 2017-12-04Bibliographically approved

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de Gier, Jan-Willem
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