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Bacteriophage Sf6 Tailspike Protein for Detection of Shigella flexneri Pathogens

Authors :
Kunstmann, Sonja
Scheidt, Tom
Buchwald, Saskia
Helm, Alexandra
Mulard, Laurence A.
Fruth, Angelika
Barbirz, Stefanie
University of Potsdam
Chimie des Biomolécules - Chemistry of Biomolecules
Centre National de la Recherche Scientifique (CNRS)-Institut Pasteur [Paris]
Robert Koch Institute [Berlin] (RKI)
This research was funded by Deutsche Forschungsgemeinschaft, grant number BA 4046/1-2 (Stefanie Barbirz) and the International Max Planck Research School on Multiscale Biosystems (Sonja Kunstmann).
We thank Nils Carlin (Scandinavian Biopharma) for providing us with S. flexneri LPS preparations. We are grateful to Catherine Guerreiro (Chemistry of Biomolecules Laboratory, Institut Pasteur, France) for her contribution to the chemical synthesis of S. flexneri 2a oligosaccharides. We thank Jörg Fettke for assistance with MALDI-TOF MS and CE-LIF. We thank Mandy Schietke and Melanie Anding for excellent technical assistance. We acknowledge the support of the Deutsche Forschungsgemeinschaft and Open Access Publishing Fund of University of Potsdam.
University of Potsdam = Universität Potsdam
Institut Pasteur [Paris] (IP)-Centre National de la Recherche Scientifique (CNRS)
Source :
Viruses, Viruses, MDPI, 2018, 10 (8), pp.431. ⟨10.3390/v10080431⟩, Viruses, Vol 10, Iss 8, p 431 (2018), Viruses, 2018, 10 (8), pp.431. ⟨10.3390/v10080431⟩
Publication Year :
2018
Publisher :
HAL CCSD, 2018.

Abstract

International audience; Bacteriophage research is gaining more importance due to increasing antibiotic resistance. However, for treatment with bacteriophages, diagnostics have to be improved. Bacteriophages carry adhesion proteins, which bind to the bacterial cell surface, for example tailspike proteins (TSP) for specific recognition of bacterial O-antigen polysaccharide. TSP are highly stable proteins and thus might be suitable components for the integration into diagnostic tools. We used the TSP of bacteriophage Sf6 to establish two applications for detecting Shigella flexneri (S. flexneri), a highly contagious pathogen causing dysentery. We found that Sf6TSP not only bound O-antigen of S. flexneri serotype Y, but also the glucosylated O-antigen of serotype 2a. Moreover, mass spectrometry glycan analyses showed that Sf6TSP tolerated various O-acetyl modifications on these O-antigens. We established a microtiter plate-based ELISA like tailspike adsorption assay (ELITA) using a Strep-tag®II modified Sf6TSP. As sensitive screening alternative we produced a fluorescently labeled Sf6TSP via coupling to an environment sensitive dye. Binding of this probe to the S. flexneri O-antigen Y elicited a fluorescence intensity increase of 80% with an emission maximum in the visible light range. The Sf6TSP probes thus offer a promising route to a highly specific and sensitive bacteriophage TSP-based Shigella detection system.

Details

Language :
English
ISSN :
19994915
Database :
OpenAIRE
Journal :
Viruses, Viruses, MDPI, 2018, 10 (8), pp.431. ⟨10.3390/v10080431⟩, Viruses, Vol 10, Iss 8, p 431 (2018), Viruses, 2018, 10 (8), pp.431. ⟨10.3390/v10080431⟩
Accession number :
edsair.dedup.wf.001..b73ac4f22e36f25a48e566dca1a5cb4b