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Bacteriophage Sf6 Tailspike Protein for Detection of Shigella flexneri Pathogens
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...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6116271/ https://www.ncbi.nlm.nih.gov/pubmed/30111705 http://dx.doi.org/10.3390/v10080431 |
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author | Kunstmann, Sonja Scheidt, Tom Buchwald, Saskia Helm, Alexandra Mulard, Laurence A. Fruth, Angelika Barbirz, Stefanie |
author_facet | Kunstmann, Sonja Scheidt, Tom Buchwald, Saskia Helm, Alexandra Mulard, Laurence A. Fruth, Angelika Barbirz, Stefanie |
author_sort | Kunstmann, Sonja |
collection | PubMed |
description | 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. |
format | Online Article Text |
id | pubmed-6116271 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-61162712018-08-31 Bacteriophage Sf6 Tailspike Protein for Detection of Shigella flexneri Pathogens Kunstmann, Sonja Scheidt, Tom Buchwald, Saskia Helm, Alexandra Mulard, Laurence A. Fruth, Angelika Barbirz, Stefanie Viruses Communication 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. MDPI 2018-08-15 /pmc/articles/PMC6116271/ /pubmed/30111705 http://dx.doi.org/10.3390/v10080431 Text en © 2018 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Communication Kunstmann, Sonja Scheidt, Tom Buchwald, Saskia Helm, Alexandra Mulard, Laurence A. Fruth, Angelika Barbirz, Stefanie Bacteriophage Sf6 Tailspike Protein for Detection of Shigella flexneri Pathogens |
title | Bacteriophage Sf6 Tailspike Protein for Detection of Shigella flexneri Pathogens |
title_full | Bacteriophage Sf6 Tailspike Protein for Detection of Shigella flexneri Pathogens |
title_fullStr | Bacteriophage Sf6 Tailspike Protein for Detection of Shigella flexneri Pathogens |
title_full_unstemmed | Bacteriophage Sf6 Tailspike Protein for Detection of Shigella flexneri Pathogens |
title_short | Bacteriophage Sf6 Tailspike Protein for Detection of Shigella flexneri Pathogens |
title_sort | bacteriophage sf6 tailspike protein for detection of shigella flexneri pathogens |
topic | Communication |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6116271/ https://www.ncbi.nlm.nih.gov/pubmed/30111705 http://dx.doi.org/10.3390/v10080431 |
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