Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: Kunstmann, Sonja, Scheidt, Tom, Buchwald, Saskia, Helm, Alexandra, Mulard, Laurence A., Fruth, Angelika, Barbirz, Stefanie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2018
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
_version_ 1783351567717498880
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
work_keys_str_mv AT kunstmannsonja bacteriophagesf6tailspikeproteinfordetectionofshigellaflexneripathogens
AT scheidttom bacteriophagesf6tailspikeproteinfordetectionofshigellaflexneripathogens
AT buchwaldsaskia bacteriophagesf6tailspikeproteinfordetectionofshigellaflexneripathogens
AT helmalexandra bacteriophagesf6tailspikeproteinfordetectionofshigellaflexneripathogens
AT mulardlaurencea bacteriophagesf6tailspikeproteinfordetectionofshigellaflexneripathogens
AT fruthangelika bacteriophagesf6tailspikeproteinfordetectionofshigellaflexneripathogens
AT barbirzstefanie bacteriophagesf6tailspikeproteinfordetectionofshigellaflexneripathogens