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Combined Staining Techniques for Demonstration of Staphylococcus aureus Biofilm in Routine Histopathology

Aim: Visualization of Staphylococcus aureus biofilm using histochemical staining and combined histochemistry (HC) and immunohistochemistry (IHC). Methods: The ability of S. aureus S54F9 to form biofilm was tested in vitro. Hereafter, infected bone tissue was collected from two different porcine mode...

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Autores principales: Jensen, Louise Kruse, Henriksen, Nicole Lind, Bjarnsholt, Thomas, Kragh, Kasper Nørskov, Jensen, Henrik Elvang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Ivyspring International Publisher 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5852845/
https://www.ncbi.nlm.nih.gov/pubmed/29545993
http://dx.doi.org/10.7150/jbji.22799
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author Jensen, Louise Kruse
Henriksen, Nicole Lind
Bjarnsholt, Thomas
Kragh, Kasper Nørskov
Jensen, Henrik Elvang
author_facet Jensen, Louise Kruse
Henriksen, Nicole Lind
Bjarnsholt, Thomas
Kragh, Kasper Nørskov
Jensen, Henrik Elvang
author_sort Jensen, Louise Kruse
collection PubMed
description Aim: Visualization of Staphylococcus aureus biofilm using histochemical staining and combined histochemistry (HC) and immunohistochemistry (IHC). Methods: The ability of S. aureus S54F9 to form biofilm was tested in vitro. Hereafter, infected bone tissue was collected from two different porcine models of osteomyelitis inoculated with S. aureus strain S54F9. The infection time was five and fifteen days, respectively. Twenty-five different histochemical staining protocols were tested in order to find the stains that could identify extracellular biofilm matrix. Protocols with an optimal visualization of biofilm extracellular matrix were combined with an immunohistochemical protocol based on a specific antibody against S. aureus. The combined protocols were applied to the tissue from the porcine models and to infected bone tissue from a child suffering from chronic staphylococcal osteomyelitis for more than a year. Results: S. aureus S54F9 showed an ability to form biofilm in vitro. Visualization of biofilm, i.e. bacterial cells and extracellular matrix in different colours, was seen when the immunohistochemical protocol was combined with Alcian Blue pH3, Luna and Methyl-pyronin green. The bacterial cells were red to light brown and the extracellular matrix either light blue, blue or orange depending on the histochemical stain. In the porcine models and the human case 10 and 90 percent, respectively, of the bacterial aggregates in a 100x magnification field displayed both the extracellular matrix and the bacterial cells simultaneously in two different colours. Conclusions: A combination of HC and IHC can be used to diagnose and characterise biofilm infections on a routine basis.
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spelling pubmed-58528452018-03-15 Combined Staining Techniques for Demonstration of Staphylococcus aureus Biofilm in Routine Histopathology Jensen, Louise Kruse Henriksen, Nicole Lind Bjarnsholt, Thomas Kragh, Kasper Nørskov Jensen, Henrik Elvang J Bone Jt Infect Research Paper Aim: Visualization of Staphylococcus aureus biofilm using histochemical staining and combined histochemistry (HC) and immunohistochemistry (IHC). Methods: The ability of S. aureus S54F9 to form biofilm was tested in vitro. Hereafter, infected bone tissue was collected from two different porcine models of osteomyelitis inoculated with S. aureus strain S54F9. The infection time was five and fifteen days, respectively. Twenty-five different histochemical staining protocols were tested in order to find the stains that could identify extracellular biofilm matrix. Protocols with an optimal visualization of biofilm extracellular matrix were combined with an immunohistochemical protocol based on a specific antibody against S. aureus. The combined protocols were applied to the tissue from the porcine models and to infected bone tissue from a child suffering from chronic staphylococcal osteomyelitis for more than a year. Results: S. aureus S54F9 showed an ability to form biofilm in vitro. Visualization of biofilm, i.e. bacterial cells and extracellular matrix in different colours, was seen when the immunohistochemical protocol was combined with Alcian Blue pH3, Luna and Methyl-pyronin green. The bacterial cells were red to light brown and the extracellular matrix either light blue, blue or orange depending on the histochemical stain. In the porcine models and the human case 10 and 90 percent, respectively, of the bacterial aggregates in a 100x magnification field displayed both the extracellular matrix and the bacterial cells simultaneously in two different colours. Conclusions: A combination of HC and IHC can be used to diagnose and characterise biofilm infections on a routine basis. Ivyspring International Publisher 2018-02-20 /pmc/articles/PMC5852845/ /pubmed/29545993 http://dx.doi.org/10.7150/jbji.22799 Text en © Ivyspring International Publisher This is an open access article distributed under the terms of the Creative Commons Attribution (CC BY-NC) license (https://creativecommons.org/licenses/by-nc/4.0/). See http://ivyspring.com/terms for full terms and conditions.
spellingShingle Research Paper
Jensen, Louise Kruse
Henriksen, Nicole Lind
Bjarnsholt, Thomas
Kragh, Kasper Nørskov
Jensen, Henrik Elvang
Combined Staining Techniques for Demonstration of Staphylococcus aureus Biofilm in Routine Histopathology
title Combined Staining Techniques for Demonstration of Staphylococcus aureus Biofilm in Routine Histopathology
title_full Combined Staining Techniques for Demonstration of Staphylococcus aureus Biofilm in Routine Histopathology
title_fullStr Combined Staining Techniques for Demonstration of Staphylococcus aureus Biofilm in Routine Histopathology
title_full_unstemmed Combined Staining Techniques for Demonstration of Staphylococcus aureus Biofilm in Routine Histopathology
title_short Combined Staining Techniques for Demonstration of Staphylococcus aureus Biofilm in Routine Histopathology
title_sort combined staining techniques for demonstration of staphylococcus aureus biofilm in routine histopathology
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5852845/
https://www.ncbi.nlm.nih.gov/pubmed/29545993
http://dx.doi.org/10.7150/jbji.22799
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