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A novel human skin chamber model to study wound infection ex vivo

Wound infections with multi-drug resistant bacteria increase morbidity and mortality and have considerable socioeconomic impact. They can lead to impaired wound healing, resulting in rising treatment costs. The aim of this study was to investigate an ex vivo human wound infection model. Human full-t...

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Autores principales: Steinstraesser, Lars, Sorkin, M., Niederbichler, A. D., Becerikli, M., Stupka, J., Daigeler, A., Kesting, M. R., Stricker, I., Jacobsen, F., Schulte, M.
Formato: Texto
Lenguaje:English
Publicado: Springer-Verlag 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2876270/
https://www.ncbi.nlm.nih.gov/pubmed/19956960
http://dx.doi.org/10.1007/s00403-009-1009-8
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author Steinstraesser, Lars
Sorkin, M.
Niederbichler, A. D.
Becerikli, M.
Stupka, J.
Daigeler, A.
Kesting, M. R.
Stricker, I.
Jacobsen, F.
Schulte, M.
author_facet Steinstraesser, Lars
Sorkin, M.
Niederbichler, A. D.
Becerikli, M.
Stupka, J.
Daigeler, A.
Kesting, M. R.
Stricker, I.
Jacobsen, F.
Schulte, M.
author_sort Steinstraesser, Lars
collection PubMed
description Wound infections with multi-drug resistant bacteria increase morbidity and mortality and have considerable socioeconomic impact. They can lead to impaired wound healing, resulting in rising treatment costs. The aim of this study was to investigate an ex vivo human wound infection model. Human full-thickness skin from the operating room (OR) was placed into the Bo-Drum(®) and cultivated for 7 days in an air–liquid interphase. On day 8, the skin was inoculated with either (1) Pseudomonas aeruginosa, (2) Staphylococcus aureus (10(5) CFU, n = 3) or (3) carrier control. 1, 3 and 7 days after inoculation colony forming units in the tissue/media were determined and cytokine expression was quantified. A reliable and reproducible wound infection could be established for 7 days. At this timepoint, 1.8 × 10(8) CFU/g tissue of P. aeruginosa and 2 × 10(7) CFU/g tissue of S. aureus were detected. Immunohistochemical analysis demonstrated bacterial infection and epidermolysis in infected skin. RT-PCR analysis exhibited a significant induction of proinflammatory cytokines after infection. The BO-drum(®) is a robust, easy-to-use, sterilizable and reusable ex vivo full-skin culture system. For investigation of wound infection, treatment and healing, the BO-drum(®) presents a convenient model and may help to standardize wound research.
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spelling pubmed-28762702010-06-10 A novel human skin chamber model to study wound infection ex vivo Steinstraesser, Lars Sorkin, M. Niederbichler, A. D. Becerikli, M. Stupka, J. Daigeler, A. Kesting, M. R. Stricker, I. Jacobsen, F. Schulte, M. Arch Dermatol Res Original Paper Wound infections with multi-drug resistant bacteria increase morbidity and mortality and have considerable socioeconomic impact. They can lead to impaired wound healing, resulting in rising treatment costs. The aim of this study was to investigate an ex vivo human wound infection model. Human full-thickness skin from the operating room (OR) was placed into the Bo-Drum(®) and cultivated for 7 days in an air–liquid interphase. On day 8, the skin was inoculated with either (1) Pseudomonas aeruginosa, (2) Staphylococcus aureus (10(5) CFU, n = 3) or (3) carrier control. 1, 3 and 7 days after inoculation colony forming units in the tissue/media were determined and cytokine expression was quantified. A reliable and reproducible wound infection could be established for 7 days. At this timepoint, 1.8 × 10(8) CFU/g tissue of P. aeruginosa and 2 × 10(7) CFU/g tissue of S. aureus were detected. Immunohistochemical analysis demonstrated bacterial infection and epidermolysis in infected skin. RT-PCR analysis exhibited a significant induction of proinflammatory cytokines after infection. The BO-drum(®) is a robust, easy-to-use, sterilizable and reusable ex vivo full-skin culture system. For investigation of wound infection, treatment and healing, the BO-drum(®) presents a convenient model and may help to standardize wound research. Springer-Verlag 2009-12-03 2010 /pmc/articles/PMC2876270/ /pubmed/19956960 http://dx.doi.org/10.1007/s00403-009-1009-8 Text en © The Author(s) 2009 https://creativecommons.org/licenses/by-nc/4.0/ This article is distributed under the terms of the Creative Commons Attribution Noncommercial License which permits any noncommercial use, distribution, and reproduction in any medium, provided the original author(s) and source are credited.
spellingShingle Original Paper
Steinstraesser, Lars
Sorkin, M.
Niederbichler, A. D.
Becerikli, M.
Stupka, J.
Daigeler, A.
Kesting, M. R.
Stricker, I.
Jacobsen, F.
Schulte, M.
A novel human skin chamber model to study wound infection ex vivo
title A novel human skin chamber model to study wound infection ex vivo
title_full A novel human skin chamber model to study wound infection ex vivo
title_fullStr A novel human skin chamber model to study wound infection ex vivo
title_full_unstemmed A novel human skin chamber model to study wound infection ex vivo
title_short A novel human skin chamber model to study wound infection ex vivo
title_sort novel human skin chamber model to study wound infection ex vivo
topic Original Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2876270/
https://www.ncbi.nlm.nih.gov/pubmed/19956960
http://dx.doi.org/10.1007/s00403-009-1009-8
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