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Dynamics of a Staphylococcus aureus infective endocarditis simulation model
Infective endocarditis (IE) is a serious infection of the inner surface of heart, resulting from minor lesions in the endocardium. The damage induces a healing reaction, which leads to recruitment of fibrin and immune cells. This sterile healing vegetation can be colonized during temporary bacteremi...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9545761/ https://www.ncbi.nlm.nih.gov/pubmed/35460117 http://dx.doi.org/10.1111/apm.13231 |
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author | Schwartz, Franziska A. Nielsen, Luna Struve Andersen, Jessica Bock, Magnus Christophersen, Lars Sunnerhagen, Torgny Lerche, Christian Johann Bay, Lene Bundgaard, Henning Høiby, Niels Moser, Claus |
author_facet | Schwartz, Franziska A. Nielsen, Luna Struve Andersen, Jessica Bock, Magnus Christophersen, Lars Sunnerhagen, Torgny Lerche, Christian Johann Bay, Lene Bundgaard, Henning Høiby, Niels Moser, Claus |
author_sort | Schwartz, Franziska A. |
collection | PubMed |
description | Infective endocarditis (IE) is a serious infection of the inner surface of heart, resulting from minor lesions in the endocardium. The damage induces a healing reaction, which leads to recruitment of fibrin and immune cells. This sterile healing vegetation can be colonized during temporary bacteremia, inducing IE. We have previously established a novel in vitro IE model using a simulated IE vegetation (IEV) model produced from whole venous blood, on which we achieved stable bacterial colonization after 24 h. The bacteria were organized in biofilm aggregates and displayed increased tolerance toward antibiotics. In this current study, we aimed at further characterizing the time course of biofilm formation and the impact on antibiotic tolerance development. We found that a Staphylococcus aureus reference strain, as well as three clinical IE isolates formed biofilms on the IEV after 6 h. When treatment was initiated immediately after infection, the antibiotic effect was significantly higher than when treatment was started after the biofilm was allowed to mature. We could follow the biofilm development microscopically by visualizing growing bacterial aggregates on the IEV. The findings indicate that mature, antibiotic‐tolerant biofilms can be formed in our model already after 6 h, accelerating the screening for optimal treatment strategies for IE. |
format | Online Article Text |
id | pubmed-9545761 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-95457612022-10-14 Dynamics of a Staphylococcus aureus infective endocarditis simulation model Schwartz, Franziska A. Nielsen, Luna Struve Andersen, Jessica Bock, Magnus Christophersen, Lars Sunnerhagen, Torgny Lerche, Christian Johann Bay, Lene Bundgaard, Henning Høiby, Niels Moser, Claus APMIS Original Articles Infective endocarditis (IE) is a serious infection of the inner surface of heart, resulting from minor lesions in the endocardium. The damage induces a healing reaction, which leads to recruitment of fibrin and immune cells. This sterile healing vegetation can be colonized during temporary bacteremia, inducing IE. We have previously established a novel in vitro IE model using a simulated IE vegetation (IEV) model produced from whole venous blood, on which we achieved stable bacterial colonization after 24 h. The bacteria were organized in biofilm aggregates and displayed increased tolerance toward antibiotics. In this current study, we aimed at further characterizing the time course of biofilm formation and the impact on antibiotic tolerance development. We found that a Staphylococcus aureus reference strain, as well as three clinical IE isolates formed biofilms on the IEV after 6 h. When treatment was initiated immediately after infection, the antibiotic effect was significantly higher than when treatment was started after the biofilm was allowed to mature. We could follow the biofilm development microscopically by visualizing growing bacterial aggregates on the IEV. The findings indicate that mature, antibiotic‐tolerant biofilms can be formed in our model already after 6 h, accelerating the screening for optimal treatment strategies for IE. John Wiley and Sons Inc. 2022-05-27 2022-08 /pmc/articles/PMC9545761/ /pubmed/35460117 http://dx.doi.org/10.1111/apm.13231 Text en © 2022 The Authors. APMIS published by John Wiley & Sons Ltd on behalf of Scandinavian Societies for Medical Microbiology and Pathology. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
spellingShingle | Original Articles Schwartz, Franziska A. Nielsen, Luna Struve Andersen, Jessica Bock, Magnus Christophersen, Lars Sunnerhagen, Torgny Lerche, Christian Johann Bay, Lene Bundgaard, Henning Høiby, Niels Moser, Claus Dynamics of a Staphylococcus aureus infective endocarditis simulation model |
title | Dynamics of a Staphylococcus aureus infective endocarditis simulation model |
title_full | Dynamics of a Staphylococcus aureus infective endocarditis simulation model |
title_fullStr | Dynamics of a Staphylococcus aureus infective endocarditis simulation model |
title_full_unstemmed | Dynamics of a Staphylococcus aureus infective endocarditis simulation model |
title_short | Dynamics of a Staphylococcus aureus infective endocarditis simulation model |
title_sort | dynamics of a staphylococcus aureus infective endocarditis simulation model |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9545761/ https://www.ncbi.nlm.nih.gov/pubmed/35460117 http://dx.doi.org/10.1111/apm.13231 |
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