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Real‐time detection of volatile metabolites enabling species‐level discrimination of bacterial biofilms associated with wound infection
AIMS: The main aim of this study was to investigate the real‐time detection of volatile metabolites for the species‐level discrimination of pathogens associated with clinically relevant wound infection, when grown in a collagen wound biofilm model. METHODS AND RESULTS: This work shows that Staphyloc...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9298000/ https://www.ncbi.nlm.nih.gov/pubmed/34617369 http://dx.doi.org/10.1111/jam.15313 |
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author | Slade, Elisabeth A. Thorn, Robin M. S. Young, Amber E. Reynolds, Darren M. |
author_facet | Slade, Elisabeth A. Thorn, Robin M. S. Young, Amber E. Reynolds, Darren M. |
author_sort | Slade, Elisabeth A. |
collection | PubMed |
description | AIMS: The main aim of this study was to investigate the real‐time detection of volatile metabolites for the species‐level discrimination of pathogens associated with clinically relevant wound infection, when grown in a collagen wound biofilm model. METHODS AND RESULTS: This work shows that Staphylococcus aureus, Pseudomonas aeruginosa and Streptococcus pyogenes produce a multitude of volatile compounds when grown as biofilms in a collagen‐based biofilm model. The real‐time detection of these complex volatile profiles using selected ion flow tube mass spectrometry and the use of multivariate statistical analysis on the resulting data can be used to successfully differentiate between the pathogens studied. CONCLUSIONS: The range of bacterial volatile compounds detected between the species studied vary and are distinct. Discrimination between bacterial species using real‐time detection of volatile metabolites and multivariate statistical analysis was successfully demonstrated. SIGNIFICANCE AND IMPACT OF THE STUDY: Development of rapid point‐of‐care diagnostics for wound infection would improve diagnosis and patient care. Such technological approaches would also facilitate the appropriate use of antimicrobials, minimizing the emergence of antimicrobial resistance. This study further develops the use of volatile metabolite detection as a new diagnostic approach for wound infection. |
format | Online Article Text |
id | pubmed-9298000 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-92980002022-07-21 Real‐time detection of volatile metabolites enabling species‐level discrimination of bacterial biofilms associated with wound infection Slade, Elisabeth A. Thorn, Robin M. S. Young, Amber E. Reynolds, Darren M. J Appl Microbiol Editor's Choice AIMS: The main aim of this study was to investigate the real‐time detection of volatile metabolites for the species‐level discrimination of pathogens associated with clinically relevant wound infection, when grown in a collagen wound biofilm model. METHODS AND RESULTS: This work shows that Staphylococcus aureus, Pseudomonas aeruginosa and Streptococcus pyogenes produce a multitude of volatile compounds when grown as biofilms in a collagen‐based biofilm model. The real‐time detection of these complex volatile profiles using selected ion flow tube mass spectrometry and the use of multivariate statistical analysis on the resulting data can be used to successfully differentiate between the pathogens studied. CONCLUSIONS: The range of bacterial volatile compounds detected between the species studied vary and are distinct. Discrimination between bacterial species using real‐time detection of volatile metabolites and multivariate statistical analysis was successfully demonstrated. SIGNIFICANCE AND IMPACT OF THE STUDY: Development of rapid point‐of‐care diagnostics for wound infection would improve diagnosis and patient care. Such technological approaches would also facilitate the appropriate use of antimicrobials, minimizing the emergence of antimicrobial resistance. This study further develops the use of volatile metabolite detection as a new diagnostic approach for wound infection. John Wiley and Sons Inc. 2021-10-19 2022-03 /pmc/articles/PMC9298000/ /pubmed/34617369 http://dx.doi.org/10.1111/jam.15313 Text en © 2021 The Authors. Journal of Applied Microbiology published by John Wiley & Sons Ltd on behalf of Society for Applied Microbiology. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Editor's Choice Slade, Elisabeth A. Thorn, Robin M. S. Young, Amber E. Reynolds, Darren M. Real‐time detection of volatile metabolites enabling species‐level discrimination of bacterial biofilms associated with wound infection |
title | Real‐time detection of volatile metabolites enabling species‐level discrimination of bacterial biofilms associated with wound infection |
title_full | Real‐time detection of volatile metabolites enabling species‐level discrimination of bacterial biofilms associated with wound infection |
title_fullStr | Real‐time detection of volatile metabolites enabling species‐level discrimination of bacterial biofilms associated with wound infection |
title_full_unstemmed | Real‐time detection of volatile metabolites enabling species‐level discrimination of bacterial biofilms associated with wound infection |
title_short | Real‐time detection of volatile metabolites enabling species‐level discrimination of bacterial biofilms associated with wound infection |
title_sort | real‐time detection of volatile metabolites enabling species‐level discrimination of bacterial biofilms associated with wound infection |
topic | Editor's Choice |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9298000/ https://www.ncbi.nlm.nih.gov/pubmed/34617369 http://dx.doi.org/10.1111/jam.15313 |
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