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Analysis of Pathogenic Bacterial and Yeast Biofilms Using the Combination of Synchrotron ATR-FTIR Microspectroscopy and Chemometric Approaches
Biofilms are assemblages of microbial cells, extracellular polymeric substances (EPS), and other components extracted from the environment in which they develop. Within biofilms, the spatial distribution of these components can vary. Here we present a fundamental characterization study to show diffe...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8271424/ https://www.ncbi.nlm.nih.gov/pubmed/34202224 http://dx.doi.org/10.3390/molecules26133890 |
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author | Cheeseman, Samuel Shaw, Z. L. Vongsvivut, Jitraporn Crawford, Russell J. Dupont, Madeleine F. Boyce, Kylie J. Gangadoo, Sheeana Bryant, Saffron J. Bryant, Gary Cozzolino, Daniel Chapman, James Elbourne, Aaron Truong, Vi Khanh |
author_facet | Cheeseman, Samuel Shaw, Z. L. Vongsvivut, Jitraporn Crawford, Russell J. Dupont, Madeleine F. Boyce, Kylie J. Gangadoo, Sheeana Bryant, Saffron J. Bryant, Gary Cozzolino, Daniel Chapman, James Elbourne, Aaron Truong, Vi Khanh |
author_sort | Cheeseman, Samuel |
collection | PubMed |
description | Biofilms are assemblages of microbial cells, extracellular polymeric substances (EPS), and other components extracted from the environment in which they develop. Within biofilms, the spatial distribution of these components can vary. Here we present a fundamental characterization study to show differences between biofilms formed by Gram-positive methicillin-resistant Staphylococcus aureus (MRSA), Gram-negative Pseudomonas aeruginosa, and the yeast-type Candida albicans using synchrotron macro attenuated total reflectance-Fourier transform infrared (ATR-FTIR) microspectroscopy. We were able to characterise the pathogenic biofilms’ heterogeneous distribution, which is challenging to do using traditional techniques. Multivariate analyses revealed that the polysaccharides area (1200–950 cm(−1)) accounted for the most significant variance between biofilm samples, and other spectral regions corresponding to amides, lipids, and polysaccharides all contributed to sample variation. In general, this study will advance our understanding of microbial biofilms and serve as a model for future research on how to use synchrotron source ATR-FTIR microspectroscopy to analyse their variations and spatial arrangements. |
format | Online Article Text |
id | pubmed-8271424 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-82714242021-07-11 Analysis of Pathogenic Bacterial and Yeast Biofilms Using the Combination of Synchrotron ATR-FTIR Microspectroscopy and Chemometric Approaches Cheeseman, Samuel Shaw, Z. L. Vongsvivut, Jitraporn Crawford, Russell J. Dupont, Madeleine F. Boyce, Kylie J. Gangadoo, Sheeana Bryant, Saffron J. Bryant, Gary Cozzolino, Daniel Chapman, James Elbourne, Aaron Truong, Vi Khanh Molecules Article Biofilms are assemblages of microbial cells, extracellular polymeric substances (EPS), and other components extracted from the environment in which they develop. Within biofilms, the spatial distribution of these components can vary. Here we present a fundamental characterization study to show differences between biofilms formed by Gram-positive methicillin-resistant Staphylococcus aureus (MRSA), Gram-negative Pseudomonas aeruginosa, and the yeast-type Candida albicans using synchrotron macro attenuated total reflectance-Fourier transform infrared (ATR-FTIR) microspectroscopy. We were able to characterise the pathogenic biofilms’ heterogeneous distribution, which is challenging to do using traditional techniques. Multivariate analyses revealed that the polysaccharides area (1200–950 cm(−1)) accounted for the most significant variance between biofilm samples, and other spectral regions corresponding to amides, lipids, and polysaccharides all contributed to sample variation. In general, this study will advance our understanding of microbial biofilms and serve as a model for future research on how to use synchrotron source ATR-FTIR microspectroscopy to analyse their variations and spatial arrangements. MDPI 2021-06-25 /pmc/articles/PMC8271424/ /pubmed/34202224 http://dx.doi.org/10.3390/molecules26133890 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/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 (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Cheeseman, Samuel Shaw, Z. L. Vongsvivut, Jitraporn Crawford, Russell J. Dupont, Madeleine F. Boyce, Kylie J. Gangadoo, Sheeana Bryant, Saffron J. Bryant, Gary Cozzolino, Daniel Chapman, James Elbourne, Aaron Truong, Vi Khanh Analysis of Pathogenic Bacterial and Yeast Biofilms Using the Combination of Synchrotron ATR-FTIR Microspectroscopy and Chemometric Approaches |
title | Analysis of Pathogenic Bacterial and Yeast Biofilms Using the Combination of Synchrotron ATR-FTIR Microspectroscopy and Chemometric Approaches |
title_full | Analysis of Pathogenic Bacterial and Yeast Biofilms Using the Combination of Synchrotron ATR-FTIR Microspectroscopy and Chemometric Approaches |
title_fullStr | Analysis of Pathogenic Bacterial and Yeast Biofilms Using the Combination of Synchrotron ATR-FTIR Microspectroscopy and Chemometric Approaches |
title_full_unstemmed | Analysis of Pathogenic Bacterial and Yeast Biofilms Using the Combination of Synchrotron ATR-FTIR Microspectroscopy and Chemometric Approaches |
title_short | Analysis of Pathogenic Bacterial and Yeast Biofilms Using the Combination of Synchrotron ATR-FTIR Microspectroscopy and Chemometric Approaches |
title_sort | analysis of pathogenic bacterial and yeast biofilms using the combination of synchrotron atr-ftir microspectroscopy and chemometric approaches |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8271424/ https://www.ncbi.nlm.nih.gov/pubmed/34202224 http://dx.doi.org/10.3390/molecules26133890 |
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