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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...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
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.
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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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