Shaun N. Robertson
Probing Interkingdom Signaling Molecules via Liquid Extraction Surface Analysis-Mass Spectrometry
Robertson, Shaun N.; Soukarieh, Fadi; White, Thomas M.; Camara, Miguel; Romero, Manuel; Griffiths, Rian L.
Authors
Dr FADI SOUKARIEH Fadi.Soukarieh@nottingham.ac.uk
RESEARCH FELLOW
Thomas M. White
Professor MIGUEL CAMARA MIGUEL.CAMARA@NOTTINGHAM.AC.UK
PROFESSOR OF MOLECULAR MICROBIOLOGY
Manuel Romero
Dr RIAN GRIFFITHS Rian.Griffiths@nottingham.ac.uk
ASSISTANT PROFESSOR
Abstract
Previously, metabolites diffused or secreted from microbial samples have been analyzed via liquid chromatography–mass spectrometry (LC–MS) approaches following lengthy extraction protocols. Here, we present a model system for growing biofilms on discs before utilizing rapid and direct surface sampling MS, namely, liquid extraction surface analysis, to study the microbial exometabolome. One of the benefits of this approach is its surface-specific nature, enabling mimicking biofilm formation in a way that the study of planktonic liquid cultures cannot imitate. Even though Pseudomonas aeruginosa (P. aeruginosa), Staphylococcus aureus (S. aureus), and Candida albicans (C. albicans) have been studied previously in isolation, very few studies consider the complexity of the interplay between these pathogens, which are commonly combined causative agents of infection. Our model system provides a route to investigate changes in the exometabolome, such as metabolites that become circulatory in the presence of multiple pathogens. Our results agree with previous reports showing that 2-alkyl-4(1H)-quinolone signal molecules produced by P. aeruginosa are important markers of infection and suggest that methods for monitoring levels of 2-heptyl-4-hydroxyquinoline and 2,4-dihydroxyquinoline, as well as pyocyanin, could be beneficial in the determination of causative agents in interkingdom infection including P. aeruginosa. Furthermore, studying changes in exometabolome metabolites between pqs quorum sensing antagonists in treated and nontreated samples suggests suppression of phenazine production by P. aeruginosa. Hence, our model provides a rapid analytical approach to gaining a mechanistic understanding of bacterial signaling.
Citation
Robertson, S. N., Soukarieh, F., White, T. M., Camara, M., Romero, M., & Griffiths, R. L. (2023). Probing Interkingdom Signaling Molecules via Liquid Extraction Surface Analysis-Mass Spectrometry. Analytical Chemistry, 95(11), 5079-5086. https://doi.org/10.1021/acs.analchem.2c05703
Journal Article Type | Article |
---|---|
Acceptance Date | Feb 21, 2023 |
Online Publication Date | Mar 7, 2023 |
Publication Date | Mar 21, 2023 |
Deposit Date | Mar 10, 2023 |
Publicly Available Date | Mar 8, 2024 |
Journal | Analytical Chemistry |
Print ISSN | 0003-2700 |
Electronic ISSN | 1520-6882 |
Publisher | American Chemical Society |
Peer Reviewed | Peer Reviewed |
Volume | 95 |
Issue | 11 |
Pages | 5079-5086 |
DOI | https://doi.org/10.1021/acs.analchem.2c05703 |
Keywords | Biofilms, Computer simulations, Infectious diseases, Inhibitors, Molecules |
Public URL | https://nottingham-repository.worktribe.com/output/18236138 |
Publisher URL | https://pubs.acs.org/doi/10.1021/acs.analchem.2c05703 |
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Probing Interkingdom Signaling Molecules via Liquid Extraction Surface Analysis–Mass Spectrometry
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Licence
https://creativecommons.org/licenses/by/4.0/
Publisher Licence URL
https://creativecommons.org/licenses/by/4.0/
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