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Toward Comprehensive Analysis of the 3D Chemistry of Pseudomonas aeruginosa Biofilms

Kotowska, Anna M.; Zhang, Junting; Carabelli, Alessandro; Watts, Julie; Aylott, Jonathan W.; Gilmore, Ian S.; Williams, Paul; Scurr, David J.; Alexander, Morgan R.

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Authors

Junting Zhang

Dr ALE CARABELLI Ale.Carabelli@nottingham.ac.uk
MIT Postdoctoral Fellowshipin Biomaterials

Julie Watts

Ian S. Gilmore



Abstract

Bacterial biofilms are structured communities consisting of cells enmeshed in a self-generated extracellular matrix usually attached to a surface. They contain diverse classes of molecules including polysaccharides, lipids, proteins, nucleic acids, and diverse small organic molecules (primary and secondary metabolites) which are organized to optimize survival and facilitate dispersal to new colonization sites. In situ characterization of the chemical composition and structure of bacterial biofilms is necessary to fully understand their development on surfaces relevant to biofouling in health, industry, and the environment. Biofilm development has been extensively studied using confocal microscopy using targeted fluorescent labels providing important insights into the architecture of biofilms. Recently, cryopreparation has been used to undertake targeted in situ chemical characterization using Orbitrap secondary ion mass spectrometry (OrbiSIMS), providing a label-free method for imaging biofilms in their native state. Although the high mass resolution of OrbiSIMS enables more confident peak assignments, it is still very challenging to assign most of the peaks in the spectra due to complexity of SIMS spectra and lack of automatic peak assignment methods. Here, we analyze the same OrbiSIMS depth profile data generated from the frozen-hydrated biofilm, but employ a new untargeted chemical filtering process utilizing mass spectral databases to assign secondary ions to decipher the large number of fragments present in the SIMS spectra. To move towards comprehensive analysis of different chemistries in the sample, we apply a molecular formula prediction approach which putatively assigns 81% of peaks in the 3D OrbiSIMS depth profile analysis. This enables us to catalog over 1000 lipids and their fragments, 3500 protein fragments, 71 quorum sensing-related molecules (2-alkyl-4-quinolones and N-acylhomoserine lactones), 150 polysaccharide fragments, and glycolipids simultaneously from one data set and map these separated molecular classes spatially through a Pseudomonas aeruginosa biofilm. Assignment of different chemistries in this sample facilitates identification of differences between biofilms grown on biofilm-promoting and biofilm-resistant polymers.

Citation

Kotowska, A. M., Zhang, J., Carabelli, A., Watts, J., Aylott, J. W., Gilmore, I. S., Williams, P., Scurr, D. J., & Alexander, M. R. (2023). Toward Comprehensive Analysis of the 3D Chemistry of Pseudomonas aeruginosa Biofilms. Analytical Chemistry, 95(49), 18287-18294. https://doi.org/10.1021/acs.analchem.3c04443

Journal Article Type Article
Acceptance Date Nov 20, 2023
Online Publication Date Dec 3, 2023
Publication Date Dec 12, 2023
Deposit Date Dec 8, 2023
Publicly Available Date Dec 10, 2023
Journal Analytical Chemistry
Print ISSN 0003-2700
Electronic ISSN 1520-6882
Publisher American Chemical Society
Peer Reviewed Peer Reviewed
Volume 95
Issue 49
Pages 18287-18294
DOI https://doi.org/10.1021/acs.analchem.3c04443
Keywords Biofilms, Carbohydrates, Ions, Lipids, Molecules
Public URL https://nottingham-repository.worktribe.com/output/28151510
Publisher URL https://pubs.acs.org/doi/10.1021/acs.analchem.3c04443

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