Alessandro M. Carabelli
Single-Cell Tracking on Polymer Microarrays Reveals the Impact of Surface Chemistry on Pseudomonas aeruginosa Twitching Speed and Biofilm Development
Carabelli, Alessandro M.; Isgr�, Marco; Sanni, Olutoba; Figueredo, Grazziela P.; Winkler, David A.; Burroughs, Laurence; Blok, Andrew J.; Dubern, Jean Fr�d�ric; Pappalardo, Francesco; Hook, Andrew L.; Williams, Paul; Alexander, Morgan R.
Authors
Marco Isgr�
Olutoba Sanni
GRAZZIELA FIGUEREDO G.Figueredo@nottingham.ac.uk
Associate Professor
David A. Winkler
Laurence Burroughs
Andrew J. Blok
JEAN DUBERN JEAN.DUBERN@NOTTINGHAM.AC.UK
Senior Research Fellow
Francesco Pappalardo
ANDREW HOOK ANDREW.HOOK@NOTTINGHAM.AC.UK
Associate Professor
PAUL WILLIAMS PAUL.WILLIAMS@NOTTINGHAM.AC.UK
Professor of Molecular Microbiology
MORGAN ALEXANDER MORGAN.ALEXANDER@NOTTINGHAM.AC.UK
Professor of Biomedical Surfaces
Abstract
© 2020 American Chemical Society. Bacterial biofilms exhibit up to 1000 times greater resistance to antibiotic or host immune clearance than planktonic cells. Pseudomonas aeruginosa produces retractable type IV pili (T4P) that facilitate twitching motility on surfaces. The deployment of pili is one of the first responses of bacteria to surface interactions and because of their ability to contribute to cell surface adhesion and biofilm formation, this has relevance to medical device-associated infections. While polymer chemistry is known to influence biofilm development, its impact on twitching motility is not understood. Here, we combine a polymer microarray format with time-lapse automated microscopy to simultaneously assess P. aeruginosa twitching motility on 30 different methacrylate/acrylate polymers over 60 min post inoculation using a high-throughput system. During this critical initial period where the decision to form a biofilm is thought to occur, similar numbers of bacterial cells accumulate on each polymer. Twitching motility is observed on all polymers irrespective of their chemistry and physical surface properties, in contrast to the differential biofilm formation noted after 24 h of incubation. However, on the microarray polymers, P. aeruginosa cells twitch at significantly different speeds, ranging from 5 to ∼13 nm/s, associated with crawling or walking and are distinguishable from the different cell surface tilt angles observed. Chemometric analysis using partial least-squares (PLS) regression identifies correlations between surface chemistry, as measured by time-of-flight secondary ion mass spectrometry (ToF-SIMS), and both biofilm formation and single-cell twitching speed. The relationships between surface chemistry and these two responses are different for each process. There is no correlation between polymer surface stiffness and roughness as determined by atomic force measurement (AFM), or water contact angle (WCA), and twitching speed or biofilm formation. This reinforces the dominant and distinct contributions of material surface chemistry to twitching speed and biofilm formation.
Citation
Carabelli, A. M., Isgró, M., Sanni, O., Figueredo, G. P., Winkler, D. A., Burroughs, L., …Alexander, M. R. (2020). Single-Cell Tracking on Polymer Microarrays Reveals the Impact of Surface Chemistry on Pseudomonas aeruginosa Twitching Speed and Biofilm Development. ACS Applied Bio Materials, 3(12), 8471–8480. https://doi.org/10.1021/acsabm.0c00849
Journal Article Type | Article |
---|---|
Acceptance Date | Oct 21, 2020 |
Online Publication Date | Nov 6, 2020 |
Publication Date | Dec 21, 2020 |
Deposit Date | Nov 2, 2020 |
Publicly Available Date | Nov 7, 2021 |
Journal | ACS Applied Bio Materials |
Print ISSN | 2576-6422 |
Electronic ISSN | 2576-6422 |
Publisher | American Chemical Society |
Peer Reviewed | Peer Reviewed |
Volume | 3 |
Issue | 12 |
Pages | 8471–8480 |
DOI | https://doi.org/10.1021/acsabm.0c00849 |
Keywords | Polymers; high-throughput screening; Pseudomonas aeruginosa; twitching motility; biofilm *Joint corresponding authors |
Public URL | https://nottingham-repository.worktribe.com/output/5012853 |
Publisher URL | https://pubs.acs.org/doi/pdf/10.1021/acsabm.0c00849 |
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