Evidence map›Paper›PMID 40533450›Full record

ArticleNature communications2025

Combinatorial discovery of microtopographical landscapes that resist biofilm formation through quorum sensing mediated autolubrication.

Manuel Romero, Jeni Luckett, Jean-Frédéric Dubern, Grazziela P Figueredo, Elizabeth Ison, Alessandro M Carabelli, David J Scurr, Andrew L Hook, Lisa Kammerling, Ana C da Silva and 11 more

Abstract read
In one paragraph

Article in Nature communications, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

7 citing papers in PubMed.

  1. Review
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

21 authors.

Manuel RomeroSchool of Life Sciences, University of Nottingham, Nottingham, United Kingdom.ORCID http://orcid.org/0000-0001-6902-6776
Jeni LuckettSchool of Life Sciences, University of Nottingham, Nottingham, United Kingdom.
Jean-Frédéric DubernSchool of Life Sciences, University of Nottingham, Nottingham, United Kingdom.ORCID http://orcid.org/0000-0002-9951-6925
Grazziela P FigueredoSchool of Computer Science, University of Nottingham, Nottingham, United Kingdom.
Elizabeth IsonSchool of Life Sciences, University of Nottingham, Nottingham, United Kingdom.
Alessandro M CarabelliSchool of Pharmacy, University of Nottingham, Nottingham, United Kingdom.ORCID http://orcid.org/0000-0003-3625-4021
David J ScurrSchool of Pharmacy, University of Nottingham, Nottingham, United Kingdom.ORCID http://orcid.org/0000-0003-0859-3886
Andrew L HookSchool of Pharmacy, University of Nottingham, Nottingham, United Kingdom.ORCID http://orcid.org/0000-0001-7756-8444
Lisa KammerlingSchool of Life Sciences, University of Nottingham, Nottingham, United Kingdom.
Ana C da SilvaSchool of Life Sciences, University of Nottingham, Nottingham, United Kingdom.
Xuan XueSchool of Pharmacy, University of Nottingham, Nottingham, United Kingdom.
Chester BlackburnSchool of Pharmacy, University of Nottingham, Nottingham, United Kingdom.
Aurélie CarlierMERLN Institute for Technology-Inspired Regenerative Medicine, Maastricht University, Maastricht, The Netherlands.ORCID http://orcid.org/0000-0002-2305-5667
Aliaksei VasilevichDepartment of Biomedical Engineering, Eindhoven University of Technology, Eindhoven, The Netherlands.
Phani K SudarsanamDepartment of Biomedical Engineering, Eindhoven University of Technology, Eindhoven, The Netherlands.
Steven VermeulenMERLN Institute for Technology-Inspired Regenerative Medicine, Maastricht University, Maastricht, The Netherlands.ORCID http://orcid.org/0000-0001-6797-7084
David A WinklerDepartment of Biochemistry and Genetics, La Trobe Institute for Molecular Science, La Trobe University, Melbourne, VIC, Australia.ORCID http://orcid.org/0000-0002-7301-6076
Amir M GhaemmaghamiSchool of Life Sciences, University of Nottingham, Nottingham, United Kingdom.
Jan de BoerDepartment of Biomedical Engineering, Eindhoven University of Technology, Eindhoven, The Netherlands.
Morgan R AlexanderSchool of Pharmacy, University of Nottingham, Nottingham, United Kingdom. morgan.alexander@nottingham.ac.uk.ORCID http://orcid.org/0000-0001-5182-493X
Paul WilliamsSchool of Life Sciences, University of Nottingham, Nottingham, United Kingdom. paul.williams@nottingham.ac.uk.ORCID http://orcid.org/0000-0002-1920-5036

Funding

EC | Horizon 2020 Framework Programme (EU Framework Programme for Research and Innovation H2020) H2020-MSCA-ITN-2015;676338RCUK | Biotechnology and Biological Sciences Research Council (BBSRC) BB/R012415/1RCUK | Engineering and Physical Sciences Research Council (EPSRC) EP/K005138/1RCUK | Engineering and Physical Sciences Research Council (EPSRC) EP/N006615/1RCUK | Engineering and Physical Sciences Research Council (EPSRC) EP/P029868/1RCUK | Engineering and Physical Sciences Research Council (EPSRC) EP/X001156/1Wellcome TrustWellcome Trust 103882Wellcome Trust 103884
6 · The paper itself

Abstract

Bio-instructive materials that intrinsically inhibit biofilm formation have significant anti-biofouling potential in industrial and healthcare settings. Since bacterial surface attachment is sensitive to surface topography, we experimentally surveyed 2176 combinatorially generated shapes embossed into polymers using an unbiased screen. This identified microtopographies that, in vitro, reduce colonization by pathogens associated with medical device-related infections by up to 15-fold compared to a flat polymer surface. Machine learning provided design rules, based on generalisable descriptors, for predicting biofilm-resistant microtopographies. On tracking single bacterial cells we observed that the motile behaviour of Pseudomonas aeruginosa is markedly different on anti-attachment microtopographies compared with pro-attachment or flat surfaces. Inactivation of Rhl-dependent quorum sensing in P. aeruginosa through deletion of rhlI or rhlR restored biofilm formation on the anti-attachment topographies due to the loss of rhamnolipid biosurfactant production. Exogenous provision of N-butanoyl-homoserine lactone to the rhlI mutant inhibited biofilm formation, as did genetic complementation of the rhlI, rhlR or rhlA mutants. These data are consistent with confinement-induced anti-adhesive rhamnolipid biosurfactant 'autolubrication'. In a murine foreign body infection model, anti-attachment topographies are refractory to P. aeruginosa colonization. Our findings highlight the potential of simple topographical patterning of implanted medical devices for preventing biofilm associated infections.

Indexed as

BiofilmsPseudomonas aeruginosaQuorum Sensing4-ButyrolactoneAnimalsBacterial AdhesionBacterial ProteinsBiofoulingFemaleGlycolipidsLigasesMicePolymersPseudomonas InfectionsSurface PropertiesTranscription Factors4-ButyrolactoneBacterial ProteinsGlycolipidsLigasesPolymersrhamnolipidRHLI protein, Pseudomonas aeruginosaRhlR protein, Pseudomonas aeruginosaTranscription Factors

Identifiers

PMID40533450
PMCPMC12177056

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.