Evidence map›Paper›PMID 40341406›Full record

ArticleNPJ biofilms and microbiomes2025

Analysis of biofilm assembly by large area automated AFM.

Ruben Millan-Solsona, Spenser R Brown, Lance Zhang, Sita Sirisha Madugula, HuanHuan Zhao, Blythe Dumerer, Amber N Bible, Nickolay V Lavrik, Rama K Vasudevan, Arpan Biswas and 4 more

Abstract read
In one paragraph

Article in NPJ biofilms and microbiomes, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
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

14 authors.

Ruben Millan-SolsonaCenter for Nanophase Materials Sciences, Oak Ridge National Laboratory, Oak Ridge, TN, 37831, USA. solsonarm@ornl.gov.
Spenser R BrownBiosciences Division, Oak Ridge National Laboratory, Oak Ridge, TN, 37831, USA.
Lance ZhangBiosciences Division, Oak Ridge National Laboratory, Oak Ridge, TN, 37831, USA.
Sita Sirisha MadugulaCenter for Nanophase Materials Sciences, Oak Ridge National Laboratory, Oak Ridge, TN, 37831, USA.
HuanHuan ZhaoBredesen Center for Interdisciplinary Research, University of Tennessee, Knoxville, USA.
Blythe DumererCenter for Nanophase Materials Sciences, Oak Ridge National Laboratory, Oak Ridge, TN, 37831, USA.
Amber N BibleBiosciences Division, Oak Ridge National Laboratory, Oak Ridge, TN, 37831, USA.
Nickolay V LavrikCenter for Nanophase Materials Sciences, Oak Ridge National Laboratory, Oak Ridge, TN, 37831, USA.
Rama K VasudevanCenter for Nanophase Materials Sciences, Oak Ridge National Laboratory, Oak Ridge, TN, 37831, USA.
Arpan BiswasUniversity of Tennessee-Oak Ridge Innovation Institute, Knoxville, TN, 37996, USA.
Jennifer L Morrell-FalveyBiosciences Division, Oak Ridge National Laboratory, Oak Ridge, TN, 37831, USA.
Scott RettererCenter for Nanophase Materials Sciences, Oak Ridge National Laboratory, Oak Ridge, TN, 37831, USA.
Martí ChecaCenter for Nanophase Materials Sciences, Oak Ridge National Laboratory, Oak Ridge, TN, 37831, USA.
Liam CollinsCenter for Nanophase Materials Sciences, Oak Ridge National Laboratory, Oak Ridge, TN, 37831, USA. collinslf@ornl.gov.

Funding

U.S. Department of Energy FWP ERKCZ64
6 · The paper itself

Abstract

Biofilms are complex microbial communities critical in medical, industrial, and environmental contexts. Understanding their assembly, structure, genetic regulation, interspecies interactions, and environmental responses is key to developing effective control and mitigation strategies. While atomic force microscopy (AFM) offers critically important high-resolution insights on structural and functional properties at the cellular and even sub-cellular level, its limited scan range and labor-intensive nature restricts the ability to link these smaller scale features to the functional macroscale organization of the films. We begin to address this limitation by introducing an automated large area AFM approach capable of capturing high-resolution images over millimeter-scale areas, aided by machine learning for seamless image stitching, cell detection, and classification. Large area AFM is shown to provide a very detailed view of spatial heterogeneity and cellular morphology during the early stages of biofilm formation which were previously obscured. Using this approach, we examined the organization of Pantoea sp. YR343 on PFOTS-treated glass surfaces. Our findings reveal a preferred cellular orientation among surface-attached cells, forming a distinctive honeycomb pattern. Detailed mapping of flagella interactions suggests that flagellar coordination plays a role in biofilm assembly beyond initial attachment. Additionally, we use large-area AFM to characterize surface modifications on silicon substrates, observing a significant reduction in bacterial density. This highlights the potential of this method for studying surface modifications to better understand and control bacterial adhesion and biofilm formation.

Indexed as

BiofilmsMicroscopy, Atomic ForceFlagellaImage Processing, Computer-AssistedMachine Learning

Identifiers

PMID40341406
PMCPMC12062311

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.