Evidence map›Paper›PMID 27842347›Full record

ArticleJournal of visualized experiments : JoVE2016

Monitoring Spatial Segregation in Surface Colonizing Microbial Populations.

Theresa Hölscher, Anna Dragoš, Ramses Gallegos-Monterrosa, Marivic Martin, Eisha Mhatre, Anne Richter, Ákos T Kovács

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In one paragraph

Article in Journal of visualized experiments : JoVE, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing 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

14 citing papers in PubMed.

  1. Review
  2. Swarming Motility Assays in Salmonella.Methods in molecular biology (Clifton, N.J.) · 2023
    Article
  3. Article
  4. Article
  5. International journal of molecular sciences · 2022
    Article
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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

7 authors.

Theresa HölscherTerrestrial Biofilms Group, Institute of Microbiology, Friedrich Schiller University, Jena.
Anna DragošTerrestrial Biofilms Group, Institute of Microbiology, Friedrich Schiller University, Jena.
Ramses Gallegos-MonterrosaTerrestrial Biofilms Group, Institute of Microbiology, Friedrich Schiller University, Jena.
Marivic MartinTerrestrial Biofilms Group, Institute of Microbiology, Friedrich Schiller University, Jena.
Eisha MhatreTerrestrial Biofilms Group, Institute of Microbiology, Friedrich Schiller University, Jena.
Anne RichterTerrestrial Biofilms Group, Institute of Microbiology, Friedrich Schiller University, Jena.
Ákos T KovácsTerrestrial Biofilms Group, Institute of Microbiology, Friedrich Schiller University, Jena; akos-tibor.kovacs@uni-jena.de.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Microbes provide an intriguing system to study social interaction among individuals within a population. The short generation times and relatively simple genetic modification procedures of microbes facilitate the development of the sociomicrobiology field. To assess the fitness of certain microbial species, selected strains or their genetically modified derivatives within one population, can be fluorescently labelled and tracked using microscopy adapted with appropriate fluorescence filters. Expanding colonies of diverse microbial species on agar media can be used to monitor the spatial distribution of cells producing distinctive fluorescent proteins. Here, we present a detailed protocol for the use of green- and red-fluorescent protein producing bacterial strains to follow spatial arrangement during surface colonization, including flagellum-driven community movement (swarming), exopolysaccharide- and hydrophobin-dependent growth mediated spreading (sliding), and complex colony biofilm formation. Non-domesticated isolates of the Gram-positive bacterium, Bacillus subtilis can be utilized to scrutinize certain surface spreading traits and their effect on two-dimensional distribution on the agar-solidified medium. By altering the number of cells used to initiate colony biofilms, the assortment levels can be varied on a continuous scale. Time-lapse fluorescent microscopy can be used to witness the interaction between different phenotypes and genotypes at a certain assortment level and to determine the relative success of either.

Indexed as

Bacillus subtilisBiofilmsMicroscopy, FluorescenceCulture MediaLuminescent ProteinsCulture MediaLuminescent Proteins

Identifiers

PMID27842347
PMCPMC5226080

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.