Evidence map›Paper›PMID 32210351›Full record

ArticleScientific reports2020

A live-cell super-resolution technique demonstrated by imaging germinosomes in wild-type bacterial spores.

R M P Breedijk, J Wen, V Krishnaswami, T Bernas, E M M Manders, P Setlow, N O E Vischer, S Brul

Abstract read
In one paragraph

Article in Scientific reports, 2020. 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
  2. Article
  3. Article
  4. Predicting the Structure and Dynamics of Membrane Protein GerAB fromInternational journal of molecular sciences · 2021
    Article
  5. Super-Resolution Live Cell Imaging of Subcellular Structures.Journal of visualized experiments : JoVE · 2021
    Article
  6. Review
  7. Visualization of Germination Proteins in PutativeInternational journal of molecular sciences · 2020
    Article
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

8 authors.

R M P Breedijk *Van Leeuwenhoek Centre for Advanced Microscopy, Molecular Cytology, Swammerdam Institute for Life Sciences, University of Amsterdam, Amsterdam, Science Park 904, 1098 XH, The Netherlands.
J Wen *Molecular Biology and Microbial Food Safety, Swammerdam Institute for Life Sciences, University of Amsterdam, Amsterdam, Science Park 904, 1098 XH, The Netherlands.
V Krishnaswami *Van Leeuwenhoek Centre for Advanced Microscopy, Molecular Cytology, Swammerdam Institute for Life Sciences, University of Amsterdam, Amsterdam, Science Park 904, 1098 XH, The Netherlands.
T BernasDepartment of Anatomy and Neurobiology, Virginia Commonwealth University, PO Box 980709, 1101 East Marshall Street, Richmond, VA, 23298, United States of America.
E M M MandersVan Leeuwenhoek Centre for Advanced Microscopy, Molecular Cytology, Swammerdam Institute for Life Sciences, University of Amsterdam, Amsterdam, Science Park 904, 1098 XH, The Netherlands.
P SetlowDepartment of Molecular Biology and Biophysics, UConn Health, 263 Farmington Avenue, Farmington, CT, 06030-3305, United States of America.
N O E VischerMolecular Biology and Microbial Food Safety, Swammerdam Institute for Life Sciences, University of Amsterdam, Amsterdam, Science Park 904, 1098 XH, The Netherlands.
S BrulMolecular Biology and Microbial Food Safety, Swammerdam Institute for Life Sciences, University of Amsterdam, Amsterdam, Science Park 904, 1098 XH, The Netherlands. s.brul@uva.nl.ORCID http://orcid.org/0000-0001-5706-8768

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Time-lapse fluorescence imaging of live cells at super-resolution remains a challenge, especially when the photon budget is limited. Current super-resolution techniques require either the use of special exogenous probes, high illumination doses or multiple image acquisitions with post-processing or combinations of the aforementioned. Here, we describe a new approach by combining annular illumination with rescan confocal microscopy. This optics-only technique generates images in a single scan, thereby avoiding any potential risks of reconstruction related artifacts. The lateral resolution is comparable to that of linear structured illumination microscopy and the axial resolution is similar to that of a standard confocal microscope. As a case study, we present super-resolution time-lapse imaging of wild-type Bacillus subtilis spores, which contain low numbers of germination receptor proteins in a focus (a germinosome) surrounded by an autofluorescent coat layer. Here, we give the first evidence for the existence of germinosomes in wild-type spores, show their spatio-temporal dynamics upon germinant addition and visualize spores coming to life.

Indexed as

FluorescenceBacillus subtilisBacterial ProteinsCell MembraneMicroscopy, FluorescenceSpores, BacterialTime-Lapse ImagingBacterial Proteins

Identifiers

PMID32210351
PMCPMC7093444

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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.