Evidence map›Paper›PMID 30188886›Full record

ArticlePLoS biology2018

Hook length of the bacterial flagellum is optimized for maximal stability of the flagellar bundle.

Imke Spöring, Vincent A Martinez, Christian Hotz, Jana Schwarz-Linek, Keara L Grady, Josué M Nava-Sedeño, Teun Vissers, Hanna M Singer, Manfred Rohde, Carole Bourquin and 4 more

Abstract read
In one paragraph

Article in PLoS biology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing 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

18 citing papers in PubMed.

  1. Article
  2. Article
  3. Run-and-tumble dynamics ofJournal of the Royal Society, Interface · 2025
    Article
  4. Article
  5. Article
  6. Review
  7. Review
  8. Review
  9. Article
  10. An overview of the structure and function of the flagellar hook FlgE protein.World journal of microbiology & biotechnology · 2023
    Review
  11. Article
  12. Article
  13. Article
  14. Article
  15. Amylases: Biofilm Inducer or Biofilm Inhibitor?Frontiers in cellular and infection microbiology · 2021
    Review
  16. Article
  17. Article
  18. 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.

Imke SpöringInstitute for Biology - Bacterial Physiology, Humboldt-Universität zu Berlin, Berlin, Germany.
Vincent A MartinezSchool of Physics and Astronomy, The University of Edinburgh, Edinburgh, United Kingdom.
Christian HotzDepartment of Medicine/MED3 - Pharmacology, University of Fribourg, Fribourg, Switzerland.
Jana Schwarz-LinekSchool of Physics and Astronomy, The University of Edinburgh, Edinburgh, United Kingdom.
Keara L GradyMicrobiology and Molecular Genetics, Michigan State University, East Lansing, Michigan, United States of America.
Josué M Nava-SedeñoBraunschweig Integrated Centre of Systems Biology (BRICS), Braunschweig, Germany.
Teun VissersSchool of Physics and Astronomy, The University of Edinburgh, Edinburgh, United Kingdom.
Hanna M SingerDepartment of Medicine/MED3 - Microbiologie, University of Fribourg, Fribourg, Switzerland.
Manfred RohdeCentral Facility for Microscopy, Helmholtz Centre for Infection Research, Braunschweig, Germany.
Carole BourquinDepartment of Medicine/MED3 - Pharmacology, University of Fribourg, Fribourg, Switzerland.
Haralampos HatzikirouBraunschweig Integrated Centre of Systems Biology (BRICS), Braunschweig, Germany.
Wilson C K PoonSchool of Physics and Astronomy, The University of Edinburgh, Edinburgh, United Kingdom.
Yann S DufourMicrobiology and Molecular Genetics, Michigan State University, East Lansing, Michigan, United States of America.
Marc ErhardtInstitute for Biology - Bacterial Physiology, Humboldt-Universität zu Berlin, Berlin, Germany.ORCID 0000-0001-6292-619X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Most bacteria swim in liquid environments by rotating one or several flagella. The long external filament of the flagellum is connected to a membrane-embedded basal body by a flexible universal joint, the hook, which allows the transmission of motor torque to the filament. The length of the hook is controlled on a nanometer scale by a sophisticated molecular ruler mechanism. However, why its length is stringently controlled has remained elusive. We engineered and studied a diverse set of hook-length variants of Salmonella enterica. Measurements of plate-assay motility, single-cell swimming speed, and directional persistence in quasi-2D and population-averaged swimming speed and body angular velocity in 3D revealed that the motility performance is optimal around the wild-type hook length. We conclude that too-short hooks may be too stiff to function as a junction and too-long hooks may buckle and create instability in the flagellar bundle. Accordingly, peritrichously flagellated bacteria move most efficiently as the distance travelled per body rotation is maximal and body wobbling is minimized. Thus, our results suggest that the molecular ruler mechanism evolved to control flagellar hook growth to the optimal length consistent with efficient bundle formation. The hook-length control mechanism is therefore a prime example of how bacteria evolved elegant but robust mechanisms to maximize their fitness under specific environmental constraints.

Indexed as

Bacterial ProteinsFlagellaMovementMutationSalmonella entericaSingle-Cell AnalysisBacterial Proteins

Identifiers

PMID30188886
PMCPMC6126814

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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.