Evidence map›Paper›PMID 25569823›Full record

ArticlePLoS computational biology2015

Simulating the complex cell design of Trypanosoma brucei and its motility.

Davod Alizadehrad, Timothy Krüger, Markus Engstler, Holger Stark

Open access · goldAbstract read
In one paragraph

Article in PLoS computational biology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
7.0field-weighted citation impact, top 3% of its field
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

22 citing papers in PubMed, 63 citations in OpenAlex.

  1. Article
  2. Article
  3. Modelling motility of Trypanosoma brucei.PLoS computational biology · 2025
    Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Microgel that swims to the beat of light.The European physical journal. E, Soft matter · 2021
    Article
  9. Article
  10. Single-cell motile behaviour ofThe European physical journal. E, Soft matter · 2021
    Article
  11. Review
  12. Article
  13. Flagellum couples cell shape to motility inProceedings of the National Academy of Sciences of the United States of America · 2018
    Article
  14. Simulating squirmers with multiparticle collision dynamics.The European physical journal. E, Soft matter · 2018
    Article
  15. Review
  16. Article
  17. Article
  18. Article
  19. Article
  20. 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

4 authors at 2 institutions in 1 country.

Davod AlizadehradInstitute of Theoretical Physics, Technische Universität Berlin, Berlin, Germany.
Timothy KrügerDepartment of Cell and Developmental Biology, Biocenter, University of Würzburg, Würzburg, Germany.
Markus EngstlerDepartment of Cell and Developmental Biology, Biocenter, University of Würzburg, Würzburg, Germany.
Holger StarkInstitute of Theoretical Physics, Technische Universität Berlin, Berlin, Germany.
Technische Universität Berlin · DEUniversity of Würzburg · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The flagellate Trypanosoma brucei, which causes the sleeping sickness when infecting a mammalian host, goes through an intricate life cycle. It has a rather complex propulsion mechanism and swims in diverse microenvironments. These continuously exert selective pressure, to which the trypanosome adjusts with its architecture and behavior. As a result, the trypanosome assumes a diversity of complex morphotypes during its life cycle. However, although cell biology has detailed form and function of most of them, experimental data on the dynamic behavior and development of most morphotypes is lacking. Here we show that simulation science can predict intermediate cell designs by conducting specific and controlled modifications of an accurate, nature-inspired cell model, which we developed using information from live cell analyses. The cell models account for several important characteristics of the real trypanosomal morphotypes, such as the geometry and elastic properties of the cell body, and their swimming mechanism using an eukaryotic flagellum. We introduce an elastic network model for the cell body, including bending rigidity and simulate swimming in a fluid environment, using the mesoscale simulation technique called multi-particle collision dynamics. The in silico trypanosome of the bloodstream form displays the characteristic in vivo rotational and translational motility pattern that is crucial for survival and virulence in the vertebrate host. Moreover, our model accurately simulates the trypanosome's tumbling and backward motion. We show that the distinctive course of the attached flagellum around the cell body is one important aspect to produce the observed swimming behavior in a viscous fluid, and also required to reach the maximal swimming velocity. Changing details of the flagellar attachment generates less efficient swimmers. We also simulate different morphotypes that occur during the parasite's development in the tsetse fly, and predict a flagellar course we have not been able to measure in experiments so far.

Indexed as

Models, BiologicalCell MovementComputational BiologyComputer SimulationTrypanosoma brucei brucei

Identifiers

PMID25569823
PMCPMC4288712
OpenAlexW2025005952

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.