Evidence map›Paper›PMID 32248844›Full record

ArticleParasites & vectors2020

Timing and original features of flagellum assembly in trypanosomes during development in the tsetse fly.

Moara Lemos, Adeline Mallet, Eloïse Bertiaux, Albane Imbert, Brice Rotureau, Philippe Bastin

Open access · goldAbstract read
In one paragraph

Article in Parasites & vectors, 2020. 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
1.3field-weighted citation impact, top 19% 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

3 citing papers in PubMed, 10 citations in OpenAlex.

  1. 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

6 authors at 2 institutions in 1 country.

Moara LemosTrypanosome Cell Biology Unit, Institut Pasteur & INSERM U1201, 25, rue du Docteur Roux, 75015, Paris, France.
Adeline MalletTrypanosome Cell Biology Unit, Institut Pasteur & INSERM U1201, 25, rue du Docteur Roux, 75015, Paris, France.
Eloïse BertiauxTrypanosome Cell Biology Unit, Institut Pasteur & INSERM U1201, 25, rue du Docteur Roux, 75015, Paris, France.
Albane ImbertFab Lab, Institut Pasteur, 75015, Paris, France.
Brice RotureauTrypanosome Cell Biology Unit, Institut Pasteur & INSERM U1201, 25, rue du Docteur Roux, 75015, Paris, France.
Philippe BastinTrypanosome Cell Biology Unit, Institut Pasteur & INSERM U1201, 25, rue du Docteur Roux, 75015, Paris, France. pbastin@pasteur.fr.ORCID http://orcid.org/0000-0002-3042-8679
Inserm · FRInstitut Pasteur · FR

Funding

ANR ANR-10-LABX-62-IBEIDANR ANR-18-CE13-0014FRM FRM DEQ20150734356
6 · The paper itself

Abstract

backgroundTrypanosoma brucei exhibits a complex life-cycle alternating between tsetse flies and mammalian hosts. When parasites infect the fly, cells differentiate to adapt to life in various tissues, which is accompanied by drastic morphological and biochemical modifications especially in the proventriculus. This key step represents a bottleneck for salivary gland infection.

methodsHere, we monitored flagellum assembly in trypanosomes during differentiation from the trypomastigote to the epimastigote stage, i.e. when the nucleus migrates to the posterior end of the cell, by using three-dimensional electron microscopy (focused ion beam scanning electron microscopy, FIB-SEM) and immunofluorescence assays.

resultsThe combination of light and electron microscopy approaches provided structural and molecular evidence that the new flagellum is assembled while the nucleus migrates towards the posterior region of the body. Two major differences with well-known procyclic cells are reported. First, growth of the new flagellum begins when the associated basal body is found in a posterior position relative to the mature flagellum. Secondly, the new flagellum acquires its own flagellar pocket before rotating on the left side of the anterior-posterior axis. FIB-SEM revealed the presence of a structure connecting the new and mature flagellum and serial sectioning confirmed morphological similarities with the flagella connector of procyclic cells. We discuss the potential function of the flagella connector in trypanosomes from the proventriculus.

conclusionsThese findings show that T. brucei finely modulates its cytoskeletal components to generate highly variable morphologies.

Indexed as

AnimalsCell DifferentiationCytoskeletonFlagellaFluorescent Antibody TechniqueLife Cycle StagesMaleMicroscopy, ElectronProtozoan ProteinsTrypanosoma brucei bruceiTsetse FliesProtozoan ProteinsDifferentiationFocused ion beam scanning electron microscopyProventriculusTrypanosoma bruceiTsetse fly

Identifiers

PMID32248844
PMCPMC7132888
OpenAlexW3014696249

What OpenQuestion holds

Textmetadata
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.