Evidence map›Paper›PMID 34355698›Full record

ArticleeLife2021

Unexpected plasticity in the life cycle of

Sarah Schuster, Jaime Lisack, Ines Subota, Henriette Zimmermann, Christian Reuter, Tobias Mueller, Brooke Morriswood, Markus Engstler

Abstract read
In one paragraph

Article in eLife, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing 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

26 citing papers in PubMed.

  1. Article
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  8. A limitation lifted: A conditional knockdown system reveals essential roles for Polo-like kinase and Aurora kinase 1 inProceedings of the National Academy of Sciences of the United States of America · 2025
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  9. Article
  10. Review
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  14. Cell-cell communication in African trypanosomes.Microbiology (Reading, England) · 2023
    Review
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

8 authors.

Sarah Schuster *Lehrstuhl für Zell- und Entwicklungsbiologie, Biozentrum, Julius-Maximilians-Universität, Würzburg, Germany.
Jaime Lisack *Lehrstuhl für Zell- und Entwicklungsbiologie, Biozentrum, Julius-Maximilians-Universität, Würzburg, Germany.ORCID https://orcid.org/0000-0001-9621-4000
Ines Subota *Lehrstuhl für Zell- und Entwicklungsbiologie, Biozentrum, Julius-Maximilians-Universität, Würzburg, Germany.
Henriette ZimmermannLehrstuhl für Zell- und Entwicklungsbiologie, Biozentrum, Julius-Maximilians-Universität, Würzburg, Germany.
Christian ReuterLehrstuhl für Zell- und Entwicklungsbiologie, Biozentrum, Julius-Maximilians-Universität, Würzburg, Germany.
Tobias MuellerLehrstuhl für Bioinformatik, Biozentrum, Julius-Maximilians-Universität, Würzburg, Germany.
Brooke MorriswoodLehrstuhl für Zell- und Entwicklungsbiologie, Biozentrum, Julius-Maximilians-Universität, Würzburg, Germany.ORCID https://orcid.org/0000-0001-7031-3801
Markus EngstlerLehrstuhl für Zell- und Entwicklungsbiologie, Biozentrum, Julius-Maximilians-Universität, Würzburg, Germany.ORCID https://orcid.org/0000-0003-1436-5759

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

African trypanosomes cause sleeping sickness in humans and nagana in cattle. These unicellular parasites are transmitted by the bloodsucking tsetse fly. In the mammalian host's circulation, proliferating slender stage cells differentiate into cell cycle-arrested stumpy stage cells when they reach high population densities. This stage transition is thought to fulfil two main functions: first, it auto-regulates the parasite load in the host; second, the stumpy stage is regarded as the only stage capable of successful vector transmission. Here, we show that proliferating slender stage trypanosomes express the mRNA and protein of a known stumpy stage marker, complete the complex life cycle in the fly as successfully as the stumpy stage, and require only a single parasite for productive infection. These findings suggest a reassessment of the traditional view of the trypanosome life cycle. They may also provide a solution to a long-lasting paradox, namely the successful transmission of parasites in chronic infections, despite low parasitemia.

Indexed as

Trypanosoma brucei bruceiAnimalsFemaleGastrointestinal TractHost-Parasite InteractionsLife Cycle StagesMaleProtozoan ProteinsRNA, MessengerRNA, ProtozoanTsetse FliesProtozoan ProteinsRNA, MessengerRNA, Protozoandevelopmentinfectious diseaselife cyclemicrobiologysleeping sicknesstransmissiontrypanosomatsetse fly

Identifiers

PMID34355698
PMCPMC8448533

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.