Evidence map›Paper›PMID 30778051›Full record

ArticleNature communications2019

Flagellar cAMP signaling controls trypanosome progression through host tissues.

Sebastian Shaw, Stephanie F DeMarco, Ruth Rehmann, Tanja Wenzler, Francesca Florini, Isabel Roditi, Kent L Hill

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 40 papers.

0numbers the graph read from it
0cells of the map it votes in
40citing papers in PubMed
6.9field-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

40 citing papers in PubMed, 67 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. FAP20 is required for flagellum assembly inMolecular biology of the cell · 2024
    Article
  10. Article
  11. FAP20 is required for flagellum assembly inbioRxiv : the preprint server for biology · 2024
    Article
  12. Article
  13. Review
  14. Article
  15. Cell-cell communication in African trypanosomes.Microbiology (Reading, England) · 2023
    Review
  16. Article
  17. Review
  18. Article
  19. Review
  20. 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

7 authors at 3 institutions in 2 countries.

Sebastian ShawInstitute of Cell Biology, University of Bern, Baltzerstrasse 4, CH-3012, Bern, Switzerland.ORCID http://orcid.org/0000-0001-7163-5650
Stephanie F DeMarcoMolecular Biology Institute, University of California, Los Angeles, CA, 90095, USA.ORCID http://orcid.org/0000-0001-8010-8027
Ruth RehmannInstitute of Cell Biology, University of Bern, Baltzerstrasse 4, CH-3012, Bern, Switzerland.
Tanja WenzlerInstitute of Cell Biology, University of Bern, Baltzerstrasse 4, CH-3012, Bern, Switzerland.
Francesca FloriniInstitute of Cell Biology, University of Bern, Baltzerstrasse 4, CH-3012, Bern, Switzerland.
Isabel RoditiInstitute of Cell Biology, University of Bern, Baltzerstrasse 4, CH-3012, Bern, Switzerland. isabel.roditi@izb.unibe.ch.ORCID http://orcid.org/0000-0003-2812-6513
Kent L HillMolecular Biology Institute, University of California, Los Angeles, CA, 90095, USA. kenthill@microbio.ucla.edu.ORCID http://orcid.org/0000-0001-6529-1273
University of Bern · CHCalifornia NanoSystems Institute · USUniversity of California, Los Angeles · US

Funding

UCLA NIGMS T32 Program AssessmentT32GM007185 · NIGMS · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI TORRES, JORGE · 1985 to 2020
$21.7M
MULTIDISCIPLINARY TRAINING IN MICROBIAL PATHOGENESIST32AI007323 · NIAID · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI Peter John Bradley · 1988 to 2026
$8.6M
Biochemical and Functional Analysis of TrypaninR01AI052348 · NIAID · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI HILL, KENT L · 2002 to 2023
$7.4M
Biochemical and Functional Analysis of TrypaninR56AI052348 · NIAID · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI HILL, KENT L · 2007 to 2007
$374k
NIAID NIH HHS R01 AI052348NIAID NIH HHS R56 AI052348NIAID NIH HHS T32 AI007323NIGMS NIH HHS T32 GM007185
6 · The paper itself

Abstract

The unicellular parasite Trypanosoma brucei is transmitted between mammals by tsetse flies. Following the discovery that flagellar phosphodiesterase PDEB1 is required for trypanosomes to move in response to signals in vitro (social motility), we investigated its role in tsetse flies. Here we show that PDEB1 knockout parasites exhibit subtle changes in movement, reminiscent of bacterial chemotaxis mutants. Infecting flies with the knockout, followed by live confocal microscopy of fluorescent parasites within dual-labelled insect tissues, shows that PDEB1 is important for traversal of the peritrophic matrix, which separates the midgut lumen from the ectoperitrophic space. Without PDEB1, parasites are trapped in the lumen and cannot progress through the cycle. This demonstrates that the peritrophic matrix is a barrier that must be actively overcome and that the parasite's flagellar cAMP signaling pathway facilitates this. Migration may depend on perception of chemotactic cues, which could stem from co-infecting parasites and/or the insect host.

Indexed as

3',5'-Cyclic-AMP PhosphodiesterasesAnimalsCyclic AMPDigestive SystemFlagellaGene Knockout TechniquesHost-Parasite InteractionsMutationProtozoan ProteinsSignal TransductionTrypanosoma brucei bruceiTrypanosomiasis, AfricanTsetse Flies3',5'-Cyclic-AMP PhosphodiesterasesCyclic AMPPDEB1 protein, Trypanosoma bruceiProtozoan Proteins

Identifiers

PMID30778051
PMCPMC6379439
OpenAlexW2913042128

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.