Evidence map›Paper›PMID 35012338›Full record

ArticlemBio2022

Genomic and Phenotypic Characterization of Experimentally Selected Resistant Leishmania donovani Reveals a Role for Dynamin-1-Like Protein in the Mechanism of Resistance to a Novel Antileishmanial Compound.

Aya Hefnawy, Gabriel Negreira, Marlene Jara, James A Cotton, Ilse Maes, Erika D'Haenens, Hideo Imamura, Bart Cuypers, Pieter Monsieurs, Christina Mouchtoglou and 10 more

Open access · goldAbstract read
In one paragraph

Article in mBio, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
2.4field-weighted citation impact, top 12% 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

7 citing papers in PubMed, 12 citations in OpenAlex.

  1. Article
  2. The trypanosomatid dynamin-like protein associates with glycosomes.bioRxiv : the preprint server for biology · 2026
    Article
  3. 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

20 authors at 4 institutions in 3 countries.

Aya HefnawyMolecular Parasitology Unit, Institute of Tropical Medicine, Antwerp, Belgium.
Gabriel NegreiraMolecular Parasitology Unit, Institute of Tropical Medicine, Antwerp, Belgium.
Marlene JaraMolecular Parasitology Unit, Institute of Tropical Medicine, Antwerp, Belgium.
James A CottonWellcome Sanger Institutegrid.10306.34, Wellcome Genome Campus, Hinxton, United Kingdom.
Ilse MaesMolecular Parasitology Unit, Institute of Tropical Medicine, Antwerp, Belgium.
Erika D'HaenensMolecular Parasitology Unit, Institute of Tropical Medicine, Antwerp, Belgium.
Hideo ImamuraMolecular Parasitology Unit, Institute of Tropical Medicine, Antwerp, Belgium.
Bart CuypersMolecular Parasitology Unit, Institute of Tropical Medicine, Antwerp, Belgium.ORCID 0000-0002-7198-1470
Pieter MonsieursMolecular Parasitology Unit, Institute of Tropical Medicine, Antwerp, Belgium.
Christina MouchtoglouMolecular Parasitology Unit, Institute of Tropical Medicine, Antwerp, Belgium.
Hans De WinterLaboratory of Medicinal Chemistry, University of Antwerpgrid.5284.b, Antwerp, Belgium.
Isabel PintelonDepartment of Veterinary Sciences, University of Antwerpgrid.5284.b, Antwerp, Belgium.
Jean-Pierre TimmermansDepartment of Veterinary Sciences, University of Antwerpgrid.5284.b, Antwerp, Belgium.
Matt BerrimanWellcome Sanger Institutegrid.10306.34, Wellcome Genome Campus, Hinxton, United Kingdom.
Mandy SandersWellcome Sanger Institutegrid.10306.34, Wellcome Genome Campus, Hinxton, United Kingdom.
Julio MartinGlobal Health R&D, GlaxoSmithKline, Tres Cantos, Madrid, Spain.
Geraldine de MuylderMolecular Parasitology Unit, Institute of Tropical Medicine, Antwerp, Belgium.
Jean-Claude DujardinMolecular Parasitology Unit, Institute of Tropical Medicine, Antwerp, Belgium.ORCID 0000-0002-9217-5240
Yann G-J SterckxLaboratory of Medical Biochemistry, University of Antwerpgrid.5284.b, Antwerp, Belgium.
Malgorzata Anna DomagalskaMolecular Parasitology Unit, Institute of Tropical Medicine, Antwerp, Belgium.
Instituut voor Tropische Geneeskunde · BEUniversity of Antwerp · BEWellcome Sanger Institute · GBGlaxoSmithKline (Spain) · ES

Funding

Wellcome TrustWellcome Trust 206194
6 · The paper itself

Abstract

The implementation of prospective drug resistance (DR) studies in the research-and-development (R&D) pipeline is a common practice for many infectious diseases but not for neglected tropical diseases (NTDs). Here, we explored and demonstrated the importance of this approach using as paradigms Leishmania donovani, the etiological agent of visceral leishmaniasis (VL), and TCMDC-143345, a promising compound of the GlaxoSmithKline (GSK) "Leishbox" to treat VL. We experimentally selected resistance to TCMDC-143345

Indexed as

Antiprotozoal AgentsDrug ResistanceDynamin ILeishmania donovaniLeishmaniasis, VisceralGenomicsHumansPhylogenyRetrospective StudiesAntiprotozoal AgentsDynamin ICRISPR-Cas9drug resistance mechanismsdynamingenomicsLeishmania

Identifiers

PMID35012338
PMCPMC8749414
OpenAlexW4220728458

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.