Evidence map›Paper›PMID 42401745›Full record

Articlenpj antimicrobials and resistance2026

A cell surface transporter mediates phenanthridine resistance in African trypanosomes.

Pieter C Steketee, Marzuq A Ungogo, Edith Paxton, Ella Maria Rogerson, Furaha Mramba, Michael C Pearce, Harriet K Auty, Jan Van Den Abbeele, Harry P de Koning, Catarina Gadelha and 2 more

Abstract read
In one paragraph

Article in npj antimicrobials and resistance, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

12 authors.

Pieter C Steketee *The Roslin Institute, Royal (Dick) School of Veterinary Studies, University of Edinburgh, Edinburgh, UK. Pieter.Steketee@ed.ac.uk.
Marzuq A Ungogo *The Roslin Institute, Royal (Dick) School of Veterinary Studies, University of Edinburgh, Edinburgh, UK.
Edith PaxtonThe Roslin Institute, Royal (Dick) School of Veterinary Studies, University of Edinburgh, Edinburgh, UK.
Ella Maria RogersonSchool of Life Sciences, University of Nottingham, Nottingham, UK.
Furaha MrambaTanzania Veterinary Laboratory Agency, Dar es Salaam, Tanzania.
Michael C PearceGlobal Alliance for Livestock Veterinary Medicines, Edinburgh, UK.
Harriet K AutySchool of Biodiversity, One Health and Veterinary Medicine, College of Medical, Veterinary and Life Sciences, University of Glasgow, Glasgow, UK.
Jan Van Den AbbeeleTrypanosoma Unit, Department of Biomedical Sciences, Institute of Tropical Medicine Antwerp, Antwerp, Belgium.
Harry P de KoningSchool of Infection and Immunity, University of Glasgow, Glasgow, UK.
Catarina GadelhaSchool of Life Sciences, University of Nottingham, Nottingham, UK.
Michael P BarrettSchool of Infection and Immunity, University of Glasgow, Glasgow, UK.
Liam J MorrisonThe Roslin Institute, Royal (Dick) School of Veterinary Studies, University of Edinburgh, Edinburgh, UK.

Funding

Biotechnology and Biological Sciences Research Council BB/S00243X/1Biotechnology and Biological Sciences Research Council BB/W005867/1Biotechnology and Biological Sciences Research Council BB/X009807/7
6 · The paper itself

Abstract

African animal trypanosomosis poses a significant threat to livestock health and agricultural productivity across sub-Saharan Africa. Isometamidium chloride is the only available drug that is both prophylactic and curative. Despite sustained reports of resistance since the 1970s, a definitive molecular mechanism of resistance remains unresolved in the clinically relevant pathogen species Trypanosoma congolense. In this study, the role of a putative drug/metabolite transporter protein, TcoDMT, was validated via the analysis of in vitro-derived mutants, showing that expression levels of this protein correlated strongly with isometamidium sensitivity. Functional analyses revealed that the protein is a cell surface phenanthridine transporter and, notably, copy number variation correlates with isometamidium sensitivity in T. congolense field isolates. This study validates, for the first time, a plasma membrane transporter with a defined role in phenanthridine action and resistance, advancing our understanding of drug resistance mechanisms in parasitic protists, and informing strategies to combat animal trypanosomosis.

Identifiers

PMID42401745
PMCPMC13642254

What OpenQuestion holds

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Read underepoch 390

Registered trials

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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.