Evidence map›Paper›PMID 32413766›Full record

ArticleInternational journal for parasitology. Drugs and drug resistance2020

MRPA-independent mechanisms of antimony resistance in Leishmania infantum.

Noélie Douanne, Victoria Wagner, Gaetan Roy, Philippe Leprohon, Marc Ouellette, Christopher Fernandez-Prada

Open access · goldAbstract read
In one paragraph

Article in International journal for parasitology. Drugs and drug resistance, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
4.7field-weighted citation impact, top 5% 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

18 citing papers in PubMed, 34 citations in OpenAlex.

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  12. Simvastatin Resistance ofMicroorganisms · 2022
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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 3 institutions in 1 country.

Noélie DouanneDépartement de Pathologie et Microbiologie, Faculté de Médecine Vétérinaire Université de Montréal, Saint-Hyacinthe, Québec, Canada.
Victoria WagnerDépartement de Pathologie et Microbiologie, Faculté de Médecine Vétérinaire Université de Montréal, Saint-Hyacinthe, Québec, Canada.
Gaetan RoyCentre de Recherche en Infectiologie du Centre de Recherche du CHU Québec and Département de Microbiologie, Infectiologie et Immunologie, Faculté de Médecine, Université Laval, Québec, Québec, Canada.
Philippe LeprohonCentre de Recherche en Infectiologie du Centre de Recherche du CHU Québec and Département de Microbiologie, Infectiologie et Immunologie, Faculté de Médecine, Université Laval, Québec, Québec, Canada.
Marc OuelletteCentre de Recherche en Infectiologie du Centre de Recherche du CHU Québec and Département de Microbiologie, Infectiologie et Immunologie, Faculté de Médecine, Université Laval, Québec, Québec, Canada.
Christopher Fernandez-PradaDépartement de Pathologie et Microbiologie, Faculté de Médecine Vétérinaire Université de Montréal, Saint-Hyacinthe, Québec, Canada; Department of Microbiology and Immunology, Faculty of Medicine, McGill University, Montréal, Québec, Canada. Electronic address: christopher.fernandez.prada@umontreal.ca.
Centre hospitalier de l'Université Laval · CAUniversité de Montréal · CAMcGill University · CA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Control of both human and canine leishmaniasis is based on a very short list of chemotherapeutic agents, headed by antimonial derivatives (Sb). The utility of these molecules is severely threatened by high rates of drug resistance. The ABC transporter MRPA is one of the few key Sb resistance proteins described to date, whose role in detoxification has been thoroughly studied in Leishmania parasites. Nonetheless, its rapid amplification during drug selection complicates the discovery of other mechanisms potentially involved in Sb resistance. In this study, stepwise drug-resistance selection and next-generation sequencing were combined in the search for novel Sb-resistance mechanisms deployed by parasites when MRPA is abolished by targeted gene disruption. The gene mrpA is not essential in L. infantum, and its disruption leads to an Sb hypersensitive phenotype in both promastigotes and amastigotes. Five independent mrpA

Indexed as

Leishmania infantumAnimalsAntimonyAntiprotozoal AgentsATP-Binding Cassette TransportersDogsDrug ResistanceGenes, ProtozoanHumansLeishmaniasisMembrane Transport ProteinsMultidrug Resistance-Associated Protein 2MutationProtozoan ProteinsSerine O-AcetyltransferaseWhole Genome SequencingABCC2 protein, humanAntimonyAntiprotozoal AgentsATP-Binding Cassette TransportersMembrane Transport ProteinsMultidrug Resistance-Associated Protein 2Protozoan ProteinsSerine O-AcetyltransferaseAntimonyDrug resistanceGene disruptionLeishmania infantumMRPAWhole-genome sequencing

Identifiers

PMID32413766
PMCPMC7225602
OpenAlexW3014716530

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.