Evidence map›Paper›PMID 27457482›Full record

ArticleParasitology research2016

Deep-sequencing revealing mutation dynamics in the miltefosine transporter gene in Leishmania infantum selected for miltefosine resistance.

Marie-Claude N Laffitte, Philippe Leprohon, Danielle Légaré, Marc Ouellette

Abstract read
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In one paragraph

Article in Parasitology research, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
3.0field-weighted citation impact, top 8% 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

17 citing papers in PubMed, 26 citations in OpenAlex.

  1. Review
  2. CRISPR-Cas13b mediated gene knockdowns in Leishmania infantum.International journal for parasitology. Drugs and drug resistance · 2025
    Article
  3. Molecular Mechanisms of Drug Resistance inPathogens (Basel, Switzerland) · 2024
    Review
  4. Article
  5. Article
  6. Review
  7. Impact of Genetic Diversity and Genome Plasticity ofFrontiers in cellular and infection microbiology · 2022
    Review
  8. Article
  9. Article
  10. Computational and structural biotechnology journal · 2020
    Review
  11. Article
  12. Article
  13. Article
  14. Article
  15. Leishmaniasis in humans: drug or vaccine therapy?Drug design, development and therapy · 2018
    Review
  16. Article
  17. Plasticity of theF1000Research · 2016
    Review
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

4 authors at 1 institution in 1 country.

Marie-Claude N LaffitteCentre de Recherche en Infectiologie, CRCHU de Québec, 2705 Boul. Laurier, Québec, Qc, G1V 4G2, Canada.
Philippe LeprohonCentre de Recherche en Infectiologie, CRCHU de Québec, 2705 Boul. Laurier, Québec, Qc, G1V 4G2, Canada.
Danielle LégaréCentre de Recherche en Infectiologie, CRCHU de Québec, 2705 Boul. Laurier, Québec, Qc, G1V 4G2, Canada.
Marc OuelletteCentre de Recherche en Infectiologie, CRCHU de Québec, 2705 Boul. Laurier, Québec, Qc, G1V 4G2, Canada. marc.ouellette@crchul.ulaval.ca.
Centre de Recherche en Sciences Animales de Deschambault · CA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Miltefosine is the first oral drug used in chemotherapy against leishmaniasis. In vitro studies found that resistance to miltefosine in Leishmania is often associated with the acquisition of point mutations in the miltefosine transporter, leading to a decrease in drug uptake. In this study, the dynamics of mutations upon miltefosine selection was studied by deep-sequencing of the miltefosine transporter gene. Deep-sequencing data revealed that no mutation was detected in the miltefosine transporter at sub-inhibitory concentrations of miltefosine. We show that the prevalence of mutated alleles was increasing when the drug pressure heightened, that more mutations were observed in highly resistant mutants, and that most mutations remained when parasites were cultured for a few passages in the absence of miltefosine.

Indexed as

AllelesAnimalsAntiprotozoal AgentsHigh-Throughput Nucleotide SequencingHumansLeishmania infantumLeishmaniasisMembrane Transport ProteinsPhosphorylcholinePoint MutationSequence Analysis, DNAAntiprotozoal AgentsMembrane Transport ProteinsmiltefosinePhosphorylcholineDeep-sequencingLeishmaniaMiltefosine transporterResistance

Identifiers

PMID27457482
OpenAlexW2483272154

What OpenQuestion holds

Textmetadata
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.