Evidence map›Paper›PMID 24913173›Full record

ArticleAntimicrobial agents and chemotherapy2014

Heterogeneity of molecular resistance patterns in antimony-resistant field isolates of Leishmania species from the western Mediterranean area.

Fakhri Jeddi, Charles Mary, Karim Aoun, Zoubir Harrat, Aïda Bouratbine, Françoise Faraut, Rezika Benikhlef, Christelle Pomares, Francine Pratlong, Pierre Marty and 1 more

Abstract read
In one paragraph

Article in Antimicrobial agents and chemotherapy, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing 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

20 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Genome analyses of amphotericin B-susceptible and -resistant strains ofCurrent research in parasitology & vector-borne diseases · 2025
    Article
  5. Review
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  10. Regulation of Translation in the Protozoan ParasiteInternational journal of molecular sciences · 2020
    Review
  11. Molecular Analysis ofJournal of arthropod-borne diseases · 2019
    Article
  12. Journal of parasitic diseases : official organ of the Indian Society for Parasitology · 2019
    Article
  13. Article
  14. Article
  15. Reverse Epidemiology: An Experimental Framework to DriveFrontiers in cellular and infection microbiology · 2018
    Review
  16. Article
  17. Article
  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

11 authors.

Fakhri JeddiLaboratoire de Parasitologie-Mycologie, CHU Timone, UMR MD3 Aix-Marseille Université, Marseille, France fjeddi2@yahoo.fr.
Charles MaryLaboratoire de Parasitologie-Mycologie, CHU Timone, UMR MD3 Aix-Marseille Université, Marseille, France.
Karim AounLaboratoire de recherche parasitoses médicales, Biotechnologie & Biomolécules, LR 11 IPT 06, Institut Pasteur de Tunis, Tunis, Tunisia.
Zoubir HarratService Eco-épidémiologie Parasitaire et Génétique des Populations, Institut Pasteur d'Algérie, Algiers, Algeria Laboratoire Biodiversité et Environnement, Interactions, Génomes, USTHB, Algiers, Algeria.
Aïda BouratbineLaboratoire de recherche parasitoses médicales, Biotechnologie & Biomolécules, LR 11 IPT 06, Institut Pasteur de Tunis, Tunis, Tunisia.
Françoise FarautLaboratoire de Parasitologie-Mycologie, CHU Timone, UMR MD3 Aix-Marseille Université, Marseille, France.
Rezika BenikhlefService Eco-épidémiologie Parasitaire et Génétique des Populations, Institut Pasteur d'Algérie, Algiers, Algeria.
Christelle PomaresINSERM, U1065, Centre Méditerranéen de Médecine Moléculaire, C3M, Toxines Microbiennes dans la relation hôte pathogènes, Nice, France Service de Parasitologie-Mycologie, Centre Hospitalier Universitaire de Nice, Nice, France.
Francine PratlongMontpellier Université 1, UMR MIVEGEC (CNRS 5290/IRD 224/UM1/UM2), Montpellier, France CHRU de Montpellier, Montpellier, France.
Pierre MartyINSERM, U1065, Centre Méditerranéen de Médecine Moléculaire, C3M, Toxines Microbiennes dans la relation hôte pathogènes, Nice, France Service de Parasitologie-Mycologie, Centre Hospitalier Universitaire de Nice, Nice, France.
Renaud PiarrouxLaboratoire de Parasitologie-Mycologie, CHU Timone, UMR MD3 Aix-Marseille Université, Marseille, France.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Antimonials remain the first-line treatment for the various manifestations of leishmaniasis in most areas where the disease is endemic, and increasing cases of therapeutic failure associated with parasite resistance have been reported. In this study, we assessed the molecular status of 47 clinical isolates of Leishmania causing visceral and cutaneous leishmaniasis from Algeria, Tunisia, and southern France. In total, we examined 14 genes that have been shown to exhibit significant variations in DNA amplification, mRNA levels, or protein expression with respect to resistance to antimonials. The gene status of each clinical isolate was assessed via qPCR and qRT-PCR. We then compared the molecular pattern against the phenotype determined via an in vitro sensitivity test of the clinical isolates against meglumine antimoniate, which is considered the reference technique. Our results demonstrate significant DNA amplification and/or RNA overexpression in 56% of the clinical isolates with the resistant phenotype. All clinical isolates that exhibited significant overexpression of at least 2 genes displayed a resistant phenotype. Among the 14 genes investigated, 10 genes displayed either significant amplification or overexpression in at least 1 clinical isolate; these genes are involved in several metabolic pathways. Moreover, various gene associations were observed depending on the clinical isolates, supporting the multifactorial nature of Leishmania resistance. Molecular resistance features were found in the 3 Leishmania species investigated (Leishmania infantum, Leishmania major, and Leishmania killicki). To our knowledge, this is the first report of the involvement of molecular resistance genes in field isolates of Leishmania major and Leishmania killicki with the resistance phenotype.

Indexed as

AlgeriaAntiprotozoal AgentsDrug ResistanceFranceGene Expression RegulationGenotypeHumansLeishmania infantumLeishmania majorLeishmaniasis, CutaneousLeishmaniasis, VisceralMeglumineMeglumine AntimoniateMetabolic Networks and PathwaysOrganometallic CompoundsParasitic Sensitivity TestsAntiprotozoal AgentsMeglumineMeglumine AntimoniateOrganometallic CompoundsProtozoan Proteins

Identifiers

PMID24913173
PMCPMC4136049

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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.