Evidence map›Paper›PMID 27317865›Full record

ArticleInternational journal for parasitology. Drugs and drug resistance2016

Decreased antimony uptake and overexpression of genes of thiol metabolism are associated with drug resistance in a canine isolate of Leishmania infantum.

Verónica Gómez Pérez, Raquel García-Hernandez, Victoriano Corpas-López, Ana M Tomás, Joaquina Martín-Sanchez, Santiago Castanys, Francisco Gamarro

Open access · goldAbstract read
In one paragraph

Article in International journal for parasitology. Drugs and drug resistance, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed, 1 pooled it
3.3field-weighted citation impact, top 7% 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

22 citing papers in PubMed, 1 synthesis or guideline pooled it, 45 citations in OpenAlex.

  1. Guideline
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  11. Polyamine Metabolism inMedical sciences (Basel, Switzerland) · 2022
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  13. Tongue nodules in an atypical canine leishmaniasis in Brazil.The Journal of veterinary medical science · 2021
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  14. Article
  15. Article
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  17. RSC medicinal chemistry · 2020
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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

7 authors at 3 institutions in 2 countries.

Verónica Gómez PérezInstituto de Parasitología y Biomedicina "López-Neyra", CSIC, (IPBLN-CSIC), Parque Tecnológico de Ciencias de la Salud, Granada, Spain.
Raquel García-HernandezInstituto de Parasitología y Biomedicina "López-Neyra", CSIC, (IPBLN-CSIC), Parque Tecnológico de Ciencias de la Salud, Granada, Spain.
Victoriano Corpas-LópezDepartamento de Parasitología, Facultad de Farmacia, Universidad de Granada, Granada, Spain.
Ana M TomásIBMC - Institute for Molecular and Cell Biology, Porto, Portugal.
Joaquina Martín-SanchezDepartamento de Parasitología, Facultad de Farmacia, Universidad de Granada, Granada, Spain.
Santiago CastanysInstituto de Parasitología y Biomedicina "López-Neyra", CSIC, (IPBLN-CSIC), Parque Tecnológico de Ciencias de la Salud, Granada, Spain.
Francisco GamarroInstituto de Parasitología y Biomedicina "López-Neyra", CSIC, (IPBLN-CSIC), Parque Tecnológico de Ciencias de la Salud, Granada, Spain. Electronic address: gamarro@ipb.csic.es.
Instituto de Parasitología y Biomedicina "López - Neyra" · ESUniversidad de Granada · ESInstituto de Biologia Molecular e Celular

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Visceral leishmaniasis (VL) caused by the protozoan parasite Leishmania infantum, is one of the most important zoonotic diseases affecting dogs and humans in the Mediterranean area. The presence of infected dogs as the main reservoir host of L. infantum is regarded as the most significant risk for potential human infection. We have studied the susceptibility profile to antimony and other anti-leishmania drugs (amphotericin B, miltefosine, paromomycin) in Leishmania infantum isolates extracted from a dog before and after two therapeutic interventions with meglumine antimoniate (subcutaneous Glucantime(®), 100 mg/kg/day for 28 days). After the therapeutic intervention, these parasites were significantly less susceptible to antimony than pretreatment isolate, presenting a resistance index of 6-fold to Sb(III) for promastigotes and >3-fold to Sb(III) and 3-fold to Sb(V) for intracellular amastigotes. The susceptibility profile of this resistant L. infantum line is related to a decreased antimony uptake due to lower aquaglyceroporin-1 expression levels. Additionally, other mechanisms including an increase in thiols and overexpression of enzymes involved in thiol metabolism, such as ornithine decarboxylase, trypanothione reductase, mitochondrial tryparedoxin and mitochondrial tryparedoxin peroxidase, could contribute to the resistance as antimony detoxification mechanisms. A major contribution of this study in a canine L. infantum isolate is to find an antimony-resistant mechanism similar to that previously described in other human clinical isolates.

Indexed as

Drug ResistanceAnimalsAntimonyAntiprotozoal AgentsAquaglyceroporinsDog DiseasesDogsGene ExpressionLeishmania infantumLeishmaniasis, VisceralMeglumineMeglumine AntimoniateOrganometallic CompoundsParasitic Sensitivity TestsSulfhydryl CompoundsAntimonyAntiprotozoal AgentsAquaglyceroporinsMeglumineMeglumine AntimoniateOrganometallic CompoundsSulfhydryl CompoundsAntimony resistanceAntimony uptakeAquaglyceroporinCanine leishmaniasisLeishmaniaPeroxiredoxinsTherapeutic failureThiols

Identifiers

PMID27317865
PMCPMC4919363
OpenAlexW2418993425

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.