Evidence map›Paper›PMID 25714343›Full record

ArticlePLoS neglected tropical diseases2015

Species-specific antimonial sensitivity in Leishmania is driven by post-transcriptional regulation of AQP1.

Goutam Mandal, Srotoswati Mandal, Mansi Sharma, Karen Santos Charret, Barbara Papadopoulou, Hiranmoy Bhattacharjee, Rita Mukhopadhyay

Open access · goldAbstract read
In one paragraph

Article in PLoS neglected tropical diseases, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
5.3field-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

25 citing papers in PubMed, 45 citations in OpenAlex.

  1. Trial
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  10. New Vistas in the Biology of the Flagellum-Pathogens (Basel, Switzerland) · 2022
    Review
  11. Review
  12. Review
  13. Advances in UnderstandingFrontiers in cell and developmental biology · 2021
    Review
  14. Article
  15. Computational and structural biotechnology journal · 2020
    Review
  16. Article
  17. Article
  18. Article
  19. Article
  20. Gene Expression inmBio · 2017
    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

7 authors at 2 institutions in 2 countries.

Goutam MandalDepartment of Cellular Biology and Pharmacology, Florida International University, Herbert Wertheim College of Medicine, Florida, United States of America.
Srotoswati MandalDepartment of Cellular Biology and Pharmacology, Florida International University, Herbert Wertheim College of Medicine, Florida, United States of America.
Mansi SharmaDepartment of Cellular Biology and Pharmacology, Florida International University, Herbert Wertheim College of Medicine, Florida, United States of America.
Karen Santos CharretCHU de Quebec Research Center and Department of Microbiology-Infectious Disease and Immunology, University Laval, Quebec, Canada.
Barbara PapadopoulouCHU de Quebec Research Center and Department of Microbiology-Infectious Disease and Immunology, University Laval, Quebec, Canada.
Hiranmoy BhattacharjeeDepartment of Cellular Biology and Pharmacology, Florida International University, Herbert Wertheim College of Medicine, Florida, United States of America.
Rita MukhopadhyayDepartment of Cellular Biology and Pharmacology, Florida International University, Herbert Wertheim College of Medicine, Florida, United States of America.
Florida International University · USUniversité Laval · CA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Leishmania is a digenetic protozoan parasite causing leishmaniasis in humans. The different clinical forms of leishmaniasis are caused by more than twenty species of Leishmania that are transmitted by nearly thirty species of phlebotomine sand flies. Pentavalent antimonials (such as Pentostam or Glucantime) are the first line drugs for treating leishmaniasis. Recent studies suggest that pentavalent antimony (Sb(V)) acts as a pro-drug, which is converted to the more active trivalent form (Sb(III)). However, sensitivity to trivalent antimony varies among different Leishmania species. In general, Leishmania species causing cutaneous leishmaniasis (CL) are more sensitive to Sb(III) than the species responsible for visceral leishmaniasis (VL). Leishmania aquaglyceroporin (AQP1) facilitates the adventitious passage of antimonite down a concentration gradient. In this study, we show that Leishmania species causing CL accumulate more antimonite, and therefore exhibit higher sensitivity to antimonials, than the species responsible for VL. This species-specific differential sensitivity to antimonite is directly proportional to the expression levels of AQP1 mRNA. We show that the stability of AQP1 mRNA in different Leishmania species is regulated by their respective 3'-untranslated regions. The differential regulation of AQP1 mRNA explains the distinct antimonial sensitivity of each species.

Indexed as

3' Untranslated RegionsAntimonyAntimony Sodium GluconateAntiprotozoal AgentsAquaglyceroporinsAquaporin 1Cell MovementDrug ResistanceGene Expression RegulationHumansLeishmaniaLeishmaniasis, CutaneousLeishmaniasis, VisceralMeglumineMeglumine AntimoniateOrganometallic Compounds3' Untranslated RegionsantimoniteAntimonyAntimony Sodium GluconateAntiprotozoal AgentsAquaglyceroporinsAquaporin 1MeglumineMeglumine AntimoniateOrganometallic CompoundsRNA, MessengerRNA, Protozoan

Identifiers

PMID25714343
PMCPMC4340957
OpenAlexW1987222318

What Socratic holds

Textmetadata
LicenceCC BY
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 Socratic graph.