Evidence map›Paper›PMID 22479507›Full record

ArticlePloS one2012

Leishmania amazonensis arginase compartmentalization in the glycosome is important for parasite infectivity.

Maria Fernanda Laranjeira da Silva, Ricardo Andrade Zampieri, Sandra M Muxel, Stephen M Beverley, Lucile M Floeter-Winter

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 47 papers.

0numbers the graph read from it
0cells of the map it votes in
47citing papers in PubMed
3.9field-weighted citation impact, top 6% 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

47 citing papers in PubMed, 99 citations in OpenAlex.

  1. Review
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  9. Polyamine Metabolism inMedical sciences (Basel, Switzerland) · 2022
    Review
  10. Article
  11. Review
  12. Metabolomic Reprogramming of C57BL/6-Macrophages during Early Infection withInternational journal of molecular sciences · 2021
    Article
  13. Article
  14. Review
  15. Review
  16. SystematicFrontiers in chemistry · 2021
    Article
  17. Article
  18. Review
  19. Article
  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

5 authors at 2 institutions in 2 countries.

Maria Fernanda Laranjeira da SilvaDepartamento de Fisiologia, Instituto de Biociências, Universidade de São Paulo, São Paulo, São Paulo, Brazil.
Ricardo Andrade Zampieri
Sandra M Muxel
Stephen M Beverley
Lucile M Floeter-Winter
Universidade de São Paulo · BRWashington University in St. Louis · US

Funding

MOLECULAR GENETICS OF LEISHMANIA USING DNA TRANSFECTIONR01AI029646 · NIAID · WASHINGTON UNIVERSITY · PI BEVERLEY, STEPHEN M · 1990 to 2015
$9.3M
MECHANISM OF GENE AMPLIFICATION IN LEISHMANIAR01AI021903 · NIAID · WASHINGTON UNIVERSITY · PI BEVERLEY, STEPHEN M · 1985 to 2010
$2.6M
DRUG RESISTANCE AND GENE AMPLIFICATION IN LEISHMANIAR37AI021903 · NIAID · WASHINGTON UNIVERSITY · PI BEVERLEY, STEPHEN M · 1993 to 2002
$960k
NIAID NIH HHS AI 21903NIAID NIH HHS AI 29646NIAID NIH HHS R01 AI021903NIAID NIH HHS R01 AI029646NIAID NIH HHS R37 AI021903
6 · The paper itself

Abstract

In Leishmania, de novo polyamine synthesis is initiated by the cleavage of L-arginine to urea and L-ornithine by the action of arginase (ARG, E.C. 3.5.3.1). Previous studies in L. major and L. mexicana showed that ARG is essential for in vitro growth in the absence of polyamines and needed for full infectivity in animal infections. The ARG protein is normally found within the parasite glycosome, and here we examined whether this localization is required for survival and infectivity. First, the localization of L. amazonensis ARG in the glycosome was confirmed in both the promastigote and amastigote stages. As in other species, arg(-) L. amazonensis required putrescine for growth and presented an attenuated infectivity. Restoration of a wild type ARG to the arg(-) mutant restored ARG expression, growth and infectivity. In contrast, restoration of a cytosol-targeted ARG lacking the glycosomal SKL targeting sequence (argΔSKL) restored growth but failed to restore infectivity. Further study showed that the ARGΔSKL protein was found in the cytosol as expected, but at very low levels. Our results indicate that the proper compartmentalization of L. amazonensis arginase in the glycosome is important for enzyme activity and optimal infectivity. Our conjecture is that parasite arginase participates in a complex equilibrium that defines the fate of L-arginine and that its proper subcellular location may be essential for this physiological orchestration.

Indexed as

Gene Expression RegulationAnimalsArginaseArginineCell LineCytosolLeishmaniaLeishmaniasisMacrophagesMiceMice, Inbred BALB CMicrobodiesMutationOpen Reading FramesArginaseArginine

Identifiers

PMID22479507
PMCPMC3316525
OpenAlexW2063862054

What OpenQuestion 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 OpenQuestion graph.