Evidence map›Paper›PMID 23980754›Full record

ArticleMolecular microbiology2013

Sphingosine kinase A is a pleiotropic and essential enzyme for Leishmania survival and virulence.

Ou Zhang, Fong-Fu Hsu, Wei Xu, Mattie Pawlowic, Kai Zhang

Open access · greenAbstract read
In one paragraph

Article in Molecular microbiology, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
1.0field-weighted citation impact, top 21% 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

6 citing papers in PubMed, 12 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Sphingolipid biosynthesis in man and microbes.Natural product reports · 2018
    Review
  5. Article
  6. 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 1 country.

Ou ZhangDepartment of Biological Sciences, Texas Tech University, Lubbock, TX, 79409, USA.
Fong-Fu Hsu
Wei Xu
Mattie Pawlowic
Kai Zhang
Texas Tech University · USWashington University in St. Louis · US

Funding

Washington University Nutrition Obesity Research CenterP30DK056341 · NIDDK · WASHINGTON UNIVERSITY · PI Dominic N Reeds · 1999 to 2026
$30.2M
YOGA LIFESTYLE INTERVENTION REDUCES BLOOD PRESSURE IN HIV-INFECTED ADULTSP41RR000954 · NCRR · WASHINGTON UNIVERSITY · PI TAYLOR, JOHN-STEPHEN ADOLFINO · 1985 to 2011
$16.0M
TrainingP41GM103422 · NIGMS · WASHINGTON UNIVERSITY · PI YARASHESKI, KEVIN E · 2012 to 2019
$12.0M
A Biomedical Mass Spectrometry Resource: Ongoing Driving Biomedical ProjectsR24GM136766 · NIGMS · WASHINGTON UNIVERSITY · PI GROSS, MICHAEL L · 2020 to 2022
$2.3M
Exploring an Essential and Dangerous Pathway in Leishmania ParasitesR01AI099380 · NIAID · TEXAS TECH UNIVERSITY · PI ZHANG, KAI · 2013 to 2017
$1.8M
Identification of a Parasite-Specific, Lipid-Metabolic Pathway Essential for LeisR56AI081781 · NIAID · TEXAS TECH UNIVERSITY · PI ZHANG, KAI · 2009 to 2009
$339k
NCRR NIH HHS P41 RR000954NIAID NIH HHS R01 AI099380NIAID NIH HHS R56 AI081781NIDDK NIH HHS P30 DK056341NIGMS NIH HHS P41 GM103422NIGMS NIH HHS R24 GM136766
6 · The paper itself

Abstract

Sphingosine kinase is a key enzyme in sphingolipid metabolism, catalysing the conversion of sphingosine or dihydrosphingosine into sphingosine-1-phosphate or dihydrosphingosine-1-phosphate respectively. In mammals, sphingosine-1-phosphate is a powerful signalling molecule regulating cell growth, differentiation, apoptosis and immunity. Functions of sphingosine kinase or sphingosine-1-phosphate in pathogenic protozoans are virtually unknown. While most organisms possess two closely related sphingosine kinases, only one sphingosine kinase homologue (SKa) can be identified in Leishmania, which are vector-borne protozoan parasites responsible for leishmaniasis. Leishmania SKa is a large, cytoplasmic enzyme capable of phosphorylating both sphingosine and dihydrosphingosine. Remarkably, deletion of SKa leads to catastrophic defects in both the insect stage and mammalian stage of Leishmania parasites. Genetic and biochemical analyses demonstrate that proper expression of SKa is essential for Leishmania parasites to remove toxic metabolites, to survive stressful conditions, and to cause disease in mice. Therefore, SKa is a pleiotropic enzyme with vital roles throughout the life cycle of Leishmania. The essentiality of SKa and its apparent divergence from mammalian counterparts suggests that this enzyme can be selectively targeted to reduce Leishmania infection.

Indexed as

AnimalsAntifungal AgentsDNA, ProtozoanDNA ReplicationEthanolamineFatty Acids, MonounsaturatedGenes, ProtozoanLeishmaniaLeishmaniasisLysophospholipidsMiceMice, Inbred BALB CPhosphotransferases (Alcohol Group Acceptor)SphingosineSphingosine KinaseVirulenceAntifungal AgentsDNA, ProtozoanEthanolamineFatty Acids, MonounsaturatedLysophospholipidsPhosphotransferases (Alcohol Group Acceptor)Sphingosinesphingosine 1-phosphateSphingosine Kinasethermozymocidin

Identifiers

PMID23980754
PMCPMC3938578
OpenAlexW1946325796

What OpenQuestion holds

Textmetadata
LicenceTDM
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.