Literature DB >> 10589986

Substrate depletion upregulates uptake of myo-inositol, glucose and adenosine in Leishmania.

A Seyfang1, S M Landfear.   

Abstract

Leishmania flagellates undergo a digenetic life cycle in the gut of the sandfly insect vector and in macrophage phagolysosomes of the mammalian host. This involves vast changes of the environment to which the parasite has to adapt, including temperature, pH and concentration of nutrients between different types of meals of the insect vector or within the enclosed intracellular environment of the phagolysosome. The regulation of transporters for important organic substrates in Leishmania donovani, Leishmania mexicana and Leishmania enriettii has been investigated. A pronounced upregulation of inositol (25-fold), adenosine (11-fold) or glucose (5-fold) uptake activities was found when cells were depleted of the respective substrates during culture. Inositol-depleted cells showed a half-maximal uptake rate at nanomolar inositol concentration. Depletion of inositol only affected inositol uptake but did not affect uptake of glucose analog or proline in control experiments, indicating the specificity of the mechanism(s) underlying transport regulation. Adenosine-depleted cells showed an approximately 10-fold increase in both adenosine and uridine uptake, both mediated by the L. donovani nucleoside transporter 1 (LdNT1), but no change in guanosine uptake, which is mediated by the L. donovani nucleoside transporter 2 (LdNT2). These results suggest that extracellular adenosine concentration specifically regulates LdNT1 transport activity and does not affect LdNT2. The data imply that upregulation of transport activities by substrate depletion is a general phenomenon in protozoan flagellates, which is in remarkable contrast to bacteria where upregulation typically follows an increase of extracellular organic substrate. Hence, the parasites can maximize the uptake of important nutrients from the host even under limiting conditions, whereas bacteria often have dormant stages (spores) to overcome unfavorable environmental conditions or are heterotrophic for organic substrates.

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Year:  1999        PMID: 10589986     DOI: 10.1016/s0166-6851(99)00138-3

Source DB:  PubMed          Journal:  Mol Biochem Parasitol        ISSN: 0166-6851            Impact factor:   1.759


  9 in total

1.  Adaptive responses to purine starvation in Leishmania donovani.

Authors:  Nicola S Carter; Phillip A Yates; Sarah K Gessford; Sean R Galagan; Scott M Landfear; Buddy Ullman
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Review 2.  Nucleoside and nucleobase transporters in parasitic protozoa.

Authors:  Scott M Landfear; Buddy Ullman; Nicola S Carter; Marco A Sanchez
Journal:  Eukaryot Cell       Date:  2004-04

3.  Lysosomal degradation of Leishmania hexose and inositol transporters is regulated in a stage-, nutrient- and ubiquitin-dependent manner.

Authors:  James E Vince; Dedreia Tull; Scott Landfear; Malcolm J McConville
Journal:  Int J Parasitol       Date:  2011-04-09       Impact factor: 3.981

4.  A high-affinity putrescine-cadaverine transporter from Trypanosoma cruzi.

Authors:  Marie-Pierre Hasne; Isabelle Coppens; Radika Soysa; Buddy Ullman
Journal:  Mol Microbiol       Date:  2010-02-10       Impact factor: 3.501

5.  Purine restriction induces pronounced translational upregulation of the NT1 adenosine/pyrimidine nucleoside transporter in Leishmania major.

Authors:  Diana Ortiz; Raquel Valdés; Marco A Sanchez; Johanna Hayenga; Carolyn Elya; Siegfried Detke; Scott M Landfear
Journal:  Mol Microbiol       Date:  2010-08-02       Impact factor: 3.501

Review 6.  Lipid synthesis in protozoan parasites: a comparison between kinetoplastids and apicomplexans.

Authors:  Srinivasan Ramakrishnan; Mauro Serricchio; Boris Striepen; Peter Bütikofer
Journal:  Prog Lipid Res       Date:  2013-07-01       Impact factor: 16.195

7.  Glucose transporters in parasitic protozoa.

Authors:  Scott M Landfear
Journal:  Methods Mol Biol       Date:  2010

8.  Regulation and biological function of a flagellar glucose transporter in Leishmania mexicana: a potential glucose sensor.

Authors:  Dayana Rodriguez-Contreras; Hamide Aslan; Xiuhong Feng; Khoa Tran; Phillip A Yates; Shaden Kamhawi; Scott M Landfear
Journal:  FASEB J       Date:  2014-10-09       Impact factor: 5.191

9.  Tamoxifen inhibits the biosynthesis of inositolphosphorylceramide in Leishmania.

Authors:  Cristiana T Trinconi; Danilo C Miguel; Ariel M Silber; Christopher Brown; John G M Mina; Paul W Denny; Norton Heise; Silvia R B Uliana
Journal:  Int J Parasitol Drugs Drug Resist       Date:  2018-10-24       Impact factor: 4.077

  9 in total

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