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Glucose Starvation Boosts Entamoeba histolytica Virulence

The unicellular parasite, Entamoeba histolytica, is exposed to numerous adverse conditions, such as nutrient deprivation, during its life cycle stages in the human host. In the present study, we examined whether the parasite virulence could be influenced by glucose starvation (GS). The migratory beh...

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Autores principales: Tovy, Ayala, Hertz, Rivka, Siman-Tov, Rama, Syan, Sylvie, Faust, Daniela, Guillen, Nancy, Ankri, Serge
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3149018/
https://www.ncbi.nlm.nih.gov/pubmed/21829737
http://dx.doi.org/10.1371/journal.pntd.0001247
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author Tovy, Ayala
Hertz, Rivka
Siman-Tov, Rama
Syan, Sylvie
Faust, Daniela
Guillen, Nancy
Ankri, Serge
author_facet Tovy, Ayala
Hertz, Rivka
Siman-Tov, Rama
Syan, Sylvie
Faust, Daniela
Guillen, Nancy
Ankri, Serge
author_sort Tovy, Ayala
collection PubMed
description The unicellular parasite, Entamoeba histolytica, is exposed to numerous adverse conditions, such as nutrient deprivation, during its life cycle stages in the human host. In the present study, we examined whether the parasite virulence could be influenced by glucose starvation (GS). The migratory behaviour of the parasite and its capability to kill mammalian cells and to lyse erythrocytes is strongly enhanced following GS. In order to gain insights into the mechanism underlying the GS boosting effects on virulence, we analyzed differences in protein expression levels in control and glucose-starved trophozoites, by quantitative proteomic analysis. We observed that upstream regulatory element 3-binding protein (URE3-BP), a transcription factor that modulates E.histolytica virulence, and the lysine-rich protein 1 (KRiP1) which is induced during liver abscess development, are upregulated by GS. We also analyzed E. histolytica membrane fractions and noticed that the Gal/GalNAc lectin light subunit LgL1 is up-regulated by GS. Surprisingly, amoebapore A (Ap-A) and cysteine proteinase A5 (CP-A5), two important E. histolytica virulence factors, were strongly down-regulated by GS. While the boosting effect of GS on E. histolytica virulence was conserved in strains silenced for Ap-A and CP-A5, it was lost in LgL1 and in KRiP1 down-regulated strains. These data emphasize the unexpected role of GS in the modulation of E.histolytica virulence and the involvement of KRiP1 and Lgl1 in this phenomenon.
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spelling pubmed-31490182011-08-09 Glucose Starvation Boosts Entamoeba histolytica Virulence Tovy, Ayala Hertz, Rivka Siman-Tov, Rama Syan, Sylvie Faust, Daniela Guillen, Nancy Ankri, Serge PLoS Negl Trop Dis Research Article The unicellular parasite, Entamoeba histolytica, is exposed to numerous adverse conditions, such as nutrient deprivation, during its life cycle stages in the human host. In the present study, we examined whether the parasite virulence could be influenced by glucose starvation (GS). The migratory behaviour of the parasite and its capability to kill mammalian cells and to lyse erythrocytes is strongly enhanced following GS. In order to gain insights into the mechanism underlying the GS boosting effects on virulence, we analyzed differences in protein expression levels in control and glucose-starved trophozoites, by quantitative proteomic analysis. We observed that upstream regulatory element 3-binding protein (URE3-BP), a transcription factor that modulates E.histolytica virulence, and the lysine-rich protein 1 (KRiP1) which is induced during liver abscess development, are upregulated by GS. We also analyzed E. histolytica membrane fractions and noticed that the Gal/GalNAc lectin light subunit LgL1 is up-regulated by GS. Surprisingly, amoebapore A (Ap-A) and cysteine proteinase A5 (CP-A5), two important E. histolytica virulence factors, were strongly down-regulated by GS. While the boosting effect of GS on E. histolytica virulence was conserved in strains silenced for Ap-A and CP-A5, it was lost in LgL1 and in KRiP1 down-regulated strains. These data emphasize the unexpected role of GS in the modulation of E.histolytica virulence and the involvement of KRiP1 and Lgl1 in this phenomenon. Public Library of Science 2011-08-02 /pmc/articles/PMC3149018/ /pubmed/21829737 http://dx.doi.org/10.1371/journal.pntd.0001247 Text en Tovy et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Tovy, Ayala
Hertz, Rivka
Siman-Tov, Rama
Syan, Sylvie
Faust, Daniela
Guillen, Nancy
Ankri, Serge
Glucose Starvation Boosts Entamoeba histolytica Virulence
title Glucose Starvation Boosts Entamoeba histolytica Virulence
title_full Glucose Starvation Boosts Entamoeba histolytica Virulence
title_fullStr Glucose Starvation Boosts Entamoeba histolytica Virulence
title_full_unstemmed Glucose Starvation Boosts Entamoeba histolytica Virulence
title_short Glucose Starvation Boosts Entamoeba histolytica Virulence
title_sort glucose starvation boosts entamoeba histolytica virulence
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3149018/
https://www.ncbi.nlm.nih.gov/pubmed/21829737
http://dx.doi.org/10.1371/journal.pntd.0001247
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