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Glucose starvation boosts Entamoeba histolytica virulence

Authors :
Nancy Guillén
Ayala Tovy
Serge Ankri
Rama Siman-Tov
Daniela M. Faust
Sylvie Syan
Rivka Hertz
Department of Molecular Microbiology
The Bruce Rappaport Faculty of Medicine
Biologie Cellulaire du Parasitisme
Institut Pasteur [Paris] (IP)-Institut National de la Santé et de la Recherche Médicale (INSERM)
This study was supported by grants to SA from the Israel Science Foundation, the Israel Ministry of Health, the Rappaport Family Institute for Research in the Medical Sciences, and the Deutsche Forschungsgemeinschaft (DFG) and from the French National Research Agency grant (Intestinalamibe) to NG.
Autard, Delphine
Institut Pasteur [Paris]-Institut National de la Santé et de la Recherche Médicale (INSERM)
Source :
PLoS Neglected Tropical Diseases, PLoS Neglected Tropical Diseases, 2011, 5 (8), pp.e1247. ⟨10.1371/journal.pntd.0001247⟩, PLoS Neglected Tropical Diseases, Vol 5, Iss 8, p e1247 (2011), PLoS Neglected Tropical Diseases, Public Library of Science, 2011, 5 (8), pp.e1247. ⟨10.1371/journal.pntd.0001247⟩
Publication Year :
2011
Publisher :
HAL CCSD, 2011.

Abstract

International audience; 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.

Details

Language :
English
ISSN :
19352727 and 19352735
Database :
OpenAIRE
Journal :
PLoS Neglected Tropical Diseases, PLoS Neglected Tropical Diseases, 2011, 5 (8), pp.e1247. ⟨10.1371/journal.pntd.0001247⟩, PLoS Neglected Tropical Diseases, Vol 5, Iss 8, p e1247 (2011), PLoS Neglected Tropical Diseases, Public Library of Science, 2011, 5 (8), pp.e1247. ⟨10.1371/journal.pntd.0001247⟩
Accession number :
edsair.doi.dedup.....2e1584d919411054cd9b2011e4c282be
Full Text :
https://doi.org/10.1371/journal.pntd.0001247⟩