Phosphorylation of Eukaryotic Initiation Factor-2α during Stress and Encystation in Entamoeba Species

dc.contributor.authorHendrick, Holland M.
dc.contributor.authorWelter, Brenda H.
dc.contributor.authorHapstack, Matthew A.
dc.contributor.authorSykes, Steven E.
dc.contributor.authorSullivan, William J., Jr.
dc.contributor.authorTemesvari, Lesly A.
dc.contributor.departmentPharmacology and Toxicology, School of Medicine
dc.date.accessioned2024-08-28T14:18:39Z
dc.date.available2024-08-28T14:18:39Z
dc.date.issued2016-12-08
dc.description.abstractEntamoeba histolytica is an enteric pathogen responsible for amoebic dysentery and liver abscess. It alternates between the host-restricted trophozoite form and the infective environmentally-stable cyst stage. Throughout its lifecycle E. histolytica experiences stress, in part, from host immune pressure. Conversion to cysts is presumed to be a stress-response. In other systems, stress induces phosphorylation of a serine residue on eukaryotic translation initiation factor-2α (eIF2α). This inhibits eIF2α activity resulting in a general decline in protein synthesis. Genomic data reveal that E. histolytica possesses eIF2α (EheIF2α) with a conserved phosphorylatable serine at position 59 (Ser59). Thus, this pathogen may have the machinery for stress-induced translational control. To test this, we exposed cells to different stress conditions and measured the level of total and phospho-EheIF2α. Long-term serum starvation, long-term heat shock, and oxidative stress induced an increase in the level of phospho-EheIF2α, while short-term serum starvation, short-term heat shock, or glucose deprivation did not. Long-term serum starvation also caused a decrease in polyribosome abundance, which is in accordance with the observation that this condition induces phosphorylation of EheIF2α. We generated transgenic cells that overexpress wildtype EheIF2α, a non-phosphorylatable variant of eIF2α in which Ser59 was mutated to alanine (EheIF2α-S59A), or a phosphomimetic variant of eIF2α in which Ser59 was mutated to aspartic acid (EheIF2α-S59D). Consistent with the known functions of eIF2α, cells expressing wildtype or EheIF2α-S59D exhibited increased or decreased translation, respectively. Surprisingly, cells expressing EheIF2α-S59A also exhibited reduced translation. Cells expressing EheIF2α-S59D were more resistant to long-term serum starvation underscoring the significance of EheIF2α phosphorylation in managing stress. Finally, phospho-eIF2α accumulated during encystation in E. invadens, a model encystation system. Together, these data demonstrate that the eIF2α-dependent stress response system is operational in Entamoeba species.
dc.eprint.versionFinal published version
dc.identifier.citationHendrick HM, Welter BH, Hapstack MA, Sykes SE, Sullivan WJ Jr, Temesvari LA. Phosphorylation of Eukaryotic Initiation Factor-2α during Stress and Encystation in Entamoeba Species. PLoS Pathog. 2016;12(12):e1006085. Published 2016 Dec 8. doi:10.1371/journal.ppat.1006085
dc.identifier.urihttps://hdl.handle.net/1805/43005
dc.language.isoen_US
dc.publisherPublic Library of Science
dc.relation.isversionof10.1371/journal.ppat.1006085
dc.relation.journalPLoS Pathogens
dc.rightsAttribution 4.0 Internationalen
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.sourcePMC
dc.subjectEntamoeba
dc.subjectEukaryotic initiation factor-2
dc.subjectParasite encystment
dc.subjectPhosphorylation
dc.titlePhosphorylation of Eukaryotic Initiation Factor-2α during Stress and Encystation in Entamoeba Species
dc.typeArticle
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