Phosphorylation of Eukaryotic Initiation Factor-2α during Stress and Encystation in Entamoeba Species
dc.contributor.author | Hendrick, Holland M. | |
dc.contributor.author | Welter, Brenda H. | |
dc.contributor.author | Hapstack, Matthew A. | |
dc.contributor.author | Sykes, Steven E. | |
dc.contributor.author | Sullivan, William J., Jr. | |
dc.contributor.author | Temesvari, Lesly A. | |
dc.contributor.department | Pharmacology and Toxicology, School of Medicine | |
dc.date.accessioned | 2024-08-28T14:18:39Z | |
dc.date.available | 2024-08-28T14:18:39Z | |
dc.date.issued | 2016-12-08 | |
dc.description.abstract | Entamoeba 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.version | Final published version | |
dc.identifier.citation | Hendrick 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.uri | https://hdl.handle.net/1805/43005 | |
dc.language.iso | en_US | |
dc.publisher | Public Library of Science | |
dc.relation.isversionof | 10.1371/journal.ppat.1006085 | |
dc.relation.journal | PLoS Pathogens | |
dc.rights | Attribution 4.0 International | en |
dc.rights.uri | http://creativecommons.org/licenses/by/4.0/ | |
dc.source | PMC | |
dc.subject | Entamoeba | |
dc.subject | Eukaryotic initiation factor-2 | |
dc.subject | Parasite encystment | |
dc.subject | Phosphorylation | |
dc.title | Phosphorylation of Eukaryotic Initiation Factor-2α during Stress and Encystation in Entamoeba Species | |
dc.type | Article |