Phosphorylation of eukaryotic initiation factor-2α promotes the extracellular survival of obligate intracellular parasite Toxoplasma gondii

被引:64
作者
Joyce, Bradley R. [1 ,2 ]
Queener, Sherry F. [2 ]
Wek, Ronald C. [1 ]
Sullivan, William J., Jr. [2 ]
机构
[1] Indiana Univ, Sch Med, Dept Biochem & Mol Biol, Indianapolis, IN 46202 USA
[2] Indiana Univ, Sch Med, Dept Pharmacol & Toxicol, Indianapolis, IN 46202 USA
关键词
Apicomplexa; toxoplasmosis; stress; translation control; elF2; UNFOLDED PROTEIN RESPONSE; TRANSLATIONAL CONTROL; MAMMALIAN-CELLS; PLASMODIUM-FALCIPARUM; TRANSCRIPTION FACTORS; STRESS; KINASE; MECHANISMS; RESISTANCE; INVASION;
D O I
10.1073/pnas.1007610107
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
While seeking a new host cell, obligate intracellular parasites, such as the protozoan Toxoplasma gondii, must be able to endure the stress of an extracellular environment. The mechanisms Toxoplasma use to remain viable while deprived of a host cell are not understood. We have previously shown that phosphorylation of Toxoplasma eukaryotic initiation factor-2 alpha (TgIF2 alpha) is a conserved response to stress. Here we report the characterization of Toxoplasma harboring a point mutation (S71A) in TgIF2 alpha that prevents phosphorylation. Results show that TgIF2 alpha phosphorylation is critical for parasite viability because the TgIF2 alpha-S71A mutants are ill-equipped to cope with life outside the host cell. The TgIF2 alpha-S71A mutants also showed a significant delay in producing acute toxoplasmosis in vivo. We conclude that the phosphorylation of TgIF2 alpha plays a crucial role during the lytic cycle by ameliorating the stress of the extracellular environment while the parasite searches for a new host cell.
引用
收藏
页码:17200 / 17205
页数:6
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