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

被引:65
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
相关论文
共 28 条
[1]   Lytic cycle of Toxoplasma gondii [J].
Black, MW ;
Boothroyd, JC .
MICROBIOLOGY AND MOLECULAR BIOLOGY REVIEWS, 2000, 64 (03) :607-+
[2]   Ionophore-resistant mutants of Toxoplasma gondii reveal host cell permeabilization as an early event in egress [J].
Black, MW ;
Arrizabalaga, G ;
Boothroyd, JC .
MOLECULAR AND CELLULAR BIOLOGY, 2000, 20 (24) :9399-9408
[3]   Identification of STAT4-dependent and independent mechanisms of resistance to Toxoplasma gondii [J].
Cai, GF ;
Radzanowski, T ;
Villegas, EN ;
Kastelein, R ;
Hunter, CA .
JOURNAL OF IMMUNOLOGY, 2000, 165 (05) :2619-2627
[4]   Specific DNA-binding by Apicomplexan AP2 transcription factors [J].
De Silva, Erandi K. ;
Gehrke, Andrew R. ;
Olszewski, Kellen ;
Leon, Ilsa ;
Chahal, Jasdave S. ;
Bulyk, Martha L. ;
Llinas, Manuel .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2008, 105 (24) :8393-8398
[5]   PHOSPHORYLATION OF INITIATION FACTOR-2-ALPHA BY PROTEIN-KINASE GCN2 MEDIATES GENE-SPECIFIC TRANSLATIONAL CONTROL OF GCN4 IN YEAST [J].
DEVER, TE ;
FENG, L ;
WEK, RC ;
CIGAN, AM ;
DONAHUE, TF ;
HINNEBUSCH, AG .
CELL, 1992, 68 (03) :585-596
[6]   Toxoplasma invasion of mammalian cells is powered by the actin cytoskeleton of the parasite [J].
Dobrowolski, JM ;
Sibley, LD .
CELL, 1996, 84 (06) :933-939
[7]   PfeIK1, a eukaryotic initiation factor 2α kinase of the human malaria parasite Plasmodium falciparum, regulates stress-response to amino-acid starvation [J].
Fennell, Clare ;
Babbitt, Shalon ;
Russo, Ilaria ;
Wilkes, Jonathan ;
Ranford-Cartwright, Lisa ;
Goldberg, Daniel E. ;
Doerig, Christian .
MALARIA JOURNAL, 2009, 8
[8]   IN-VITRO ASSAYS ELUCIDATE PECULIAR KINETICS OF CLINDAMYCIN ACTION AGAINST TOXOPLASMA-GONDII [J].
FICHERA, ME ;
BHOPALE, MK ;
ROOS, DS .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1995, 39 (07) :1530-1537
[9]   Fitness effects of DHFR-TS mutations associated with pyrimethamine resistance in apicomplexan parasites [J].
Fohl, LM ;
Roos, DS .
MOLECULAR MICROBIOLOGY, 2003, 50 (04) :1319-1327
[10]   Efficient Gene Replacements in Toxoplasma gondii Strains Deficient for Nonhomologous End Joining [J].
Fox, Barbara A. ;
Ristuccia, Jessica G. ;
Gigley, Jason P. ;
Bzik, David J. .
EUKARYOTIC CELL, 2009, 8 (04) :520-529