A Toxoplasma gondii mutant highlights the importance of translational regulation in the apicoplast during animal infection

Mol Microbiol. 2011 Nov 7. doi: 10.1111/j.1365-2958.2011.07879.x. [Epub ahead of print]

A Toxoplasma gondii mutant highlights the importance of translational regulation in the apicoplast during animal infection.

Payne TM, Payne AJ, Knoll LJ.

SourceDepartment of Medical Microbiology and Immunology, University of Wisconsin-Madison, 1550 Linden Drive, Madison, WI 53706, USA.

Abstract
Toxoplasma gondii is an obligate intracellular parasite of all warm-blooded animals. We previously described a forward genetic screen to identify T. gondii mutants defective in the establishment of a chronic infection. One of the mutants isolated was disrupted in the 3' untranslated region (3'UTR) of an orthologue of bacterial translation elongation factor G (EFG). The mutant does not have a growth defect in tissue culture. Genetic complementation of this mutant with the genomic locus of TgEFG restores virulence in an acute infection mouse model. Epitope tagged TgEFG localized to the apicoplast, via a non-canonical targeting signal, where it functions as an elongation factor for translation in the apicoplast. Comparisons of TgEFG expression constructs with wild-type or mutant 3'UTRs showed that a wild-type 3'UTR is necessary for translation of TgEFG. In tissue culture, the TgEFG transcript is equally abundant in wild-type and mutant parasites; however, during an animal infection, the TgEFG transcript is increased more than threefold in the mutant. These results highlight that in tissue culture, translation in the apicoplast can be diminished, but during an animal infection, translation in the apicoplast must be fully functional.

© 2011 Blackwell Publishing Ltd.

PMID:22059956[PubMed - as supplied by publisher]