| Literature DB >> 27457282 |
Érica S Martins-Duarte1, Maira Carias2, Rossiane Vommaro2, Namita Surolia3, Wanderley de Souza1.
Abstract
The apicomplexan protozoan Toxoplasma gondii, the causative agent of toxoplasmosis, harbors an apicoplast, a plastid-like organelle with essential metabolic functions. Although the FASII fatty acid biosynthesis pathway located in the apicoplast is essential for parasite survival, the cellular effects of FASII disruption in T. gondii had not been examined in detail. Here, we combined light and electron microscopy techniques - including focused ion beam scanning electron microscopy (FIB-SEM) - to characterize the effect of FASII disruption in T. gondii, by treatment with the FASII inhibitor triclosan or by inducible knockdown of the FASII component acyl carrier protein. Morphological analyses showed that FASII disruption prevented cytokinesis completion in T. gondii tachyzoites, leading to the formation of large masses of 'tethered' daughter cells. FIB-SEM showed that tethered daughters had a mature basal complex, but a defect in new membrane addition between daughters resulted in incomplete pellicle formation. Addition of exogenous fatty acids to medium suppressed the formation of tethered daughter cells and supports the notion that FASII is essential to generate lipid substrates required for the final step of parasite division.Entities:
Keywords: Apicomplexa; Bradyzoite; Cell division; Cleavage furrow; Triclosan
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Year: 2016 PMID: 27457282 DOI: 10.1242/jcs.185223
Source DB: PubMed Journal: J Cell Sci ISSN: 0021-9533 Impact factor: 5.285