Dissecting apicoplast functions through continuous cultivation of Toxoplasma gondii devoid of the organelle

The apicoplast, a relic plastid organelle derived from secondary endosymbiosis, is crucial for many medically relevant Apicomplexa. While it no longer performs photosynthesis, the organelle retains several essential metabolic pathways. In this study, we examine the four primary metabolic pathways in the Toxoplasma gondii apicoplast, along with an accessory pathway, and identify conditions that can bypass these. Contrary to the prevailing view that the apicoplast is indispensable for T. gondii, we demonstrate that bypassing all pathways renders the apicoplast non-essential. We further show that T. gondii lacking an apicoplast (T. gondii<sup>-Apico</sup>) can be maintained indefinitely in culture, establishing a unique model to study the functions of this organelle. Through comprehensive metabolomic, transcriptomic, and proteomic analyses of T. gondii<sup>-Apico</sup> we uncover significant adaptation mechanisms following loss of the organelle and identify numerous putative apicoplast proteins revealed by their decreased abundance in T. gondii<sup>-Apico</sup>. Moreover, T. gondii<sup>-Apico</sup> parasites exhibit reduced sensitivity to apicoplast targeting compounds, providing a valuable tool for discovering new drugs acting on the organelle. The capability to culture T. gondii without its plastid offers new avenues for exploring apicoplast biology and developing novel therapeutic strategies against apicomplexan parasites.

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Publication Details

Journal
Nature Communications
Published
2025-03-01
DOI
https://doi.org/10.1038/s41467-025-57302-x
Citations
5
Primary Topic
Toxoplasma gondii Research Studies
Type
article
Field-Weighted Citation Impact
10.24

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article

Dissecting apicoplast functions through continuous cultivation of Toxoplasma gondii devoid of the organelle

Dominique Soldati‐Favre, Bohumil Maco, Min Chen, Joachim Kloehn et al.
5 citations
Nature Communications
Toxoplasma gondii Research Studies
10.24
article

Dissecting apicoplast functions through continuous cultivation of Toxoplasma gondii devoid of the organelle

Dominique Soldati‐Favre, Bohumil Maco, Min Chen, Joachim Kloehn, Hong‐Juan Peng, Alessandro Bonavoglia, Olivier Rohr, Szilamér Gyula Koszti
article en
5 citations

Abstract

The apicoplast, a relic plastid organelle derived from secondary endosymbiosis, is crucial for many medically relevant Apicomplexa. While it no longer performs photosynthesis, the organelle retains several essential metabolic pathways. In this study, we examine the four primary metabolic pathways in the Toxoplasma gondii apicoplast, along with an accessory pathway, and identify conditions that can bypass these. Contrary to the prevailing view that the apicoplast is indispensable for T. gondii, we demonstrate that bypassing all pathways renders the apicoplast non-essential. We further show that T. gondii lacking an apicoplast (T. gondii<sup>-Apico</sup>) can be maintained indefinitely in culture, establishing a unique model to study the functions of this organelle. Through comprehensive metabolomic, transcriptomic, and proteomic analyses of T. gondii<sup>-Apico</sup> we uncover significant adaptation mechanisms following loss of the organelle and identify numerous putative apicoplast proteins revealed by their decreased abundance in T. gondii<sup>-Apico</sup>. Moreover, T. gondii<sup>-Apico</sup> parasites exhibit reduced sensitivity to apicoplast targeting compounds, providing a valuable tool for discovering new drugs acting on the organelle. The capability to culture T. gondii without its plastid offers new avenues for exploring apicoplast biology and developing novel therapeutic strategies against apicomplexan parasites.

Nature CommunicationsVol. 16(1)
University of Geneva (CH), Southern Medical University (CN)
Schweizerischer Nationalfonds zur Förderung der Wissenschaftlichen Forschung, Novartis Stiftung für Medizinisch-Biologische Forschung, Gertrude von Meissner-Stiftung
Openalex Percentile: Top 2%
Toxoplasma gondii Research Studies
10.24
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