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. 2023 Jul 27;19(7):e1011522.
doi: 10.1371/journal.ppat.1011522. eCollection 2023 Jul.

How much (ATP) does it cost to build a trypanosome? A theoretical study on the quantity of ATP needed to maintain and duplicate a bloodstream-form Trypanosoma brucei cell

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How much (ATP) does it cost to build a trypanosome? A theoretical study on the quantity of ATP needed to maintain and duplicate a bloodstream-form Trypanosoma brucei cell

Janaina F Nascimento et al. PLoS Pathog. .

Erratum in

Abstract

ATP hydrolysis is required for the synthesis, transport and polymerization of monomers for macromolecules as well as for the assembly of the latter into cellular structures. Other cellular processes not directly related to synthesis of biomass, such as maintenance of membrane potential and cellular shape, also require ATP. The unicellular flagellated parasite Trypanosoma brucei has a complex digenetic life cycle. The primary energy source for this parasite in its bloodstream form (BSF) is glucose, which is abundant in the host's bloodstream. Here, we made a detailed estimation of the energy budget during the BSF cell cycle. As glycolysis is the source of most produced ATP, we calculated that a single parasite produces 6.0 x 1011 molecules of ATP/cell cycle. Total biomass production (which involves biomass maintenance and duplication) accounts for ~63% of the total energy budget, while the total biomass duplication accounts for the remaining ~37% of the ATP consumption, with in both cases translation being the most expensive process. These values allowed us to estimate a theoretical YATP of 10.1 (g biomass)/mole ATP and a theoretical [Formula: see text] of 28.6 (g biomass)/mole ATP. Flagellar motility, variant surface glycoprotein recycling, transport and maintenance of transmembrane potential account for less than 30% of the consumed ATP. Finally, there is still ~5.5% available in the budget that is being used for other cellular processes of as yet unknown cost. These data put a new perspective on the assumptions about the relative energetic weight of the processes a BSF trypanosome undergoes during its cell cycle.

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Conflict of interest statement

The authors have declared that no competing interests exist.

Figures

Fig 1
Fig 1. Summary of the most energetically costly biological processes in bloodstream form T. brucei. For underlying values see text and S5 Table.

References

    1. Flamholz A, Phillips R, Milo R. The quantified cell. Mol Biol Cell. 2014;25: 3497–3500. doi: 10.1091/mbc.E14-09-1347 - DOI - PMC - PubMed
    1. Gadelha C, Holden JM, Allison HC, Field MC. Specializations in a successful parasite: What makes the bloodstream-form African trypanosome so deadly? Mol Biochem Parasitol. 2011;179: 51–58. doi: 10.1016/j.molbiopara.2011.06.006 - DOI - PubMed
    1. Lamour N, Riviere L, Coustou V, Coombs GH, Barrett MP, Bringaud FF. Proline metabolism in procyclic Trypanosoma brucei is down-regulated in the presence of glucose. Journal of Biological Chemistry. 2005;280: 11902–11910. doi: 10.1074/jbc.M414274200 - DOI - PubMed
    1. Mantilla BS, Marchese L, Casas-Sánchez A, Dyer NA, Ejeh N, Biran M, et al.. Proline metabolism is essential for Trypanosoma brucei brucei survival in the tsetse vector. PLoS Pathog. 2017;13: 1–29. doi: 10.1371/journal.ppat.1006158 - DOI - PMC - PubMed
    1. Rojas F, Silvester E, Young J, Milne R, Tettey M, Houston DR, et al.. Oligopeptide signaling through TbGPR89 drives trypanosome quorum sensing. Cell. 2019;176: 306–317.e16. doi: 10.1016/j.cell.2018.10.041 - DOI - PMC - PubMed

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