The Acidocalcisome Vacuolar Transporter Chaperone 4 Catalyzes the Synthesis of Polyphosphate in Insect‐stages of <i>Trypanosoma brucei</i> and <i>T. cruzi</i>

Paul N. Ulrich(University of Georgia), Noelia Lander(University of Georgia), Samarchith P. Kurup(University of Georgia), Laura Reiss(University of Georgia), Jessica V. Brewer(University of Georgia), Lia Carolina Soares Medeiros(Universidade Federal do Rio de Janeiro), Kildare Miranda(Universidade Federal do Rio de Janeiro), Roberto Docampo(University of Georgia)
Journal of Eukaryotic Microbiology
November 25, 2013
Cited by 45

Abstract

Polyphosphate is a polymer of inorganic phosphate found in both prokaryotes and eukaryotes. Polyphosphate typically accumulates in acidic, calcium-rich organelles known as acidocalcisomes, and recent research demonstrated that vacuolar transporter chaperone 4 catalyzes its synthesis in yeast. The human pathogens Trypanosoma brucei and T. cruzi possess vacuolar transporter chaperone 4 homologs. We demonstrate that T. cruzi vacuolar transporter chaperone 4 localizes to acidocalcisomes of epimastigotes by immunofluorescence and immuno-electron microscopy and that the recombinant catalytic region of the T. cruzi enzyme is a polyphosphate kinase. RNA interference of the T. brucei enzyme in procyclic form parasites reduced short chain polyphosphate levels and resulted in accumulation of pyrophosphate. These results suggest that this trypanosome enzyme is an important component of a polyphosphate synthase complex that utilizes ATP to synthesize and translocate polyphosphate to acidocalcisomes in insect stages of these parasites.


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