4.1 Article

Inorganic phosphate transporter in Giardia duodenalis and its possible role in ATP synthesis

Journal

MOLECULAR AND BIOCHEMICAL PARASITOLOGY
Volume 251, Issue -, Pages -

Publisher

ELSEVIER
DOI: 10.1016/j.molbiopara.2022.111504

Keywords

Giardia duodenalis; P-i uptake; P-i metabolism; Glycolytic pathway; Energetic metabolism; ATP synthesis

Funding

  1. Brazilian agency Conselho Nacional de Desenvolvimento Cientifico e Tecnologico (CNPq) [401134/2014-8]
  2. Brazilian agency Coordenacao de Aperfeicoamento de Pessoal de Nivel superior (CAPES) [0012017]
  3. Brazilian agency Fundacao Carlos Chagas Filho de Amparo a Pesquisa do Estado do Rio de Janeiro (FAPERJ) [e-26/201.300/2014]

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Giardia duodenalis, a protozoan parasite causing giardiasis, relies on environmental phosphate resources for survival. The Pi transporter in G. duodenalis is H+ dependent and demonstrates high affinity for Pi uptake, powered by an intracellular H+ gradient.
Giardia duodenalis is a flagellated protozoan that inhabits vertebrate host intestines, causing the disease known as giardiasis. Similar to other parasites, G. duodenalis must take advantage of environmental resources to survive, such as inorganic phosphate (Pi) availability. P-i is an anionic molecule and an essential nutrient for all organisms because it participates in the biosynthesis of biomolecules, energy storage, and cellular structure formation. The first step in P-i metabolism is its uptake through specific transporters on the plasma membrane. We identified a symporter H+:Pi-type ORF sequence in the G. duodenalis genome (GenBank ID: GL50803_5164), named GdPho84, which is homologous to Saccharomyces cerevisiae PHO84. In trophozoites, P-i transport was linear for up to 15 min, and the cell density was 3 x 10(7 )cells/ml. Physiological variations in pH (6.4-8.0) did not influence Pi uptake. This Pi transporter had a high affinity, with K-0.5 = 67.7 +/- 7.1 mu M Pi. SCH28080 (inhibitor of H+, K+- ATPase), bafilomycin A1 (inhibitor of vacuolar H+-ATPase), and FCCP (H+ ionophore) were able to inhibit Pi transport, indicating that an H(+ )gradient in the cell powered uphill P-i movement. PAA, an H+-dependent Pi transport inhibitor, reduced cell proliferation, P-i transport activity, and GdPHO48 mRNA levels. Pi starvation stimulated membrane potential-sensitive P-i uptake coupled to H+ fluxes, increased GdPho84 expression, and reduced intracellular ATP levels. These events indicate that these cells had an increased capacity to internalize P(i )as a compensatory mechanism compared to cells maintained in control medium conditions. Internalized Pi can be used in glycolytic metabolism once iodoacetamide (GAPDH inhibitor) inhibits P-i influx. Together, these results reinforce the hypothesis that P-i is a crucial nutrient for G. duodenalis energy metabolism.

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