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PMID: 9528801 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Ca2+ content and expression of an acidocalcisomal calcium pump are elevated in intracellular forms of Trypanosoma cruzi.

Molecular and cellular biology ·Vol. 18 ·No. 4 ·1998-04-00 ·Pages 2309-23

Lu HG, Zhong L, de Souza W, Benchimol M, Moreno S, Docampo R

Abstract

The survival of a eukaryotic protozoan as an obligate parasite in the interior of a eukaryotic host cell implies its adaptation to an environment with a very different ionic composition from that of its extracellular habitat. This is particularly important in the case of Ca2+, the intracellular concentration of which is 3 orders of magnitude lower than the extracellular value. Ca2+ entry across the plasma membrane is a widely recognized mechanism for Ca2+ signaling, needed for a number of intracellular processes, and obviously, it would be restricted in the case of intracellular parasites. Here we show that Trypanosoma cruzi amastigotes possess a higher Ca2+ content than the extracellular stages of the parasite. This correlates with the higher expression of a calcium pump, the gene for which was cloned and sequenced. The deduced protein product (Tca1) of this gene has a calculated molecular mass of 121,141 Da and exhibits 34 to 38% identity with vacuolar Ca2+-ATPases of Saccharomyces cerevisiae and Dictyostelium discoideum, respectively. The tca1 gene suppresses the Ca2+ hypersensitivity of a mutant of S. cerevisiae that has a defect in vacuolar Ca2+ accumulation. Indirect immunofluorescence and immunoelectron microscopy analysis indicate that Tca1 colocalizes with the vacuolar H+-ATPase to the plasma membrane and to intracellular vacuoles of T. cruzi. These vacuoles were shown to have the same size and distribution as the calcium-containing vacuoles identified by the potassium pyroantimoniate-osmium technique and as the electron-dense vacuoles observed in whole unfixed parasites by transmission electron microscopy and identified in a previous work (D. A. Scott, R. Docampo, J. A. Dvorak, S. Shi, and R. D. Leapman, J. Biol. Chem. 272:28020-28029, 1997) as being acidic and possessing a high calcium content (i.e., acidocalcisomes). Together, these results suggest that acidocalcisomes are distinct from other previously recognized organelles present in these parasites and underscore the ability of intracellular parasites to adapt to the hostile environment of their hosts.

MeSH Terms
Amino Acid Sequence Animals Base Sequence Calcium/metabolism Calcium-Transporting ATPases/biosynthesis,genetics,metabolism Carrier Proteins/genetics,metabolism Cloning, Molecular DNA, Protozoan Fungal Proteins/genetics Gene Expression Genes, Protozoan Genetic Complementation Test Life Cycle Stages/genetics Membrane Proteins/genetics,metabolism Microscopy, Confocal Microscopy, Fluorescence Molecular Sequence Data Plasma Membrane Calcium-Transporting ATPases Protozoan Proteins/biosynthesis,genetics,metabolism Saccharomyces cerevisiae/enzymology,genetics Saccharomyces cerevisiae Proteins Trypanosoma cruzi/growth & development,metabolism,ultrastructure Vacuoles/enzymology,ultrastructure
Chemicals
Carrier Proteins DNA, Protozoan Fungal Proteins Membrane Proteins PMC1 protein, S cerevisiae Protozoan Proteins Saccharomyces cerevisiae Proteins Plasma Membrane Calcium-Transporting ATPases Calcium-Transporting ATPases Calcium
Authors & Affiliations
6 authors, click to expand affiliations / ORCID
Lu H G
Department of Pathobiology, University of Illinois at Urbana-Champaign, Urbana 61802, USA.
Zhong L
de Souza W
Benchimol M
Moreno S
Docampo R
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Article Info
Journal
Molecular and cellular biology
Abbr.
Mol Cell Biol
ISSN
0270-7306
Published
1998-04-00
Pages
2309-23
Language
English
Region
United States
NLM ID
8109087
PMCID
PMC121484
Subset
IM
Grants
NIAID NIH HHS · AI-23259 · United States
FIC NIH HHS · TW00476 · United States
Databases
GENBANK
U70620
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