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Presence of a plant-like proton-translocating pyrophosphatase in a scuticociliate parasite and its role as a possible drug target

Published online by Cambridge University Press:  14 August 2014

NATALIA MALLO ,
JESÚS LAMAS ,
CARLA PIAZZON  and
JOSÉ M. LEIRO
NATALIA MALLO
Affiliation:
Department of Microbiology and Parasitology, Laboratory of Parasitology, Institute of Research and Food Analysis, University of Santiago de Compostela, c/Constantino Candeira s/n, 15782, Santiago de Compostela, La Coruña, Spain
JESÚS LAMAS
Affiliation:
Department of Cell Biology and Ecology, Faculty of Biology, University of Santiago de Compostela, La Coruña, Spain
CARLA PIAZZON
Affiliation:
Department of Cell Biology and Ecology, Faculty of Biology, University of Santiago de Compostela, La Coruña, Spain
JOSÉ M. LEIRO*
Affiliation:
Department of Microbiology and Parasitology, Laboratory of Parasitology, Institute of Research and Food Analysis, University of Santiago de Compostela, c/Constantino Candeira s/n, 15782, Santiago de Compostela, La Coruña, Spain
*
* Corresponding author: Laboratorio de Parasitología, Instituto de Investigación y Análisis Alimentarios, c/Constantino Candeira s/n, 15782, Santiago de Compostela, La Coruña, Spain. E-mail: [email protected]
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Summary

The proton-translocating inorganic pyrophosphatases (H+-PPases) are primary electrogenic H+ pumps that derive energy from the hydrolysis of inorganic pyrophosphate (PPi). They are widely distributed among most land plants and have also been found in several species of protozoan parasites. Here we describe, for the first time, the molecular cloning and functional characterization of a gene encoding an H+-pyrophosphatase in the protozoan scuticociliate parasite Philasterides dicentrarchi, which infects turbot. The predicted P. dicentrarchi PPase (PdPPase) consists of 587 amino acids of molecular mass 61·7 kDa and an isoelectric point of 5·0. Several motifs characteristic of plant vacuolar H+-PPases (V–H+-PPases) were also found in the PdPPase, which contains all the sequence motifs of the prototypical type I V–H+-PPase from Arabidopsis thaliana vacuolar pyrophosphatase type I (AVP1) plant. The PdPPase has a characteristic residue that determines strict K+-dependence, but unlike AVP1, PdPPase contains an N-terminal signal peptide (SP) sequence. Antibodies generated by vaccination of mice with a genetic or recombinant protein containing a partial sequence of the PdPPase and a common motif with the polyclonal antibody PABHK specific to AVP1 recognized a single band of about 62 kDa in western blots. These antibodies specifically stained both vacuole and the alveolar membranes of trophozoites of P. dicentrarchi. H+ transport was partially inhibited by the bisphosphonate pamidronate (PAM) and completely inhibited by NaF. The bisphosphonate PAM inhibited both H+-translocation and gene expression. PdPPase and PAM also inhibited in vitro growth of the ciliates. The apparent lack of V–H+-PPases in vertebrates and the parasite sensitivity to PPI analogues may provide a molecular target for developing new drugs to control scuticociliatosis.

Keywords

Philasterides dicentrarchiscuticociliatesinorganic pyrophosphataseproton pumpbisphosphonates
Type
Research Article
Information
Parasitology , Volume 142 , Issue 3 , March 2015 , pp. 449 - 462
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Copyright
Copyright © Cambridge University Press 2014 

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