Abstract
Entamoeba histolytica
, the protozoan responsible for human amoebiasis, presents the multidrug resistant phenotype due to the expression of the
E. histolytica
P-glycoproteins EhPgp1 and EhPgp5.
Here, we studied the protein EhPgp5 encoded by the
EhPgp5
gene in emetine-sensitive trophozoites transfected with the
pEhNEOPgp5
plasmid carrying the
EhPgp5
gene. The transfected trophozoites
increased their drug resistance slightly, but became bigger and globular. To investigate other EhPgp5 functions further, we microinjected the
EhPgp5
mRNA in
Xenopus laevis
oocytes. Microinjected
oocytes expressed EhPgp5 protein in their membranes and exhibited an ion current not present in the control oocytes. The antisense
EhPgp5AS
transcript, co-injected with the
EhPgp5
mRNA, abolished
the exogenous current, showing its specificity. Exogenous current was outward during depolarizing pulses. Reduction of the extracellular Cl
-
concentration displayed a reversible decrease of the
current amplitude. Niflumic acid, 4,4-diisothiocyanatostilbene-2, 2′-disulfonic acid, and other Cl
-
channel blockers abolished the exogenous current, which was poorly modified by verapamil
and changes in osmolarity of the medium. Our results suggest that the EhPgp5 protein could function as a Cl
-
current inductor and as a coadjuvant factor to avoid drug accumulation in the cell.