INHIBITION OF Na,K-ATPASE ACTIVITY REDUCES BABESIA GIBSONI INFECTION OF CANINE ERYTHROCYTES WITH INHERITED HIGH K, LOW Na CONCENTRATIONS

Babesia gibsoni multiplies well in canine red blood cells (RBCs) containing high concentrations of potassium (HK), reduced glutathione, and free amino acids as a result of an inherited high Na,K-ATPase activity, i.e., HK RBCs. To determine the role of Na,K-ATPase in the multiplication of B. gibsoni, the effect of ouabain on the proliferation of the parasites in HK RBCs was investigated. To determine the direct effect of ouabain on the parasites, the proliferation of the parasites in normal canine RBCs containing low potassium (LK) and high sodium concentrations, i.e., LK RBCs, which completely lack Na,K-ATPase activity, was observed. Ouabain at 0.1 mM significantly suppressed the multiplication of B. gibsoni in HK RBCs in vitro, whereas it had no effect on the parasites in LK RBCs. The results suggest that the multiplication of B. gibsoni in HK RBCs depends mainly on the presence of Na,K-ATPase in the cells. Therefore, the effects of ouabain on the intracellular cation and free amino acid composition of the HK RBCs were examined. In HK RBCs incubated with ouabain, a marked decrease in the concentration of potassium and an increase in sodium were observed, together with a decrease in the number of parasitized cells. These results suggest that the intracellular cation composition maintained by Na,K-ATPase might be advantageous to the parasites. Moreover, the concentrations of some free amino acids, i.e., asparagine, aspartate, glutamate, glutamine, glycine, and histidine, were markedly decreased in HK RBCs incubated with ouabain. Decreased concentrations of the free amino acids induced by inhibition of Na,K-ATPase seemed to affect the multiplication of B. gibsoni in HK RBCs. Based on these results, it is clear that the high Na,K-ATPase activity in HK RBCs contributes to the proliferation of B. gibsoni by maintaining high potassium and low sodium concentrations, as well as high concentrations of some free amino acids in the cells.

[1]  T. Murase,et al.  Direct evidence for preferential multiplication ofBabesia gibsoni in young erythrocytes , 2004, Parasitology Research.

[2]  H. Ginsburg,et al.  Effects of red blood cell potassium and hypertonicity on the growth ofPlasmodium falciparum in culture , 2004, Zeitschrift für Parasitenkunde.

[3]  M. A. Hossain,et al.  BABESIA GIBSONI–SPECIFIC ISOENZYMES RELATED TO ENERGY METABOLISM OF THE PARASITE IN INFECTED ERYTHROCYTES , 2003, The Journal of parasitology.

[4]  S. Krishna,et al.  Expression and Functional Characterization of a Plasmodium falciparum Ca2+-ATPase (PfATP4) Belonging to a Subclass Unique to Apicomplexan Organisms* , 2001, The Journal of Biological Chemistry.

[5]  Y. Maede,et al.  Use of canine red blood cell with high concentrations of potassium, reduced glutathione, and free amino acid as host cells for in vitro cultivation of Babesia gibsoni. , 2000, American journal of veterinary research.

[6]  Y. Maede,et al.  The cause of the predilection of Babesia gibsoni for reticulocytes. , 2000, The Journal of veterinary medical science.

[7]  R. Mikkelsen,et al.  Membrane potential of erythrocytic stages of Plasmodium chabaudi free of the host cell membrane. , 1986, Molecular and biochemical parasitology.

[8]  M. Inaba,et al.  (Na,K)-ATPase and Ouabain binding in reticulocytes from dogs with high K and low K erythrocytes and their changes during maturation. , 1985, The Journal of biological chemistry.

[9]  M. Inaba,et al.  Increase of Na+ gradient-dependent L-glutamate and L-aspartate transport in high K+ dog erythrocytes associated with high activity of (Na+, K+)-ATPase. , 1984, The Journal of biological chemistry.

[10]  N. Taniguchi,et al.  Increase of Na-K-ATPase activity, glutamate, and aspartate uptake in dog erythrocytes associated with hereditary high accumulation of GSH, glutamate, glutamine, and aspartate , 1983 .

[11]  N. Taniguchi,et al.  Increase of Na-K-ATPase activity, glutamate, and aspartate uptake in dog erythrocytes associated with hereditary high accumulation of GSH, glutamate, glutamine, and aspartate. , 1983, Blood.

[12]  K. Yagi,et al.  Assay for lipid peroxides in animal tissues by thiobarbituric acid reaction. , 1979, Analytical biochemistry.

[13]  C. Winterbourn,et al.  Protection by Ascorbate against Acetylphenylhydrazine‐Induced Heinz Body Formation in Glucose‐6‐Phosphate Dehydrogenase Deficient Erythrocytes , 1979, British journal of haematology.

[14]  Coulter Db,et al.  Sodium and potassium concentrations of erythrocytes from perinatal, immature, and adult dogs. , 1973 .

[15]  W. Trager,et al.  Malaria parasites (Plasmodium lophurae) developing extracellularly in vitro: incorporation of labeled precursors. , 1971, The Journal of protozoology.

[16]  H. Shuval,et al.  A sensitive micromethod for the determination of methemoglobin in blood. , 1970, Clinica chimica acta; international journal of clinical chemistry.

[17]  W. Trager,et al.  The nutrition of an intracellular parasite ( avian malaria ) , 2017 .