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1.
J Biol Chem ; 288(21): 15256-67, 2013 May 24.
Article in English | MEDLINE | ID: mdl-23525104

ABSTRACT

Polyamine biosynthesis is a key drug target in African trypanosomes. The "resurrection drug" eflornithine (difluoromethylornithine), which is used clinically to treat human African trypanosomiasis, inhibits the first step in polyamine (spermidine) biosynthesis, a highly regulated pathway in most eukaryotic cells. Previously, we showed that activity of a key trypanosomatid spermidine biosynthetic enzyme, S-adenosylmethionine decarboxylase, is regulated by heterodimer formation with a catalytically dead paralog (a prozyme). Here, we describe an expansion of this prozyme paradigm to the enzyme deoxyhypusine synthase, which is required for spermidine-dependent hypusine modification of a lysine residue in the essential translation factor eIF5A. Trypanosoma brucei encodes two deoxyhypusine synthase paralogs, one that is catalytically functional but grossly impaired, and the other is inactive. Co-expression in Escherichia coli results in heterotetramer formation with a 3000-fold increase in enzyme activity. This functional complex is also present in T. brucei, and conditional knock-out studies indicate that both DHS genes are essential for in vitro growth and infectivity in mice. The recurrent evolution of paralogous, catalytically dead enzyme-based activating mechanisms may be a consequence of the unusual gene expression in the parasites, which lack transcriptional regulation. Our results suggest that this mechanism may be more widely used by trypanosomatids to control enzyme activity and ultimately influence pathogenesis than currently appreciated.


Subject(s)
Lysine/analogs & derivatives , Oxidoreductases Acting on CH-NH Group Donors/metabolism , Protozoan Proteins/metabolism , Spermidine/metabolism , Trypanosoma brucei brucei/enzymology , Animals , Cattle , Escherichia coli , Gene Knockdown Techniques , Humans , Lysine/chemistry , Lysine/genetics , Lysine/metabolism , Mice , Oxidoreductases Acting on CH-NH Group Donors/chemistry , Oxidoreductases Acting on CH-NH Group Donors/genetics , Protozoan Proteins/chemistry , Protozoan Proteins/genetics , Recombinant Proteins/chemistry , Recombinant Proteins/genetics , Recombinant Proteins/metabolism , Spermidine/chemistry , Trypanosoma brucei brucei/genetics , Trypanosoma brucei brucei/pathogenicity , Trypanosomiasis, Bovine/enzymology , Trypanosomiasis, Bovine/genetics
2.
Infect Immun ; 67(6): 2797-803, 1999 Jun.
Article in English | MEDLINE | ID: mdl-10338483

ABSTRACT

Clearance of trypanosomes from the blood of infected Cape buffalo was associated with the development of two responses: (i) complement-dependent and clone-specific lytic activity and (ii) complement-independent trypanocidal activity that was not restricted by trypanosome clone or species. This latter activity was mediated by H2O2 and required the presence of xanthine oxidase in serum but not the addition of purine substrates. Expression of the xanthine oxidase-dependent trypanocidal activity in Cape buffalo serum was coincident with, and required, a decline in its H2O2 catabolic activity. The H2O2 catabolic activity of Cape buffalo serum was due solely to catalase and declined by eightfold around the time that trypanosomes were cleared from the blood, accompanied by a fivefold drop in erythrocyte-associated catalase activity. The Cape buffalo did not develop subsequent parasitemic waves. Clearance of parasitemia in similarly infected cattle was also associated with development of trypanosome clone-specific lytic activity, but not with the acquisition of H2O2-dependent trypanocidal activity in serum, and the cattle supported recurring parasitemia. The lack of trypanocidal activity in pre- and postinfection cattle sera was due to their low content of xanthine oxidase and sustained catalase activity. These data strongly suggest that an infection-induced serum oxidative response, the efficacy of which is amplified by a decline in blood catalase, contributes to suppression of recurring parasitemia in Cape buffalo.


Subject(s)
Catalase/immunology , Trypanocidal Agents/immunology , Trypanosoma brucei brucei/immunology , Trypanosoma congolense/immunology , Trypanosomiasis, African/immunology , Trypanosomiasis, Bovine/immunology , Animals , Antibodies, Protozoan/immunology , Buffaloes , Catalase/metabolism , Cattle , Hydrogen Peroxide/metabolism , Rabbits , Trypanosomiasis, African/enzymology , Trypanosomiasis, Bovine/enzymology
3.
Exp Parasitol ; 64(3): 401-9, 1987 Dec.
Article in English | MEDLINE | ID: mdl-3678446

ABSTRACT

Trypanosoma brucei brucei are lysed when incubated in vitro in a mixture of bovine serum and polyamine. Normal bovine serum alone or polyamine alone does not show any trypanocidal activity. The bovine serum in the mixture can be replaced by purified polyamine oxidase, and addition of polyamine oxidase inhibitors blocks trypanolysis. Using this in vitro lysis test, it is shown that West African cattle which are resistant naturally to trypanosomiasis have a higher trypanolytic activity in their serum than do trypanosensitive cattle (P less than 10(-5]. Seric trypanolytic activity of individual animals remains stable when tested over a period of 18 months; moreover, it is not modified by trypanosome infection. Higher levels of seric polyamine oxidase in resistant cattle were demonstrated also by enzymatic analysis. The factors responsible for trypanolysis have been analyzed. Oxidation of spermidine by polyamine oxidase leads to the production of unstable aldehydes, acrolein, ammonia, O2-, HO, and H2O2. Acrolein and H2O2 show strong trypanolytic activity while the other products do not appear to be toxic for trypanosomes. The physiological importance of polyamine oxidase mediated trypanolysis is unclear; even at peak parasitemia in cattle (10(7) organisms/ml) it can be calculated that trypanosomes would not release enough spermidine for the generation of sufficient quantities of toxic degradation products. Additional polyamines could be released in serum from tissues damaged as a result of the infection.


Subject(s)
Oxidoreductases Acting on CH-NH Group Donors/metabolism , Trypanosomiasis, Bovine/immunology , Acrolein/pharmacology , Ammonia/pharmacology , Animals , Cattle/immunology , Cattle/parasitology , Hydrogen Peroxide/pharmacology , Immunity, Innate , Polyamines/pharmacology , Trypanosoma brucei brucei/drug effects , Trypanosomiasis, African/veterinary , Trypanosomiasis, Bovine/enzymology , Polyamine Oxidase
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