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1.
Mem. Inst. Oswaldo Cruz ; 113(9): e180162, 2018. graf
Article Dans Anglais | LILACS | ID: biblio-1040603

Résumé

Eukaryotic initiation factor 5A (eIF5A) is a conserved protein with an essential role in translation elongation. Using one and two-dimensional western blotting, we showed that the eIF5A protein level was 2-fold lower in benznidazole (BZ)-resistant (BZR and 17LER) Trypanosoma cruzi populations than in their respective susceptible counterparts (BZS and 17WTS). To confirm the role of eIF5A in BZ resistance, we transfected BZS and 17WTS with the wild-type eIF5A or mutant eIF5A-S2A (in which serine 2 was replaced by alanine). Upon overexpressing eIF5A, both susceptible lines became approximately 3- and 5-fold more sensitive to BZ. In contrast, the eIF5A-S2A mutant did not alter its susceptibility to BZ. These data suggest that BZ resistance might arise from either decreasing the translation of proteins that require eIF5A, or as a consequence of differential levels of precursors for the hypusination reactions (e.g., spermidine and trypanothione), both of which alter BZ's effects in the parasite.


Sujets)
Humains , Trypanocides/pharmacologie , Trypanosoma cruzi/effets des médicaments et des substances chimiques , Trypanosoma cruzi/enzymologie , Résistance aux substances/génétique , Facteurs initiation chaîne peptidique/métabolisme , Protéines de liaison à l'ARN/métabolisme , Nitroimidazoles/pharmacologie , Trypanosoma cruzi/génétique , Expression des gènes , Facteurs initiation chaîne peptidique/analyse , Facteurs initiation chaîne peptidique/effets des médicaments et des substances chimiques , Protéines de liaison à l'ARN/analyse , Protéines de liaison à l'ARN/effets des médicaments et des substances chimiques
2.
Mem. Inst. Oswaldo Cruz ; 106(7): 837-843, Nov. 2011. ilus, tab
Article Dans Anglais | LILACS | ID: lil-606647

Résumé

The development of a more sensitive diagnostic test for schistosomiasis is needed to overcome the limitations of the use of stool examination in low endemic areas. Using parasite antigens in enzyme linked immunosorbent assay is a promising strategy, however a more rational selection of parasite antigens is necessary. In this study we performed in silico analysis of the Schistosoma mansoni genome, using SchistoDB database and bioinformatic tools for screening immunogenic antigens. Based on evidence of expression in all parasite life stage within the definitive host, extracellular or plasmatic membrane localization, low similarity to human and other helminthic proteins and presence of predicted B cell epitopes, six candidates were selected: a glycosylphosphatidylinositol-anchored 200 kDa protein, two putative cytochrome oxidase subunits, two expressed proteins and one hypothetical protein. The recognition in unidimensional and bidimensional Western blot of protein with similar molecular weight and isoelectric point to the selected antigens by sera from S. mansoni infected mice indicate a good correlation between these two approaches in selecting immunogenic proteins.


Sujets)
Animaux , Humains , Souris , Antigènes d'helminthe , Schistosoma mansoni/immunologie , Schistosomiase à Schistosoma mansoni/diagnostic , Technique de Western , Test ELISA/méthodes , Sensibilité et spécificité , Schistosomiase à Schistosoma mansoni/immunologie
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