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1.
Int J Biol Macromol ; 167: 267-278, 2021 Jan 15.
Artículo en Inglés | MEDLINE | ID: mdl-33242552

RESUMEN

This study aims to examine whether two L-amino acid oxidases isolated from Bothrops snake venom (SV-LAAOs) were cytotoxic to Leishmania (Leishmania) amazonensis and Leishmania (Viannia) braziliensis, two causative agents of leishmaniasis, which is an endemic disease in tropical and subtropical countries. The SV-LAAOs BjussuLAAO-II and BmooLAAO-II were isolated from Bothrops jararacussu and Bothrops moojeni venom, respectively, through a three-step chromatography process that used molecular exclusion, hydrophobic interaction, and affinity columns. BmooLAAO-II is a new SV-LAAO isoform that we isolated in this study. The purified BjussuLAAO-II and BmooLAAO-II had high L-amino acid oxidase-specific activity: 3481.17 and 4924.77 U/mg/min, respectively. Both SV-LAAOs were strongly cytotoxic to the two Leishmania species, even at low concentrations. At the same concentration, BjussuLAAO-II and BmooLAAO-II exerted different cytotoxic effects on the parasites. We reported for the first time that the SV-LAAOs suppressed cell proliferation and altered the mitochondrial membrane potential of the two Leishmania species. Surprisingly, BjussuLAAO-II increased the intracellular reactive oxygen species production only in L. (L.) amazonensis, while BmooLAAO-II increased the intracellular reactive oxygen species production only in L. (V.) braziliensis, indicating that these SV-LAAOs had a certain specificity of action.


Asunto(s)
Antiprotozoarios/aislamiento & purificación , Antiprotozoarios/farmacología , Bothrops , Venenos de Crotálidos/enzimología , L-Aminoácido Oxidasa/aislamiento & purificación , L-Aminoácido Oxidasa/farmacología , Leishmania/efectos de los fármacos , Secuencia de Aminoácidos , Animales , Brasil , Cromatografía , Activación Enzimática , L-Aminoácido Oxidasa/química , Potencial de la Membrana Mitocondrial/efectos de los fármacos , Mitocondrias/efectos de los fármacos , Mitocondrias/genética , Mitocondrias/metabolismo , Pruebas de Sensibilidad Parasitaria , Especies Reactivas de Oxígeno/metabolismo
2.
Int J Biol Macromol ; 112: 333-342, 2018 Jun.
Artículo en Inglés | MEDLINE | ID: mdl-29391226

RESUMEN

Activities of phospholipases (PLAs) have been linked to pathogenesis in various microorganisms, and implicated in cell invasion and so the interest in these enzymes as potential targets that could contribute to the control of parasite survival and proliferation. Chicken eggs immunized with BnSP-7, a Lys49 phospholipase A2 (PLA2) homologue from Bothrops pauloensis snake venom, represent an excellent source of polyclonal antibodies with potential inhibitory activity on parasite PLAs. Herein, we report the production, characterization and anti-parasitic effect of IgY antibodies from egg yolks of hens immunized with BnSP-7. Produced antibodies presented increasing avidity and affinity for antigenic toxin epitopes throughout immunization, attaining a plateau after 4weeks. Pooled egg yolks-purified anti-BnSP-7 IgY antibodies were able to specifically recognize different PLA2s from Bothrops pauloensis and Bothrops jararacussu venom. Antibodies also neutralized BnSP-7 cytotoxic activity in C2C12 cells. Also, the antibodies recognized targets in Leishmania (Leishmania) amazonensis and Toxoplasma gondii extracts by ELISA and immunofluorescence assays. Anti-BnSP-7 IgY antibodies were cytotoxic to T. gondii tachyzoite and L. (L.) amazonensis promastigotes, and were able to decrease proliferation of both parasites treated before infection. These data suggest that the anti-BnSP-7 IgY is an important tool for discovering new parasite targets and blocking parasitic effects.


Asunto(s)
Anticuerpos Antiidiotipos/administración & dosificación , Inmunoglobulinas/administración & dosificación , Inhibidores de Fosfolipasa A2/administración & dosificación , Fosfolipasas A2/química , Secuencia de Aminoácidos , Animales , Anticuerpos Antiidiotipos/inmunología , Antiparasitarios/administración & dosificación , Antiparasitarios/inmunología , Bothrops/inmunología , Pollos , Venenos de Crotálidos/antagonistas & inhibidores , Venenos de Crotálidos/inmunología , Inmunoglobulinas/inmunología , Leishmania/efectos de los fármacos , Leishmania/patogenicidad , Inhibidores de Fosfolipasa A2/inmunología , Toxoplasma/efectos de los fármacos , Toxoplasma/patogenicidad
3.
Toxicon ; 119: 84-91, 2016 Sep 01.
Artículo en Inglés | MEDLINE | ID: mdl-27212627

RESUMEN

Toxoplasmosis affects a third of the global population and presents high incidence in tropical areas. Its great relevance in public health has led to a search for new therapeutic approaches. Herein, we report the antiparasitic effects of BnSP-7 toxin, a Lys49 phospholipase A2 (PLA2) homologue from Bothrops pauloensis snake venom, on Toxoplasma gondii. In an MTT assay, BnSP-7 presented significant cytotoxicity against host HeLa cells at higher doses (200 µg/mL to 50 µg/mL), whereas lower doses (25 µg/mL to 1.56 µg/mL) produced low cytotoxicity. Furthermore, the toxin showed no effect on T. gondii tachyzoite viability when evaluated by trypan blue exclusion, but decreased both adhesion and parasite proliferation when tachyzoites were treated before infection. We also measured cytokines in supernatants collected from HeLa cells infected with T. gondii tachyzoites previously treated with RPMI or BnSP-7, which revealed enhancement of only MIF and IL-6 cytokines levels in supernatants of HeLa cells after BnSP-7 treatment. Our results showed that the BnSP-7 PLA2 exerts an anti-Toxoplasma effect at a lower dose than that required to induce cytotoxicity in HeLa cells, and also modulates the immune response of host cells. In this sense, the anti-parasitic effect of BnSP-7 PLA2 demonstrated in the present study opens perspectives for use of this toxin as a tool for future studies on toxoplasmosis.


Asunto(s)
Venenos de Crotálidos/toxicidad , Lisina/química , Fosfolipasas A2/toxicidad , Toxoplasma/efectos de los fármacos , Secuencia de Aminoácidos , Cromatografía Líquida de Alta Presión , Venenos de Crotálidos/enzimología , Electroforesis en Gel de Poliacrilamida , Células HeLa , Humanos , Fosfolipasas A2/química , Homología de Secuencia de Aminoácido
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