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1.
Exp Parasitol ; 210: 107842, 2020 Mar.
Artículo en Inglés | MEDLINE | ID: mdl-31978393

RESUMEN

Free-living amoebae of the genus Acanthamoeba have been associated with keratitis and encephalitis. Some factors related to their pathogenic potential have been described, including the release of hydrolytic enzymes, and the adhesion and phagocytosis processes. However, other factors such as their effect over the hemodynamics and microcirculation elements have not been fully investigated. This work determines the in vitro activity of potentially pathogenic environmental isolates of Acanthamoeba genotype T4 and T5 over erythrocytes and platelets. The hemolytic activity (dependent and independent of contact), as well as the production of ADP of ten environmental isolates of Acanthamoeba obtained from dental units, combined emergency showers, dust, and hospital water, were measured. Tests were carried out over erythrocytes in suspension and blood agar plates, incubated at 4 °C, room temperature and 37 °C. Erythrophagocytosis and platelet aggregation assays were also performed. Live trophozoites of all of the isolates tested showed a hemolytic activity that was temperature-dependent. Over erythrocytes in suspension, variable hemolysis percentages were obtained: a maximum of 41% and a minimum of 15%. Regarding hemolysis over agar plates, two patterns of hemolysis were observed: double and simple halos. Conditioned medium and crude extracts of trophozoites did not show hemolytic activity. Erythrophagocytosis by Acanthamoeba was also observed; however, no production of ADP was determined by the employed methodology.


Asunto(s)
Acanthamoeba/fisiología , Plaquetas/parasitología , Ambiente , Eritrocitos/parasitología , Acanthamoeba/clasificación , Acanthamoeba/genética , Acanthamoeba/patogenicidad , Adenosina Difosfato/metabolismo , Enfermedades Transmisibles Emergentes/parasitología , Medios de Cultivo Condicionados , Eritrocitos/fisiología , Genotipo , Hemólisis , Humanos , Fagocitosis , Agregación Plaquetaria , Temperatura , Trofozoítos/clasificación , Trofozoítos/genética , Trofozoítos/patogenicidad , Trofozoítos/fisiología
2.
Colloids Surf B Biointerfaces ; 173: 725-732, 2019 Jan 01.
Artículo en Inglés | MEDLINE | ID: mdl-30384269

RESUMEN

Acanthamoeba keratitis is an ophthalmic disease with no specific treatment that specially affects contact lens users. The silencing of serine phosphatase (SP) and glycogen phosphorylase (GP) proteins produced by Acanthamoeba has been shown to significantly reduce the cytopathic effect, although no vehicle was proposed yet to deliver the siRNA sequences to the trophozoites. In this study, PEGylated cationic liposomes were proposed and optimized using Box-Behnken design. The influence of DOTAP:DOPE ratio, DSPE-PEG concentration, and siRNA/DOTAP charge ratio were evaluated over both biological response and physicochemical properties of liposomes. The ratio of DOTAP:DOPE had an effect in the trophozoite activity whereas the charge ratio influenced both size and protease activity. The predicted values were very close to the observed values, yielding a formulation with good activity and toxicity profile, which was used in the following experiments. A murine model of ocular keratitis was treated with siGP + siSP-loaded liposomes, as well as their respective controls, and combined treatment of liposomes and chlorhexidine. After 15 days of eight daily administrations, the liposomal complex combined with chlorhexidine was the only treatment able to reverse the more severe lesions associated with keratitis. There was 60% complete regression in corneal damage, with histological sections demonstrating the presence of an integral epithelium, without lymphocytic infiltrate. The set of results demonstrate the efficacy of a combined therapy based on siRNA with classical drugs for a better prognosis of keratitis caused by Acanthamoeba.


Asunto(s)
Queratitis por Acanthamoeba/terapia , Acanthamoeba/efectos de los fármacos , Clorhexidina/farmacología , Sistemas de Liberación de Medicamentos/métodos , Liposomas/química , Proteínas Protozoarias/antagonistas & inhibidores , Trofozoítos/efectos de los fármacos , Acanthamoeba/enzimología , Acanthamoeba/patogenicidad , Queratitis por Acanthamoeba/parasitología , Queratitis por Acanthamoeba/patología , Animales , Córnea/efectos de los fármacos , Córnea/parasitología , Córnea/patología , Modelos Animales de Enfermedad , Esquema de Medicación , Composición de Medicamentos/métodos , Quimioterapia Combinada , Análisis Factorial , Ácidos Grasos Monoinsaturados/química , Regulación de la Expresión Génica , Glucógeno Fosforilasa/antagonistas & inhibidores , Glucógeno Fosforilasa/genética , Glucógeno Fosforilasa/metabolismo , Humanos , Liposomas/metabolismo , Fosfatidiletanolaminas/química , Monoéster Fosfórico Hidrolasas/antagonistas & inhibidores , Monoéster Fosfórico Hidrolasas/genética , Monoéster Fosfórico Hidrolasas/metabolismo , Polietilenglicoles/química , Proteínas Protozoarias/genética , Proteínas Protozoarias/metabolismo , Compuestos de Amonio Cuaternario/química , ARN Interferente Pequeño/genética , ARN Interferente Pequeño/metabolismo , Ratas , Ratas Wistar , Trofozoítos/enzimología , Trofozoítos/patogenicidad
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