Your browser doesn't support javascript.
loading
Mostrar: 20 | 50 | 100
Resultados 1 - 3 de 3
Filtrar
Más filtros

Bases de datos
Tipo del documento
Intervalo de año de publicación
1.
Infect Immun ; 85(12)2017 12.
Artículo en Inglés | MEDLINE | ID: mdl-28993457

RESUMEN

Small-colony variants (SCVs) of Staphylococcus aureus typically lack a functional electron transport chain and cannot produce virulence factors such as leukocidins, hemolysins, or the antioxidant staphyloxanthin. Despite this, SCVs are associated with persistent infections of the bloodstream, bones, and prosthetic devices. The survival of SCVs in the host has been ascribed to intracellular residency, biofilm formation, and resistance to antibiotics. However, the ability of SCVs to resist host defenses is largely uncharacterized. To address this, we measured the survival of wild-type and SCV S. aureus in whole human blood, which contains high numbers of neutrophils, the key defense against staphylococcal infection. Despite the loss of leukocidin production and staphyloxanthin biosynthesis, SCVs defective for heme or menaquinone biosynthesis were significantly more resistant to the oxidative burst than wild-type bacteria in human blood or the presence of purified neutrophils. Supplementation of the culture medium of the heme-auxotrophic SCV with heme, but not iron, restored growth, hemolysin and staphyloxanthin production, and sensitivity to the oxidative burst. Since Enterococcus faecalis is a natural heme auxotroph and cause of bloodstream infection, we explored whether restoration of the electron transport chain in this organism also affected survival in blood. Incubation of E. faecalis with heme increased growth and restored catalase activity but resulted in decreased survival in human blood via increased sensitivity to the oxidative burst. Therefore, the lack of functional electron transport chains in SCV S. aureus and wild-type E. faecalis results in reduced growth rate but provides resistance to a key immune defense mechanism.


Asunto(s)
Antibacterianos/metabolismo , Transporte de Electrón , Enterococcus faecalis/fisiología , Viabilidad Microbiana/efectos de los fármacos , Estallido Respiratorio , Staphylococcus aureus/fisiología , Superóxidos/metabolismo , Sangre/microbiología , Actividad Bactericida de la Sangre , Enterococcus faecalis/genética , Humanos , Neutrófilos/inmunología , Staphylococcus aureus/genética
2.
Viruses ; 9(7)2017 06 23.
Artículo en Inglés | MEDLINE | ID: mdl-28644404

RESUMEN

Dengue virus (DENV) is a mosquito-borne flavivirus that causes significant global human disease and mortality. One approach to develop treatments for DENV infection and the prevention of severe disease is through investigation of natural medicines. Inflammation plays both beneficial and harmful roles during DENV infection. Studies have proposed that the oxidative stress response may be one mechanism responsible for triggering inflammation during DENV infection. Thus, blocking the oxidative stress response could reduce inflammation and the development of severe disease. Garlic has been shown to both reduce inflammation and affect the oxidative stress response. Here, we show that the garlic active compounds diallyl disulfide (DADS), diallyl sulfide (DAS) and alliin reduced inflammation during DENV infection and show that this reduction is due to the effects on the oxidative stress response. These results suggest that garlic could be used as an alternative treatment for DENV infection and for the prevention of severe disease development.


Asunto(s)
Compuestos Alílicos/farmacología , Antiinflamatorios/farmacología , Antioxidantes/farmacología , Cisteína/análogos & derivados , Virus del Dengue/crecimiento & desarrollo , Disulfuros/farmacología , Ajo/química , Sulfuros/farmacología , Compuestos Alílicos/aislamiento & purificación , Antiinflamatorios/aislamiento & purificación , Antioxidantes/aislamiento & purificación , Línea Celular , Cisteína/aislamiento & purificación , Cisteína/farmacología , Disulfuros/aislamiento & purificación , Interacciones Huésped-Patógeno , Humanos , Estrés Oxidativo/efectos de los fármacos , Sulfuros/aislamiento & purificación
3.
Appl Environ Microbiol ; 78(16): 5646-52, 2012 Aug.
Artículo en Inglés | MEDLINE | ID: mdl-22660719

RESUMEN

Interest in using bacteriophages to treat bacterial infections (phage therapy) is growing, but there have been few experiments comparing the effects of different treatment strategies on both bacterial densities and resistance evolution. While it is established that multiphage therapy is typically more effective than the application of a single phage type, it is not clear if it is best to apply phages simultaneously or sequentially. We tried single- and multiphage therapy against Pseudomonas aeruginosa PAO1 in vitro, using different combinations of phages either simultaneously or sequentially. Across different phage combinations, simultaneous application was consistently equal or superior to sequential application in terms of reducing bacterial population density, and there was no difference (on average) in terms of minimizing resistance. Phage-resistant bacteria emerged in all experimental treatments and incurred significant fitness costs, expressed as reduced growth rate in the absence of phages. Finally, phage therapy increased the life span of wax moth larvae infected with P. aeruginosa, and a phage cocktail was the most effective short-term treatment. When the ratio of phages to bacteria was very high, phage cocktails cured otherwise lethal infections. These results suggest that while adding all available phages simultaneously tends to be the most successful short-term strategy, there are sequential strategies that are equally effective and potentially better over longer time scales.


Asunto(s)
Terapia Biológica/métodos , Infecciones por Pseudomonas/terapia , Fagos Pseudomonas/crecimiento & desarrollo , Pseudomonas aeruginosa/crecimiento & desarrollo , Pseudomonas aeruginosa/virología , Animales , Modelos Animales de Enfermedad , Larva/microbiología , Mariposas Nocturnas/microbiología , Análisis de Supervivencia
SELECCIÓN DE REFERENCIAS
DETALLE DE LA BÚSQUEDA