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1.
Virulence ; 10(1): 600-609, 2019 12.
Artículo en Inglés | MEDLINE | ID: mdl-31230520

RESUMEN

Streptococcus agalactiae, or group B Streptococcus (GBS), infects diverse hosts including humans and economically important species such as cattle and fishes. In the context of human health, GBS is a major cause of neonatal infections and an emerging cause of invasive disease in adults and of foodborne disease in Southeast Asia. Here we show that GBS is able to establish a systemic infection in Galleria mellonella larvae that is associated with extensive bacterial replication and dose-dependent larval survival. This infection model is suitable for use with GBS isolates from both homeothermic and poikilothermic hosts. Hypervirulent sequence types (ST) associated with invasive human disease in neonates (ST17) or adults (ST283) show increased virulence in this model, indicating it may be useful in studying GBS virulence determinants, albeit with limitations for some host-specific virulence factors. In addition, we demonstrate that larval survival can be afforded by antibiotic treatment and so the model may also be useful in the development of novel anti-GBS strategies. The use of G. mellonella in GBS research has the potential to provide a low-cost infection model that could reduce the number of vertebrates used in the study of GBS infection.


Asunto(s)
Modelos Animales de Enfermedad , Lepidópteros/microbiología , Infecciones Estreptocócicas/microbiología , Streptococcus agalactiae/patogenicidad , Animales , Interacciones Huésped-Patógeno , Humanos , Larva/microbiología , Virulencia , Factores de Virulencia
2.
Artículo en Inglés | MEDLINE | ID: mdl-19323031

RESUMEN

A multiplex polymerase chain reaction (PCR) has been developed for simultaneous detection of canine blood parasites, Ehrlichia canis, Babesia spp and Hepatozoon canis, from blood samples in a single reaction. The multiplex PCR primers were specific to E. canis VirB9, Babesia spp 16S rRNA and H. canis 16S rRNA genes. Specificity of the amplicons was confirmed by DNA sequencing. The assay was evaluated using normal canine and infected blood samples, which were detected by microscopic examination. This multiplex PCR offers scope for simultaneous detection of three important canine blood parasites and should be valuable in monitoring parasite infections in dogs and ticks.


Asunto(s)
Apicomplexa/genética , Babesia/genética , Babesiosis/veterinaria , Enfermedades de los Perros/diagnóstico , Ehrlichia canis/genética , Ehrlichiosis/veterinaria , Reacción en Cadena de la Polimerasa/veterinaria , Animales , Apicomplexa/aislamiento & purificación , Babesia/clasificación , Babesia/aislamiento & purificación , Babesiosis/diagnóstico , Babesiosis/genética , Babesiosis/parasitología , Secuencia de Bases , Cartilla de ADN/genética , ADN Protozoario/sangre , ADN Protozoario/genética , Enfermedades de los Perros/genética , Enfermedades de los Perros/parasitología , Perros , Ehrlichia canis/aislamiento & purificación , Ehrlichiosis/diagnóstico , Ehrlichiosis/genética , Ehrlichiosis/microbiología , Genes Bacterianos , Datos de Secuencia Molecular , Reacción en Cadena de la Polimerasa/métodos , Polimorfismo de Longitud del Fragmento de Restricción , ARN Ribosómico 16S/genética , Sensibilidad y Especificidad , Análisis de Secuencia de ADN
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