Your browser doesn't support javascript.
loading
Mostrar: 20 | 50 | 100
Resultados 1 - 2 de 2
Filtrar
Mais filtros










Base de dados
Intervalo de ano de publicação
1.
Virulence ; 10(1): 600-609, 2019 12.
Artigo em Inglês | MEDLINE | ID: mdl-31230520

RESUMO

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.


Assuntos
Modelos Animais de Doenças , Lepidópteros/microbiologia , Infecções Estreptocócicas/microbiologia , Streptococcus agalactiae/patogenicidade , Animais , Interações Hospedeiro-Patógeno , Humanos , Larva/microbiologia , Virulência , Fatores de Virulência
2.
Artigo em Inglês | MEDLINE | ID: mdl-19323031

RESUMO

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.


Assuntos
Apicomplexa/genética , Babesia/genética , Babesiose/veterinária , Doenças do Cão/diagnóstico , Ehrlichia canis/genética , Ehrlichiose/veterinária , Reação em Cadeia da Polimerase/veterinária , Animais , Apicomplexa/isolamento & purificação , Babesia/classificação , Babesia/isolamento & purificação , Babesiose/diagnóstico , Babesiose/genética , Babesiose/parasitologia , Sequência de Bases , Primers do DNA/genética , DNA de Protozoário/sangue , DNA de Protozoário/genética , Doenças do Cão/genética , Doenças do Cão/parasitologia , Cães , Ehrlichia canis/isolamento & purificação , Ehrlichiose/diagnóstico , Ehrlichiose/genética , Ehrlichiose/microbiologia , Genes Bacterianos , Dados de Sequência Molecular , Reação em Cadeia da Polimerase/métodos , Polimorfismo de Fragmento de Restrição , RNA Ribossômico 16S/genética , Sensibilidade e Especificidade , Análise de Sequência de DNA
SELEÇÃO DE REFERÊNCIAS
DETALHE DA PESQUISA
...