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1.
J Thromb Haemost ; 13(2): 271-82, 2015 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-25393316

RESUMO

BACKGROUND: To further understand the role of platelets in the pathogenesis of viral infections we explored platelet interaction with Coxsackieviruses B (CVB) 1 and 3. CVB is a group of viruses that cause the majority of human enterovirus-related viral myocarditis; their receptor (CAR) is expressed on the platelet surface and there is a well-characterized CVB3-induced myocarditis murine model. METHODS: Human platelets were infected with CVB1 and 3 and viruses were detected in pellets and in supernatants. C57BL/6J mice with or without platelet depletion were inoculated with CVB3 and peripheral blood and heart samples collected at different times post-infection. RESULTS: CVB1 and 3 RNA and a capsid protein were detected in infected platelets. Despite the fact that titration assays in Vero cells showed increasing infectivity titers over time, supernatants and pellets from infected platelets showed similar levels, suggesting that platelets were not susceptible to a replicative infectivity cycle. CVB binding was CAR-independent and resulted in P-selectin and phosphatidylserine (PS) exposure. CVB3-infected mice showed a rapid thrombocytopenia that correlated with an increase in platelet PS exposure and platelet-leukocyte aggregates without modification of platelet P-selectin expression or von Willebrand factor levels. Mortality, viremia, heart viral titers and myocarditis were significantly higher in platelet-depleted than normal animals. Type I IFN levels were not changed but IgG levels were lower in infected and platelet-depleted mice. CONCLUSIONS: Our data reveal that platelets play a critical role in host survival and immune response against CVB3 infection.


Assuntos
Plaquetas/virologia , Infecções por Coxsackievirus/sangue , Infecções por Coxsackievirus/virologia , Enterovirus Humano B/patogenicidade , Miocardite/sangue , Miocardite/virologia , Animais , Plaquetas/imunologia , Plaquetas/metabolismo , Proteínas do Capsídeo/sangue , Proteínas do Capsídeo/genética , Chlorocebus aethiops , Infecções por Coxsackievirus/imunologia , Modelos Animais de Doenças , Enterovirus Humano B/genética , Enterovirus Humano B/imunologia , Enterovirus Humano B/metabolismo , Feminino , Interações Hospedeiro-Patógeno , Humanos , Imunoglobulina G/sangue , Masculino , Camundongos Endogâmicos C57BL , Miocardite/imunologia , Selectina-P/sangue , Fosfatidilserinas/sangue , RNA Viral/sangue , Trombocitopenia/sangue , Trombocitopenia/virologia , Fatores de Tempo , Células Vero , Replicação Viral
2.
J Gen Virol ; 92(Pt 8): 1769-1777, 2011 Aug.
Artigo em Inglês | MEDLINE | ID: mdl-21471319

RESUMO

Camel papillomatosis has been described previously, but the genome of the suspected papillomavirus (PV) has not been identified. An outbreak of papillomatosis occurred in a dromedary farm of 55 animals in Sudan during August 2009. The disease was only present in young animals aged about 3-7 months, of which 44 % (11/25) were affected with lesions, mainly on the lips and lower jaw. This study reports for the first time the complete genomes of Camelus dromedarius papillomavirus types 1 (CdPV1) and 2 (CdPV2), isolated from a cauliflower-like nodule and a round oval raised nodule, respectively. Pairwise comparisons of their L1 nucleotide sequences revealed 69.2 % identity, and phylogenetic analyses suggested that these two PV types are grouped within the genus Deltapapillomavirus. Both viruses were isolated from fibropapillomas, although no putative E5 proteins homologous to that of bovine papillomavirus type 1 were identified. The genetic information will be useful for evolutionary studies of the family Papillomaviridae, as well as for the development of diagnostic methods for surveillance of the disease in dromedaries.


Assuntos
Genoma Viral , Papiloma/veterinária , Papillomaviridae/genética , Infecções por Papillomavirus/veterinária , Animais , Camelus , Dados de Sequência Molecular , Papiloma/virologia , Papillomaviridae/classificação , Papillomaviridae/isolamento & purificação , Infecções por Papillomavirus/virologia , Filogenia , Proteínas Virais/genética
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