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1.
J Gen Virol ; 91(Pt 2): 452-62, 2010 Feb.
Artículo en Inglés | MEDLINE | ID: mdl-19846671

RESUMEN

Koi herpesvirus, also known as cyprinid herpesvirus 3 (CyHV-3), is the aetiological agent of an emerging and mortal disease in common and koi carp. CyHV-3 virions present the characteristic morphology of other members of the order Herpesvirales, being composed of an envelope, a capsid containing the genome and a tegument. This study identified CyHV-3 structural proteins and the corresponding encoding genes using liquid chromatography tandem mass spectrometry-based proteomic approaches. In addition, exponentially modified protein abundance index analyses were used to estimate the relative abundance of the identified proteins in CyHV-3 virions. These analyses resulted in the identification of 40 structural proteins, which were classified based on bioinformatic analyses as capsid (three), envelope (13), tegument (two) and unclassified (22) structural proteins. Finally, a search for host proteins in purified CyHV-3 virions indicated the potential incorporation of up to 18 distinct cellular proteins. The identification of the proteins incorporated into CyHV-3 virions and determination of the viral genes encoding these proteins are key milestones for further fundamental and applied research on this virus.


Asunto(s)
Infecciones por Virus ADN/veterinaria , Enfermedades de los Peces/virología , Genoma Viral , Proteínas Estructurales Virales/metabolismo , Virión/metabolismo , Virus/metabolismo , Animales , Carpas/virología , Células Cultivadas , Infecciones por Virus ADN/genética , Infecciones por Virus ADN/metabolismo , Infecciones por Virus ADN/virología , Enfermedades de los Peces/genética , Enfermedades de los Peces/metabolismo , Interacciones Huésped-Patógeno , Datos de Secuencia Molecular , Proteínas Estructurales Virales/química , Proteínas Estructurales Virales/genética , Virión/química , Virión/genética , Virión/aislamiento & purificación , Virus/genética , Virus/aislamiento & purificación
2.
J Gen Virol ; 88(Pt 12): 3224-3233, 2007 Dec.
Artículo en Inglés | MEDLINE | ID: mdl-18024890

RESUMEN

Many gammaherpesviruses encode G-protein-coupled receptors (GPCRs). Several in vivo studies have revealed that gammaherpesvirus GPCRs are important for viral replication and for virus-induced pathogenesis. The gammaherpesvirus alcelaphine herpesvirus 1 (AlHV-1) is carried asymptomatically by wildebeest, but causes malignant catarrhal fever (MCF) following cross-species transmission to a variety of susceptible species. The A5 ORF of the AlHV-1 genome encodes a putative GPCR. In the present study, we investigated whether A5 encodes a functional GPCR and addressed its role in viral replication and in the pathogenesis of MCF. In silico analysis supported the hypothesis that A5 could encode a functional GPCR as its expression product contained several hallmark features of GPCRs. Expression of A5 as tagged proteins in various cell lines revealed that A5 localizes in cell membranes, including the plasma membrane. Using [35S]GTPgammaS and reporter gene assays, we found that A5 is able to constitutively couple to alpha i-type G-proteins in transfected cells, and that this interaction is able to inhibit forskolin-triggered cAMP response element-binding protein (CREB) activation. Finally, using an AlHV-1 BAC clone, we produced a strain deleted for A5 and a revertant strain. Interestingly, the strain deleted for A5 replicated comparably to the wild-type parental strain and induced MCF in rabbits that was indistinguishable from that of the parental strain. The present study is the first to investigate the role of an individual gene of AlHV-1 in MCF pathogenesis.


Asunto(s)
Gammaherpesvirinae/fisiología , Genes Virales/fisiología , Fiebre Catarral Maligna/metabolismo , Receptores Acoplados a Proteínas G/metabolismo , Secuencia de Aminoácidos , Animales , Bovinos , Línea Celular , Membrana Celular/metabolismo , Subunidades alfa de la Proteína de Unión al GTP/metabolismo , Gammaherpesvirinae/patogenicidad , Fiebre Catarral Maligna/virología , Datos de Secuencia Molecular , Sistemas de Lectura Abierta/genética , Conejos , Virulencia , Replicación Viral
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