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Development of a fluorescent ASFV strain that retains the ability to cause disease in swine.
Borca, Manuel V; O'Donnell, Vivian; Holinka, Lauren G; Sanford, Brent; Azzinaro, Paul A; Risatti, Guillermo R; Gladue, Douglas P.
Afiliación
  • Borca MV; Agricultural Research Service Plum Island Animal Disease Center, Greenport, NY 11944, US.
  • O'Donnell V; Agricultural Research Service Plum Island Animal Disease Center, Greenport, NY 11944, US.
  • Holinka LG; Departments of Pathobiology and Veterinary Science, University of Connecticut, Storrs, CT 06269, USA.
  • Sanford B; Agricultural Research Service Plum Island Animal Disease Center, Greenport, NY 11944, US.
  • Azzinaro PA; Department of Homeland Security, Plum Island Animal Disease Center, Greenport, NY 11944, USA.
  • Risatti GR; Agricultural Research Service Plum Island Animal Disease Center, Greenport, NY 11944, US.
  • Gladue DP; Oak Ridge Institute for Science and Education (ORISE), Oak Ridge, TN 37831, USA.
Sci Rep ; 7: 46747, 2017 04 24.
Article en En | MEDLINE | ID: mdl-28436458
ABSTRACT
African swine fever is a contagious and often lethal disease for domestic pigs with a significant economic impact for the swine industry. The etiological agent, African swine fever virus (ASFV), is a highly structurally complex double stranded DNA virus. No effective vaccines or antiviral treatment are currently commercially available. We present here the development of a strain of ASFV that has been shown to retain its ability to cause disease in swine, efficiently replicate in swine macrophage and that is fluorescently tagged. The insertion of an EGFP cassette replacing the reading frames for two neighboring genes, MGF360-13L and MGF360-14L, in highly virulent field isolate Georgia/2007, did not affect virus replication in cell cultures and did not affect disease progression in swine, the natural host for ASFV. A virulent fluorescently tagged ASFV is a suitable tool to conduct pathogenesis studies in swine, study on virus-macrophage interaction and to run large scale screens that require a sensitive high throughput output. Utilizing an EGFP reporter system for observing ASFV replication and infectivity can circumvent the time and labor-intensive steps associated with viral antigen-based assays such as the observation of hemadsorption or cytopathic effect.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Virus de la Fiebre Porcina Africana / Proteínas Fluorescentes Verdes / Macrófagos Límite: Animals Idioma: En Revista: Sci Rep Año: 2017 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Virus de la Fiebre Porcina Africana / Proteínas Fluorescentes Verdes / Macrófagos Límite: Animals Idioma: En Revista: Sci Rep Año: 2017 Tipo del documento: Article País de afiliación: Estados Unidos