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Inhibiting avian influenza virus shedding using a novel RNAi antiviral vector technology: proof of concept in an avian cell model.
Linke, Lyndsey M; Wilusz, Jeffrey; Pabilonia, Kristy L; Fruehauf, Johannes; Magnuson, Roberta; Olea-Popelka, Francisco; Triantis, Joni; Landolt, Gabriele; Salman, Mo.
Afiliação
  • Linke LM; Animal Population Health Institute, Colorado State University, Fort Collins, CO, USA. Lyndsey.Linke@colostate.edu.
  • Wilusz J; Department of Clinical Sciences, Colorado State University, Fort Collins, CO, USA. Lyndsey.Linke@colostate.edu.
  • Pabilonia KL; Department of Microbiology, Immunology and Pathology, Colorado State University, Fort Collins, CO, USA.
  • Fruehauf J; Animal Population Health Institute, Colorado State University, Fort Collins, CO, USA.
  • Magnuson R; Department of Microbiology, Immunology and Pathology, Colorado State University, Fort Collins, CO, USA.
  • Olea-Popelka F; Cambridge Biolabs, Cambridge, MA, USA.
  • Triantis J; Animal Population Health Institute, Colorado State University, Fort Collins, CO, USA.
  • Landolt G; Department of Clinical Sciences, Colorado State University, Fort Collins, CO, USA.
  • Salman M; Department of Clinical Sciences, Colorado State University, Fort Collins, CO, USA.
AMB Express ; 6(1): 16, 2016 Mar.
Article em En | MEDLINE | ID: mdl-26910902
ABSTRACT
Influenza A viruses pose significant health and economic threats to humans and animals. Outbreaks of avian influenza virus (AIV) are a liability to the poultry industry and increase the risk for transmission to humans. There are limitations to using the AIV vaccine in poultry, creating barriers to controlling outbreaks and a need for alternative effective control measures. Application of RNA interference (RNAi) techniques hold potential; however, the delivery of RNAi-mediating agents is a well-known obstacle to harnessing its clinical application. We introduce a novel antiviral approach using bacterial vectors that target avian mucosal epithelial cells and deliver (small interfering RNA) siRNAs against two AIV genes, nucleoprotein (NP) and polymerase acidic protein (PA). Using a red fluorescent reporter, we first demonstrated vector delivery and intracellular expression in avian epithelial cells. Subsequently, we demonstrated significant reductions in AIV shedding when applying these anti-AIV vectors prophylactically. These antiviral vectors provided up to a 10,000-fold reduction in viral titers shed, demonstrating in vitro proof-of-concept for using these novel anti-AIV vectors to inhibit AIV shedding. Our results indicate this siRNA vector technology could represent a scalable and clinically applicable antiviral technology for avian and human influenza and a prototype for RNAi-based vectors against other viruses.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2016 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2016 Tipo de documento: Article