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Reovirus intermediate subviral particles constitute a strategy to infect intestinal epithelial cells by exploiting TGF-ß dependent pro-survival signaling.
Stanifer, Megan L; Rippert, Anja; Kazakov, Alexander; Willemsen, Joschka; Bucher, Delia; Bender, Silke; Bartenschlager, Ralf; Binder, Marco; Boulant, Steeve.
Afiliación
  • Stanifer ML; Schaller research group at CellNetworks, Department of Infectious Diseases, Virology, Heidelberg University, Germany.
  • Rippert A; Schaller research group at CellNetworks, Department of Infectious Diseases, Virology, Heidelberg University, Germany.
  • Kazakov A; Schaller research group at CellNetworks, Department of Infectious Diseases, Virology, Heidelberg University, Germany.
  • Willemsen J; Research Group 'Dynamics of early viral infection and the innate antiviral response'.
  • Bucher D; Division Virus-associated Carcinogenesis (F170), German Cancer Research Center (DKFZ), Heidelberg, Germany.
  • Bender S; Schaller research group at CellNetworks, Department of Infectious Diseases, Virology, Heidelberg University, Germany.
  • Bartenschlager R; Division Virus-associated Carcinogenesis (F170), German Cancer Research Center (DKFZ), Heidelberg, Germany.
  • Binder M; Division Virus-associated Carcinogenesis (F170), German Cancer Research Center (DKFZ), Heidelberg, Germany.
  • Boulant S; Research Group 'Dynamics of early viral infection and the innate antiviral response'.
Cell Microbiol ; 18(12): 1831-1845, 2016 Dec.
Article en En | MEDLINE | ID: mdl-27279006
ABSTRACT
Intestinal epithelial cells (IECs) constitute the primary barrier that separates us from the outside environment. These cells, lining the surface of the intestinal tract, represent a major challenge that enteric pathogens have to face. How IECs respond to viral infection and whether enteric viruses have developed strategies to subvert IECs innate immune response remains poorly characterized. Using mammalian reovirus (MRV) as a model enteric virus, we found that the intermediate subviral particles (ISVPs), which are formed in the gut during the natural course of infection by proteolytic digestion of the reovirus virion, trigger reduced innate antiviral immune response in IECs. On the contrary, infection of IECs by virions induces a strong antiviral immune response that leads to cellular death. Additionally, we determined that virions can be sensed by both TLR and RLR pathways while ISVPs are sensed by RLR pathways only. Interestingly, we found that ISVP infected cells secrete TGF-ß acting as a pro-survival factor that protects IECs against virion induced cellular death. We propose that ISVPs represent a reovirus strategy to initiate primary infection of the gut by subverting IECs innate immune system and by counteracting cellular-death pathways.
Asunto(s)

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Virión / Factor de Crecimiento Transformador beta / Colon / Orthoreovirus de los Mamíferos / Células Epiteliales / Interacciones Huésped-Patógeno Tipo de estudio: Prognostic_studies Límite: Humans Idioma: En Año: 2016 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Virión / Factor de Crecimiento Transformador beta / Colon / Orthoreovirus de los Mamíferos / Células Epiteliales / Interacciones Huésped-Patógeno Tipo de estudio: Prognostic_studies Límite: Humans Idioma: En Año: 2016 Tipo del documento: Article