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Turnip Mosaic Virus Counteracts Selective Autophagy of the Viral Silencing Suppressor HCpro.
Hafrén, Anders; Üstün, Suayib; Hochmuth, Anton; Svenning, Steingrim; Johansen, Terje; Hofius, Daniel.
Afiliación
  • Hafrén A; Department of Plant Biology, Uppsala BioCenter, Swedish University of Agricultural Sciences (SLU) and Linnean Center for Plant Biology, 75007 Uppsala, Sweden.
  • Üstün S; Department of Plant Biology, Uppsala BioCenter, Swedish University of Agricultural Sciences (SLU) and Linnean Center for Plant Biology, 75007 Uppsala, Sweden.
  • Hochmuth A; Department of Plant Biology, Uppsala BioCenter, Swedish University of Agricultural Sciences (SLU) and Linnean Center for Plant Biology, 75007 Uppsala, Sweden.
  • Svenning S; Molecular Cancer Research Group, Institute of Medical Biology, University of Tromsø - The Arctic University of Norway, 9037 Tromsø, Norway.
  • Johansen T; Molecular Cancer Research Group, Institute of Medical Biology, University of Tromsø - The Arctic University of Norway, 9037 Tromsø, Norway.
  • Hofius D; Department of Plant Biology, Uppsala BioCenter, Swedish University of Agricultural Sciences (SLU) and Linnean Center for Plant Biology, 75007 Uppsala, Sweden daniel.hofius@slu.se.
Plant Physiol ; 176(1): 649-662, 2018 01.
Article en En | MEDLINE | ID: mdl-29133371
ABSTRACT
Autophagy is a conserved intracellular degradation pathway and has emerged as a key mechanism of antiviral immunity in metazoans, including the selective elimination of viral components. In turn, some animal viruses are able to escape and modulate autophagy for enhanced pathogenicity. Whether host autophagic responses and viral countermeasures play similar roles in plant-virus interactions is not well understood. Here, we have identified selective autophagy as antiviral pathway during plant infection with turnip mosaic virus (TuMV), a positive-stranded RNA potyvirus. We show that the autophagy cargo receptor NBR1 suppresses viral accumulation by targeting the viral RNA silencing suppressor helper-component proteinase (HCpro), presumably in association with virus-induced RNA granules. Intriguingly, TuMV seems to antagonize NBR1-dependent autophagy during infection by the activity of distinct viral proteins, thereby limiting its antiviral capacity. We also found that NBR1-independent bulk autophagy prevents premature plant death, thus extending the lifespan of virus reservoirs and particle production. Together, our study highlights a conserved role of selective autophagy in antiviral immunity and suggests the evolvement of viral protein functions to inhibit autophagy processes, despite a potential trade-off in host survival.
Asunto(s)

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Autofagia / Proteínas Virales / Potyvirus / Interferencia de ARN Tipo de estudio: Prognostic_studies Idioma: En Año: 2018 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Autofagia / Proteínas Virales / Potyvirus / Interferencia de ARN Tipo de estudio: Prognostic_studies Idioma: En Año: 2018 Tipo del documento: Article