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Viperin targets flavivirus virulence by inducing assembly of non-infectious capsid particles

Vonderstein, Kirstin, 1986- (author)
Umeå universitet,Virologi,Molekylär Infektionsmedicin, Sverige (MIMS),Anna Överby Wernstedt
Nilsson, Emma, 1979- (author)
Umeå universitet,Virologi,Molekylär Infektionsmedicin, Sverige (MIMS),Anna Överby Wernstedt
Hubel, Philipp (author)
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Nygård Skalman, Lars (author)
Umeå universitet,Institutionen för medicinsk kemi och biofysik,Institutionen för integrativ medicinsk biologi (IMB)
Upadhyay, Arunkumar, 1984- (author)
Umeå universitet,Virologi,Molekylär Infektionsmedicin, Sverige (MIMS),Anna Överby Wernstedt
Pasto, Jenny, 1987- (author)
Umeå universitet,Virologi,Molekylär Infektionsmedicin, Sverige (MIMS),Anna Överby Wernstedt
Pichlmair, Andreas (author)
Lundmark, Richard (author)
Umeå universitet,Molekylär Infektionsmedicin, Sverige (MIMS),Institutionen för medicinsk kemi och biofysik,Institutionen för integrativ medicinsk biologi (IMB)
Överby, Anna K., 1978- (author)
Umeå universitet,Virologi,Molekylär Infektionsmedicin, Sverige (MIMS),Anna Överby Wernstedt
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 (creator_code:org_t)
American Society of Microbiology, 2018
2018
English.
In: Journal of Virology. - : American Society of Microbiology. - 0022-538X .- 1098-5514. ; 92:1
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • Efficient antiviral immunity requires interference with virus replication at multiple layers targeting diverse steps in the viral life cycle. Here we describe a novel flavivirus inhibition mechanism that results in interferon-mediated obstruction of tick-borne encephalitis virus particle assembly, and involves release of malfunctional membrane associated capsid (C) particles. This mechanism is controlled by the activity of the interferon-induced protein viperin, a broad spectrum antiviral interferon stimulated gene. Through analysis of the viperin-interactome, we identified the Golgi Brefeldin A resistant guanine nucleotide exchange factor 1 (GBF1), as the cellular protein targeted by viperin. Viperin-induced antiviral activity as well as C-particle release was stimulated by GBF1 inhibition and knock down, and reduced by elevated levels of GBF1. Our results suggest that viperin targets flavivirus virulence by inducing the secretion of unproductive non-infectious virus particles, by a GBF1-dependent mechanism. This yet undescribed antiviral mechanism allows potential therapeutic intervention.Importance The interferon response can target viral infection on almost every level, however, very little is known about interference of flavivirus assembly. Here we show that interferon, through the action of viperin, can disturb assembly of tick-borne encephalitis virus. The viperin protein is highly induced after viral infection and exhibit broad-spectrum antiviral activity. However, the mechanism of action is still elusive and appear to vary between the different viruses, indicating that cellular targets utilized by several viruses might be involved. In this study we show that viperin induce capsid particle release by interacting and inhibiting the function of the cellular protein Golgi Brefeldin A resistant guanine nucleotide exchange factor 1 (GBF1). GBF1 is a key protein in the cellular secretory pathway and essential in the life cycle of many viruses, also targeted by viperin, implicating GBF1 as a novel putative drug target.

Subject headings

MEDICIN OCH HÄLSOVETENSKAP  -- Medicinska och farmaceutiska grundvetenskaper -- Mikrobiologi inom det medicinska området (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Basic Medicine -- Microbiology in the medical area (hsv//eng)
NATURVETENSKAP  -- Biologi -- Biokemi och molekylärbiologi (hsv//swe)
NATURAL SCIENCES  -- Biological Sciences -- Biochemistry and Molecular Biology (hsv//eng)

Keyword

COPI
COPII
GBF1
assembly
capsid
flavivirus
interferon
tick-borne encephalitis virus
viperi

Publication and Content Type

ref (subject category)
art (subject category)

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