Treatment of norovirus particles with citrate

Human norovirus is a dominant cause of acute gastroenteritis around the world. Several norovirus disinfectants label citric acid as an active ingredient. In this study, we showed that norovirus virus-like particles (VLPs) treated with citrate buffer caused the particles to alter their morphology, in...

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Bibliographic Details
Main Authors: Koromyslova, Anna D. (Author) , White, Peter A. (Author) , Hansman, Grant S. (Author)
Format: Article (Journal)
Language:English
Published: 25 August 2015
In: Virology
Year: 2015, Volume: 485, Pages: 199-204
ISSN:1096-0341
DOI:10.1016/j.virol.2015.07.009
Online Access:Resolving-System, lizenzpflichtig, Volltext: https://doi.org/10.1016/j.virol.2015.07.009
Verlag, lizenzpflichtig, Volltext: http://www.sciencedirect.com/science/article/pii/S0042682215003281
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Author Notes:Anna D. Koromyslova, Peter A. White, Grant S. Hansman
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Summary:Human norovirus is a dominant cause of acute gastroenteritis around the world. Several norovirus disinfectants label citric acid as an active ingredient. In this study, we showed that norovirus virus-like particles (VLPs) treated with citrate buffer caused the particles to alter their morphology, including increased diameters associated with a new ring-like structure. We also found that epitopes on the protruding (P) domain on these particles were more readily accessible to antibodies after the citrate treatment. These results suggested that citrate had a direct effect on the norovirus particles. Using X-ray crystallography, we showed that the P domain bound citrate from lemon juice and a disinfectant containing citric acid. Importantly, citrate binds at the histo-blood group antigen binding pocket, which are attachment factors for norovirus infections. Taken together, these new findings suggested that it might be possible to treat/reduce norovirus infections with citrate, although further studies are needed.
Item Description:Gesehen am 22.07.2020
Physical Description:Online Resource
ISSN:1096-0341
DOI:10.1016/j.virol.2015.07.009