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Human norovirus binding to select bacteria representative of the human gut microbiota

Recent reports describe the ability of select bacterial strains to bind human norovirus, although the specificity of such interactions is unknown. The purpose of this work was to determine if a select group of bacterial species representative of human gut microbiota bind to human norovirus, and if s...

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Autores principales: Almand, Erin A., Moore, Matthew D., Outlaw, Janie, Jaykus, Lee-Ann
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5336261/
https://www.ncbi.nlm.nih.gov/pubmed/28257478
http://dx.doi.org/10.1371/journal.pone.0173124
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author Almand, Erin A.
Moore, Matthew D.
Outlaw, Janie
Jaykus, Lee-Ann
author_facet Almand, Erin A.
Moore, Matthew D.
Outlaw, Janie
Jaykus, Lee-Ann
author_sort Almand, Erin A.
collection PubMed
description Recent reports describe the ability of select bacterial strains to bind human norovirus, although the specificity of such interactions is unknown. The purpose of this work was to determine if a select group of bacterial species representative of human gut microbiota bind to human norovirus, and if so, to characterize the intensity and location of that binding. The bacteria screened included naturally occurring strains isolated from human stool (Klebsiella spp., Citrobacter spp., Bacillus spp., Enterococcus faecium and Hafnia alvei) and select reference strains (Staphylococcus aureus and Enterobacter cloacae). Binding in PBS was evaluated to three human norovirus strains (GII.4 New Orleans 2009 and Sydney 2012, GI.6) and two surrogate viruses (Tulane virus and Turnip Crinkle Virus (TCV)) using a suspension assay format linked to RT-qPCR for quantification. The impact of different overnight culture media prior to washing on binding efficiency in PBS was also evaluated, and binding was visualized using transmission electron microscopy. All bacteria tested bound the representative human norovirus strains with high efficiency (<1 log(10) of input virus remained unbound or <10% unbound and >90% binding efficiency) (p>0.05); there was selective binding for Tulane virus and no binding observed for TCV. Binding efficiency was highest when bacteria were cultured in minimal media (<1 log(10) of input virus remained unbound, so >90% bound), but notably decreased when cultured in enriched media (1–3 log(10) unbound or 0.01 –<90% bound)) (p<0.05). The norovirus-bacteria binding occurred around the outer cell surfaces and pili structures, without apparent localization. The findings reported here further elucidate and inform the dynamics between human noroviruses and enteric bacteria with implications for norovirus pathogenesis.
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spelling pubmed-53362612017-03-10 Human norovirus binding to select bacteria representative of the human gut microbiota Almand, Erin A. Moore, Matthew D. Outlaw, Janie Jaykus, Lee-Ann PLoS One Research Article Recent reports describe the ability of select bacterial strains to bind human norovirus, although the specificity of such interactions is unknown. The purpose of this work was to determine if a select group of bacterial species representative of human gut microbiota bind to human norovirus, and if so, to characterize the intensity and location of that binding. The bacteria screened included naturally occurring strains isolated from human stool (Klebsiella spp., Citrobacter spp., Bacillus spp., Enterococcus faecium and Hafnia alvei) and select reference strains (Staphylococcus aureus and Enterobacter cloacae). Binding in PBS was evaluated to three human norovirus strains (GII.4 New Orleans 2009 and Sydney 2012, GI.6) and two surrogate viruses (Tulane virus and Turnip Crinkle Virus (TCV)) using a suspension assay format linked to RT-qPCR for quantification. The impact of different overnight culture media prior to washing on binding efficiency in PBS was also evaluated, and binding was visualized using transmission electron microscopy. All bacteria tested bound the representative human norovirus strains with high efficiency (<1 log(10) of input virus remained unbound or <10% unbound and >90% binding efficiency) (p>0.05); there was selective binding for Tulane virus and no binding observed for TCV. Binding efficiency was highest when bacteria were cultured in minimal media (<1 log(10) of input virus remained unbound, so >90% bound), but notably decreased when cultured in enriched media (1–3 log(10) unbound or 0.01 –<90% bound)) (p<0.05). The norovirus-bacteria binding occurred around the outer cell surfaces and pili structures, without apparent localization. The findings reported here further elucidate and inform the dynamics between human noroviruses and enteric bacteria with implications for norovirus pathogenesis. Public Library of Science 2017-03-03 /pmc/articles/PMC5336261/ /pubmed/28257478 http://dx.doi.org/10.1371/journal.pone.0173124 Text en https://creativecommons.org/publicdomain/zero/1.0/ This is an open access article, free of all copyright, and may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose. The work is made available under the Creative Commons CC0 (https://creativecommons.org/publicdomain/zero/1.0/) public domain dedication.
spellingShingle Research Article
Almand, Erin A.
Moore, Matthew D.
Outlaw, Janie
Jaykus, Lee-Ann
Human norovirus binding to select bacteria representative of the human gut microbiota
title Human norovirus binding to select bacteria representative of the human gut microbiota
title_full Human norovirus binding to select bacteria representative of the human gut microbiota
title_fullStr Human norovirus binding to select bacteria representative of the human gut microbiota
title_full_unstemmed Human norovirus binding to select bacteria representative of the human gut microbiota
title_short Human norovirus binding to select bacteria representative of the human gut microbiota
title_sort human norovirus binding to select bacteria representative of the human gut microbiota
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5336261/
https://www.ncbi.nlm.nih.gov/pubmed/28257478
http://dx.doi.org/10.1371/journal.pone.0173124
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