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The Role of the Gut Microbiome in Resisting Norovirus Infection as Revealed by a Human Challenge Study

Norovirus infections take a heavy toll on worldwide public health. While progress has been made toward understanding host responses to infection, the role of the gut microbiome in determining infection outcome is unknown. Moreover, data are lacking on the nature and duration of the microbiome respon...

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Autores principales: Patin, N. V., Peña-Gonzalez, A., Hatt, J. K., Moe, C., Kirby, A., Konstantinidis, K. T.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society for Microbiology 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7683401/
https://www.ncbi.nlm.nih.gov/pubmed/33203758
http://dx.doi.org/10.1128/mBio.02634-20
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author Patin, N. V.
Peña-Gonzalez, A.
Hatt, J. K.
Moe, C.
Kirby, A.
Konstantinidis, K. T.
author_facet Patin, N. V.
Peña-Gonzalez, A.
Hatt, J. K.
Moe, C.
Kirby, A.
Konstantinidis, K. T.
author_sort Patin, N. V.
collection PubMed
description Norovirus infections take a heavy toll on worldwide public health. While progress has been made toward understanding host responses to infection, the role of the gut microbiome in determining infection outcome is unknown. Moreover, data are lacking on the nature and duration of the microbiome response to norovirus infection, which has important implications for diagnostics and host recovery. Here, we characterized the gut microbiomes of subjects enrolled in a norovirus challenge study. We analyzed microbiome features of asymptomatic and symptomatic individuals at the genome (population) and gene levels and assessed their response over time in symptomatic individuals. We show that the preinfection microbiomes of subjects with asymptomatic infections were enriched in Bacteroidetes and depleted in Clostridia relative to the microbiomes of symptomatic subjects. These compositional differences were accompanied by differences in genes involved in the metabolism of glycans and sphingolipids that may aid in host resilience to infection. We further show that microbiomes shifted in composition following infection and that recovery times were variable among human hosts. In particular, Firmicutes increased immediately following the challenge, while Bacteroidetes and Proteobacteria decreased over the same time. Genes enriched in the microbiomes of symptomatic subjects, including the adenylyltransferase glgC, were linked to glycan metabolism and cell-cell signaling, suggesting as-yet unknown roles for these processes in determining infection outcome. These results provide important context for understanding the gut microbiome role in host susceptibility to symptomatic norovirus infection and long-term health outcomes.
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spelling pubmed-76834012020-11-30 The Role of the Gut Microbiome in Resisting Norovirus Infection as Revealed by a Human Challenge Study Patin, N. V. Peña-Gonzalez, A. Hatt, J. K. Moe, C. Kirby, A. Konstantinidis, K. T. mBio Research Article Norovirus infections take a heavy toll on worldwide public health. While progress has been made toward understanding host responses to infection, the role of the gut microbiome in determining infection outcome is unknown. Moreover, data are lacking on the nature and duration of the microbiome response to norovirus infection, which has important implications for diagnostics and host recovery. Here, we characterized the gut microbiomes of subjects enrolled in a norovirus challenge study. We analyzed microbiome features of asymptomatic and symptomatic individuals at the genome (population) and gene levels and assessed their response over time in symptomatic individuals. We show that the preinfection microbiomes of subjects with asymptomatic infections were enriched in Bacteroidetes and depleted in Clostridia relative to the microbiomes of symptomatic subjects. These compositional differences were accompanied by differences in genes involved in the metabolism of glycans and sphingolipids that may aid in host resilience to infection. We further show that microbiomes shifted in composition following infection and that recovery times were variable among human hosts. In particular, Firmicutes increased immediately following the challenge, while Bacteroidetes and Proteobacteria decreased over the same time. Genes enriched in the microbiomes of symptomatic subjects, including the adenylyltransferase glgC, were linked to glycan metabolism and cell-cell signaling, suggesting as-yet unknown roles for these processes in determining infection outcome. These results provide important context for understanding the gut microbiome role in host susceptibility to symptomatic norovirus infection and long-term health outcomes. American Society for Microbiology 2020-11-17 /pmc/articles/PMC7683401/ /pubmed/33203758 http://dx.doi.org/10.1128/mBio.02634-20 Text en Copyright © 2020 Patin et al. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Research Article
Patin, N. V.
Peña-Gonzalez, A.
Hatt, J. K.
Moe, C.
Kirby, A.
Konstantinidis, K. T.
The Role of the Gut Microbiome in Resisting Norovirus Infection as Revealed by a Human Challenge Study
title The Role of the Gut Microbiome in Resisting Norovirus Infection as Revealed by a Human Challenge Study
title_full The Role of the Gut Microbiome in Resisting Norovirus Infection as Revealed by a Human Challenge Study
title_fullStr The Role of the Gut Microbiome in Resisting Norovirus Infection as Revealed by a Human Challenge Study
title_full_unstemmed The Role of the Gut Microbiome in Resisting Norovirus Infection as Revealed by a Human Challenge Study
title_short The Role of the Gut Microbiome in Resisting Norovirus Infection as Revealed by a Human Challenge Study
title_sort role of the gut microbiome in resisting norovirus infection as revealed by a human challenge study
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7683401/
https://www.ncbi.nlm.nih.gov/pubmed/33203758
http://dx.doi.org/10.1128/mBio.02634-20
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