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Taxonomical and functional changes in COVID‐19 faecal microbiome could be related to SARS‐CoV‐2 faecal load

Since the beginning of the pandemic caused by the severe acute respiratory syndrome coronavirus 2 (SARS‐CoV‐2) the gastrointestinal (GI) tract has emerged as an important organ influencing the propensity to and potentially the severity of the related COVID‐19 disease. However, the contribution of th...

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Autores principales: Grenga, Lucia, Pible, Olivier, Miotello, Guylaine, Culotta, Karen, Ruat, Sylvie, Roncato, Marie‐Anne, Gas, Fabienne, Bellanger, Laurent, Claret, Pierre‐Géraud, Dunyach‐Remy, Catherine, Laureillard, Didier, Sotto, Albert, Lavigne, Jean‐Philippe, Armengaud, Jean
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons, Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9347659/
https://www.ncbi.nlm.nih.gov/pubmed/35506300
http://dx.doi.org/10.1111/1462-2920.16028
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author Grenga, Lucia
Pible, Olivier
Miotello, Guylaine
Culotta, Karen
Ruat, Sylvie
Roncato, Marie‐Anne
Gas, Fabienne
Bellanger, Laurent
Claret, Pierre‐Géraud
Dunyach‐Remy, Catherine
Laureillard, Didier
Sotto, Albert
Lavigne, Jean‐Philippe
Armengaud, Jean
author_facet Grenga, Lucia
Pible, Olivier
Miotello, Guylaine
Culotta, Karen
Ruat, Sylvie
Roncato, Marie‐Anne
Gas, Fabienne
Bellanger, Laurent
Claret, Pierre‐Géraud
Dunyach‐Remy, Catherine
Laureillard, Didier
Sotto, Albert
Lavigne, Jean‐Philippe
Armengaud, Jean
author_sort Grenga, Lucia
collection PubMed
description Since the beginning of the pandemic caused by the severe acute respiratory syndrome coronavirus 2 (SARS‐CoV‐2) the gastrointestinal (GI) tract has emerged as an important organ influencing the propensity to and potentially the severity of the related COVID‐19 disease. However, the contribution of the SARS‐CoV‐2 intestinal infection on COVID‐19 pathogenesis remains to be clarified. In this exploratory study, we highlighted a possible link between alterations in the composition of the gut microbiota and the levels of SARS‐CoV‐2 RNA in the gastrointestinal tract, which could be more important than the presence of SARS‐CoV‐2 in the respiratory tract, COVID‐19 severity and GI symptoms. As established by metaproteomics, altered molecular functions in the microbiota profiles of high SARS‐CoV‐2 RNA level faeces highlight mechanisms such as inflammation‐induced enterocyte damage, increased intestinal permeability and activation of immune response that may contribute to vicious cycles. Uncovering the role of this gut microbiota dysbiosis could drive the investigation of alternative therapeutic strategies to favour the clearance of the virus and potentially mitigate the effect of the SARS‐CoV‐2 infection.
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spelling pubmed-93476592022-08-03 Taxonomical and functional changes in COVID‐19 faecal microbiome could be related to SARS‐CoV‐2 faecal load Grenga, Lucia Pible, Olivier Miotello, Guylaine Culotta, Karen Ruat, Sylvie Roncato, Marie‐Anne Gas, Fabienne Bellanger, Laurent Claret, Pierre‐Géraud Dunyach‐Remy, Catherine Laureillard, Didier Sotto, Albert Lavigne, Jean‐Philippe Armengaud, Jean Environ Microbiol Special Issue on Pathogen and Antimicrobial Resistance Ecology Since the beginning of the pandemic caused by the severe acute respiratory syndrome coronavirus 2 (SARS‐CoV‐2) the gastrointestinal (GI) tract has emerged as an important organ influencing the propensity to and potentially the severity of the related COVID‐19 disease. However, the contribution of the SARS‐CoV‐2 intestinal infection on COVID‐19 pathogenesis remains to be clarified. In this exploratory study, we highlighted a possible link between alterations in the composition of the gut microbiota and the levels of SARS‐CoV‐2 RNA in the gastrointestinal tract, which could be more important than the presence of SARS‐CoV‐2 in the respiratory tract, COVID‐19 severity and GI symptoms. As established by metaproteomics, altered molecular functions in the microbiota profiles of high SARS‐CoV‐2 RNA level faeces highlight mechanisms such as inflammation‐induced enterocyte damage, increased intestinal permeability and activation of immune response that may contribute to vicious cycles. Uncovering the role of this gut microbiota dysbiosis could drive the investigation of alternative therapeutic strategies to favour the clearance of the virus and potentially mitigate the effect of the SARS‐CoV‐2 infection. John Wiley & Sons, Inc. 2022-05-09 2022-09 /pmc/articles/PMC9347659/ /pubmed/35506300 http://dx.doi.org/10.1111/1462-2920.16028 Text en © 2022 The Authors. Environmental Microbiology published by Society for Applied Microbiology and John Wiley & Sons Ltd. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Special Issue on Pathogen and Antimicrobial Resistance Ecology
Grenga, Lucia
Pible, Olivier
Miotello, Guylaine
Culotta, Karen
Ruat, Sylvie
Roncato, Marie‐Anne
Gas, Fabienne
Bellanger, Laurent
Claret, Pierre‐Géraud
Dunyach‐Remy, Catherine
Laureillard, Didier
Sotto, Albert
Lavigne, Jean‐Philippe
Armengaud, Jean
Taxonomical and functional changes in COVID‐19 faecal microbiome could be related to SARS‐CoV‐2 faecal load
title Taxonomical and functional changes in COVID‐19 faecal microbiome could be related to SARS‐CoV‐2 faecal load
title_full Taxonomical and functional changes in COVID‐19 faecal microbiome could be related to SARS‐CoV‐2 faecal load
title_fullStr Taxonomical and functional changes in COVID‐19 faecal microbiome could be related to SARS‐CoV‐2 faecal load
title_full_unstemmed Taxonomical and functional changes in COVID‐19 faecal microbiome could be related to SARS‐CoV‐2 faecal load
title_short Taxonomical and functional changes in COVID‐19 faecal microbiome could be related to SARS‐CoV‐2 faecal load
title_sort taxonomical and functional changes in covid‐19 faecal microbiome could be related to sars‐cov‐2 faecal load
topic Special Issue on Pathogen and Antimicrobial Resistance Ecology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9347659/
https://www.ncbi.nlm.nih.gov/pubmed/35506300
http://dx.doi.org/10.1111/1462-2920.16028
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