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Temporal changes in fecal microbiota of patients infected with COVID-19: a longitudinal cohort
BACKGROUND: Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) is a multifaceted disease potentially responsible for various clinical manifestations including gastro-intestinal symptoms. Several evidences suggest that the intestine is a critical site of immune cell development, gut microbi...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10436399/ https://www.ncbi.nlm.nih.gov/pubmed/37596518 http://dx.doi.org/10.1186/s12879-023-08511-6 |
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author | Galperine, Tatiana Choi, Yangji Pagani, Jean-Luc Kritikos, Antonios Papadimitriou-Olivgeris, Matthaios Méan, Marie Scherz, Valentin Opota, Onya Greub, Gilbert Guery, Benoit Bertelli, Claire |
author_facet | Galperine, Tatiana Choi, Yangji Pagani, Jean-Luc Kritikos, Antonios Papadimitriou-Olivgeris, Matthaios Méan, Marie Scherz, Valentin Opota, Onya Greub, Gilbert Guery, Benoit Bertelli, Claire |
author_sort | Galperine, Tatiana |
collection | PubMed |
description | BACKGROUND: Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) is a multifaceted disease potentially responsible for various clinical manifestations including gastro-intestinal symptoms. Several evidences suggest that the intestine is a critical site of immune cell development, gut microbiota could therefore play a key role in lung immune response. We designed a monocentric longitudinal observational study to describe the gut microbiota profile in COVID-19 patients and compare it to a pre-existing cohort of ventilated non-COVID-19 patients. METHODS: From March to December 2020, we included patients admitted for COVID-19 in medicine (43 not ventilated) or intensive care unit (ICU) (14 ventilated) with a positive SARS-CoV-2 RT-PCR assay in a respiratory tract sample. 16S metagenomics was performed on rectal swabs from these 57 COVID-19 patients, 35 with one and 22 with multiple stool collections. Nineteen non-COVID-19 ICU controls were also enrolled, among which 14 developed ventilator-associated pneumonia (pneumonia group) and five remained without infection (control group). SARS-CoV-2 viral loads in fecal samples were measured by qPCR. RESULTS: Although similar at inclusion, Shannon alpha diversity appeared significantly lower in COVID-19 and pneumonia groups than in the control group at day 7. Furthermore, the microbiota composition became distinct between COVID-19 and non-COVID-19 groups. The fecal microbiota of COVID-19 patients was characterized by increased Bacteroides and the pneumonia group by Prevotella. In a distance-based redundancy analysis, only COVID-19 presented significant effects on the microbiota composition. Moreover, patients in ICU harbored increased Campylobacter and decreased butyrate-producing bacteria, such as Lachnospiraceae, Roseburia and Faecalibacterium as compared to patients in medicine. Both the stay in ICU and patient were significant factors affecting the microbiota composition. SARS-CoV-2 viral loads were higher in ICU than in non-ICU patients. CONCLUSIONS: Overall, we identified distinct characteristics of the gut microbiota in COVID-19 patients compared to control groups. COVID-19 patients were primarily characterized by increased Bacteroides and decreased Prevotella. Moreover, disease severity showed a negative correlation with butyrate-producing bacteria. These features could offer valuable insights into potential targets for modulating the host response through the microbiota and contribute to a better understanding of the disease's pathophysiology. TRIAL REGISTRATION: CER-VD 2020–00755 (05.05.2020) & 2017–01820 (08.06.2018). SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12879-023-08511-6. |
format | Online Article Text |
id | pubmed-10436399 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-104363992023-08-19 Temporal changes in fecal microbiota of patients infected with COVID-19: a longitudinal cohort Galperine, Tatiana Choi, Yangji Pagani, Jean-Luc Kritikos, Antonios Papadimitriou-Olivgeris, Matthaios Méan, Marie Scherz, Valentin Opota, Onya Greub, Gilbert Guery, Benoit Bertelli, Claire BMC Infect Dis Research BACKGROUND: Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) is a multifaceted disease potentially responsible for various clinical manifestations including gastro-intestinal symptoms. Several evidences suggest that the intestine is a critical site of immune cell development, gut microbiota could therefore play a key role in lung immune response. We designed a monocentric longitudinal observational study to describe the gut microbiota profile in COVID-19 patients and compare it to a pre-existing cohort of ventilated non-COVID-19 patients. METHODS: From March to December 2020, we included patients admitted for COVID-19 in medicine (43 not ventilated) or intensive care unit (ICU) (14 ventilated) with a positive SARS-CoV-2 RT-PCR assay in a respiratory tract sample. 16S metagenomics was performed on rectal swabs from these 57 COVID-19 patients, 35 with one and 22 with multiple stool collections. Nineteen non-COVID-19 ICU controls were also enrolled, among which 14 developed ventilator-associated pneumonia (pneumonia group) and five remained without infection (control group). SARS-CoV-2 viral loads in fecal samples were measured by qPCR. RESULTS: Although similar at inclusion, Shannon alpha diversity appeared significantly lower in COVID-19 and pneumonia groups than in the control group at day 7. Furthermore, the microbiota composition became distinct between COVID-19 and non-COVID-19 groups. The fecal microbiota of COVID-19 patients was characterized by increased Bacteroides and the pneumonia group by Prevotella. In a distance-based redundancy analysis, only COVID-19 presented significant effects on the microbiota composition. Moreover, patients in ICU harbored increased Campylobacter and decreased butyrate-producing bacteria, such as Lachnospiraceae, Roseburia and Faecalibacterium as compared to patients in medicine. Both the stay in ICU and patient were significant factors affecting the microbiota composition. SARS-CoV-2 viral loads were higher in ICU than in non-ICU patients. CONCLUSIONS: Overall, we identified distinct characteristics of the gut microbiota in COVID-19 patients compared to control groups. COVID-19 patients were primarily characterized by increased Bacteroides and decreased Prevotella. Moreover, disease severity showed a negative correlation with butyrate-producing bacteria. These features could offer valuable insights into potential targets for modulating the host response through the microbiota and contribute to a better understanding of the disease's pathophysiology. TRIAL REGISTRATION: CER-VD 2020–00755 (05.05.2020) & 2017–01820 (08.06.2018). SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12879-023-08511-6. BioMed Central 2023-08-18 /pmc/articles/PMC10436399/ /pubmed/37596518 http://dx.doi.org/10.1186/s12879-023-08511-6 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Galperine, Tatiana Choi, Yangji Pagani, Jean-Luc Kritikos, Antonios Papadimitriou-Olivgeris, Matthaios Méan, Marie Scherz, Valentin Opota, Onya Greub, Gilbert Guery, Benoit Bertelli, Claire Temporal changes in fecal microbiota of patients infected with COVID-19: a longitudinal cohort |
title | Temporal changes in fecal microbiota of patients infected with COVID-19: a longitudinal cohort |
title_full | Temporal changes in fecal microbiota of patients infected with COVID-19: a longitudinal cohort |
title_fullStr | Temporal changes in fecal microbiota of patients infected with COVID-19: a longitudinal cohort |
title_full_unstemmed | Temporal changes in fecal microbiota of patients infected with COVID-19: a longitudinal cohort |
title_short | Temporal changes in fecal microbiota of patients infected with COVID-19: a longitudinal cohort |
title_sort | temporal changes in fecal microbiota of patients infected with covid-19: a longitudinal cohort |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10436399/ https://www.ncbi.nlm.nih.gov/pubmed/37596518 http://dx.doi.org/10.1186/s12879-023-08511-6 |
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