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Oropharyngeal and intestinal concentrations of opportunistic pathogens are independently associated with death of SARS-CoV-2 critically ill adults

BACKGROUND: The composition of the digestive microbiota may be associated with outcome and infections in patients admitted to the intensive care unit (ICU). The dominance by opportunistic pathogens (such as Enterococcus) has been associated with death. However, whether this association remains all t...

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Autores principales: Patrier, Juliette, Villageois-Tran, Khanh, Szychowiak, Piotr, Ruckly, Stéphane, Gschwind, Rémi, Wicky, Paul-Henri, Gueye, Signara, Armand-Lefevre, Laurence, Marzouk, Mehdi, Sonneville, Romain, Bouadma, Lila, Petitjean, Marie, Lamara, Fariza, de Montmollin, Etienne, Timsit, Jean-Francois, Ruppé, Etienne
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9527714/
https://www.ncbi.nlm.nih.gov/pubmed/36192756
http://dx.doi.org/10.1186/s13054-022-04164-0
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author Patrier, Juliette
Villageois-Tran, Khanh
Szychowiak, Piotr
Ruckly, Stéphane
Gschwind, Rémi
Wicky, Paul-Henri
Gueye, Signara
Armand-Lefevre, Laurence
Marzouk, Mehdi
Sonneville, Romain
Bouadma, Lila
Petitjean, Marie
Lamara, Fariza
de Montmollin, Etienne
Timsit, Jean-Francois
Ruppé, Etienne
author_facet Patrier, Juliette
Villageois-Tran, Khanh
Szychowiak, Piotr
Ruckly, Stéphane
Gschwind, Rémi
Wicky, Paul-Henri
Gueye, Signara
Armand-Lefevre, Laurence
Marzouk, Mehdi
Sonneville, Romain
Bouadma, Lila
Petitjean, Marie
Lamara, Fariza
de Montmollin, Etienne
Timsit, Jean-Francois
Ruppé, Etienne
author_sort Patrier, Juliette
collection PubMed
description BACKGROUND: The composition of the digestive microbiota may be associated with outcome and infections in patients admitted to the intensive care unit (ICU). The dominance by opportunistic pathogens (such as Enterococcus) has been associated with death. However, whether this association remains all throughout the hospitalization are lacking. METHODS: We performed a single-center observational prospective cohort study in critically ill patients admitted with severe SARS-CoV-2 infection. Oropharyngeal and rectal swabs were collected at admission and then twice weekly until discharge or death. Quantitative cultures for opportunistic pathogens were performed on oropharyngeal and rectal swabs. The composition of the intestinal microbiota was assessed by 16S rDNA sequencing. Oropharyngeal and intestinal concentrations of opportunistic pathogens, intestinal richness and diversity were entered into a multivariable Cox model as time-dependent covariates. The primary outcome was death at day 90. RESULTS: From March to September 2020, 95 patients (765 samples) were included. The Simplified Acute Physiology Score 2 (SAPS 2) at admission was 33 [24; 50] and a Sequential Organ Failure Assessment score (SOFA score) at 6 [4; 8]. Day 90 all-cause mortality was 44.2% (42/95). We observed that the oropharyngeal and rectal concentrations of Enterococcus spp., Staphylococcus aureus and Candida spp. were associated with a higher risk of death. This association remained significant after adjustment for prognostic covariates (age, chronic disease, daily antimicrobial agent use and daily SOFA score). A one-log increase in Enterococcus spp., S. aureus and Candida spp. in oropharyngeal or rectal swabs was associated with a 17% or greater increase in the risk of death. CONCLUSION: We found that elevated oropharyngeal/intestinal Enterococcus spp. S. aureus and Candida spp. concentrations, assessed by culture, are associated with mortality, independent of age, organ failure, and antibiotic therapy, opening prospects for simple and inexpensive microbiota-based markers for the prognosis of critically ill SARS-CoV-2 patients. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13054-022-04164-0.
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spelling pubmed-95277142022-10-03 Oropharyngeal and intestinal concentrations of opportunistic pathogens are independently associated with death of SARS-CoV-2 critically ill adults Patrier, Juliette Villageois-Tran, Khanh Szychowiak, Piotr Ruckly, Stéphane Gschwind, Rémi Wicky, Paul-Henri Gueye, Signara Armand-Lefevre, Laurence Marzouk, Mehdi Sonneville, Romain Bouadma, Lila Petitjean, Marie Lamara, Fariza de Montmollin, Etienne Timsit, Jean-Francois Ruppé, Etienne Crit Care Research BACKGROUND: The composition of the digestive microbiota may be associated with outcome and infections in patients admitted to the intensive care unit (ICU). The dominance by opportunistic pathogens (such as Enterococcus) has been associated with death. However, whether this association remains all throughout the hospitalization are lacking. METHODS: We performed a single-center observational prospective cohort study in critically ill patients admitted with severe SARS-CoV-2 infection. Oropharyngeal and rectal swabs were collected at admission and then twice weekly until discharge or death. Quantitative cultures for opportunistic pathogens were performed on oropharyngeal and rectal swabs. The composition of the intestinal microbiota was assessed by 16S rDNA sequencing. Oropharyngeal and intestinal concentrations of opportunistic pathogens, intestinal richness and diversity were entered into a multivariable Cox model as time-dependent covariates. The primary outcome was death at day 90. RESULTS: From March to September 2020, 95 patients (765 samples) were included. The Simplified Acute Physiology Score 2 (SAPS 2) at admission was 33 [24; 50] and a Sequential Organ Failure Assessment score (SOFA score) at 6 [4; 8]. Day 90 all-cause mortality was 44.2% (42/95). We observed that the oropharyngeal and rectal concentrations of Enterococcus spp., Staphylococcus aureus and Candida spp. were associated with a higher risk of death. This association remained significant after adjustment for prognostic covariates (age, chronic disease, daily antimicrobial agent use and daily SOFA score). A one-log increase in Enterococcus spp., S. aureus and Candida spp. in oropharyngeal or rectal swabs was associated with a 17% or greater increase in the risk of death. CONCLUSION: We found that elevated oropharyngeal/intestinal Enterococcus spp. S. aureus and Candida spp. concentrations, assessed by culture, are associated with mortality, independent of age, organ failure, and antibiotic therapy, opening prospects for simple and inexpensive microbiota-based markers for the prognosis of critically ill SARS-CoV-2 patients. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13054-022-04164-0. BioMed Central 2022-10-03 /pmc/articles/PMC9527714/ /pubmed/36192756 http://dx.doi.org/10.1186/s13054-022-04164-0 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis 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
Patrier, Juliette
Villageois-Tran, Khanh
Szychowiak, Piotr
Ruckly, Stéphane
Gschwind, Rémi
Wicky, Paul-Henri
Gueye, Signara
Armand-Lefevre, Laurence
Marzouk, Mehdi
Sonneville, Romain
Bouadma, Lila
Petitjean, Marie
Lamara, Fariza
de Montmollin, Etienne
Timsit, Jean-Francois
Ruppé, Etienne
Oropharyngeal and intestinal concentrations of opportunistic pathogens are independently associated with death of SARS-CoV-2 critically ill adults
title Oropharyngeal and intestinal concentrations of opportunistic pathogens are independently associated with death of SARS-CoV-2 critically ill adults
title_full Oropharyngeal and intestinal concentrations of opportunistic pathogens are independently associated with death of SARS-CoV-2 critically ill adults
title_fullStr Oropharyngeal and intestinal concentrations of opportunistic pathogens are independently associated with death of SARS-CoV-2 critically ill adults
title_full_unstemmed Oropharyngeal and intestinal concentrations of opportunistic pathogens are independently associated with death of SARS-CoV-2 critically ill adults
title_short Oropharyngeal and intestinal concentrations of opportunistic pathogens are independently associated with death of SARS-CoV-2 critically ill adults
title_sort oropharyngeal and intestinal concentrations of opportunistic pathogens are independently associated with death of sars-cov-2 critically ill adults
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9527714/
https://www.ncbi.nlm.nih.gov/pubmed/36192756
http://dx.doi.org/10.1186/s13054-022-04164-0
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