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An integrative understanding of the large metabolic shifts induced by antibiotics in critical illness

Antibiotics are commonly used in the Intensive Care Unit (ICU); however, several studies showed that the impact of antibiotics to prevent infection, multi-organ failure, and death in the ICU is less clear than their benefit on course of infection in the absence of organ dysfunction. We characterized...

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Autores principales: Marfil-Sánchez, Andrea, Zhang, Lu, Alonso-Pernas, Pol, Mirhakkak, Mohammad, Mueller, Melinda, Seelbinder, Bastian, Ni, Yueqiong, Santhanam, Rakesh, Busch, Anne, Beemelmanns, Christine, Ermolaeva, Maria, Bauer, Michael, Panagiotou, Gianni
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8604395/
https://www.ncbi.nlm.nih.gov/pubmed/34793277
http://dx.doi.org/10.1080/19490976.2021.1993598
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author Marfil-Sánchez, Andrea
Zhang, Lu
Alonso-Pernas, Pol
Mirhakkak, Mohammad
Mueller, Melinda
Seelbinder, Bastian
Ni, Yueqiong
Santhanam, Rakesh
Busch, Anne
Beemelmanns, Christine
Ermolaeva, Maria
Bauer, Michael
Panagiotou, Gianni
author_facet Marfil-Sánchez, Andrea
Zhang, Lu
Alonso-Pernas, Pol
Mirhakkak, Mohammad
Mueller, Melinda
Seelbinder, Bastian
Ni, Yueqiong
Santhanam, Rakesh
Busch, Anne
Beemelmanns, Christine
Ermolaeva, Maria
Bauer, Michael
Panagiotou, Gianni
author_sort Marfil-Sánchez, Andrea
collection PubMed
description Antibiotics are commonly used in the Intensive Care Unit (ICU); however, several studies showed that the impact of antibiotics to prevent infection, multi-organ failure, and death in the ICU is less clear than their benefit on course of infection in the absence of organ dysfunction. We characterized here the compositional and metabolic changes of the gut microbiome induced by critical illness and antibiotics in a cohort of 75 individuals in conjunction with 2,180 gut microbiome samples representing 16 different diseases. We revealed an “infection-vulnerable” gut microbiome environment present only in critically ill treated with antibiotics (ICU(+)). Feeding of Caenorhabditis elegans with Bifidobacterium animalis and Lactobacillus crispatus, species that expanded in ICU(+) patients, revealed a significant negative impact of these microbes on host viability and developmental homeostasis. These results suggest that antibiotic administration can dramatically impact essential functional activities in the gut related to immune responses more than critical illness itself, which might explain in part untoward effects of antibiotics in the critically ill.
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spelling pubmed-86043952021-11-20 An integrative understanding of the large metabolic shifts induced by antibiotics in critical illness Marfil-Sánchez, Andrea Zhang, Lu Alonso-Pernas, Pol Mirhakkak, Mohammad Mueller, Melinda Seelbinder, Bastian Ni, Yueqiong Santhanam, Rakesh Busch, Anne Beemelmanns, Christine Ermolaeva, Maria Bauer, Michael Panagiotou, Gianni Gut Microbes Research Paper Antibiotics are commonly used in the Intensive Care Unit (ICU); however, several studies showed that the impact of antibiotics to prevent infection, multi-organ failure, and death in the ICU is less clear than their benefit on course of infection in the absence of organ dysfunction. We characterized here the compositional and metabolic changes of the gut microbiome induced by critical illness and antibiotics in a cohort of 75 individuals in conjunction with 2,180 gut microbiome samples representing 16 different diseases. We revealed an “infection-vulnerable” gut microbiome environment present only in critically ill treated with antibiotics (ICU(+)). Feeding of Caenorhabditis elegans with Bifidobacterium animalis and Lactobacillus crispatus, species that expanded in ICU(+) patients, revealed a significant negative impact of these microbes on host viability and developmental homeostasis. These results suggest that antibiotic administration can dramatically impact essential functional activities in the gut related to immune responses more than critical illness itself, which might explain in part untoward effects of antibiotics in the critically ill. Taylor & Francis 2021-11-18 /pmc/articles/PMC8604395/ /pubmed/34793277 http://dx.doi.org/10.1080/19490976.2021.1993598 Text en © 2021 The Author(s). Published with license by Taylor & Francis Group, LLC. https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial License (http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) ), which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Paper
Marfil-Sánchez, Andrea
Zhang, Lu
Alonso-Pernas, Pol
Mirhakkak, Mohammad
Mueller, Melinda
Seelbinder, Bastian
Ni, Yueqiong
Santhanam, Rakesh
Busch, Anne
Beemelmanns, Christine
Ermolaeva, Maria
Bauer, Michael
Panagiotou, Gianni
An integrative understanding of the large metabolic shifts induced by antibiotics in critical illness
title An integrative understanding of the large metabolic shifts induced by antibiotics in critical illness
title_full An integrative understanding of the large metabolic shifts induced by antibiotics in critical illness
title_fullStr An integrative understanding of the large metabolic shifts induced by antibiotics in critical illness
title_full_unstemmed An integrative understanding of the large metabolic shifts induced by antibiotics in critical illness
title_short An integrative understanding of the large metabolic shifts induced by antibiotics in critical illness
title_sort integrative understanding of the large metabolic shifts induced by antibiotics in critical illness
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8604395/
https://www.ncbi.nlm.nih.gov/pubmed/34793277
http://dx.doi.org/10.1080/19490976.2021.1993598
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