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Identification and Analysis of Gut Microbiota and Functional Metabolism in Decompensated Cirrhosis with Infection

BACKGROUND AND AIMS: Intestinal dysbiosis play a role in the adverse outcomes of sepsis and septic shock. However, variations in bacterial diversity and microbiota-related functional metabolic alterations within the gut microbiome in decompensated cirrhosis (DC) patients with infection remain unknow...

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Autores principales: Philips, Cyriac Abby, Ahamed, Rizwan, Abduljaleel, Jinsha K.P., Rajesh, Sasidharan, Augustine, Philip
Formato: Online Artículo Texto
Lenguaje:English
Publicado: XIA & HE Publishing Inc. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9647106/
https://www.ncbi.nlm.nih.gov/pubmed/36406325
http://dx.doi.org/10.14218/JCTH.2021.00428
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author Philips, Cyriac Abby
Ahamed, Rizwan
Abduljaleel, Jinsha K.P.
Rajesh, Sasidharan
Augustine, Philip
author_facet Philips, Cyriac Abby
Ahamed, Rizwan
Abduljaleel, Jinsha K.P.
Rajesh, Sasidharan
Augustine, Philip
author_sort Philips, Cyriac Abby
collection PubMed
description BACKGROUND AND AIMS: Intestinal dysbiosis play a role in the adverse outcomes of sepsis and septic shock. However, variations in bacterial diversity and microbiota-related functional metabolic alterations within the gut microbiome in decompensated cirrhosis (DC) patients with infection remain unknown. METHODS: We conducted 16-srRNA sequencing on stool samples (n=51: sepsis, 27/no sepsis, 24) collected from consecutive DC patients upon admission. Bacterial diversity, significant taxa, and respective metabolic profiling were performed based on subgroup comparisons. Conet/Cytoscape was utilized to identify significant non-random patterns of bacterial copresence and mutual exclusion for clinical events. RESULTS: Genera associated with pathogenicity in conditions of immune exhaustion (Corynebacterium, Lautropia) were predominant in patients with sepsis. Metabolic pathways associated with oxidative stress and endotoxemia [lipopolysaccharide (LPS) synthesis and sulfur relay] were significantly upregulated in sepsis. Specific taxa were associated with sites of infection in DC patients. Protective oxidant pathways that increase glutathione were upregulated in those without sepsis. Gammaproteobacteria family of sulfur-metabolizing bacteria, exaggeration of orally predominant pathogens (Prevotella), and pathways of severe LPS-related hyperinflammatory stress were notable in those with interleukin-6 levels >1,000 pg/dL. Pathogenic genera related to an immune deficient state was significant in DC with ≥2 infection episodes. Megamonas was associated with survival during the same admission. CONCLUSIONS: Specific gut microbiota and their metabolites were associated with sepsis and related events in patients with DC. Identifying beneficial strains that reduce immune exhaustion and supplementation of favorable metabolites could improve therapeutics for DC and sepsis, for which larger prospective, well controlled population-based studies remain an unmet need.
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spelling pubmed-96471062022-11-18 Identification and Analysis of Gut Microbiota and Functional Metabolism in Decompensated Cirrhosis with Infection Philips, Cyriac Abby Ahamed, Rizwan Abduljaleel, Jinsha K.P. Rajesh, Sasidharan Augustine, Philip J Clin Transl Hepatol Original Article BACKGROUND AND AIMS: Intestinal dysbiosis play a role in the adverse outcomes of sepsis and septic shock. However, variations in bacterial diversity and microbiota-related functional metabolic alterations within the gut microbiome in decompensated cirrhosis (DC) patients with infection remain unknown. METHODS: We conducted 16-srRNA sequencing on stool samples (n=51: sepsis, 27/no sepsis, 24) collected from consecutive DC patients upon admission. Bacterial diversity, significant taxa, and respective metabolic profiling were performed based on subgroup comparisons. Conet/Cytoscape was utilized to identify significant non-random patterns of bacterial copresence and mutual exclusion for clinical events. RESULTS: Genera associated with pathogenicity in conditions of immune exhaustion (Corynebacterium, Lautropia) were predominant in patients with sepsis. Metabolic pathways associated with oxidative stress and endotoxemia [lipopolysaccharide (LPS) synthesis and sulfur relay] were significantly upregulated in sepsis. Specific taxa were associated with sites of infection in DC patients. Protective oxidant pathways that increase glutathione were upregulated in those without sepsis. Gammaproteobacteria family of sulfur-metabolizing bacteria, exaggeration of orally predominant pathogens (Prevotella), and pathways of severe LPS-related hyperinflammatory stress were notable in those with interleukin-6 levels >1,000 pg/dL. Pathogenic genera related to an immune deficient state was significant in DC with ≥2 infection episodes. Megamonas was associated with survival during the same admission. CONCLUSIONS: Specific gut microbiota and their metabolites were associated with sepsis and related events in patients with DC. Identifying beneficial strains that reduce immune exhaustion and supplementation of favorable metabolites could improve therapeutics for DC and sepsis, for which larger prospective, well controlled population-based studies remain an unmet need. XIA & HE Publishing Inc. 2023-02-28 2022-06-13 /pmc/articles/PMC9647106/ /pubmed/36406325 http://dx.doi.org/10.14218/JCTH.2021.00428 Text en © 2023 Authors. https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-Noncommercial 4.0 International License (CC BY-NC 4.0), permitting all non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Philips, Cyriac Abby
Ahamed, Rizwan
Abduljaleel, Jinsha K.P.
Rajesh, Sasidharan
Augustine, Philip
Identification and Analysis of Gut Microbiota and Functional Metabolism in Decompensated Cirrhosis with Infection
title Identification and Analysis of Gut Microbiota and Functional Metabolism in Decompensated Cirrhosis with Infection
title_full Identification and Analysis of Gut Microbiota and Functional Metabolism in Decompensated Cirrhosis with Infection
title_fullStr Identification and Analysis of Gut Microbiota and Functional Metabolism in Decompensated Cirrhosis with Infection
title_full_unstemmed Identification and Analysis of Gut Microbiota and Functional Metabolism in Decompensated Cirrhosis with Infection
title_short Identification and Analysis of Gut Microbiota and Functional Metabolism in Decompensated Cirrhosis with Infection
title_sort identification and analysis of gut microbiota and functional metabolism in decompensated cirrhosis with infection
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9647106/
https://www.ncbi.nlm.nih.gov/pubmed/36406325
http://dx.doi.org/10.14218/JCTH.2021.00428
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