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Antibiotics and probiotics impact gut antimicrobial resistance gene reservoir in COVID-19 patients

Dysbiosis of gut microbiota is well-described in patients with coronavirus 2019 (COVID-19), but the dynamics of antimicrobial resistance genes (ARGs) reservoir, known as resistome, is less known. Here, we performed longitudinal fecal metagenomic profiling of 142 patients with COVID-19, characterized...

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Autores principales: Su, Qi, Liu, Qin, Zhang, Lin, Xu, Zhilu, Liu, Chenyu, Lu, Wenqi, Ching, Jessica YL, Li, Amy, Mak, Joyce Wing Yan, Lui, Grace Chung Yan, Ng, Susanna So Shan, Chow, Kai Ming, Hui, David SC, Chan, Paul KS, Chan, Francis Ka Leung, Ng, Siew C
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9543044/
https://www.ncbi.nlm.nih.gov/pubmed/36201636
http://dx.doi.org/10.1080/19490976.2022.2128603
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author Su, Qi
Liu, Qin
Zhang, Lin
Xu, Zhilu
Liu, Chenyu
Lu, Wenqi
Ching, Jessica YL
Li, Amy
Mak, Joyce Wing Yan
Lui, Grace Chung Yan
Ng, Susanna So Shan
Chow, Kai Ming
Hui, David SC
Chan, Paul KS
Chan, Francis Ka Leung
Ng, Siew C
author_facet Su, Qi
Liu, Qin
Zhang, Lin
Xu, Zhilu
Liu, Chenyu
Lu, Wenqi
Ching, Jessica YL
Li, Amy
Mak, Joyce Wing Yan
Lui, Grace Chung Yan
Ng, Susanna So Shan
Chow, Kai Ming
Hui, David SC
Chan, Paul KS
Chan, Francis Ka Leung
Ng, Siew C
author_sort Su, Qi
collection PubMed
description Dysbiosis of gut microbiota is well-described in patients with coronavirus 2019 (COVID-19), but the dynamics of antimicrobial resistance genes (ARGs) reservoir, known as resistome, is less known. Here, we performed longitudinal fecal metagenomic profiling of 142 patients with COVID-19, characterized the dynamics of resistome from diagnosis to 6 months after viral clearance, and reported the impact of antibiotics or probiotics on the ARGs reservoir. Antibiotic-naive patients with COVID-19 showed increased abundance and types, and higher prevalence of ARGs compared with non-COVID-19 controls at baseline. Expansion in resistome was mainly driven by tetracycline, vancomycin, and multidrug-resistant genes and persisted for at least 6 months after clearance of SARS-CoV-2. Patients with expanded resistome exhibited increased prevalence of Klebsiella sp. and post-acute COVID-19 syndrome. Antibiotic treatment resulted in further increased abundance of ARGs whilst oral probiotics (synbiotic formula, SIM01) significantly reduced the ARGs reservoir in the gut microbiota of COVID-19 patients during the acute infection and recovery phase. Collectively, these findings shed new insights on the dynamic of ARGs reservoir in COVID-19 patients and the potential role of microbiota-directed therapies in reducing the burden of accumulated ARGs.
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spelling pubmed-95430442022-10-08 Antibiotics and probiotics impact gut antimicrobial resistance gene reservoir in COVID-19 patients Su, Qi Liu, Qin Zhang, Lin Xu, Zhilu Liu, Chenyu Lu, Wenqi Ching, Jessica YL Li, Amy Mak, Joyce Wing Yan Lui, Grace Chung Yan Ng, Susanna So Shan Chow, Kai Ming Hui, David SC Chan, Paul KS Chan, Francis Ka Leung Ng, Siew C Gut Microbes Research Paper Dysbiosis of gut microbiota is well-described in patients with coronavirus 2019 (COVID-19), but the dynamics of antimicrobial resistance genes (ARGs) reservoir, known as resistome, is less known. Here, we performed longitudinal fecal metagenomic profiling of 142 patients with COVID-19, characterized the dynamics of resistome from diagnosis to 6 months after viral clearance, and reported the impact of antibiotics or probiotics on the ARGs reservoir. Antibiotic-naive patients with COVID-19 showed increased abundance and types, and higher prevalence of ARGs compared with non-COVID-19 controls at baseline. Expansion in resistome was mainly driven by tetracycline, vancomycin, and multidrug-resistant genes and persisted for at least 6 months after clearance of SARS-CoV-2. Patients with expanded resistome exhibited increased prevalence of Klebsiella sp. and post-acute COVID-19 syndrome. Antibiotic treatment resulted in further increased abundance of ARGs whilst oral probiotics (synbiotic formula, SIM01) significantly reduced the ARGs reservoir in the gut microbiota of COVID-19 patients during the acute infection and recovery phase. Collectively, these findings shed new insights on the dynamic of ARGs reservoir in COVID-19 patients and the potential role of microbiota-directed therapies in reducing the burden of accumulated ARGs. Taylor & Francis 2022-10-06 /pmc/articles/PMC9543044/ /pubmed/36201636 http://dx.doi.org/10.1080/19490976.2022.2128603 Text en © 2022 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
Su, Qi
Liu, Qin
Zhang, Lin
Xu, Zhilu
Liu, Chenyu
Lu, Wenqi
Ching, Jessica YL
Li, Amy
Mak, Joyce Wing Yan
Lui, Grace Chung Yan
Ng, Susanna So Shan
Chow, Kai Ming
Hui, David SC
Chan, Paul KS
Chan, Francis Ka Leung
Ng, Siew C
Antibiotics and probiotics impact gut antimicrobial resistance gene reservoir in COVID-19 patients
title Antibiotics and probiotics impact gut antimicrobial resistance gene reservoir in COVID-19 patients
title_full Antibiotics and probiotics impact gut antimicrobial resistance gene reservoir in COVID-19 patients
title_fullStr Antibiotics and probiotics impact gut antimicrobial resistance gene reservoir in COVID-19 patients
title_full_unstemmed Antibiotics and probiotics impact gut antimicrobial resistance gene reservoir in COVID-19 patients
title_short Antibiotics and probiotics impact gut antimicrobial resistance gene reservoir in COVID-19 patients
title_sort antibiotics and probiotics impact gut antimicrobial resistance gene reservoir in covid-19 patients
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9543044/
https://www.ncbi.nlm.nih.gov/pubmed/36201636
http://dx.doi.org/10.1080/19490976.2022.2128603
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