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Altered gut microbiota composition in children and their caregivers infected with the SARS-CoV-2 Omicron variant

BACKGROUND: Gut microbiota alterations have been implicated in the pathogenesis of coronavirus disease 2019 (COVID-19). This study aimed to explore gut microbiota changes in a prospective cohort of COVID-19 children and their asymptomatic caregivers infected with the severe acute respiratory syndrom...

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Autores principales: Wang, Yi-Zhong, Zhou, Jian-Guo, Lu, Yan-Ming, Hu, Hui, Xiao, Fang-Fei, Ge, Ting, Wang, Xing, Zheng, Lu, Yu, Lian-Hu, Le, Jun, Yu, Hui, Yu, Guang-Jun, Xia, Qiang, Zhang, Ting, Zhou, Wen-Hao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Nature Singapore 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9838448/
https://www.ncbi.nlm.nih.gov/pubmed/36627507
http://dx.doi.org/10.1007/s12519-022-00659-6
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author Wang, Yi-Zhong
Zhou, Jian-Guo
Lu, Yan-Ming
Hu, Hui
Xiao, Fang-Fei
Ge, Ting
Wang, Xing
Zheng, Lu
Yu, Lian-Hu
Le, Jun
Yu, Hui
Yu, Guang-Jun
Xia, Qiang
Zhang, Ting
Zhou, Wen-Hao
author_facet Wang, Yi-Zhong
Zhou, Jian-Guo
Lu, Yan-Ming
Hu, Hui
Xiao, Fang-Fei
Ge, Ting
Wang, Xing
Zheng, Lu
Yu, Lian-Hu
Le, Jun
Yu, Hui
Yu, Guang-Jun
Xia, Qiang
Zhang, Ting
Zhou, Wen-Hao
author_sort Wang, Yi-Zhong
collection PubMed
description BACKGROUND: Gut microbiota alterations have been implicated in the pathogenesis of coronavirus disease 2019 (COVID-19). This study aimed to explore gut microbiota changes in a prospective cohort of COVID-19 children and their asymptomatic caregivers infected with the severe acute respiratory syndrome coronavirus type 2 (SARS-CoV-2) Omicron variant. METHODS: A total of 186 participants, including 59 COVID-19 children, 50 asymptomatic adult caregivers, 52 healthy children (HC), and 25 healthy adults (HA), were recruited between 15 April and 31 May 2022. The gut microbiota composition was determined by 16S rRNA gene sequencing in fecal samples collected from the participants. Gut microbiota functional profiling was performed by using Phylogenetic Investigation of Communities by Reconstruction of Unobserved States (PICRUSt) software. RESULTS: The gut microbiota analysis of beta diversity revealed that the fecal microbial community of COVID-19 children remained far distantly related to HC. The relative abundances of the phyla Actinobacteria and Firmicutes were decreased, whereas Bacteroidetes, Proteobacteria, and Verrucomicrobiota were increased in COVID-19 children. Feces from COVID-19 children exhibited notably lower abundances of the genera Blautia, Bifidobacterium, Fusicatenibacter, Streptococcus, and Romboutsia and higher abundances of the genera Prevotella, Lachnoclostridium, Escherichia-Shigella, and Bacteroides than those from HC. The enterotype distributions of COVID-19 children were characterized by a high prevalence of enterotype Bacteroides. Similar changes in gut microbiota compositions were observed in asymptomatic caregivers. Furthermore, the microbial metabolic activities of KEGG (Kyoto Encyclopedia of Genes and Genomes) and COG (cluster of orthologous groups of proteins) pathways were perturbed in feces from subjects infected with the SARS-CoV-2 Omicron variant. CONCLUSION: Our data reveal altered gut microbiota compositions in both COVID-19 children and their asymptomatic caregivers infected with the SARS-CoV-2 Omicron variant, which further implicates the critical role of gut microbiota in COVID-19 pathogenesis. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s12519-022-00659-6.
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spelling pubmed-98384482023-01-17 Altered gut microbiota composition in children and their caregivers infected with the SARS-CoV-2 Omicron variant Wang, Yi-Zhong Zhou, Jian-Guo Lu, Yan-Ming Hu, Hui Xiao, Fang-Fei Ge, Ting Wang, Xing Zheng, Lu Yu, Lian-Hu Le, Jun Yu, Hui Yu, Guang-Jun Xia, Qiang Zhang, Ting Zhou, Wen-Hao World J Pediatr Original Article BACKGROUND: Gut microbiota alterations have been implicated in the pathogenesis of coronavirus disease 2019 (COVID-19). This study aimed to explore gut microbiota changes in a prospective cohort of COVID-19 children and their asymptomatic caregivers infected with the severe acute respiratory syndrome coronavirus type 2 (SARS-CoV-2) Omicron variant. METHODS: A total of 186 participants, including 59 COVID-19 children, 50 asymptomatic adult caregivers, 52 healthy children (HC), and 25 healthy adults (HA), were recruited between 15 April and 31 May 2022. The gut microbiota composition was determined by 16S rRNA gene sequencing in fecal samples collected from the participants. Gut microbiota functional profiling was performed by using Phylogenetic Investigation of Communities by Reconstruction of Unobserved States (PICRUSt) software. RESULTS: The gut microbiota analysis of beta diversity revealed that the fecal microbial community of COVID-19 children remained far distantly related to HC. The relative abundances of the phyla Actinobacteria and Firmicutes were decreased, whereas Bacteroidetes, Proteobacteria, and Verrucomicrobiota were increased in COVID-19 children. Feces from COVID-19 children exhibited notably lower abundances of the genera Blautia, Bifidobacterium, Fusicatenibacter, Streptococcus, and Romboutsia and higher abundances of the genera Prevotella, Lachnoclostridium, Escherichia-Shigella, and Bacteroides than those from HC. The enterotype distributions of COVID-19 children were characterized by a high prevalence of enterotype Bacteroides. Similar changes in gut microbiota compositions were observed in asymptomatic caregivers. Furthermore, the microbial metabolic activities of KEGG (Kyoto Encyclopedia of Genes and Genomes) and COG (cluster of orthologous groups of proteins) pathways were perturbed in feces from subjects infected with the SARS-CoV-2 Omicron variant. CONCLUSION: Our data reveal altered gut microbiota compositions in both COVID-19 children and their asymptomatic caregivers infected with the SARS-CoV-2 Omicron variant, which further implicates the critical role of gut microbiota in COVID-19 pathogenesis. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s12519-022-00659-6. Springer Nature Singapore 2023-01-10 2023 /pmc/articles/PMC9838448/ /pubmed/36627507 http://dx.doi.org/10.1007/s12519-022-00659-6 Text en © Children's Hospital, Zhejiang University School of Medicine 2023, Springer Nature or its licensor (e.g. a society or other partner) holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law. This article is made available via the PMC Open Access Subset for unrestricted research re-use and secondary analysis in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the World Health Organization (WHO) declaration of COVID-19 as a global pandemic.
spellingShingle Original Article
Wang, Yi-Zhong
Zhou, Jian-Guo
Lu, Yan-Ming
Hu, Hui
Xiao, Fang-Fei
Ge, Ting
Wang, Xing
Zheng, Lu
Yu, Lian-Hu
Le, Jun
Yu, Hui
Yu, Guang-Jun
Xia, Qiang
Zhang, Ting
Zhou, Wen-Hao
Altered gut microbiota composition in children and their caregivers infected with the SARS-CoV-2 Omicron variant
title Altered gut microbiota composition in children and their caregivers infected with the SARS-CoV-2 Omicron variant
title_full Altered gut microbiota composition in children and their caregivers infected with the SARS-CoV-2 Omicron variant
title_fullStr Altered gut microbiota composition in children and their caregivers infected with the SARS-CoV-2 Omicron variant
title_full_unstemmed Altered gut microbiota composition in children and their caregivers infected with the SARS-CoV-2 Omicron variant
title_short Altered gut microbiota composition in children and their caregivers infected with the SARS-CoV-2 Omicron variant
title_sort altered gut microbiota composition in children and their caregivers infected with the sars-cov-2 omicron variant
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9838448/
https://www.ncbi.nlm.nih.gov/pubmed/36627507
http://dx.doi.org/10.1007/s12519-022-00659-6
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