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Changes in the intestinal microbiota of children with hand, foot, and mouth disease under 3 years old

This study aimed to clarify the characteristics of intestinal microbiota in children with hand, foot, and mouth disease (HFMD) under 3 years old. Fresh feces were collected from 54 children with HFMD and 30 healthy children. All of them were <3 years old. Sequencing of the 16S rDNA amplicons was...

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Autores principales: Zhu, Su Yue, Jiang, Ya Zhou, Shen, Nan, Li, Min, Yin, Han Jun, Qiao, Ji Bing
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Lippincott Williams & Wilkins 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10158917/
https://www.ncbi.nlm.nih.gov/pubmed/37145009
http://dx.doi.org/10.1097/MD.0000000000033687
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author Zhu, Su Yue
Jiang, Ya Zhou
Shen, Nan
Li, Min
Yin, Han Jun
Qiao, Ji Bing
author_facet Zhu, Su Yue
Jiang, Ya Zhou
Shen, Nan
Li, Min
Yin, Han Jun
Qiao, Ji Bing
author_sort Zhu, Su Yue
collection PubMed
description This study aimed to clarify the characteristics of intestinal microbiota in children with hand, foot, and mouth disease (HFMD) under 3 years old. Fresh feces were collected from 54 children with HFMD and 30 healthy children. All of them were <3 years old. Sequencing of the 16S rDNA amplicons was performed. Between the 2 groups, the richness, diversity, and structure of the intestinal microbiota were analyzed by α-diversity and β-diversity. Linear discriminant analysis and LEfSe analyses were used to compare different bacterial classifications. The sex and age of the children in the 2 groups were not statistically significant (P = .92 and P = .98, respectively). Compared to healthy children, the Shannon index, Ace index, and Chao index were lower in children with HFMD (P = .027, P = .012, and P = .012, respectively). Based on the weighted or unweighted UniFrac distance analysis, the structure of the intestinal microbiota in HFMD was also significantly changed (P = .002 and P < .001, respectively). Linear discriminant analysis and LEfSe analysis showed that the changes of key bacteria were manifested as a decrease in Prevotella and Clostridium_XIVa (P < .001 and P < .001, respectively), while Escherichia and Bifidobacterium increased (P = .025 and P = .001, respectively). Children with HFMD under 3 years of age have intestinal microbiota disorder and show a decrease in diversity and richness. The decrease in the abundance of Prevotella and Clostridium, which can produce short-chain fatty acids, is also one of the characteristics of the change. These results can offer a theoretical foundation for the pathogenesis and microecological treatment of HFMD in infants.
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spelling pubmed-101589172023-05-05 Changes in the intestinal microbiota of children with hand, foot, and mouth disease under 3 years old Zhu, Su Yue Jiang, Ya Zhou Shen, Nan Li, Min Yin, Han Jun Qiao, Ji Bing Medicine (Baltimore) 4900 This study aimed to clarify the characteristics of intestinal microbiota in children with hand, foot, and mouth disease (HFMD) under 3 years old. Fresh feces were collected from 54 children with HFMD and 30 healthy children. All of them were <3 years old. Sequencing of the 16S rDNA amplicons was performed. Between the 2 groups, the richness, diversity, and structure of the intestinal microbiota were analyzed by α-diversity and β-diversity. Linear discriminant analysis and LEfSe analyses were used to compare different bacterial classifications. The sex and age of the children in the 2 groups were not statistically significant (P = .92 and P = .98, respectively). Compared to healthy children, the Shannon index, Ace index, and Chao index were lower in children with HFMD (P = .027, P = .012, and P = .012, respectively). Based on the weighted or unweighted UniFrac distance analysis, the structure of the intestinal microbiota in HFMD was also significantly changed (P = .002 and P < .001, respectively). Linear discriminant analysis and LEfSe analysis showed that the changes of key bacteria were manifested as a decrease in Prevotella and Clostridium_XIVa (P < .001 and P < .001, respectively), while Escherichia and Bifidobacterium increased (P = .025 and P = .001, respectively). Children with HFMD under 3 years of age have intestinal microbiota disorder and show a decrease in diversity and richness. The decrease in the abundance of Prevotella and Clostridium, which can produce short-chain fatty acids, is also one of the characteristics of the change. These results can offer a theoretical foundation for the pathogenesis and microecological treatment of HFMD in infants. Lippincott Williams & Wilkins 2023-05-05 /pmc/articles/PMC10158917/ /pubmed/37145009 http://dx.doi.org/10.1097/MD.0000000000033687 Text en Copyright © 2023 the Author(s). Published by Wolters Kluwer Health, Inc. https://creativecommons.org/licenses/by-nc/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution-Non Commercial License 4.0 (CCBY-NC) (https://creativecommons.org/licenses/by-nc/4.0/) , where it is permissible to download, share, remix, transform, and buildup the work provided it is properly cited. The work cannot be used commercially without permission from the journal.
spellingShingle 4900
Zhu, Su Yue
Jiang, Ya Zhou
Shen, Nan
Li, Min
Yin, Han Jun
Qiao, Ji Bing
Changes in the intestinal microbiota of children with hand, foot, and mouth disease under 3 years old
title Changes in the intestinal microbiota of children with hand, foot, and mouth disease under 3 years old
title_full Changes in the intestinal microbiota of children with hand, foot, and mouth disease under 3 years old
title_fullStr Changes in the intestinal microbiota of children with hand, foot, and mouth disease under 3 years old
title_full_unstemmed Changes in the intestinal microbiota of children with hand, foot, and mouth disease under 3 years old
title_short Changes in the intestinal microbiota of children with hand, foot, and mouth disease under 3 years old
title_sort changes in the intestinal microbiota of children with hand, foot, and mouth disease under 3 years old
topic 4900
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10158917/
https://www.ncbi.nlm.nih.gov/pubmed/37145009
http://dx.doi.org/10.1097/MD.0000000000033687
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