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Analysis of gut microbiota alteration and application as an auxiliary prognostic marker for sepsis in children: a pilot study
BACKGROUND: Emerging evidence suggests that gut microbiota dysbiosis plays a role in sepsis. Recent advances in sequencing technology enable the characterization of the gut microbiota and can provide clues for the pathogenesis of sepsis, which may help develop biomarkers for diagnosis or prognosis p...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
AME Publishing Company
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8261590/ https://www.ncbi.nlm.nih.gov/pubmed/34295779 http://dx.doi.org/10.21037/tp-21-51 |
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author | Du, Bailu Shen, Nan Tao, Yue Sun, Sijuan Zhang, Fang Ren, Hong Cao, Qing Mo, Xi |
author_facet | Du, Bailu Shen, Nan Tao, Yue Sun, Sijuan Zhang, Fang Ren, Hong Cao, Qing Mo, Xi |
author_sort | Du, Bailu |
collection | PubMed |
description | BACKGROUND: Emerging evidence suggests that gut microbiota dysbiosis plays a role in sepsis. Recent advances in sequencing technology enable the characterization of the gut microbiota and can provide clues for the pathogenesis of sepsis, which may help develop biomarkers for diagnosis or prognosis prediction in children with sepsis. METHODS: The gut microbiota from 25 children with sepsis and 15 age- and sex-matched healthy controls were extracted and sequenced by high-throughput Illumina Hiseq, targeting the 16S rDNA genes. The differences of gut microbiota between the two groups were analyzed to assess if the gut microbiota can be used as an auxiliary prognostic marker for sepsis. RESULTS: The diversity of gut microbiota in children with sepsis was significantly lower than that of healthy controls (P<0.001). The overall community structure of gut microbiota was also altered considerably. On the genus level, children with sepsis had more opportunistic pathogens, such as Acinetobacter and Enterococcus, while fewer beneficial bacterial, such as Roseburia, Bacteroides, Clostridia, Faecalibacterium, and Blautia, were detected. Further analysis of the association between the gut microbiota and clinical features revealed that the pathogens from bacteria culture correlated to the dominant bacteria genus detected in the intestinal flora. Furthermore, the gut microbiota diversity was negatively associated with the antibiotic therapy duration, but did not correlate with type of antibiotics used. Finally, gut microbiota disturbance was correlated with increased mortality rate. CONCLUSIONS: Overall, we confirmed that gut microbiota disturbance occurred in the children with sepsis, and changes in the fecal microbiota were closely related to clinical characteristics. Elucidation of such dysbiosis could improve our understanding of sepsis pathogenesis and help develop microbiota-based diagnosis, monitoring, and therapy for sepsis. |
format | Online Article Text |
id | pubmed-8261590 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | AME Publishing Company |
record_format | MEDLINE/PubMed |
spelling | pubmed-82615902021-07-21 Analysis of gut microbiota alteration and application as an auxiliary prognostic marker for sepsis in children: a pilot study Du, Bailu Shen, Nan Tao, Yue Sun, Sijuan Zhang, Fang Ren, Hong Cao, Qing Mo, Xi Transl Pediatr Original Article BACKGROUND: Emerging evidence suggests that gut microbiota dysbiosis plays a role in sepsis. Recent advances in sequencing technology enable the characterization of the gut microbiota and can provide clues for the pathogenesis of sepsis, which may help develop biomarkers for diagnosis or prognosis prediction in children with sepsis. METHODS: The gut microbiota from 25 children with sepsis and 15 age- and sex-matched healthy controls were extracted and sequenced by high-throughput Illumina Hiseq, targeting the 16S rDNA genes. The differences of gut microbiota between the two groups were analyzed to assess if the gut microbiota can be used as an auxiliary prognostic marker for sepsis. RESULTS: The diversity of gut microbiota in children with sepsis was significantly lower than that of healthy controls (P<0.001). The overall community structure of gut microbiota was also altered considerably. On the genus level, children with sepsis had more opportunistic pathogens, such as Acinetobacter and Enterococcus, while fewer beneficial bacterial, such as Roseburia, Bacteroides, Clostridia, Faecalibacterium, and Blautia, were detected. Further analysis of the association between the gut microbiota and clinical features revealed that the pathogens from bacteria culture correlated to the dominant bacteria genus detected in the intestinal flora. Furthermore, the gut microbiota diversity was negatively associated with the antibiotic therapy duration, but did not correlate with type of antibiotics used. Finally, gut microbiota disturbance was correlated with increased mortality rate. CONCLUSIONS: Overall, we confirmed that gut microbiota disturbance occurred in the children with sepsis, and changes in the fecal microbiota were closely related to clinical characteristics. Elucidation of such dysbiosis could improve our understanding of sepsis pathogenesis and help develop microbiota-based diagnosis, monitoring, and therapy for sepsis. AME Publishing Company 2021-06 /pmc/articles/PMC8261590/ /pubmed/34295779 http://dx.doi.org/10.21037/tp-21-51 Text en 2021 Translational Pediatrics. All rights reserved. https://creativecommons.org/licenses/by-nc-nd/4.0/Open Access Statement: This is an Open Access article distributed in accordance with the Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International License (CC BY-NC-ND 4.0), which permits the non-commercial replication and distribution of the article with the strict proviso that no changes or edits are made and the original work is properly cited (including links to both the formal publication through the relevant DOI and the license). See: https://creativecommons.org/licenses/by-nc-nd/4.0 (https://creativecommons.org/licenses/by-nc-nd/4.0/) . |
spellingShingle | Original Article Du, Bailu Shen, Nan Tao, Yue Sun, Sijuan Zhang, Fang Ren, Hong Cao, Qing Mo, Xi Analysis of gut microbiota alteration and application as an auxiliary prognostic marker for sepsis in children: a pilot study |
title | Analysis of gut microbiota alteration and application as an auxiliary prognostic marker for sepsis in children: a pilot study |
title_full | Analysis of gut microbiota alteration and application as an auxiliary prognostic marker for sepsis in children: a pilot study |
title_fullStr | Analysis of gut microbiota alteration and application as an auxiliary prognostic marker for sepsis in children: a pilot study |
title_full_unstemmed | Analysis of gut microbiota alteration and application as an auxiliary prognostic marker for sepsis in children: a pilot study |
title_short | Analysis of gut microbiota alteration and application as an auxiliary prognostic marker for sepsis in children: a pilot study |
title_sort | analysis of gut microbiota alteration and application as an auxiliary prognostic marker for sepsis in children: a pilot study |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8261590/ https://www.ncbi.nlm.nih.gov/pubmed/34295779 http://dx.doi.org/10.21037/tp-21-51 |
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