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Preterm Birth Is Correlated With Increased Oral Originated Microbiome in the Gut
BACKGROUND: Preterm birth is one of the leading causes of perinatal morbidity and mortality. Gut microbiome dysbiosis is closely related to adverse pregnancy outcomes. However, the role of the gut microbiome in the pathogenesis of preterm birth remains poorly studied. METHOD: We collected fecal samp...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8248533/ https://www.ncbi.nlm.nih.gov/pubmed/34222033 http://dx.doi.org/10.3389/fcimb.2021.579766 |
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author | Yin, Chunhua Chen, Jingrui Wu, Xuena Liu, Yeling He, Quan Cao, Ying Huang, Yi-E Liu, Sisun |
author_facet | Yin, Chunhua Chen, Jingrui Wu, Xuena Liu, Yeling He, Quan Cao, Ying Huang, Yi-E Liu, Sisun |
author_sort | Yin, Chunhua |
collection | PubMed |
description | BACKGROUND: Preterm birth is one of the leading causes of perinatal morbidity and mortality. Gut microbiome dysbiosis is closely related to adverse pregnancy outcomes. However, the role of the gut microbiome in the pathogenesis of preterm birth remains poorly studied. METHOD: We collected fecal samples from 41 women (cases presenting with threatened preterm labor =19, 11 of which delivered preterm; gestational age-matched no-labor controls, all of which delivered at term = 22) were recruited for the study. We performed 16S rRNA amplicon sequencing to compare the composition of the gut microbiome in threatened preterm labor cases and controls and among women who delivered preterm and at term. By annotating taxonomic biomarkers with the Human Oral Microbiome Database, we observed an increased abundance of potential oral-to-gut bacteria in preterm patients. RESULTS: Patients with preterm birth showed a distinct gut microbiome dysbiosis compared with those who delivered at term. Opportunistic pathogens, particularly Porphyromonas, Streptococcus, Fusobacterium, and Veillonella, were enriched, whereas Coprococcus and Gemmiger were markedly depleted in the preterm group. Most of the enriched bacteria were annotated oral bacteria using the Human Oral Microbiome Database. These potential oral-to-gut bacteria were correlated with clinical parameters that reflected maternal and fetal status. CONCLUSIONS: This study suggests that patients who deliver preterm demonstrate altered gut microbiome that may contain higher common oral bacteria. |
format | Online Article Text |
id | pubmed-8248533 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-82485332021-07-02 Preterm Birth Is Correlated With Increased Oral Originated Microbiome in the Gut Yin, Chunhua Chen, Jingrui Wu, Xuena Liu, Yeling He, Quan Cao, Ying Huang, Yi-E Liu, Sisun Front Cell Infect Microbiol Cellular and Infection Microbiology BACKGROUND: Preterm birth is one of the leading causes of perinatal morbidity and mortality. Gut microbiome dysbiosis is closely related to adverse pregnancy outcomes. However, the role of the gut microbiome in the pathogenesis of preterm birth remains poorly studied. METHOD: We collected fecal samples from 41 women (cases presenting with threatened preterm labor =19, 11 of which delivered preterm; gestational age-matched no-labor controls, all of which delivered at term = 22) were recruited for the study. We performed 16S rRNA amplicon sequencing to compare the composition of the gut microbiome in threatened preterm labor cases and controls and among women who delivered preterm and at term. By annotating taxonomic biomarkers with the Human Oral Microbiome Database, we observed an increased abundance of potential oral-to-gut bacteria in preterm patients. RESULTS: Patients with preterm birth showed a distinct gut microbiome dysbiosis compared with those who delivered at term. Opportunistic pathogens, particularly Porphyromonas, Streptococcus, Fusobacterium, and Veillonella, were enriched, whereas Coprococcus and Gemmiger were markedly depleted in the preterm group. Most of the enriched bacteria were annotated oral bacteria using the Human Oral Microbiome Database. These potential oral-to-gut bacteria were correlated with clinical parameters that reflected maternal and fetal status. CONCLUSIONS: This study suggests that patients who deliver preterm demonstrate altered gut microbiome that may contain higher common oral bacteria. Frontiers Media S.A. 2021-06-17 /pmc/articles/PMC8248533/ /pubmed/34222033 http://dx.doi.org/10.3389/fcimb.2021.579766 Text en Copyright © 2021 Yin, Chen, Wu, Liu, He, Cao, Huang and Liu https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Cellular and Infection Microbiology Yin, Chunhua Chen, Jingrui Wu, Xuena Liu, Yeling He, Quan Cao, Ying Huang, Yi-E Liu, Sisun Preterm Birth Is Correlated With Increased Oral Originated Microbiome in the Gut |
title | Preterm Birth Is Correlated With Increased Oral Originated Microbiome in the Gut |
title_full | Preterm Birth Is Correlated With Increased Oral Originated Microbiome in the Gut |
title_fullStr | Preterm Birth Is Correlated With Increased Oral Originated Microbiome in the Gut |
title_full_unstemmed | Preterm Birth Is Correlated With Increased Oral Originated Microbiome in the Gut |
title_short | Preterm Birth Is Correlated With Increased Oral Originated Microbiome in the Gut |
title_sort | preterm birth is correlated with increased oral originated microbiome in the gut |
topic | Cellular and Infection Microbiology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8248533/ https://www.ncbi.nlm.nih.gov/pubmed/34222033 http://dx.doi.org/10.3389/fcimb.2021.579766 |
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