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Cesarean or Vaginal Birth Does Not Impact the Longitudinal Development of the Gut Microbiome in a Cohort of Exclusively Preterm Infants

The short and long-term impact of birth mode on the developing gut microbiome in neonates has potential implications for the health of infants. In term infants, the microbiome immediately following birth across multiple body sites corresponds to birth mode, with increased Bacteroides in vaginally de...

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Autores principales: Stewart, Christopher J., Embleton, Nicholas D., Clements, Elizabeth, Luna, Pamela N., Smith, Daniel P., Fofanova, Tatiana Y., Nelson, Andrew, Taylor, Gillian, Orr, Caroline H., Petrosino, Joseph F., Berrington, Janet E., Cummings, Stephen P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5459931/
https://www.ncbi.nlm.nih.gov/pubmed/28634475
http://dx.doi.org/10.3389/fmicb.2017.01008
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author Stewart, Christopher J.
Embleton, Nicholas D.
Clements, Elizabeth
Luna, Pamela N.
Smith, Daniel P.
Fofanova, Tatiana Y.
Nelson, Andrew
Taylor, Gillian
Orr, Caroline H.
Petrosino, Joseph F.
Berrington, Janet E.
Cummings, Stephen P.
author_facet Stewart, Christopher J.
Embleton, Nicholas D.
Clements, Elizabeth
Luna, Pamela N.
Smith, Daniel P.
Fofanova, Tatiana Y.
Nelson, Andrew
Taylor, Gillian
Orr, Caroline H.
Petrosino, Joseph F.
Berrington, Janet E.
Cummings, Stephen P.
author_sort Stewart, Christopher J.
collection PubMed
description The short and long-term impact of birth mode on the developing gut microbiome in neonates has potential implications for the health of infants. In term infants, the microbiome immediately following birth across multiple body sites corresponds to birth mode, with increased Bacteroides in vaginally delivered infants. We aimed to determine the impact of birth mode of the preterm gut microbiome over the first 100 days of life and following neonatal intensive care unit (NICU) discharge. In total, 867 stool samples from 46 preterm infants (21 cesarean and 25 vaginal), median gestational age 27 weeks, were sequenced (V4 region 16S rRNA gene, Illumina MiSeq). Of these, 776 samples passed quality filtering and were included in the analysis. The overall longitudinal alpha-diversity and within infant beta-diversity was comparable between cesarean and vaginally delivered infants. Vaginally delivered infants kept significantly more OTUs from 2 months of life and following NICU discharge, but OTUs lost, gained, and regained were not different based on birth mode. Furthermore, the temporal progression of dominant genera was comparable between birth modes and no significant difference was found for any genera following adjustment for covariates. Lastly, preterm gut community types (PGCTs) showed some moderate differences in very early life, but progressed toward a comparable pattern by week 5. No PGCT was significantly associated with cesarean or vaginal birth. Unlike term infants, birth mode was not significantly associated with changes in microbial diversity, composition, specific taxa, or overall microbial development in preterm infants. This may result from the dominating effects of NICU exposures including the universal use of antibiotics immediately following birth and/or the lack of Bacteroides colonizing preterm infants.
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spelling pubmed-54599312017-06-20 Cesarean or Vaginal Birth Does Not Impact the Longitudinal Development of the Gut Microbiome in a Cohort of Exclusively Preterm Infants Stewart, Christopher J. Embleton, Nicholas D. Clements, Elizabeth Luna, Pamela N. Smith, Daniel P. Fofanova, Tatiana Y. Nelson, Andrew Taylor, Gillian Orr, Caroline H. Petrosino, Joseph F. Berrington, Janet E. Cummings, Stephen P. Front Microbiol Microbiology The short and long-term impact of birth mode on the developing gut microbiome in neonates has potential implications for the health of infants. In term infants, the microbiome immediately following birth across multiple body sites corresponds to birth mode, with increased Bacteroides in vaginally delivered infants. We aimed to determine the impact of birth mode of the preterm gut microbiome over the first 100 days of life and following neonatal intensive care unit (NICU) discharge. In total, 867 stool samples from 46 preterm infants (21 cesarean and 25 vaginal), median gestational age 27 weeks, were sequenced (V4 region 16S rRNA gene, Illumina MiSeq). Of these, 776 samples passed quality filtering and were included in the analysis. The overall longitudinal alpha-diversity and within infant beta-diversity was comparable between cesarean and vaginally delivered infants. Vaginally delivered infants kept significantly more OTUs from 2 months of life and following NICU discharge, but OTUs lost, gained, and regained were not different based on birth mode. Furthermore, the temporal progression of dominant genera was comparable between birth modes and no significant difference was found for any genera following adjustment for covariates. Lastly, preterm gut community types (PGCTs) showed some moderate differences in very early life, but progressed toward a comparable pattern by week 5. No PGCT was significantly associated with cesarean or vaginal birth. Unlike term infants, birth mode was not significantly associated with changes in microbial diversity, composition, specific taxa, or overall microbial development in preterm infants. This may result from the dominating effects of NICU exposures including the universal use of antibiotics immediately following birth and/or the lack of Bacteroides colonizing preterm infants. Frontiers Media S.A. 2017-06-06 /pmc/articles/PMC5459931/ /pubmed/28634475 http://dx.doi.org/10.3389/fmicb.2017.01008 Text en Copyright © 2017 Stewart, Embleton, Clements, Luna, Smith, Fofanova, Nelson, Taylor, Orr, Petrosino, Berrington and Cummings. http://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) or licensor 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 Microbiology
Stewart, Christopher J.
Embleton, Nicholas D.
Clements, Elizabeth
Luna, Pamela N.
Smith, Daniel P.
Fofanova, Tatiana Y.
Nelson, Andrew
Taylor, Gillian
Orr, Caroline H.
Petrosino, Joseph F.
Berrington, Janet E.
Cummings, Stephen P.
Cesarean or Vaginal Birth Does Not Impact the Longitudinal Development of the Gut Microbiome in a Cohort of Exclusively Preterm Infants
title Cesarean or Vaginal Birth Does Not Impact the Longitudinal Development of the Gut Microbiome in a Cohort of Exclusively Preterm Infants
title_full Cesarean or Vaginal Birth Does Not Impact the Longitudinal Development of the Gut Microbiome in a Cohort of Exclusively Preterm Infants
title_fullStr Cesarean or Vaginal Birth Does Not Impact the Longitudinal Development of the Gut Microbiome in a Cohort of Exclusively Preterm Infants
title_full_unstemmed Cesarean or Vaginal Birth Does Not Impact the Longitudinal Development of the Gut Microbiome in a Cohort of Exclusively Preterm Infants
title_short Cesarean or Vaginal Birth Does Not Impact the Longitudinal Development of the Gut Microbiome in a Cohort of Exclusively Preterm Infants
title_sort cesarean or vaginal birth does not impact the longitudinal development of the gut microbiome in a cohort of exclusively preterm infants
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5459931/
https://www.ncbi.nlm.nih.gov/pubmed/28634475
http://dx.doi.org/10.3389/fmicb.2017.01008
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