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Perinatal environment shapes microbiota colonization and infant growth: impact on host response and intestinal function
BACKGROUND: Early microbial colonization triggers processes that result in intestinal maturation and immune priming. Perinatal factors, especially those associated with birth, including both mode and place of delivery are critical to shaping the infant gut microbiota with potential health consequenc...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7685601/ https://www.ncbi.nlm.nih.gov/pubmed/33228771 http://dx.doi.org/10.1186/s40168-020-00940-8 |
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author | Selma-Royo, M. Calatayud Arroyo, M. García-Mantrana, I. Parra-Llorca, A. Escuriet, R. Martínez-Costa, C. Collado, M. C. |
author_facet | Selma-Royo, M. Calatayud Arroyo, M. García-Mantrana, I. Parra-Llorca, A. Escuriet, R. Martínez-Costa, C. Collado, M. C. |
author_sort | Selma-Royo, M. |
collection | PubMed |
description | BACKGROUND: Early microbial colonization triggers processes that result in intestinal maturation and immune priming. Perinatal factors, especially those associated with birth, including both mode and place of delivery are critical to shaping the infant gut microbiota with potential health consequences. METHODS: Gut microbiota profile of 180 healthy infants (n = 23 born at home and n = 157 born in hospital, 41.7% via cesarean section [CS]) was analyzed by 16S rRNA gene sequencing at birth, 7 days, and 1 month of life. Breastfeeding habits and infant clinical data, including length, weight, and antibiotic exposure, were collected up to 18 months of life. Long-term personalized in vitro models of the intestinal epithelium and innate immune system were used to assess the link between gut microbiota composition, intestinal function, and immune response. RESULTS: Microbiota profiles were shaped by the place and mode of delivery, and they had a distinct biological impact on the immune response and intestinal function in epithelial/immune cell models. Bacteroidetes and Bifidobacterium genus were decreased in C-section infants, who showed higher z-scores BMI and W/L during the first 18 months of life. Intestinal simulated epithelium had a stronger epithelial barrier function and intestinal maturation, alongside a higher immunological response (TLR4 route activation and pro-inflammatory cytokine release), when exposed to home-birth fecal supernatants, compared with CS. Distinct host response could be associated with different microbiota profiles. CONCLUSIONS: Mode and place of birth influence the neonatal gut microbiota, likely shaping its interplay with the host through the maturation of the intestinal epithelium, regulation of the intestinal epithelial barrier, and control of the innate immune system during early life, which can affect the phenotypic responses linked to metabolic processes in infants. TRIAL REGISTRATION: NCT03552939. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s40168-020-00940-8. |
format | Online Article Text |
id | pubmed-7685601 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-76856012020-11-25 Perinatal environment shapes microbiota colonization and infant growth: impact on host response and intestinal function Selma-Royo, M. Calatayud Arroyo, M. García-Mantrana, I. Parra-Llorca, A. Escuriet, R. Martínez-Costa, C. Collado, M. C. Microbiome Research BACKGROUND: Early microbial colonization triggers processes that result in intestinal maturation and immune priming. Perinatal factors, especially those associated with birth, including both mode and place of delivery are critical to shaping the infant gut microbiota with potential health consequences. METHODS: Gut microbiota profile of 180 healthy infants (n = 23 born at home and n = 157 born in hospital, 41.7% via cesarean section [CS]) was analyzed by 16S rRNA gene sequencing at birth, 7 days, and 1 month of life. Breastfeeding habits and infant clinical data, including length, weight, and antibiotic exposure, were collected up to 18 months of life. Long-term personalized in vitro models of the intestinal epithelium and innate immune system were used to assess the link between gut microbiota composition, intestinal function, and immune response. RESULTS: Microbiota profiles were shaped by the place and mode of delivery, and they had a distinct biological impact on the immune response and intestinal function in epithelial/immune cell models. Bacteroidetes and Bifidobacterium genus were decreased in C-section infants, who showed higher z-scores BMI and W/L during the first 18 months of life. Intestinal simulated epithelium had a stronger epithelial barrier function and intestinal maturation, alongside a higher immunological response (TLR4 route activation and pro-inflammatory cytokine release), when exposed to home-birth fecal supernatants, compared with CS. Distinct host response could be associated with different microbiota profiles. CONCLUSIONS: Mode and place of birth influence the neonatal gut microbiota, likely shaping its interplay with the host through the maturation of the intestinal epithelium, regulation of the intestinal epithelial barrier, and control of the innate immune system during early life, which can affect the phenotypic responses linked to metabolic processes in infants. TRIAL REGISTRATION: NCT03552939. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s40168-020-00940-8. BioMed Central 2020-11-23 /pmc/articles/PMC7685601/ /pubmed/33228771 http://dx.doi.org/10.1186/s40168-020-00940-8 Text en © The Author(s) 2020 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Selma-Royo, M. Calatayud Arroyo, M. García-Mantrana, I. Parra-Llorca, A. Escuriet, R. Martínez-Costa, C. Collado, M. C. Perinatal environment shapes microbiota colonization and infant growth: impact on host response and intestinal function |
title | Perinatal environment shapes microbiota colonization and infant growth: impact on host response and intestinal function |
title_full | Perinatal environment shapes microbiota colonization and infant growth: impact on host response and intestinal function |
title_fullStr | Perinatal environment shapes microbiota colonization and infant growth: impact on host response and intestinal function |
title_full_unstemmed | Perinatal environment shapes microbiota colonization and infant growth: impact on host response and intestinal function |
title_short | Perinatal environment shapes microbiota colonization and infant growth: impact on host response and intestinal function |
title_sort | perinatal environment shapes microbiota colonization and infant growth: impact on host response and intestinal function |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7685601/ https://www.ncbi.nlm.nih.gov/pubmed/33228771 http://dx.doi.org/10.1186/s40168-020-00940-8 |
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