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Maternal gut microbiota during pregnancy and the composition of immune cells in infancy

BACKGROUND: Preclinical studies have shown that maternal gut microbiota during pregnancy play a key role in prenatal immune development but the relevance of these findings to humans is unknown. The aim of this prebirth cohort study was to investigate the association between the maternal gut microbio...

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Autores principales: Gao, Yuan, O’Hely, Martin, Quinn, Thomas P., Ponsonby, Anne-Louise, Harrison, Leonard C., Frøkiær, Hanne, Tang, Mimi L. K., Brix, Susanne, Kristiansen, Karsten, Burgner, Dave, Saffery, Richard, Ranganathan, Sarath, Collier, Fiona, Vuillermin, Peter
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9535361/
https://www.ncbi.nlm.nih.gov/pubmed/36211431
http://dx.doi.org/10.3389/fimmu.2022.986340
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author Gao, Yuan
O’Hely, Martin
Quinn, Thomas P.
Ponsonby, Anne-Louise
Harrison, Leonard C.
Frøkiær, Hanne
Tang, Mimi L. K.
Brix, Susanne
Kristiansen, Karsten
Burgner, Dave
Saffery, Richard
Ranganathan, Sarath
Collier, Fiona
Vuillermin, Peter
author_facet Gao, Yuan
O’Hely, Martin
Quinn, Thomas P.
Ponsonby, Anne-Louise
Harrison, Leonard C.
Frøkiær, Hanne
Tang, Mimi L. K.
Brix, Susanne
Kristiansen, Karsten
Burgner, Dave
Saffery, Richard
Ranganathan, Sarath
Collier, Fiona
Vuillermin, Peter
author_sort Gao, Yuan
collection PubMed
description BACKGROUND: Preclinical studies have shown that maternal gut microbiota during pregnancy play a key role in prenatal immune development but the relevance of these findings to humans is unknown. The aim of this prebirth cohort study was to investigate the association between the maternal gut microbiota in pregnancy and the composition of the infant’s cord and peripheral blood immune cells over the first year of life. METHODS: The Barwon Infant Study cohort (n=1074 infants) was recruited using an unselected sampling frame. Maternal fecal samples were collected at 36 weeks of pregnancy and flow cytometry was conducted on cord/peripheral blood collected at birth, 6 and 12 months of age. Among a randomly selected sub-cohort with available samples (n=293), maternal gut microbiota was characterized by sequencing the 16S rRNA V4 region. Operational taxonomic units (OTUs) were clustered based on their abundance. Associations between maternal fecal microbiota clusters and infant granulocyte, monocyte and lymphocyte subsets were explored using compositional data analysis. Partial least squares (PLS) and regression models were used to investigate the relationships/associations between environmental, maternal and infant factors, and OTU clusters. RESULTS: We identified six clusters of co-occurring OTUs. The first two components in the PLS regression explained 39% and 33% of the covariance between the maternal prenatal OTU clusters and immune cell populations in offspring at birth. A cluster in which Dialister, Escherichia, and Ruminococcus were predominant was associated with a lower proportion of granulocytes (p=0.002), and higher proportions of both central naïve CD4(+) T cells (CD4(+)/CD45RA(+)/CD31(−)) (p<0.001) and naïve regulatory T cells (Treg) (CD4(+)/CD45RA(+)/FoxP3(low)) (p=0.02) in cord blood. The association with central naïve CD4(+) T cells persisted to 12 months of age. CONCLUSION: This birth cohort study provides evidence consistent with past preclinical models that the maternal gut microbiota during pregnancy plays a role in shaping the composition of innate and adaptive elements of the infant’s immune system following birth.
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spelling pubmed-95353612022-10-07 Maternal gut microbiota during pregnancy and the composition of immune cells in infancy Gao, Yuan O’Hely, Martin Quinn, Thomas P. Ponsonby, Anne-Louise Harrison, Leonard C. Frøkiær, Hanne Tang, Mimi L. K. Brix, Susanne Kristiansen, Karsten Burgner, Dave Saffery, Richard Ranganathan, Sarath Collier, Fiona Vuillermin, Peter Front Immunol Immunology BACKGROUND: Preclinical studies have shown that maternal gut microbiota during pregnancy play a key role in prenatal immune development but the relevance of these findings to humans is unknown. The aim of this prebirth cohort study was to investigate the association between the maternal gut microbiota in pregnancy and the composition of the infant’s cord and peripheral blood immune cells over the first year of life. METHODS: The Barwon Infant Study cohort (n=1074 infants) was recruited using an unselected sampling frame. Maternal fecal samples were collected at 36 weeks of pregnancy and flow cytometry was conducted on cord/peripheral blood collected at birth, 6 and 12 months of age. Among a randomly selected sub-cohort with available samples (n=293), maternal gut microbiota was characterized by sequencing the 16S rRNA V4 region. Operational taxonomic units (OTUs) were clustered based on their abundance. Associations between maternal fecal microbiota clusters and infant granulocyte, monocyte and lymphocyte subsets were explored using compositional data analysis. Partial least squares (PLS) and regression models were used to investigate the relationships/associations between environmental, maternal and infant factors, and OTU clusters. RESULTS: We identified six clusters of co-occurring OTUs. The first two components in the PLS regression explained 39% and 33% of the covariance between the maternal prenatal OTU clusters and immune cell populations in offspring at birth. A cluster in which Dialister, Escherichia, and Ruminococcus were predominant was associated with a lower proportion of granulocytes (p=0.002), and higher proportions of both central naïve CD4(+) T cells (CD4(+)/CD45RA(+)/CD31(−)) (p<0.001) and naïve regulatory T cells (Treg) (CD4(+)/CD45RA(+)/FoxP3(low)) (p=0.02) in cord blood. The association with central naïve CD4(+) T cells persisted to 12 months of age. CONCLUSION: This birth cohort study provides evidence consistent with past preclinical models that the maternal gut microbiota during pregnancy plays a role in shaping the composition of innate and adaptive elements of the infant’s immune system following birth. Frontiers Media S.A. 2022-09-21 /pmc/articles/PMC9535361/ /pubmed/36211431 http://dx.doi.org/10.3389/fimmu.2022.986340 Text en Copyright © 2022 Gao, O’Hely, Quinn, Ponsonby, Harrison, Frøkiær, Tang, Brix, Kristiansen, Burgner, Saffery, Ranganathan, Collier and Vuillermin 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 Immunology
Gao, Yuan
O’Hely, Martin
Quinn, Thomas P.
Ponsonby, Anne-Louise
Harrison, Leonard C.
Frøkiær, Hanne
Tang, Mimi L. K.
Brix, Susanne
Kristiansen, Karsten
Burgner, Dave
Saffery, Richard
Ranganathan, Sarath
Collier, Fiona
Vuillermin, Peter
Maternal gut microbiota during pregnancy and the composition of immune cells in infancy
title Maternal gut microbiota during pregnancy and the composition of immune cells in infancy
title_full Maternal gut microbiota during pregnancy and the composition of immune cells in infancy
title_fullStr Maternal gut microbiota during pregnancy and the composition of immune cells in infancy
title_full_unstemmed Maternal gut microbiota during pregnancy and the composition of immune cells in infancy
title_short Maternal gut microbiota during pregnancy and the composition of immune cells in infancy
title_sort maternal gut microbiota during pregnancy and the composition of immune cells in infancy
topic Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9535361/
https://www.ncbi.nlm.nih.gov/pubmed/36211431
http://dx.doi.org/10.3389/fimmu.2022.986340
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