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Neonatal gut and respiratory microbiota: coordinated development through time and space

BACKGROUND: Postnatal development of early life microbiota influences immunity, metabolism, neurodevelopment, and infant health. Microbiome development occurs at multiple body sites, with distinct community compositions and functions. Associations between microbiota at multiple sites represent an un...

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Autores principales: Grier, Alex, McDavid, Andrew, Wang, Bokai, Qiu, Xing, Java, James, Bandyopadhyay, Sanjukta, Yang, Hongmei, Holden-Wiltse, Jeanne, Kessler, Haeja A, Gill, Ann L, Huyck, Heidie, Falsey, Ann R, Topham, David J, Scheible, Kristin M, Caserta, Mary T, Pryhuber, Gloria S, Gill, Steven R
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6204011/
https://www.ncbi.nlm.nih.gov/pubmed/30367675
http://dx.doi.org/10.1186/s40168-018-0566-5
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author Grier, Alex
McDavid, Andrew
Wang, Bokai
Qiu, Xing
Java, James
Bandyopadhyay, Sanjukta
Yang, Hongmei
Holden-Wiltse, Jeanne
Kessler, Haeja A
Gill, Ann L
Huyck, Heidie
Falsey, Ann R
Topham, David J
Scheible, Kristin M
Caserta, Mary T
Pryhuber, Gloria S
Gill, Steven R
author_facet Grier, Alex
McDavid, Andrew
Wang, Bokai
Qiu, Xing
Java, James
Bandyopadhyay, Sanjukta
Yang, Hongmei
Holden-Wiltse, Jeanne
Kessler, Haeja A
Gill, Ann L
Huyck, Heidie
Falsey, Ann R
Topham, David J
Scheible, Kristin M
Caserta, Mary T
Pryhuber, Gloria S
Gill, Steven R
author_sort Grier, Alex
collection PubMed
description BACKGROUND: Postnatal development of early life microbiota influences immunity, metabolism, neurodevelopment, and infant health. Microbiome development occurs at multiple body sites, with distinct community compositions and functions. Associations between microbiota at multiple sites represent an unexplored influence on the infant microbiome. Here, we examined co-occurrence patterns of gut and respiratory microbiota in pre- and full-term infants over the first year of life, a period critical to neonatal development. RESULTS: Gut and respiratory microbiota collected as longitudinal rectal, throat, and nasal samples from 38 pre-term and 44 full-term infants were first clustered into community state types (CSTs) on the basis of their compositional profiles. Multiple methods were used to relate the occurrence of CSTs to temporal microbiota development and measures of infant maturity, including gestational age (GA) at birth, week of life (WOL), and post-menstrual age (PMA). Manifestation of CSTs followed one of three patterns with respect to infant maturity: (1) chronological, with CST occurrence frequency solely a function of post-natal age (WOL), (2) idiosyncratic to maturity at birth, with the interval of CST occurrence dependent on infant post-natal age but the frequency of occurrence dependent on GA at birth, and (3) convergent, in which CSTs appear first in infants of greater maturity at birth, with occurrence frequency in pre-terms converging after a post-natal interval proportional to pre-maturity. The composition of CSTs was highly dissimilar between different body sites, but the CST of any one body site was highly predictive of the CSTs at other body sites. There were significant associations between the abundance of individual taxa at each body site and the CSTs of the other body sites, which persisted after stringent control for the non-linear effects of infant maturity. Canonical correlations exist between the microbiota composition at each pair of body sites, with the strongest correlations between proximal locations. CONCLUSION: These findings suggest that early microbiota is shaped by neonatal innate and adaptive developmental responses. Temporal progression of CST occurrence is influenced by infant maturity at birth and post-natal age. Significant associations of microbiota across body sites reveal distal connections and coordinated development of the infant microbial ecosystem. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s40168-018-0566-5) contains supplementary material, which is available to authorized users.
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spelling pubmed-62040112018-11-01 Neonatal gut and respiratory microbiota: coordinated development through time and space Grier, Alex McDavid, Andrew Wang, Bokai Qiu, Xing Java, James Bandyopadhyay, Sanjukta Yang, Hongmei Holden-Wiltse, Jeanne Kessler, Haeja A Gill, Ann L Huyck, Heidie Falsey, Ann R Topham, David J Scheible, Kristin M Caserta, Mary T Pryhuber, Gloria S Gill, Steven R Microbiome Research BACKGROUND: Postnatal development of early life microbiota influences immunity, metabolism, neurodevelopment, and infant health. Microbiome development occurs at multiple body sites, with distinct community compositions and functions. Associations between microbiota at multiple sites represent an unexplored influence on the infant microbiome. Here, we examined co-occurrence patterns of gut and respiratory microbiota in pre- and full-term infants over the first year of life, a period critical to neonatal development. RESULTS: Gut and respiratory microbiota collected as longitudinal rectal, throat, and nasal samples from 38 pre-term and 44 full-term infants were first clustered into community state types (CSTs) on the basis of their compositional profiles. Multiple methods were used to relate the occurrence of CSTs to temporal microbiota development and measures of infant maturity, including gestational age (GA) at birth, week of life (WOL), and post-menstrual age (PMA). Manifestation of CSTs followed one of three patterns with respect to infant maturity: (1) chronological, with CST occurrence frequency solely a function of post-natal age (WOL), (2) idiosyncratic to maturity at birth, with the interval of CST occurrence dependent on infant post-natal age but the frequency of occurrence dependent on GA at birth, and (3) convergent, in which CSTs appear first in infants of greater maturity at birth, with occurrence frequency in pre-terms converging after a post-natal interval proportional to pre-maturity. The composition of CSTs was highly dissimilar between different body sites, but the CST of any one body site was highly predictive of the CSTs at other body sites. There were significant associations between the abundance of individual taxa at each body site and the CSTs of the other body sites, which persisted after stringent control for the non-linear effects of infant maturity. Canonical correlations exist between the microbiota composition at each pair of body sites, with the strongest correlations between proximal locations. CONCLUSION: These findings suggest that early microbiota is shaped by neonatal innate and adaptive developmental responses. Temporal progression of CST occurrence is influenced by infant maturity at birth and post-natal age. Significant associations of microbiota across body sites reveal distal connections and coordinated development of the infant microbial ecosystem. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s40168-018-0566-5) contains supplementary material, which is available to authorized users. BioMed Central 2018-10-26 /pmc/articles/PMC6204011/ /pubmed/30367675 http://dx.doi.org/10.1186/s40168-018-0566-5 Text en © The Author(s). 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. 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.
spellingShingle Research
Grier, Alex
McDavid, Andrew
Wang, Bokai
Qiu, Xing
Java, James
Bandyopadhyay, Sanjukta
Yang, Hongmei
Holden-Wiltse, Jeanne
Kessler, Haeja A
Gill, Ann L
Huyck, Heidie
Falsey, Ann R
Topham, David J
Scheible, Kristin M
Caserta, Mary T
Pryhuber, Gloria S
Gill, Steven R
Neonatal gut and respiratory microbiota: coordinated development through time and space
title Neonatal gut and respiratory microbiota: coordinated development through time and space
title_full Neonatal gut and respiratory microbiota: coordinated development through time and space
title_fullStr Neonatal gut and respiratory microbiota: coordinated development through time and space
title_full_unstemmed Neonatal gut and respiratory microbiota: coordinated development through time and space
title_short Neonatal gut and respiratory microbiota: coordinated development through time and space
title_sort neonatal gut and respiratory microbiota: coordinated development through time and space
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6204011/
https://www.ncbi.nlm.nih.gov/pubmed/30367675
http://dx.doi.org/10.1186/s40168-018-0566-5
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