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Individuality of the Extremely Premature Infant Gut Microbiota Is Driven by Ecological Drift
The initial contact between humans and their colonizing gut microbiota after birth is thought to have expansive and long-lasting consequences for physiology and health. Premature infants are at high risk of suffering from lifelong impairments, due in part to aberrant development of gut microbiota th...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Society for Microbiology
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9238403/ https://www.ncbi.nlm.nih.gov/pubmed/35473303 http://dx.doi.org/10.1128/msystems.00163-22 |
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author | Seki, David Schauberger, Clemens Hausmann, Bela Berger, Angelika Wisgrill, Lukas Berry, David |
author_facet | Seki, David Schauberger, Clemens Hausmann, Bela Berger, Angelika Wisgrill, Lukas Berry, David |
author_sort | Seki, David |
collection | PubMed |
description | The initial contact between humans and their colonizing gut microbiota after birth is thought to have expansive and long-lasting consequences for physiology and health. Premature infants are at high risk of suffering from lifelong impairments, due in part to aberrant development of gut microbiota that can contribute to early-life infections and inflammation. Despite their importance to health, the ecological assembly and succession processes governing gut microbiome composition in premature infants remained incompletely understood. Here, we quantified these ecological processes in a spatiotemporally resolved 16S rRNA gene amplicon sequencing data set of 60 extremely premature neonates using an established mathematical framework. We found that gut colonization during the first months of life is predominantly stochastic, whereby interindividual diversification of microbiota is driven by ecological drift. Dispersal limitations are initially small but have increasing influence at later stages of succession. Furthermore, we find similar trends in a cohort of 32 healthy term-born infants. These results suggest that the uniqueness of individual gut microbiota of extremely premature infants is largely due to stochastic assembly. IMPORTANCE Our knowledge concerning the initial gut microbiome assembly in human neonates is limited, and scientific progression in this interdisciplinary field is hindered due to the individuality in composition of gut microbiota. Our study addresses the ecological processes that result in the observed individuality of microbes in the gastrointestinal tract between extremely premature and term-born infants. We find that initial assembly is mainly driven by neutral ecological processes. Interestingly, while this progression is predominantly random, limitations to the dispersal of microbiota between infants become increasingly important with age and are concomitant features of gut microbiome stability. This indicates that while we cannot predict gut microbiota assembly due to its random nature, we can expect the establishment of certain ecological features that are highly relevant for neonatal health. |
format | Online Article Text |
id | pubmed-9238403 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | American Society for Microbiology |
record_format | MEDLINE/PubMed |
spelling | pubmed-92384032022-06-29 Individuality of the Extremely Premature Infant Gut Microbiota Is Driven by Ecological Drift Seki, David Schauberger, Clemens Hausmann, Bela Berger, Angelika Wisgrill, Lukas Berry, David mSystems Research Article The initial contact between humans and their colonizing gut microbiota after birth is thought to have expansive and long-lasting consequences for physiology and health. Premature infants are at high risk of suffering from lifelong impairments, due in part to aberrant development of gut microbiota that can contribute to early-life infections and inflammation. Despite their importance to health, the ecological assembly and succession processes governing gut microbiome composition in premature infants remained incompletely understood. Here, we quantified these ecological processes in a spatiotemporally resolved 16S rRNA gene amplicon sequencing data set of 60 extremely premature neonates using an established mathematical framework. We found that gut colonization during the first months of life is predominantly stochastic, whereby interindividual diversification of microbiota is driven by ecological drift. Dispersal limitations are initially small but have increasing influence at later stages of succession. Furthermore, we find similar trends in a cohort of 32 healthy term-born infants. These results suggest that the uniqueness of individual gut microbiota of extremely premature infants is largely due to stochastic assembly. IMPORTANCE Our knowledge concerning the initial gut microbiome assembly in human neonates is limited, and scientific progression in this interdisciplinary field is hindered due to the individuality in composition of gut microbiota. Our study addresses the ecological processes that result in the observed individuality of microbes in the gastrointestinal tract between extremely premature and term-born infants. We find that initial assembly is mainly driven by neutral ecological processes. Interestingly, while this progression is predominantly random, limitations to the dispersal of microbiota between infants become increasingly important with age and are concomitant features of gut microbiome stability. This indicates that while we cannot predict gut microbiota assembly due to its random nature, we can expect the establishment of certain ecological features that are highly relevant for neonatal health. American Society for Microbiology 2022-04-27 /pmc/articles/PMC9238403/ /pubmed/35473303 http://dx.doi.org/10.1128/msystems.00163-22 Text en Copyright © 2022 Seki et al. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Research Article Seki, David Schauberger, Clemens Hausmann, Bela Berger, Angelika Wisgrill, Lukas Berry, David Individuality of the Extremely Premature Infant Gut Microbiota Is Driven by Ecological Drift |
title | Individuality of the Extremely Premature Infant Gut Microbiota Is Driven by Ecological Drift |
title_full | Individuality of the Extremely Premature Infant Gut Microbiota Is Driven by Ecological Drift |
title_fullStr | Individuality of the Extremely Premature Infant Gut Microbiota Is Driven by Ecological Drift |
title_full_unstemmed | Individuality of the Extremely Premature Infant Gut Microbiota Is Driven by Ecological Drift |
title_short | Individuality of the Extremely Premature Infant Gut Microbiota Is Driven by Ecological Drift |
title_sort | individuality of the extremely premature infant gut microbiota is driven by ecological drift |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9238403/ https://www.ncbi.nlm.nih.gov/pubmed/35473303 http://dx.doi.org/10.1128/msystems.00163-22 |
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