Cargando…

Sources of gut microbiota variation in a large longitudinal Finnish infant cohort

BACKGROUND: Although the infant gut microbiota has been extensively studied, comprehensive assessment on the microbiota determinants including technical variables has not been performed in large infant cohorts. METHODS: We studied the effect of 109 variables on the 16S rRNA gene amplicon-based gut m...

Descripción completa

Detalles Bibliográficos
Autores principales: Jokela, Roosa, Ponsero, Alise J., Dikareva, Evgenia, Wei, Xiaodong, Kolho, Kaija-Leena, Korpela, Katri, de Vos, Willem M., Salonen, Anne
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10328818/
https://www.ncbi.nlm.nih.gov/pubmed/37399600
http://dx.doi.org/10.1016/j.ebiom.2023.104695
_version_ 1785069885579067392
author Jokela, Roosa
Ponsero, Alise J.
Dikareva, Evgenia
Wei, Xiaodong
Kolho, Kaija-Leena
Korpela, Katri
de Vos, Willem M.
Salonen, Anne
author_facet Jokela, Roosa
Ponsero, Alise J.
Dikareva, Evgenia
Wei, Xiaodong
Kolho, Kaija-Leena
Korpela, Katri
de Vos, Willem M.
Salonen, Anne
author_sort Jokela, Roosa
collection PubMed
description BACKGROUND: Although the infant gut microbiota has been extensively studied, comprehensive assessment on the microbiota determinants including technical variables has not been performed in large infant cohorts. METHODS: We studied the effect of 109 variables on the 16S rRNA gene amplicon-based gut microbiota profiles of infants sampled longitudinally from three weeks to two years of life in the Finnish HELMi birth cohort. Spot faecal samples from both parents were included for intra-family analyses, totalling to 7657 samples from 985 families that were evaluated for beta-diversity patterns using permutational multivariate analysis on Bray–Curtis distances, and differential abundance testing and alpha-diversity for variables of interest. We also assessed the effect of different taxonomic levels and distance methods. FINDINGS: In time point-specific models, the largest share of variation explained, up to 2–6%, were seen in decreasing order for the DNA extraction batch, delivery mode and related perinatal exposures, defecation frequency and parity/siblings. Variables describing the infant gastrointestinal function were continuously important during the first two years, reflecting changes in e.g., feeding habits. The effect of parity/siblings on infant microbiota was modified by birth mode and exposure to intrapartum antibiotics, exemplifying the tight interlinkage of perinatal factors relevant for infant microbiota research. In total, up to 19% of the biological microbiota variation in the infant gut could be explained. Our results highlight the need to interpret variance partitioning results in the context of each cohort's characteristics and microbiota processing. INTERPRETATION: Our study provides a comprehensive report of key factors associated with infant gut microbiota composition across the two first years of life in a homogenous cohort. The study highlights possible important future research areas and confounding factors to be considered. FUNDING: This research was supported by 10.13039/501100014438Business Finland, 10.13039/501100002341Academy of Finland, Foundation for Nutrition Research and the Doctoral Program in Microbiology and Biotechnology, University of Helsinki, Finland.
format Online
Article
Text
id pubmed-10328818
institution National Center for Biotechnology Information
language English
publishDate 2023
publisher Elsevier
record_format MEDLINE/PubMed
spelling pubmed-103288182023-07-09 Sources of gut microbiota variation in a large longitudinal Finnish infant cohort Jokela, Roosa Ponsero, Alise J. Dikareva, Evgenia Wei, Xiaodong Kolho, Kaija-Leena Korpela, Katri de Vos, Willem M. Salonen, Anne eBioMedicine Articles BACKGROUND: Although the infant gut microbiota has been extensively studied, comprehensive assessment on the microbiota determinants including technical variables has not been performed in large infant cohorts. METHODS: We studied the effect of 109 variables on the 16S rRNA gene amplicon-based gut microbiota profiles of infants sampled longitudinally from three weeks to two years of life in the Finnish HELMi birth cohort. Spot faecal samples from both parents were included for intra-family analyses, totalling to 7657 samples from 985 families that were evaluated for beta-diversity patterns using permutational multivariate analysis on Bray–Curtis distances, and differential abundance testing and alpha-diversity for variables of interest. We also assessed the effect of different taxonomic levels and distance methods. FINDINGS: In time point-specific models, the largest share of variation explained, up to 2–6%, were seen in decreasing order for the DNA extraction batch, delivery mode and related perinatal exposures, defecation frequency and parity/siblings. Variables describing the infant gastrointestinal function were continuously important during the first two years, reflecting changes in e.g., feeding habits. The effect of parity/siblings on infant microbiota was modified by birth mode and exposure to intrapartum antibiotics, exemplifying the tight interlinkage of perinatal factors relevant for infant microbiota research. In total, up to 19% of the biological microbiota variation in the infant gut could be explained. Our results highlight the need to interpret variance partitioning results in the context of each cohort's characteristics and microbiota processing. INTERPRETATION: Our study provides a comprehensive report of key factors associated with infant gut microbiota composition across the two first years of life in a homogenous cohort. The study highlights possible important future research areas and confounding factors to be considered. FUNDING: This research was supported by 10.13039/501100014438Business Finland, 10.13039/501100002341Academy of Finland, Foundation for Nutrition Research and the Doctoral Program in Microbiology and Biotechnology, University of Helsinki, Finland. Elsevier 2023-07-01 /pmc/articles/PMC10328818/ /pubmed/37399600 http://dx.doi.org/10.1016/j.ebiom.2023.104695 Text en © 2023 The Author(s) https://creativecommons.org/licenses/by/4.0/This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Articles
Jokela, Roosa
Ponsero, Alise J.
Dikareva, Evgenia
Wei, Xiaodong
Kolho, Kaija-Leena
Korpela, Katri
de Vos, Willem M.
Salonen, Anne
Sources of gut microbiota variation in a large longitudinal Finnish infant cohort
title Sources of gut microbiota variation in a large longitudinal Finnish infant cohort
title_full Sources of gut microbiota variation in a large longitudinal Finnish infant cohort
title_fullStr Sources of gut microbiota variation in a large longitudinal Finnish infant cohort
title_full_unstemmed Sources of gut microbiota variation in a large longitudinal Finnish infant cohort
title_short Sources of gut microbiota variation in a large longitudinal Finnish infant cohort
title_sort sources of gut microbiota variation in a large longitudinal finnish infant cohort
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10328818/
https://www.ncbi.nlm.nih.gov/pubmed/37399600
http://dx.doi.org/10.1016/j.ebiom.2023.104695
work_keys_str_mv AT jokelaroosa sourcesofgutmicrobiotavariationinalargelongitudinalfinnishinfantcohort
AT ponseroalisej sourcesofgutmicrobiotavariationinalargelongitudinalfinnishinfantcohort
AT dikarevaevgenia sourcesofgutmicrobiotavariationinalargelongitudinalfinnishinfantcohort
AT weixiaodong sourcesofgutmicrobiotavariationinalargelongitudinalfinnishinfantcohort
AT kolhokaijaleena sourcesofgutmicrobiotavariationinalargelongitudinalfinnishinfantcohort
AT korpelakatri sourcesofgutmicrobiotavariationinalargelongitudinalfinnishinfantcohort
AT devoswillemm sourcesofgutmicrobiotavariationinalargelongitudinalfinnishinfantcohort
AT salonenanne sourcesofgutmicrobiotavariationinalargelongitudinalfinnishinfantcohort