Parity influences postpartum adaptations in the maternal gut microbiota

Abstract The gut microbiome undergoes substantial modifications during pregnancy, yet its postpartum adaptations remain poorly understood, particularly with respect to the influence of parity. Here, we investigated the impact of childbirth history on maternal gut microbiome composition and function...

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Main Authors: Zharkyn Jarmukhanov, Elizaveta Vinogradova, Nurislam Mukhanbetzhanov, Samat Kozhakhmetov, Deniza Khassenbekova, Almagul Kushugulova
Format: Article
Language:English
Published: Nature Portfolio 2025-05-01
Series:Scientific Reports
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Online Access:https://doi.org/10.1038/s41598-025-02013-y
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author Zharkyn Jarmukhanov
Elizaveta Vinogradova
Nurislam Mukhanbetzhanov
Samat Kozhakhmetov
Deniza Khassenbekova
Almagul Kushugulova
author_facet Zharkyn Jarmukhanov
Elizaveta Vinogradova
Nurislam Mukhanbetzhanov
Samat Kozhakhmetov
Deniza Khassenbekova
Almagul Kushugulova
author_sort Zharkyn Jarmukhanov
collection DOAJ
description Abstract The gut microbiome undergoes substantial modifications during pregnancy, yet its postpartum adaptations remain poorly understood, particularly with respect to the influence of parity. Here, we investigated the impact of childbirth history on maternal gut microbiome composition and function one month postpartum. By conducting metagenomic sequencing analysis on 60 participants (34 postpartum mothers and 26 controls), we demonstrated significant differences in microbial diversity and community structure between postpartum mothers and control, as well as subtle differences between first-time mothers and multiple-birth mothers. We identified parity-specific signatures, with first-time mothers showing enrichment in Dysosmobacter welbionis, Candidatus Saccharibacteria, and Anaerotruncus species. Functional analysis revealed distinct metabolic reprogramming patterns, including increased amino acid biosynthesis and modified fermentation pathways supporting postpartum recovery. We observed significant correlations between specific bacterial taxa and metabolic pathways, particularly in energy metabolism and immune modulation. Notably, the enhanced capacity for short-chain fatty acid production in primiparous mothers, mediated by Anaerotruncus and Dysosmobacter welbionis, suggests a potential role in shaping breast milk composition, which may influence neonatal development. These findings establish the concept of parity-dependent microbiome programming and provide insights into the biological mechanisms underlying maternal adaptation to pregnancy and childbirth.
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spelling doaj-art-6bba3e4df1fa459b82880eb8bd4a08302025-08-20T01:53:18ZengNature PortfolioScientific Reports2045-23222025-05-011511810.1038/s41598-025-02013-yParity influences postpartum adaptations in the maternal gut microbiotaZharkyn Jarmukhanov0Elizaveta Vinogradova1Nurislam Mukhanbetzhanov2Samat Kozhakhmetov3Deniza Khassenbekova4Almagul Kushugulova5Laboratory of Microbiome, Center for Life Sciences, National Laboratory Astana, Nazarbayev UniversityLaboratory of Microbiome, Center for Life Sciences, National Laboratory Astana, Nazarbayev UniversityLaboratory of Microbiome, Center for Life Sciences, National Laboratory Astana, Nazarbayev UniversityLaboratory of Microbiome, Center for Life Sciences, National Laboratory Astana, Nazarbayev UniversityNazarbayev Intellectual School of Physics and MathematicsLaboratory of Microbiome, Center for Life Sciences, National Laboratory Astana, Nazarbayev UniversityAbstract The gut microbiome undergoes substantial modifications during pregnancy, yet its postpartum adaptations remain poorly understood, particularly with respect to the influence of parity. Here, we investigated the impact of childbirth history on maternal gut microbiome composition and function one month postpartum. By conducting metagenomic sequencing analysis on 60 participants (34 postpartum mothers and 26 controls), we demonstrated significant differences in microbial diversity and community structure between postpartum mothers and control, as well as subtle differences between first-time mothers and multiple-birth mothers. We identified parity-specific signatures, with first-time mothers showing enrichment in Dysosmobacter welbionis, Candidatus Saccharibacteria, and Anaerotruncus species. Functional analysis revealed distinct metabolic reprogramming patterns, including increased amino acid biosynthesis and modified fermentation pathways supporting postpartum recovery. We observed significant correlations between specific bacterial taxa and metabolic pathways, particularly in energy metabolism and immune modulation. Notably, the enhanced capacity for short-chain fatty acid production in primiparous mothers, mediated by Anaerotruncus and Dysosmobacter welbionis, suggests a potential role in shaping breast milk composition, which may influence neonatal development. These findings establish the concept of parity-dependent microbiome programming and provide insights into the biological mechanisms underlying maternal adaptation to pregnancy and childbirth.https://doi.org/10.1038/s41598-025-02013-yGut MicrobiomePostpartumInfantsPregnancy
spellingShingle Zharkyn Jarmukhanov
Elizaveta Vinogradova
Nurislam Mukhanbetzhanov
Samat Kozhakhmetov
Deniza Khassenbekova
Almagul Kushugulova
Parity influences postpartum adaptations in the maternal gut microbiota
Scientific Reports
Gut Microbiome
Postpartum
Infants
Pregnancy
title Parity influences postpartum adaptations in the maternal gut microbiota
title_full Parity influences postpartum adaptations in the maternal gut microbiota
title_fullStr Parity influences postpartum adaptations in the maternal gut microbiota
title_full_unstemmed Parity influences postpartum adaptations in the maternal gut microbiota
title_short Parity influences postpartum adaptations in the maternal gut microbiota
title_sort parity influences postpartum adaptations in the maternal gut microbiota
topic Gut Microbiome
Postpartum
Infants
Pregnancy
url https://doi.org/10.1038/s41598-025-02013-y
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AT samatkozhakhmetov parityinfluencespostpartumadaptationsinthematernalgutmicrobiota
AT denizakhassenbekova parityinfluencespostpartumadaptationsinthematernalgutmicrobiota
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