Association between gut microbiota, microbial network, and immunity in pregnancy with a focus on specific bacterial clusters

The community characteristics of the gut microbiota are not well defined and are not as widely studied as the functions of individual bacteria. This study aims to investigate the community composition of intestinal flora in women of childbearing age by conducting cluster analysis of gut microbiota a...

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Published inFrontiers in microbiology Vol. 14; p. 1314257
Main Authors Yan, Hao, Liang, Xinyuan, Luo, Huijuan, Tang, Xiaomei, Xiao, Xiaomin
Format Journal Article
LanguageEnglish
Published Switzerland Frontiers Media S.A 13.12.2023
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ISSN1664-302X
1664-302X
DOI10.3389/fmicb.2023.1314257

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Abstract The community characteristics of the gut microbiota are not well defined and are not as widely studied as the functions of individual bacteria. This study aims to investigate the community composition of intestinal flora in women of childbearing age by conducting cluster analysis of gut microbiota and analyzing the relationship between different clusters and immune status. A total of 45 women of childbearing age were recruited in the study, including 15 non-pregnant women and 30 women in late pregnancy, and stool samples were collected twice during the third trimester, specifically at 32 weeks and at full term. The gut microbiota data was analyzed using 16S rRNA amplicon sequencing. Partitioning Around Medoids algorithm was employed to assess microbial clustering patterns. Microbial network for each cluster was performed and plasm cytokines were measured to analyze the relationship between specific genera and immune state in clusters. There were three distinct clusters of intestinal community composition in women of childbearing age. Cluster 1 (PAM_1) was characterized by a high abundance of , while cluster 2 (PAM_2) showed higher levels of and , along with a significantly increased Firmicutes to Bacteroidota ratio. Cluster 3 (PAM_3) displayed a high abundance of . PAM_1 was the most dominant cluster in non-pregnant women, and this dominant cluster was also one of the main in late pregnancy. At full term, the majority of subjects retained the same cluster as at 32 weeks, while a few experienced a shift. The microbial correlation networks differed across the three clusters, with PAM_1 exhibiting higher modularity and fewer connections. Analysis of the correlation between genera and plasma cytokines showed significant differences in their associations with cytokines between pregnancy and nonpregnancy within the same cluster, and the same genera had different effects in different clusters. Women of childbearing age exhibit three distribution patterns of gut microbiota, and the intestinal clusters reshaped during late pregnancy in a small population. Different clusters may have diverse immunomodulatory effects in different physiological states. When studying the gut microbiome during pregnancy, it is crucial to consider the cluster differences within healthy women.
AbstractList BackgroundThe community characteristics of the gut microbiota are not well defined and are not as widely studied as the functions of individual bacteria. This study aims to investigate the community composition of intestinal flora in women of childbearing age by conducting cluster analysis of gut microbiota and analyzing the relationship between different clusters and immune status.MethodsA total of 45 women of childbearing age were recruited in the study, including 15 non-pregnant women and 30 women in late pregnancy, and stool samples were collected twice during the third trimester, specifically at 32 weeks and at full term. The gut microbiota data was analyzed using 16S rRNA amplicon sequencing. Partitioning Around Medoids algorithm was employed to assess microbial clustering patterns. Microbial network for each cluster was performed and plasm cytokines were measured to analyze the relationship between specific genera and immune state in clusters.ResultsThere were three distinct clusters of intestinal community composition in women of childbearing age. Cluster 1 (PAM_1) was characterized by a high abundance of Bacteroides, while cluster 2 (PAM_2) showed higher levels of Bifidobacterium and Blautia, along with a significantly increased Firmicutes to Bacteroidota ratio. Cluster 3 (PAM_3) displayed a high abundance of Escherichia-shigella. PAM_1 was the most dominant cluster in non-pregnant women, and this dominant cluster was also one of the main in late pregnancy. At full term, the majority of subjects retained the same cluster as at 32 weeks, while a few experienced a shift. The microbial correlation networks differed across the three clusters, with PAM_1 exhibiting higher modularity and fewer connections. Analysis of the correlation between genera and plasma cytokines showed significant differences in their associations with cytokines between pregnancy and nonpregnancy within the same cluster, and the same genera had different effects in different clusters.ConclusionWomen of childbearing age exhibit three distribution patterns of gut microbiota, and the intestinal clusters reshaped during late pregnancy in a small population. Different clusters may have diverse immunomodulatory effects in different physiological states. When studying the gut microbiome during pregnancy, it is crucial to consider the cluster differences within healthy women.
The community characteristics of the gut microbiota are not well defined and are not as widely studied as the functions of individual bacteria. This study aims to investigate the community composition of intestinal flora in women of childbearing age by conducting cluster analysis of gut microbiota and analyzing the relationship between different clusters and immune status. A total of 45 women of childbearing age were recruited in the study, including 15 non-pregnant women and 30 women in late pregnancy, and stool samples were collected twice during the third trimester, specifically at 32 weeks and at full term. The gut microbiota data was analyzed using 16S rRNA amplicon sequencing. Partitioning Around Medoids algorithm was employed to assess microbial clustering patterns. Microbial network for each cluster was performed and plasm cytokines were measured to analyze the relationship between specific genera and immune state in clusters. There were three distinct clusters of intestinal community composition in women of childbearing age. Cluster 1 (PAM_1) was characterized by a high abundance of , while cluster 2 (PAM_2) showed higher levels of and , along with a significantly increased Firmicutes to Bacteroidota ratio. Cluster 3 (PAM_3) displayed a high abundance of . PAM_1 was the most dominant cluster in non-pregnant women, and this dominant cluster was also one of the main in late pregnancy. At full term, the majority of subjects retained the same cluster as at 32 weeks, while a few experienced a shift. The microbial correlation networks differed across the three clusters, with PAM_1 exhibiting higher modularity and fewer connections. Analysis of the correlation between genera and plasma cytokines showed significant differences in their associations with cytokines between pregnancy and nonpregnancy within the same cluster, and the same genera had different effects in different clusters. Women of childbearing age exhibit three distribution patterns of gut microbiota, and the intestinal clusters reshaped during late pregnancy in a small population. Different clusters may have diverse immunomodulatory effects in different physiological states. When studying the gut microbiome during pregnancy, it is crucial to consider the cluster differences within healthy women.
The community characteristics of the gut microbiota are not well defined and are not as widely studied as the functions of individual bacteria. This study aims to investigate the community composition of intestinal flora in women of childbearing age by conducting cluster analysis of gut microbiota and analyzing the relationship between different clusters and immune status.BackgroundThe community characteristics of the gut microbiota are not well defined and are not as widely studied as the functions of individual bacteria. This study aims to investigate the community composition of intestinal flora in women of childbearing age by conducting cluster analysis of gut microbiota and analyzing the relationship between different clusters and immune status.A total of 45 women of childbearing age were recruited in the study, including 15 non-pregnant women and 30 women in late pregnancy, and stool samples were collected twice during the third trimester, specifically at 32 weeks and at full term. The gut microbiota data was analyzed using 16S rRNA amplicon sequencing. Partitioning Around Medoids algorithm was employed to assess microbial clustering patterns. Microbial network for each cluster was performed and plasm cytokines were measured to analyze the relationship between specific genera and immune state in clusters.MethodsA total of 45 women of childbearing age were recruited in the study, including 15 non-pregnant women and 30 women in late pregnancy, and stool samples were collected twice during the third trimester, specifically at 32 weeks and at full term. The gut microbiota data was analyzed using 16S rRNA amplicon sequencing. Partitioning Around Medoids algorithm was employed to assess microbial clustering patterns. Microbial network for each cluster was performed and plasm cytokines were measured to analyze the relationship between specific genera and immune state in clusters.There were three distinct clusters of intestinal community composition in women of childbearing age. Cluster 1 (PAM_1) was characterized by a high abundance of Bacteroides, while cluster 2 (PAM_2) showed higher levels of Bifidobacterium and Blautia, along with a significantly increased Firmicutes to Bacteroidota ratio. Cluster 3 (PAM_3) displayed a high abundance of Escherichia-shigella. PAM_1 was the most dominant cluster in non-pregnant women, and this dominant cluster was also one of the main in late pregnancy. At full term, the majority of subjects retained the same cluster as at 32 weeks, while a few experienced a shift. The microbial correlation networks differed across the three clusters, with PAM_1 exhibiting higher modularity and fewer connections. Analysis of the correlation between genera and plasma cytokines showed significant differences in their associations with cytokines between pregnancy and nonpregnancy within the same cluster, and the same genera had different effects in different clusters.ResultsThere were three distinct clusters of intestinal community composition in women of childbearing age. Cluster 1 (PAM_1) was characterized by a high abundance of Bacteroides, while cluster 2 (PAM_2) showed higher levels of Bifidobacterium and Blautia, along with a significantly increased Firmicutes to Bacteroidota ratio. Cluster 3 (PAM_3) displayed a high abundance of Escherichia-shigella. PAM_1 was the most dominant cluster in non-pregnant women, and this dominant cluster was also one of the main in late pregnancy. At full term, the majority of subjects retained the same cluster as at 32 weeks, while a few experienced a shift. The microbial correlation networks differed across the three clusters, with PAM_1 exhibiting higher modularity and fewer connections. Analysis of the correlation between genera and plasma cytokines showed significant differences in their associations with cytokines between pregnancy and nonpregnancy within the same cluster, and the same genera had different effects in different clusters.Women of childbearing age exhibit three distribution patterns of gut microbiota, and the intestinal clusters reshaped during late pregnancy in a small population. Different clusters may have diverse immunomodulatory effects in different physiological states. When studying the gut microbiome during pregnancy, it is crucial to consider the cluster differences within healthy women.ConclusionWomen of childbearing age exhibit three distribution patterns of gut microbiota, and the intestinal clusters reshaped during late pregnancy in a small population. Different clusters may have diverse immunomodulatory effects in different physiological states. When studying the gut microbiome during pregnancy, it is crucial to consider the cluster differences within healthy women.
Author Yan, Hao
Liang, Xinyuan
Xiao, Xiaomin
Tang, Xiaomei
Luo, Huijuan
AuthorAffiliation 1 Department of Obstetrics and Gynecology, The First Affiliated Hospital of Jinan University , Guangzhou , China
2 Department of Obstetrics, The Second Clinical Medical College (Shenzhen People's Hospital), Jinan University , Shenzhen , China
AuthorAffiliation_xml – name: 2 Department of Obstetrics, The Second Clinical Medical College (Shenzhen People's Hospital), Jinan University , Shenzhen , China
– name: 1 Department of Obstetrics and Gynecology, The First Affiliated Hospital of Jinan University , Guangzhou , China
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CitedBy_id crossref_primary_10_1016_j_jff_2024_106620
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Cites_doi 10.1016/j.ogc.2016.07.004
10.1038/s41522-019-0101-x
10.1038/s41467-023-38558-7
10.1038/s41522-023-00383-7
10.1111/imr.13075
10.1038/s41591-018-0164-x
10.3390/nu12051474
10.1016/j.tibtech.2015.06.011
10.1136/gutjnl-2021-326789
10.3390/ijms22041778
10.1111/imr.13080
10.1038/s41586-020-2971-8
10.1186/gb-2011-12-5-r50
10.1038/s41522-021-00245-0
10.1016/j.immuni.2018.07.017
10.1016/j.cell.2021.06.019
10.1080/19490976.2021.1875796
10.1016/j.celrep.2019.03.075
10.1007/s00018-020-03674-w
10.3389/fmicb.2023.1114228
10.1038/ni.3780
10.3389/fendo.2022.970825
10.1080/19490976.2020.1730294
10.1016/j.cell.2012.07.008
10.1007/s00284-013-0491-6
10.1016/j.ebiom.2021.103602
10.1186/s40168-021-01089-8
10.1073/pnas.1502875112
10.1016/j.mib.2017.07.003
10.3109/10408369709038216
10.1038/nature11234
10.1038/ismej.2016.176
10.1186/gb-2011-12-6-r60
10.1101/gr.1239303
10.1016/j.chom.2022.05.004
10.1038/nature09944
10.1016/j.cgh.2018.08.067
10.1136/gutjnl-2022-328970
10.3389/fcimb.2022.824925
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Keywords microbial network
immunity
cluster analysis
gut microbiota
pregnancy
Language English
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References Garcia-Mantrana (ref11) 2020; 11
Menon (ref23) 2022; 308
Xiao (ref36) 2023; 72
True (ref33) 2022; 308
(ref10) 2021; 71
(ref13) 2012; 486
Nuriel-Ohayon (ref24) 2019; 27
Yang (ref37) 2023; 9
Caporaso (ref6) 2011; 12
Ozato (ref25) 2019; 5
Liu (ref18) 2021; 13
Lu (ref21) 2021; 7
Jost (ref14) 2014; 68
Vavreckova (ref34) 2022; 13
Arumugam (ref1) 2011; 473
Litvak (ref17) 2017; 39
Rio-Aige (ref27) 2021; 22
DiGiulio (ref8) 2015; 112
Schluter (ref28) 2020; 588
He (ref12) 2018; 24
Tap (ref32) 2023; 14
Bonney (ref4) 2016; 43
Berry (ref2) 2021; 9
Zakaria (ref39) 2022; 12
Shin (ref31) 2015; 33
Segata (ref29) 2011; 12
Blander (ref3) 2017; 18
Yockey (ref38) 2018; 49
Koren (ref15) 2012; 150
Lopez-Siles (ref20) 2017; 11
Lockitch (ref19) 1997; 34
Rice (ref26) 2022; 30
Shannon (ref30) 2003; 13
Wastyk (ref35) 2021; 184
Bowman (ref5) 2021; 78
Li (ref16) 2023; 14
Magne (ref22) 2020; 12
de Vos (ref7) 2022; 71
Dong (ref9) 2019; 17
References_xml – volume: 43
  start-page: 679
  year: 2016
  ident: ref4
  article-title: Immune regulation in pregnancy: a matter of perspective?
  publication-title: Obstet. Gynecol. Clin. N. Am.
  doi: 10.1016/j.ogc.2016.07.004
– volume: 5
  start-page: 28
  year: 2019
  ident: ref25
  article-title: Blautia genus associated with visceral fat accumulation in adults 20-76 years of age
  publication-title: NPJ Biofilms Microbiom.
  doi: 10.1038/s41522-019-0101-x
– volume: 14
  start-page: 3310
  year: 2023
  ident: ref32
  article-title: Global branches and local states of the human gut microbiome define associations with environmental and intrinsic factors
  publication-title: Nat. Commun.
  doi: 10.1038/s41467-023-38558-7
– volume: 9
  start-page: 14
  year: 2023
  ident: ref37
  article-title: Ecological change of the gut microbiota during pregnancy and progression to dyslipidemia
  publication-title: NPJ Biofilms Microbiom.
  doi: 10.1038/s41522-023-00383-7
– volume: 308
  start-page: 149
  year: 2022
  ident: ref23
  article-title: Fetal inflammatory response at the fetomaternal interface: a requirement for labor at term and preterm
  publication-title: Immunol. Rev.
  doi: 10.1111/imr.13075
– volume: 24
  start-page: 1532
  year: 2018
  ident: ref12
  article-title: Regional variation limits applications of healthy gut microbiome reference ranges and disease models
  publication-title: Nat. Med.
  doi: 10.1038/s41591-018-0164-x
– volume: 12
  start-page: 1474
  year: 2020
  ident: ref22
  article-title: The Firmicutes/Bacteroidetes ratio: a relevant marker of gut Dysbiosis in obese patients?
  publication-title: Nutrients
  doi: 10.3390/nu12051474
– volume: 33
  start-page: 496
  year: 2015
  ident: ref31
  article-title: Proteobacteria: microbial signature of dysbiosis in gut microbiota
  publication-title: Trends Biotechnol.
  doi: 10.1016/j.tibtech.2015.06.011
– volume: 71
  start-page: 1020
  year: 2022
  ident: ref7
  article-title: Gut microbiome and health: mechanistic insights
  publication-title: Gut
  doi: 10.1136/gutjnl-2021-326789
– volume: 22
  start-page: 1778
  year: 2021
  ident: ref27
  article-title: Association of Maternal Microbiota and Diet in cord blood cytokine and immunoglobulin profiles
  publication-title: Int. J. Mol. Sci.
  doi: 10.3390/ijms22041778
– volume: 308
  start-page: 77
  year: 2022
  ident: ref33
  article-title: Monocytes and macrophages in pregnancy: the good, the bad, and the ugly
  publication-title: Immunol. Rev.
  doi: 10.1111/imr.13080
– volume: 588
  start-page: 303
  year: 2020
  ident: ref28
  article-title: The gut microbiota is associated with immune cell dynamics in humans
  publication-title: Nature
  doi: 10.1038/s41586-020-2971-8
– volume: 12
  start-page: R50
  year: 2011
  ident: ref6
  article-title: Moving pictures of the human microbiome
  publication-title: Genome Biol.
  doi: 10.1186/gb-2011-12-5-r50
– volume: 7
  start-page: 71
  year: 2021
  ident: ref21
  article-title: Chinese gut microbiota and its associations with staple food type, ethnicity, and urbanization
  publication-title: NPJ Biofilms Microbiom.
  doi: 10.1038/s41522-021-00245-0
– volume: 49
  start-page: 397
  year: 2018
  ident: ref38
  article-title: Interferons and Proinflammatory cytokines in pregnancy and fetal development
  publication-title: Immunity
  doi: 10.1016/j.immuni.2018.07.017
– volume: 184
  start-page: 4137
  year: 2021
  ident: ref35
  article-title: Gut-microbiota-targeted diets modulate human immune status
  publication-title: Cells
  doi: 10.1016/j.cell.2021.06.019
– volume: 13
  start-page: 1
  year: 2021
  ident: ref18
  article-title: Blautia-a new functional genus with potential probiotic properties?
  publication-title: Gut Microbes
  doi: 10.1080/19490976.2021.1875796
– volume: 27
  start-page: 730
  year: 2019
  ident: ref24
  article-title: Progesterone increases Bifidobacterium relative abundance during late pregnancy
  publication-title: Cell Rep.
  doi: 10.1016/j.celrep.2019.03.075
– volume: 78
  start-page: 1455
  year: 2021
  ident: ref5
  article-title: Regulation of maternal-fetal metabolic communication
  publication-title: Cell. Mol. Life Sci.
  doi: 10.1007/s00018-020-03674-w
– volume: 14
  start-page: 1114228
  year: 2023
  ident: ref16
  article-title: Dynamic changes in gut microbiota during pregnancy among Chinese women and influencing factors: a prospective cohort study
  publication-title: Front. Microbiol.
  doi: 10.3389/fmicb.2023.1114228
– volume: 18
  start-page: 851
  year: 2017
  ident: ref3
  article-title: Regulation of inflammation by microbiota interactions with the host
  publication-title: Nat. Immunol.
  doi: 10.1038/ni.3780
– volume: 13
  start-page: 970825
  year: 2022
  ident: ref34
  article-title: Specific gut bacterial and fungal microbiota pattern in the first half of pregnancy is linked to the development of gestational diabetes mellitus in the cohort including obese women
  publication-title: Front. Endocrinol. (Lausanne)
  doi: 10.3389/fendo.2022.970825
– volume: 11
  start-page: 962
  year: 2020
  ident: ref11
  article-title: Distinct maternal microbiota clusters are associated with diet during pregnancy: impact on neonatal microbiota and infant growth during the first 18 months of life
  publication-title: Gut Microbes
  doi: 10.1080/19490976.2020.1730294
– volume: 150
  start-page: 470
  year: 2012
  ident: ref15
  article-title: Host remodeling of the gut microbiome and metabolic changes during pregnancy
  publication-title: Cells
  doi: 10.1016/j.cell.2012.07.008
– volume: 68
  start-page: 419
  year: 2014
  ident: ref14
  article-title: Stability of the maternal gut microbiota during late pregnancy and early lactation
  publication-title: Curr. Microbiol.
  doi: 10.1007/s00284-013-0491-6
– volume: 71
  start-page: 103602
  year: 2021
  ident: ref10
  article-title: The maternal microbiome: another bridge linking mothers and infants
  publication-title: EBioMedicine
  doi: 10.1016/j.ebiom.2021.103602
– volume: 9
  start-page: 146
  year: 2021
  ident: ref2
  article-title: Remodeling of the maternal gut microbiome during pregnancy is shaped by parity
  publication-title: Microbiome
  doi: 10.1186/s40168-021-01089-8
– volume: 112
  start-page: 11060
  year: 2015
  ident: ref8
  article-title: Temporal and spatial variation of the human microbiota during pregnancy
  publication-title: Proc. Natl. Acad. Sci. U. S. A.
  doi: 10.1073/pnas.1502875112
– volume: 39
  start-page: 1
  year: 2017
  ident: ref17
  article-title: Dysbiotic Proteobacteria expansion: a microbial signature of epithelial dysfunction
  publication-title: Curr. Opin. Microbiol.
  doi: 10.1016/j.mib.2017.07.003
– volume: 34
  start-page: 67
  year: 1997
  ident: ref19
  article-title: Clinical biochemistry of pregnancy
  publication-title: Crit. Rev. Clin. Lab. Sci.
  doi: 10.3109/10408369709038216
– volume: 486
  start-page: 207
  year: 2012
  ident: ref13
  article-title: Structure, function and diversity of the healthy human microbiome
  publication-title: Nature
  doi: 10.1038/nature11234
– volume: 11
  start-page: 841
  year: 2017
  ident: ref20
  article-title: Faecalibacterium prausnitzii: from microbiology to diagnostics and prognostics
  publication-title: ISME J.
  doi: 10.1038/ismej.2016.176
– volume: 12
  start-page: R60
  year: 2011
  ident: ref29
  article-title: Metagenomic biomarker discovery and explanation
  publication-title: Genome Biol.
  doi: 10.1186/gb-2011-12-6-r60
– volume: 13
  start-page: 2498
  year: 2003
  ident: ref30
  article-title: Cytoscape: a software environment for integrated models of biomolecular interaction networks
  publication-title: Genome Res.
  doi: 10.1101/gr.1239303
– volume: 30
  start-page: 988
  year: 2022
  ident: ref26
  article-title: Interspecies commensal interactions have nonlinear impacts on host immunity
  publication-title: Cell Host Microbe
  doi: 10.1016/j.chom.2022.05.004
– volume: 473
  start-page: 174
  year: 2011
  ident: ref1
  article-title: Enterotypes of the human gut microbiome
  publication-title: Nature
  doi: 10.1038/nature09944
– volume: 17
  start-page: 231
  year: 2019
  ident: ref9
  article-title: Influence of early life, diet, and the environment on the microbiome
  publication-title: Clin. Gastroenterol. Hepatol.
  doi: 10.1016/j.cgh.2018.08.067
– volume: 72
  start-page: 772
  year: 2023
  ident: ref36
  article-title: Microbial transmission, colonisation and succession: from pregnancy to infancy
  publication-title: Gut
  doi: 10.1136/gutjnl-2022-328970
– volume: 12
  start-page: 824925
  year: 2022
  ident: ref39
  article-title: Physiological changes and interactions between microbiome and the host during pregnancy
  publication-title: Front. Cell. Infect. Microbiol.
  doi: 10.3389/fcimb.2022.824925
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Snippet The community characteristics of the gut microbiota are not well defined and are not as widely studied as the functions of individual bacteria. This study aims...
BackgroundThe community characteristics of the gut microbiota are not well defined and are not as widely studied as the functions of individual bacteria. This...
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SubjectTerms cluster analysis
gut microbiota
immunity
microbial network
Microbiology
pregnancy
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Title Association between gut microbiota, microbial network, and immunity in pregnancy with a focus on specific bacterial clusters
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