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...
Saved in:
Published in | Frontiers in microbiology Vol. 14; p. 1314257 |
---|---|
Main Authors | , , , , |
Format | Journal Article |
Language | English |
Published |
Switzerland
Frontiers Media S.A
13.12.2023
|
Subjects | |
Online Access | Get full text |
ISSN | 1664-302X 1664-302X |
DOI | 10.3389/fmicb.2023.1314257 |
Cover
Loading…
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 |
Author_xml | – sequence: 1 givenname: Hao surname: Yan fullname: Yan, Hao – sequence: 2 givenname: Xinyuan surname: Liang fullname: Liang, Xinyuan – sequence: 3 givenname: Huijuan surname: Luo fullname: Luo, Huijuan – sequence: 4 givenname: Xiaomei surname: Tang fullname: Tang, Xiaomei – sequence: 5 givenname: Xiaomin surname: Xiao fullname: Xiao, Xiaomin |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/38156011$$D View this record in MEDLINE/PubMed |
BookMark | eNp9kk1vFSEUhiemxtbaP-DCsHTRe-VzZliZpvGjSRM3mrgjwBxuqTNwBabNTfzxcj_atC5kASfwnueccN7XzVGIAZrmLcFLxnr5wU3emiXFlC0JI5yK7kVzQtqWLximP4-exMfNWc63uC6Oad1fNcesJ6LFhJw0fy5yjtbr4mNABso9QECruaCKT9H4WPT5Q6xHFKoipl_nSIcB-Wmagy8b5ANaJ1gFHewG3ftygzRy0c4ZVWheg_XOW2S0LZC2FDvOuYb5TfPS6THD2eE8bX58_vT98uvi-tuXq8uL64XlrSwL3oITnLeWOSatE51hPZfQGQFSE0la2mHumB4YONMNGqBvQViHhQXDqGSnzdWeO0R9q9bJTzptVNRe7S5iWimdircjKAyMk8oXwmyLgxRyELpnxBLTY-wq6-OetZ7NBIOFUJIen0GfvwR_o1bxThHcifrv227eHwgp_p4hFzX5bGEcdYA4Z0Ul7gnltKVV-u5psccqD_OrAroX1AHlnMA9SghWW5-onU_U1ifq4JOa1P-TZH3ZOaA27Mf_pf4F-CTGgg |
CitedBy_id | crossref_primary_10_1016_j_jff_2024_106620 crossref_primary_10_1007_s43657_024_00211_8 |
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 |
ContentType | Journal Article |
Copyright | Copyright © 2023 Yan, Liang, Luo, Tang and Xiao. Copyright © 2023 Yan, Liang, Luo, Tang and Xiao. 2023 Yan, Liang, Luo, Tang and Xiao |
Copyright_xml | – notice: Copyright © 2023 Yan, Liang, Luo, Tang and Xiao. – notice: Copyright © 2023 Yan, Liang, Luo, Tang and Xiao. 2023 Yan, Liang, Luo, Tang and Xiao |
DBID | AAYXX CITATION NPM 7X8 5PM DOA |
DOI | 10.3389/fmicb.2023.1314257 |
DatabaseName | CrossRef PubMed MEDLINE - Academic PubMed Central (Full Participant titles) DOAJ Directory of Open Access Journals |
DatabaseTitle | CrossRef PubMed MEDLINE - Academic |
DatabaseTitleList | PubMed MEDLINE - Academic |
Database_xml | – sequence: 1 dbid: DOA name: DOAJ Open Access Full Text url: https://www.doaj.org/ sourceTypes: Open Website – sequence: 2 dbid: NPM name: PubMed url: https://proxy.k.utb.cz/login?url=http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed sourceTypes: Index Database |
DeliveryMethod | fulltext_linktorsrc |
Discipline | Biology |
EISSN | 1664-302X |
ExternalDocumentID | oai_doaj_org_article_0e341b3855bc469e959d5a831c1b800f PMC10753819 38156011 10_3389_fmicb_2023_1314257 |
Genre | Journal Article |
GroupedDBID | 53G 5VS 9T4 AAFWJ AAKDD AAYXX ACGFO ACGFS ACXDI ADBBV ADRAZ AENEX AFPKN ALMA_UNASSIGNED_HOLDINGS AOIJS BAWUL BCNDV CITATION DIK ECGQY GROUPED_DOAJ GX1 HYE KQ8 M48 M~E O5R O5S OK1 PGMZT RNS RPM IPNFZ NPM RIG 7X8 5PM |
ID | FETCH-LOGICAL-c469t-46ef5446c3f39cf57b3849e7b5e9a19162704f3ad3efb7daee86e5cf05ceb3293 |
IEDL.DBID | DOA |
ISSN | 1664-302X |
IngestDate | Wed Aug 27 01:25:55 EDT 2025 Thu Aug 21 18:37:20 EDT 2025 Fri Jul 11 08:19:54 EDT 2025 Thu Apr 03 07:04:05 EDT 2025 Tue Jul 01 02:18:30 EDT 2025 Thu Apr 24 23:09:35 EDT 2025 |
IsDoiOpenAccess | true |
IsOpenAccess | true |
IsPeerReviewed | true |
IsScholarly | true |
Keywords | microbial network immunity cluster analysis gut microbiota pregnancy |
Language | English |
License | Copyright © 2023 Yan, Liang, Luo, Tang and Xiao. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
LinkModel | DirectLink |
MergedId | FETCHMERGED-LOGICAL-c469t-46ef5446c3f39cf57b3849e7b5e9a19162704f3ad3efb7daee86e5cf05ceb3293 |
Notes | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 These authors have contributed equally to this work Edited by: Ricardo Araujo, Universidade do Porto, Portugal Reviewed by: Yashu Kuang, Guangzhou Medical University, China; Ji Youn Yoo, The University of Tennessee, Knoxville, United States |
OpenAccessLink | https://doaj.org/article/0e341b3855bc469e959d5a831c1b800f |
PMID | 38156011 |
PQID | 2908124262 |
PQPubID | 23479 |
ParticipantIDs | doaj_primary_oai_doaj_org_article_0e341b3855bc469e959d5a831c1b800f pubmedcentral_primary_oai_pubmedcentral_nih_gov_10753819 proquest_miscellaneous_2908124262 pubmed_primary_38156011 crossref_primary_10_3389_fmicb_2023_1314257 crossref_citationtrail_10_3389_fmicb_2023_1314257 |
ProviderPackageCode | CITATION AAYXX |
PublicationCentury | 2000 |
PublicationDate | 2023-12-13 |
PublicationDateYYYYMMDD | 2023-12-13 |
PublicationDate_xml | – month: 12 year: 2023 text: 2023-12-13 day: 13 |
PublicationDecade | 2020 |
PublicationPlace | Switzerland |
PublicationPlace_xml | – name: Switzerland |
PublicationTitle | Frontiers in microbiology |
PublicationTitleAlternate | Front Microbiol |
PublicationYear | 2023 |
Publisher | Frontiers Media S.A |
Publisher_xml | – name: Frontiers Media S.A |
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 |
SSID | ssj0000402000 |
Score | 2.371821 |
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... |
SourceID | doaj pubmedcentral proquest pubmed crossref |
SourceType | Open Website Open Access Repository Aggregation Database Index Database Enrichment Source |
StartPage | 1314257 |
SubjectTerms | cluster analysis gut microbiota immunity microbial network Microbiology pregnancy |
SummonAdditionalLinks | – databaseName: Scholars Portal Journals: Open Access dbid: M48 link: http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwrV3fi9NAEB7OE8EX8bfxFyv45qUk2WySfRBR8TiE88nCvS27m0kN1PRsE7DgH-9MNi1XOX3yLTTJdjuzk_m-dPYbgNdFhTrJbBVb68s4z3wWWw48wqaF87msFPIG5_Mvxdk8_3yhLo5g1-5oMuDmWmrH_aTm6-Xs54_tOwr4t8w4Kd-SB1rvZtwHfJbKlBfhDbhJmankQD2f4P74ZGaylCRh78xfbj3IT6OM_3XY888Syis56fQu3JnApHgfvH8PjrC7D7dCe8ntA_h1xfZiKsgSi6EX39sgv9Tbk90xDdOFivATYbtatOO-kX4r2k5crnHBuhxbwW9thRXNyg8bQYPyPk2uNRIuiD7TKH45sPbC5iHMTz99_XgWT90WYk8UuY_zAhtF5NDLRmrfqNLJKtdYOoXaEqsrsjLJG2lriY0ra4tYFah8kyhPhJxQwyM47lYdPgFBqF1R7g3yeljU2taJY-VATfTJyjyCdGdj4ycpcu6IsTRESdgvZvSLYb-YyS8RvNnfcxmEOP559Qd23f5KFtEeP1itF2aKSZMgpXD6lUo5NgFqpWtlK5n61BGObiJ4tXO8oaDjf1Jsh6thYzKdMDDKiiyCx2Eh7L9Ksv4OPTUjqA6WyMFcDs907bdR2JuouGIG_fR_zP4Z3GaLcOlNKp_Dcb8e8AUBqN69HKPiNxvoG3k priority: 102 providerName: Scholars Portal |
Title | Association between gut microbiota, microbial network, and immunity in pregnancy with a focus on specific bacterial clusters |
URI | https://www.ncbi.nlm.nih.gov/pubmed/38156011 https://www.proquest.com/docview/2908124262 https://pubmed.ncbi.nlm.nih.gov/PMC10753819 https://doaj.org/article/0e341b3855bc469e959d5a831c1b800f |
Volume | 14 |
hasFullText | 1 |
inHoldings | 1 |
isFullTextHit | |
isPrint | |
link | http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwrV1Na9wwEBUlUOglNE3TOh9Fhd4SJ7ZlydYxLU1CYXvqwt6EJI9TQ-oNWfuwkB-fGcu77JaQXnoRxpZkMTOS5tmjN4x9USXoJLNlbK0v4jzzWWxp4qFvqpzPRSmBDjhPfqqbaf5jJmcbqb4oJizQAwfBXSSA66zDNhKbKg1a6kraUqQ-dejs1LT64p63AaaGNZhgUZKEUzKIwjSqqfHunJKFn6ciJUvd2okGwv7nvMy_gyU3dp-rt2x3dBv5ZRjuHnsF7Tv2OiSSXO6zxw0p8zH0it_2Hf_TBKKlzp6trrGbNsR-n3HbVrwZToh0S960_P4BbomBY8np-yy3vJ77fsGxUzqRSVFF3AV6Z-zF3_XEsrB4z6ZX3399u4nHvAoxSbCLcwW1RBjoRS20r2WB4s01FE6CtojfVFYkeS1sJaB2RWUBSgXS14n0CL3RPzhgO-28hY-Mo38ucZcNRHqgKm2rxBFHoEagZEUesXQlY-NH0nHKfXFnEHyQXsygF0N6MaNeIna6bnMfKDderP2VVLeuSXTZww00IjMakfmXEUXs80rxBqcX_TOxLcz7hcl0Qi5QprKIfQiGsH6VIKYdXB8jVm6ZyNZYtp-0ze-BwhtBtySsfPg_Rn_E3pBEKMgmFcdsp3vo4QRdpc59GmYFltezFMtJXj4BlUEUeQ |
linkProvider | Directory of Open Access Journals |
openUrl | ctx_ver=Z39.88-2004&ctx_enc=info%3Aofi%2Fenc%3AUTF-8&rfr_id=info%3Asid%2Fsummon.serialssolutions.com&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.atitle=Association+between+gut+microbiota%2C+microbial+network%2C+and+immunity+in+pregnancy+with+a+focus+on+specific+bacterial+clusters&rft.jtitle=Frontiers+in+microbiology&rft.au=Hao+Yan&rft.au=Xinyuan+Liang&rft.au=Xinyuan+Liang&rft.au=Huijuan+Luo&rft.date=2023-12-13&rft.pub=Frontiers+Media+S.A&rft.eissn=1664-302X&rft.volume=14&rft_id=info:doi/10.3389%2Ffmicb.2023.1314257&rft.externalDBID=DOA&rft.externalDocID=oai_doaj_org_article_0e341b3855bc469e959d5a831c1b800f |
thumbnail_l | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=1664-302X&client=summon |
thumbnail_m | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=1664-302X&client=summon |
thumbnail_s | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=1664-302X&client=summon |