# Dynamic involvement of the core gut microbiome XNP_Guild1 in the evolution of gestational diabetes mellitus

**Authors:** Hualongyue Du, Qiaoxi Lin, Xiaojing He, Bin Yang, Yiyao Huang, Qianbei Li, Yudi Wang, Ruijing Wen, Wenlong Lin, Shenghui Li, Lei Zheng, Zihao Ou

PMC · DOI: 10.1080/19490976.2026.2623353 · Gut Microbes · 2026-01-31

## TL;DR

This study explores how gut microbes, especially a stable group called XNP_Guild1, are linked to the development of gestational diabetes and its effects on mothers and infants.

## Contribution

The study identifies a core gut microbial guild (XNP_Guild1) that is consistently associated with gestational diabetes progression and early pregnancy risk.

## Key findings

- A 'grey zone' group with intermediate gut microbial features was identified between healthy and GDM states.
- XNP_Guild1 showed high stability and functional cohesion across healthy, grey zone, and GDM states.
- The core guild's vertical transmission was linked to neonatal growth outcomes.

## Abstract

Integrated large-scale maternal microbiome cohort analyses are critical for understanding the development of gestational diabetes mellitus (GDM) and its impact on maternal and offspring health. Here, we analyzed the microbiomes of 2,717 mothers and infants from 9 global cohorts, including both public datasets and a prospective cohort in China, using high-throughput sequencing and multilayer network modeling. We systematically identified and characterized a group of “predicted grey zone” individuals whose gut microbial network features fell between those of healthy and GDM subjects, which represent dynamic ecological transition states in disease development. Notably, we identified and validated across cohorts a core gut microbial guild (XNP_Guild1) that remained highly stable and functionally cohesive across healthy, grey zone, and GDM states, and was significantly associated with both disease progression and early pregnancy risk. In an exploratory intergenerational network analysis, we estimated the vertical transmission effect of the core guild and its potential influence on neonatal growth outcomes. These findings highlight the tight interconnection among core functional gut microbes, transitional ecological states, disease evolution, and maternal–infant health, providing a foundation for future targeted interventions and mechanistic studies of the maternal–offspring microecosystem in GDM.

## Linked entities

- **Diseases:** gestational diabetes mellitus (MONDO:0005406)

## Full-text entities

- **Genes:** AP2B1 (adaptor related protein complex 2 subunit beta 1) [NCBI Gene 163] {aka ADTB2, AP105B, AP2-BETA, CLAPB1}, ATG5 (autophagy related 5) [NCBI Gene 9474] {aka APG5, APG5-LIKE, APG5L, ASP, SCAR25, hAPG5}, ATG10 (autophagy related 10) [NCBI Gene 83734] {aka APG10, APG10L, ATG10S, pp12616}, ATRX (ATRX chromatin remodeler) [NCBI Gene 546] {aka JMS, MRX52, RAD54, RAD54L, XH2, XNP}
- **Diseases:** organ dysfunction (MESH:D009102), type 2 diabetes (MESH:D003924), reduced head circumference (MESH:D006258), neurodevelopmental disorders (MESH:D002658), pregnancy complications (MESH:D011248), macrosomia (MESH:D005320), obesity (MESH:D009765), metabolic and developmental abnormalities (MESH:D008659), inflammation (MESH:D007249), patent ductus arteriosus (MESH:D004374), GDM (MESH:D016640), gestational hypertension (MESH:D046110), gastrointestinal disorders (MESH:D005767), diabetes (MESH:D003920), preterm birth (MESH:D047928), cardiovascular disease (MESH:D002318)
- **Chemicals:** Taxa (-), SCFA (MESH:D005232), BCAA (MESH:D000597), fatty acid (MESH:D005227), glucose (MESH:D005947), bile acid (MESH:D001647), water (MESH:D014867)
- **Species:** Anaerococcus (genus) [taxon 165779], Bifidobacterium (genus) [taxon 1678], Collinsella (genus) [taxon 102106], Homo sapiens (human, species) [taxon 9606], Bacteroides (genus) [taxon 816], Lachnoclostridium (genus) [taxon 1506553], gut metagenome (species) [taxon 749906], Escherichia coli (E. coli, species) [taxon 562]

## Full text

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## Figures

6 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12867416/full.md

## References

39 references — full list in the complete paper: https://tomesphere.com/paper/PMC12867416/full.md

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Source: https://tomesphere.com/paper/PMC12867416