Evidence map›Paper›PMID 42413498›Full record

ArticleCell reports. Medicine2026

Core gastric microbiota linked to pathogenesis and preserved across age-stratified cohorts.

Weidong Huang, Qiujin Chen, Xuejie Gao, Gaocheng Yi, Yongyuan Su, Jiayi Shen, Tao Zhang, Hao Zhang, Yanbin Chen, Yingying Yu and 4 more

Abstract read
In one paragraph

Article in Cell reports. Medicine, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

14 authors.

Weidong HuangKey Laboratory of Gastrointestinal Cancer (Fujian Medical University), Ministry of Education, Fuzhou 350122, China; Department of Gastroenterology, 900th Hospital of Joint Logistics Support Force, Fujian Medical University, Fuzhou 350001, China.
Qiujin ChenKey Laboratory of Gastrointestinal Cancer (Fujian Medical University), Ministry of Education, Fuzhou 350122, China; Department of Medical Microbiology, Fujian Key Laboratory of Tumor Microbiology, School of Basic Medical Sciences, Fujian Medical University, Fuzhou 350122, China.
Xuejie GaoDepartment of Digestive and Nutrition, College of Clinical Medicine for Obstetrics & Gynecology and Pediatrics, Fujian Medical University, Fuzhou 350014, China.
Gaocheng YiDepartment of Pathology, 900th Hospital of Joint Logistics Support Force, Fujian Medical University, Fuzhou 350001, China.
Yongyuan SuKey Laboratory of Gastrointestinal Cancer (Fujian Medical University), Ministry of Education, Fuzhou 350122, China; Department of Medical Microbiology, Fujian Key Laboratory of Tumor Microbiology, School of Basic Medical Sciences, Fujian Medical University, Fuzhou 350122, China.
Jiayi ShenKey Laboratory of Gastrointestinal Cancer (Fujian Medical University), Ministry of Education, Fuzhou 350122, China; Department of Medical Microbiology, Fujian Key Laboratory of Tumor Microbiology, School of Basic Medical Sciences, Fujian Medical University, Fuzhou 350122, China.
Tao ZhangKey Laboratory of Gastrointestinal Cancer (Fujian Medical University), Ministry of Education, Fuzhou 350122, China; Department of Medical Microbiology, Fujian Key Laboratory of Tumor Microbiology, School of Basic Medical Sciences, Fujian Medical University, Fuzhou 350122, China.
Hao ZhangKey Laboratory of Gastrointestinal Cancer (Fujian Medical University), Ministry of Education, Fuzhou 350122, China; Department of Medical Microbiology, Fujian Key Laboratory of Tumor Microbiology, School of Basic Medical Sciences, Fujian Medical University, Fuzhou 350122, China.
Yanbin ChenKey Laboratory of Gastrointestinal Cancer (Fujian Medical University), Ministry of Education, Fuzhou 350122, China; Department of Medical Microbiology, Fujian Key Laboratory of Tumor Microbiology, School of Basic Medical Sciences, Fujian Medical University, Fuzhou 350122, China.
Yingying YuKey Laboratory of Gastrointestinal Cancer (Fujian Medical University), Ministry of Education, Fuzhou 350122, China; Department of Medical Microbiology, Fujian Key Laboratory of Tumor Microbiology, School of Basic Medical Sciences, Fujian Medical University, Fuzhou 350122, China.
Wen WangDepartment of Gastroenterology, 900th Hospital of Joint Logistics Support Force, Fujian Medical University, Fuzhou 350001, China.
Hewei JiangLingang Laboratory, Shanghai 201103, China. Electronic address: jianghewei@lglab.ac.cn.
Xu LinKey Laboratory of Gastrointestinal Cancer (Fujian Medical University), Ministry of Education, Fuzhou 350122, China; Department of Medical Microbiology, Fujian Key Laboratory of Tumor Microbiology, School of Basic Medical Sciences, Fujian Medical University, Fuzhou 350122, China. Electronic address: linxu@mail.fjmu.edu.cn.
Zhaowei XuKey Laboratory of Gastrointestinal Cancer (Fujian Medical University), Ministry of Education, Fuzhou 350122, China; Department of Medical Microbiology, Fujian Key Laboratory of Tumor Microbiology, School of Basic Medical Sciences, Fujian Medical University, Fuzhou 350122, China. Electronic address: xuzw@fjmu.edu.cn.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The stomach harbors a complex microbial niche, yet the persistence and disease relevance of its core microbiota remain unclear. Using full-length 16S and ITS sequencing of 255 pediatric samples, this study identifies 11 core bacterial genera organized into two antagonistic communities, CST1A and CST1B. CST1A is enriched in non-ulcer controls, whereas CST1B is associated with gastroduodenal disease, with limited fungal involvement. Stratified analyses show that Helicobacter pylori infection depletes CST1A taxa. Functional profiling indicates that CST1A is linked to motility-related processes, while CST1B favors nucleotide and peptidoglycan biosynthesis. In vitro and in vivo experiments demonstrate that CST1A-derived Achromobacter spanius alleviates gastric mucosal injury by modulating inflammatory responses. Cross-cohort validation across eight datasets (n = 1,299) confirms the persistent relevance of the CST1A-CST1B structure across disease stages. Together, these findings define an early-life core gastric microbiota linked to disease risk and conserved across the lifespan.

Indexed as

Gastrointestinal MicrobiomeHelicobacter InfectionsStomachAdolescentAnimalsBacteriaChildChild, PreschoolCohort StudiesFemaleGastric MucosaHelicobacter pyloriHumansInfantMaleRNA, Ribosomal, 16SRNA, Ribosomal, 16Score gastric microbiotaearly lifeecological preservationH. pyloripediatric peptic ulcers

Identifiers

PMID42413498
PMCPMC13400175

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.