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ORIGINAL RESEARCH article

Front. Microbiol.

Sec. Microbial Physiology and Metabolism

16S Ribosomal Ribonucleic Acid Sequencing Reveals Bile Microbiome Features in Gallstone Disease and Their Links to Blood Lipid Subtypes

Provisionally accepted
Shijie  WangShijie Wang1*Yongxing  DingYongxing Ding2Cheng  CaiCheng Cai2Mingrui  OuMingrui Ou2Chunshen  NiuChunshen Niu2
  • 1Bengbu Third People's Hospital, Bengbu, China
  • 2The Third The People's Hospital of Bengbu, Bengbu, China

The final, formatted version of the article will be published soon.

Abstract Background: Gallstone disease (GSD) represents a major global health burden with complex pathophysiology involving bile microbiome dysbiosis and metabolic dysfunction. Although previous studies have examined bile microbial communities, the relationship between bile microbiome composition and specific lipid phenotypes remains incompletely understood. Methods: We conducted a cross-sectional study of 28 adults undergoing cholecystectomy for radiologically and pathologically confirmed gallstones. Bile samples were collected intraoperatively and subjected to 16S ribosomal ribonucleic acid V3–V4 region sequencing. Patients were stratified by lipid subtypes based on contemporary dyslipidaemia guidelines. Microbial diversity, community structure and differential abundance analyses were performed alongside machine learning classification. Results: The bile microbiome exhibited distinct compositional patterns between the hypertriglyceridaemia (HTG) and non-HTG (NTG) groups, with key phyla (Proteobacteria, Firmicutes) showing group-specific abundance trends and alpha diversity indices reflecting reduced evenness in HTG. Beta diversity analyses demonstrated mild-to-moderate separation between groups, and the linear discriminant analysis effect size technique identified discriminatory taxa with potential functional relevance. Random forest classification achieved moderate accuracy in predicting lipid subtypes based on microbial features. Conclusions: This study revealed associations between bile microbiome composition and systemic lipid metabolism in GSD, suggesting potential mechanistic links through bile acid metabolism and farnesoid X receptor–fibroblast growth factor 19 signalling pathways.

Keywords: Bile, Bile Acids and Salts, Gallstones, hypertriglyceridaemia, microbiota

Received: 07 Nov 2025; Accepted: 05 Jan 2026.

Copyright: © 2026 Wang, Ding, Cai, Ou and Niu. 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) or licensor 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.

* Correspondence: Shijie Wang

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