Microbial impact on cholesterol and bile acid metabolism: current status and future prospects
Open accessAbstract
Recently, the gut microbiota has emerged as a crucial factor that influences cholesterol metabolism. Ever since, significant interest has been shown in investigating these host-microbiome interactions to uncover microbiome-mediated functions on cholesterol and bile acid (BA) metabolism. Indeed, changes in gut microbiota composition and, hence, its derived metabolites have been previously reported to subsequently impact the metabolic processes and have been linked to several diseases. In this context, associations between a disrupted gut microbiome, impaired BA metabolism, and cholesterol dysregulation have been highlighted. Extensive advances in metagenomic and metabolomic studies in this field have allowed us to further our understanding of the role of intestinal bacteria in metabolic health and disease. However, only a few have provided mechanistic insights into their impact on cholesterol metabolism. Identifying the myriad functions and interactions of these bacteria to maintain cholesterol homeostasis remain an important challenge in such a field of research. In this review, we discuss the impact of gut microbiota on cholesterol metabolism, its association with disease settings, and the potential of modulating gut microbiota as a promising therapeutic target to lower hypercholesterolemia.
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Deconjugation ability enhances bacterial survival and colonization of the gastrointestinal tract.
“The deconjugation ability enhances bacterial survival and colonization of the gastrointestinal tract, modulates lipid metabolism, and shapes the bile acid pool, ultimately influencing host-microbiome signaling [6, 10, 11].”
From Bile Salt Hydrolase Activity in the Food-Derived Strain Levilactobacillus brevis M3R3: Genomic and Functional Characterization (2026) · cites this paper as [11]
The Deconjugation section proposes that deconjugation may enhance gastrointestinal persistence and that BSH-positive bacteria, together with bacteria that incorporate cholesterol into their membranes, may survive better in the gastrointestinal tract. The claim states this as a definite effect and extends persistence to colonization, which the passage does not establish. No page number is supplied for the passage. (LLM, conf=0.86)
Experimental — accuracy not yet measuredDeconjugation ability shapes the bile acid pool, ultimately influencing host-microbiome signaling.
“The deconjugation ability enhances bacterial survival and colonization of the gastrointestinal tract, modulates lipid metabolism, and shapes the bile acid pool, ultimately influencing host-microbiome signaling [6, 10, 11].”
From Bile Salt Hydrolase Activity in the Food-Derived Strain Levilactobacillus brevis M3R3: Genomic and Functional Characterization (2026) · cites this paper as [11]
BSH activity has been implicated in the regulation of host cholesterol levels, contributing to a potential cholesterol-lowering effect.
“Among its metabolic benefits, BSH activity has been implicated in the regulation of host cholesterol levels, contributing to its potential cholesterol-lowering effect [11–13].”
From Bile Salt Hydrolase Activity in the Food-Derived Strain Levilactobacillus brevis M3R3: Genomic and Functional Characterization (2026) · cites this paper as [11]
Deconjugation ability modulates lipid metabolism.
“The deconjugation ability enhances bacterial survival and colonization of the gastrointestinal tract, modulates lipid metabolism, and shapes the bile acid pool, ultimately influencing host-microbiome signaling [6, 10, 11].”
From Bile Salt Hydrolase Activity in the Food-Derived Strain Levilactobacillus brevis M3R3: Genomic and Functional Characterization (2026) · cites this paper as [11]
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References 138 · Cited by 264
- Authors
- Kriaa, A., Bourgin, M., Potiron, A., Mkaouar, H., Jablaoui, A., Gérard, P., Maguin, E., & Rhimi, M.
- Affiliations
- AgroParisTech (FR)
- Corresponding author
- Rhimi, Moez
- Venue
- Journal of Lipid Research
- Publisher
- Elsevier BV
- Published
- 2019-02
- Volume
- 60
- Issue
- 2
- Pages
- 323-332
- ISSN
- 0022-2275 (ISSN-L)
- PMC
- PMC6358303
- OpenAlex
- W2903267537
- Cited by
- 264
- References
- 138
- Citations by year
- 2026: 30 · 2025: 45 · 2024: 40 · 2023: 31 · 2022: 36 · 2021: 43 · 2020: 28 · 2019: 11
- FWCI
- 2.01
- Type
- journal article
- Language
- en
- Open access
- hybrid
- doi.org
- Licence
- Locations
- Journal of Lipid Research (publishedVersion, cc-by)
- Europe PMC (PubMed Central) (publishedVersion, cc-by)
- PubMed Central (publishedVersion, cc-by)
- PubMed (publishedVersion)
- HAL (submittedVersion, other-oa)
- HAL (submittedVersion, cc-by)
- HAL (submittedVersion)
- DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion, cc-by-sa)
- Funders
- Institut National de la Recherche Agronomique
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Gut microbiota and health
- Health Sciences › Medicine › Surgery › Cholesterol and Lipid Metabolism
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Steroid Chemistry and Biochemistry
- Keywords
- gut microbiota, cholesterol metabolism, bile acid metabolism, host-microbiome interactions, hypercholesterolemia, dysbiosis, cholesterol homeostasis, microbiota modulation, metabolic disorders, microbial metabolites
- MeSH terms
- Gastrointestinal Microbiome, Animals, Bile Acids and Salts, Cholesterol, Humans, Dyslipidemias, Dysbiosis
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