Target intelligence / Profile preview

Bile salt hydrolase-producing intestinal bacteria (BSH-producing bacteria)

Target
BSH-producing bacteria
Molecular classification
Enzyme, Other
01

Overview

Bile salt hydrolase (BSH)-producing intestinal bacterial taxa are a functional group of the gut microbiota, including genera such as Lactobacillus, Bifidobacterium, and Clostridium, that express the BSH enzyme (EC 3.5.1.24) (Song et al., 2019, PubMed). These bacteria play a critical role in host physiology by deconjugating primary bile acids, which is the essential first step in the transformation of bile salts into secondary bile acids (Joyce et al., 2014, PNAS). This enzymatic activity alters the bile acid pool composition, thereby influencing systemic metabolism through the activation or inhibition of nuclear receptors like the farnesoid X receptor (FXR) and membrane receptors like TGR5 (Wahlström et al., 2016, Cell Metabolism). Clinically, these taxa are targeted to manage conditions such as hypercholesterolemia, obesity, and Type 2 diabetes, as BSH activity can reduce cholesterol absorption and improve glucose tolerance (Yao et al., 2018, Nature Communications). Conversely, inhibition of BSH is being explored as a strategy to prevent Clostridioides difficile infection, as conjugated bile acids can inhibit the germination of C. difficile spores (Adhikari et al., 2020, Nature Microbiology).

Other names
BSH-active gut microbiotaBile salt hydrolase-expressing bacteriaBSH+ intestinal taxaBile salt hydrolase-producing gut microbiota
02

Mechanism of action

Catalyzes the hydrolysis of the C-24 amide bond in conjugated bile acids, releasing free amino acids (glycine or taurine) and unconjugated bile acids, which subsequently modulates host signaling through FXR and TGR5 receptors.

03

Biological functions

Bile acid metabolismCholesterol homeostasisLipid metabolismCell signalingMetabolic regulation
04

Disease associations

ObesityType 2 diabetesHypercholesterolemiaInflammatory bowel diseaseClostridioides difficile infectionNonalcoholic fatty liver disease
05

Safety considerations

Potential for increased secondary bile acid production (e.g., lithocholic acid) associated with colorectal cancer riskAlteration of fat-soluble vitamin absorptionGastrointestinal distress due to bile acid malabsorption
06

Interacting drugs

Lactobacillus acidophilus

5 more in the full profile.

07

Biomarkers

bsh gene abundanceRatio of conjugated to unconjugated bile acidsSecondary bile acid levelsFecal BSH activity

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