Target intelligence / Profile preview

Bile salt hydrolase–producing bacterium (BSH-producing bacterium)

Target
BSH-producing bacterium
Molecular classification
Enzyme (N-terminal nucleophilic hydrolase family), Microbial marker, Other (community/functional group of gut bacteria)
01

Overview

Bile salt hydrolase–producing bacteria are a broad group of gut microbes distinguished by their production of the enzyme bile salt hydrolase (BSH, EC 3.5.1.24), which catalyzes the hydrolysis (deconjugation) of glycine- or taurine-conjugated bile acids into free bile acids and amino acids. This reaction is the gateway step in gut bile acid transformation and crucial for the formation of secondary bile acids, shaping the gut microbial ecology and diverse aspects of host metabolism, immunity, and cholesterol homeostasis. Major BSH-producing taxa include species of Lactobacillus, Bifidobacterium, Clostridium, Enterococcus, and Bacteroides. The gene and protein product, BSH, is a member of the N-terminal nucleophilic hydrolase family. Interest in BSH-producing bacteria as a therapeutic target stems from their role in cholesterol lowering (via enhanced bile acid deconjugation and excretion), metabolic syndrome, and the potential to modulate gut and hepatic diseases via manipulation of the bile acid pool. However, because this "target" represents a functional microbial group rather than a single molecular entity, it is considered an imprecise molecular target for drug development.

Other names
BSH-producing bacteriaGut microbial bile salt hydrolase–positive bacteriaProbiotic bile salt hydrolase producersMicroorganisms with bile salt hydrolase activity
02

Mechanism of action

Inhibitors: Reduce BSH activity, alter bile acid pool composition, increase conjugated bile acids. Probiotic supplementation: Increases BSH activity, enhances deconjugation, may lower cholesterol.

03

Biological functions

Bile acid deconjugationModulation of bile acid poolCholesterol metabolismModulation of host metabolismColonization resistanceDetoxification of bile acidsHost–microbe signaling
04

Disease associations

Metabolic disease (e.g., dyslipidemia, atherosclerosis)Gastrointestinal infection (colonization resistance, pathogen exclusion)ObesityLiver diseaseInflammatory diseaseOther (potential cancer, neuroinflammatory roles via microbiome interaction)
05

Safety considerations

Potential for dysregulated bile acid metabolism (e.g. excessive secondary bile acid production may have pro-inflammatory, carcinogenic effects)Altered drug absorption/metabolism via changes in bile compositionPossible horizontal gene transfer of bsh and associated unintended consequences
06

Interacting drugs

Bile acid sequestrants (indirect interaction by modulating substrate availability)

1 more in the full profile.

07

Biomarkers

BSH gene abundance (metagenomic marker)Fecal bile acid deconjugation profileMicrobial taxa such as Lactobacillus, Bifidobacterium, Clostridium, Enterococcus with high BSH activity

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