Evidence map›Paper›PMID 41730843›Full record

ArticleNature communications2026

Investigation of bile salt hydrolase activity in human gut bacteria reveals production of conjugated secondary bile acids.

Lauren N Lucas, Mallikarjun Jillella, Lea E Cattaneo, Bhavana Gangwar, Qijun Zhang, A P Clay, Robert L Kerby, David M Stevenson, Helen E Blackwell, Federico E Rey and 1 more

Abstract read
In one paragraph

Article in Nature communications, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing 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

11 citing papers in PubMed.

  1. Bile acid signaling in health and disease.Molecular biomedicine · 2026
    Review
  2. Article
  3. Article
  4. Article
  5. Article
  6. Review
  7. Review
  8. Article
  9. Review
  10. Review
  11. MS/MS Mass Spectrometry Filtering Tree for Bile Acid Isomer Annotation.bioRxiv : the preprint server for biology · 2025
    Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

11 authors.

Lauren N Lucas *Department of Bacteriology, University of Wisconsin-Madison, Madison, WI, USA.ORCID http://orcid.org/0000-0001-7996-9858
Mallikarjun Jillella *Department of Bacteriology, University of Wisconsin-Madison, Madison, WI, USA.ORCID http://orcid.org/0009-0003-5689-6176
Lea E CattaneoMicrobiology Doctoral Training Program, University of Wisconsin-Madison, Madison, WI, USA.ORCID http://orcid.org/0000-0002-2920-0634
Bhavana GangwarDepartment of Bacteriology, University of Wisconsin-Madison, Madison, WI, USA.
Qijun ZhangDepartment of Bacteriology, University of Wisconsin-Madison, Madison, WI, USA.ORCID http://orcid.org/0000-0002-1003-7355
A P ClayDepartment of Chemistry, University of Wisconsin-Madison, Madison, WI, USA.
Robert L KerbyDepartment of Bacteriology, University of Wisconsin-Madison, Madison, WI, USA.
David M StevensonDepartment of Bacteriology, University of Wisconsin-Madison, Madison, WI, USA.
Helen E BlackwellDepartment of Chemistry, University of Wisconsin-Madison, Madison, WI, USA.ORCID http://orcid.org/0000-0003-4261-8194
Federico E ReyDepartment of Bacteriology, University of Wisconsin-Madison, Madison, WI, USA. ferey@wisc.edu.ORCID http://orcid.org/0000-0002-0239-7780
Daniel Amador-NoguezDepartment of Bacteriology, University of Wisconsin-Madison, Madison, WI, USA. amadornoguez@wisc.edu.ORCID http://orcid.org/0000-0002-3568-3070

Funding

Establishing mechanistic links between the gut microbiome and atherosclerosisR01HL148577 · NHLBI · UNIVERSITY OF WISCONSIN-MADISON · PI LUSIS, ALDONS JAKE, REY, FEDERICO E · 2020 to 2023
$2.6M
Gut microbiota and metabolite interactions in atherosclerosisR01HL144651 · NHLBI · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI LUSIS, ALDONS JAKE, REY, FEDERICO E · 2019 to 2022
$2.6M
Gut microbiota and MAIT cell interactions in atherosclerosisR21AG072189 · NIA · UNIVERSITY OF WISCONSIN-MADISON · PI KASAHARA, KAZUYUKI, REY, FEDERICO E · 2021 to 2022
$337k
Design and application of small molecules for the interception of quorum sensing in Staphylococcus aureusF32GM155981 · NIGMS · UNIVERSITY OF WISCONSIN-MADISON · PI Alyssa Paige Clay · 2024 to 2026
$150k
NHLBI NIH HHS R01 HL144651NHLBI NIH HHS R01 HL148577NIA NIH HHS R21 AG072189NIGMS NIH HHS F32 GM155981U.S. Department of Health & Human Services | NIH | National Heart, Lung, and Blood Institute (NHLBI) HL148577U.S. Department of Health & Human Services | NIH | National Institute of Diabetes and Digestive and Kidney Diseases (National Institute of Diabetes & Digestive & Kidney Diseases) T32 DK 007665, F32 DK142449
6 · The paper itself

Abstract

Through biochemical transformation of host-derived bile acids, gut bacteria mediate host-microbe crosstalk and function at the interface of nutrition and host metabolic regulation. Bile acids play a crucial role in human health by facilitating the absorption of dietary lipophilic nutrients, interacting with hormone receptors to regulate host physiology, and shaping gut microbiota composition through antimicrobial activity. Bile acids deconjugation by bacterial bile salt hydrolase has long been recognized as the first necessary bile acid modification required before further transformations can occur. Here, we show that bile salt hydrolase activity is common among human gut bacterial isolates spanning seven major phyla. However, we observed variation in both the extent and the specificity of deconjugation of bile acids among the tested taxa. Unexpectedly, we discovered that certain strains were capable of directly dehydrogenating conjugated bile acids via hydroxysteroid dehydrogenases to produce conjugated secondary bile acids both in vitro and in vivo. These results challenge the prevailing notion that deconjugation is a prerequisite for further bile acid modifications and lay a foundation for new hypotheses regarding how bacteria act individually or in concert to diversify the bile acid pool and influence host physiology.

Indexed as

AmidohydrolasesBacteriaBacterial ProteinsBile Acids and SaltsGastrointestinal MicrobiomeAnimalsHumansHydroxysteroid DehydrogenasesAmidohydrolasesBacterial ProteinsBile Acids and Saltscholoylglycine hydrolaseHydroxysteroid Dehydrogenases

Identifiers

PMID41730843
PMCPMC13039732

What OpenQuestion holds

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Registered trials

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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.