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Biliary Microbiota and Bile Acid Composition in Cholelithiasis

BioMed Research International, vol. 2020, pp. 1242364

Abstract

Background . A functional interplay between BAs and microbial composition in gut is a well‐documented phenomenon. In bile, this phenomenon is far less studied, and with this report, we describe the interactions between the BAs and microbiota in this complex biological matrix. Methodology . Thirty‐seven gallstone disease patients of which twenty‐one with Opisthorchis felineus infection were enrolled in the study. The bile samples were obtained during laparoscopic cholecystectomy for gallstone disease operative treatment. Common bile acid composition was measured by LC‐MS/MS. Gallbladder microbiota were previously analyzed with 16S rRNA gene sequencing on Illumina MiSeq platform. The associations between bile acid composition and microbiota were analyzed. Results . Bile acid signature and Opisthorchis felineus infection status exert influence on beta‐diversity of bile microbial community. Direct correlations were found between taurocholic acid, taurochenodeoxycholic acid concentrations, and alpha‐diversity of bile microbiota. Taurocholic acid and taurochenodeoxycholic acid both show positive associations with the presence of Chitinophagaceae family, Microbacterium and Lutibacterium genera, and Prevotella intermedia. Also, direct associations were identified for taurocholic acid concentration and the presence of Actinomycetales and Bacteroidales orders, Lautropia genus, Jeotgalicoccus psychrophilus, and Haemophilus parainfluenzae as well as for taurochenodeoxycholic acid and Acetobacteraceae family and Sphingomonas genus. There were no differences in bile acid concentrations between O. felineus- infected and noninfected patients. Conclusions/Significance . Associations between diversity, taxonomic profile of bile microbiota, and bile acid levels were evidenced in patients with cholelithiasis. Increase of taurochenodeoxycholic acid and taurocholic acid concentration correlates with bile microbiota alpha‐diversity and appearance of opportunistic pathogens.

Authors 8

  1. В. А. Петров corresponding

    Siberian State Medical University

    Affiliation as printed

    Central Research Laboratory, Siberian State Medical University, Tomsk, Russia

  2. University of Córdoba

    Affiliation as printed

    Department of Analytical Chemistry, Annex Marie Curie Building, Campus of Rabanales, University of Córdoba, E-14071 Córdoba, Spain

  3. Leiden University Medical Center

    Affiliation as printed

    Center for Proteomics and Metabolomics, Leiden University Medical Center, Leiden, Netherlands

  4. Tomsk Polytechnic University

    Affiliation as printed

    School of Core Engineering Education, National Research Tomsk Polytechnic University, Tomsk, Russia

  5. Siberian State Medical University

    Affiliation as printed

    Surgical Diseases Department of Pediatric Faculty, Siberian State Medical University, Tomsk, Russia

  6. Siberian State Medical University

    Affiliation as printed

    Central Research Laboratory, Siberian State Medical University, Tomsk, Russia

  7. National Research Tomsk State University · Leiden University Medical Center

    Affiliation as printed

    Center for Proteomics and Metabolomics, Leiden University Medical Center, Leiden, Netherlands

    Department of Chemistry, Tomsk State University, Tomsk, Russia

  8. Siberian State Medical University

    Affiliation as printed

    Central Research Laboratory, Siberian State Medical University, Tomsk, Russia

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References 34