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  1. Analyzed Page
  2. Matching Content Categories
  3. CMS
  4. Monthly Traffic Estimate
  5. How Does Link.springer.com Make Money
  6. Keywords
  7. Topics
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We are analyzing https://link.springer.com/article/10.1186/s40168-019-0628-3.

Title:
Taxonomic profiling and populational patterns of bacterial bile salt hydrolase (BSH) genes based on worldwide human gut microbiome | Microbiome
Description:
Background Bile salt hydrolase plays an important role in bile acid-mediated signaling pathways, which regulate lipid absorption, glucose metabolism, and energy homeostasis. Several reports suggest that changes in the composition of bile acids are found in many diseases caused by dysbacteriosis. Results Here, we present the taxonomic identification of bile salt hydrolase (BSH) in human microbiota and elucidate the abundance and activity differences of various bacterial BSH among 11 different populations from six continents. For the first time, we revealed that bile salt hydrolase protein sequences (BSHs) are distributed in 591 intestinal bacterial strains within 117 genera in human microbiota, and 27.52% of these bacterial strains containing BSH paralogs. Significant variations are observed in BSH distribution patterns among different populations. Based on phylogenetic analysis, we reclassified these BSHs into eight phylotypes and investigated the abundance patterns of these phylotypes among different populations. From the inspection of enzyme activity among different BSH phylotypes, BSH-T3 showed the highest enzyme activity and is only found in Lactobaclillus. The phylotypes of BSH-T5 and BSH-T6 mainly from Bacteroides with high percentage of paralogs exhibit different enzyme activity and deconjugation activity. Furthermore, we found that there were significant differences between healthy individuals and patients with atherosclerosis and diabetes in some phylotypes of BSHs though the correlations were pleiotropic. Conclusion This study revealed the taxonomic and abundance profiling of BSH in human gut microbiome and provided a phylogenetic-based system to assess BSHs activity by classifying the target sequence into specific phylotype. Furthermore, the present work disclosed the variation patterns of BSHs among different populations of geographical regions and health/disease cohorts, which is essential to understand the role of BSH in the development and progression of related diseases.
Website Age:
28 years and 1 months (reg. 1997-05-29).

Matching Content Categories {πŸ“š}

  • Education
  • Science
  • Health & Fitness

Content Management System {πŸ“}

What CMS is link.springer.com built with?

Custom-built

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Traffic Estimate {πŸ“ˆ}

What is the average monthly size of link.springer.com audience?

🌠 Phenomenal Traffic: 5M - 10M visitors per month


Based on our best estimate, this website will receive around 5,000,019 visitors per month in the current month.
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How Does Link.springer.com Make Money? {πŸ’Έ}

We can't tell how the site generates income.

While many websites aim to make money, others are created to share knowledge or showcase creativity. People build websites for various reasons. This could be one of them. Link.springer.com could be getting rich in stealth mode, or the way it's monetizing isn't detectable.

Keywords {πŸ”}

bshs, bsh, bile, article, additional, file, google, scholar, bsht, cas, figure, acid, gut, fig, activity, hydrolase, table, strains, salt, populations, microbiome, human, acids, abundance, data, analysis, microbiota, phylotypes, genera, sequences, molecular, enzyme, taxonomic, bacterial, diseases, protein, sequence, database, results, paralogs, showed, individuals, docking, studies, genes, found, diabetes, hmp, relative, total,

Topics {βœ’οΈ}

ncoi/xhoi-digested vector pet28a uk/thornton-srv/databases/pdbsum lc-ms/ms system control isopropyl Ξ²-d-thiogalactoside twin-arginine signal peptides high-performance computing resources high-performance computing center lc-ms/ms approach state key laboratory sandwiched antiparallel Ξ±-sheets 12alpha-hydroxylated bile acids 12a-hydroxylated bile acids bile salt hydrolases article download pdf world health organization screen anti-giardia lactobacilli jing shang host weight gain de vos wm ba metabolism-related diseases bile salt hydrolase human microbiome project privacy choices/manage cookies colorectal adenoma-carcinoma sequence lc-ms/ms purified bsh-lyophilized powders body mass index metagenome-wide association study bacterial taxonomic analysis read pairs mapped specific bile salt praveen kumar kalavagunta creative commons license bile acid excretion hadza hunter-gatherers increased plasma levels human intestinal tract conjugated bile salts full access public metagenomic databases raw sequencing reads bile acid metabolites ntn-hydrolase family [29 populational-level correlation analysis false discovery rate human gut microbiome bile acid metabolism typical lc spectrum cholic acid concentrations human insulin resistance

Questions {❓}

  • Bile salt hydrolase activities: a novel target to screen anti-giardia Lactobacilli?

Schema {πŸ—ΊοΈ}

WebPage:
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         headline:Taxonomic profiling and populational patterns of bacterial bile salt hydrolase (BSH) genes based on worldwide human gut microbiome
         description:Bile salt hydrolase plays an important role in bile acid-mediated signaling pathways, which regulate lipid absorption, glucose metabolism, and energy homeostasis. Several reports suggest that changes in the composition of bile acids are found in many diseases caused by dysbacteriosis. Here, we present the taxonomic identification of bile salt hydrolase (BSH) in human microbiota and elucidate the abundance and activity differences of various bacterial BSH among 11 different populations from six continents. For the first time, we revealed that bile salt hydrolase protein sequences (BSHs) are distributed in 591 intestinal bacterial strains within 117 genera in human microbiota, and 27.52% of these bacterial strains containing BSH paralogs. Significant variations are observed in BSH distribution patterns among different populations. Based on phylogenetic analysis, we reclassified these BSHs into eight phylotypes and investigated the abundance patterns of these phylotypes among different populations. From the inspection of enzyme activity among different BSH phylotypes, BSH-T3 showed the highest enzyme activity and is only found in Lactobaclillus. The phylotypes of BSH-T5 and BSH-T6 mainly from Bacteroides with high percentage of paralogs exhibit different enzyme activity and deconjugation activity. Furthermore, we found that there were significant differences between healthy individuals and patients with atherosclerosis and diabetes in some phylotypes of BSHs though the correlations were pleiotropic. This study revealed the taxonomic and abundance profiling of BSH in human gut microbiome and provided a phylogenetic-based system to assess BSHs activity by classifying the target sequence into specific phylotype. Furthermore, the present work disclosed the variation patterns of BSHs among different populations of geographical regions and health/disease cohorts, which is essential to understand the role of BSH in the development and progression of related diseases.
         datePublished:2019-01-23T00:00:00Z
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      headline:Taxonomic profiling and populational patterns of bacterial bile salt hydrolase (BSH) genes based on worldwide human gut microbiome
      description:Bile salt hydrolase plays an important role in bile acid-mediated signaling pathways, which regulate lipid absorption, glucose metabolism, and energy homeostasis. Several reports suggest that changes in the composition of bile acids are found in many diseases caused by dysbacteriosis. Here, we present the taxonomic identification of bile salt hydrolase (BSH) in human microbiota and elucidate the abundance and activity differences of various bacterial BSH among 11 different populations from six continents. For the first time, we revealed that bile salt hydrolase protein sequences (BSHs) are distributed in 591 intestinal bacterial strains within 117 genera in human microbiota, and 27.52% of these bacterial strains containing BSH paralogs. Significant variations are observed in BSH distribution patterns among different populations. Based on phylogenetic analysis, we reclassified these BSHs into eight phylotypes and investigated the abundance patterns of these phylotypes among different populations. From the inspection of enzyme activity among different BSH phylotypes, BSH-T3 showed the highest enzyme activity and is only found in Lactobaclillus. The phylotypes of BSH-T5 and BSH-T6 mainly from Bacteroides with high percentage of paralogs exhibit different enzyme activity and deconjugation activity. Furthermore, we found that there were significant differences between healthy individuals and patients with atherosclerosis and diabetes in some phylotypes of BSHs though the correlations were pleiotropic. This study revealed the taxonomic and abundance profiling of BSH in human gut microbiome and provided a phylogenetic-based system to assess BSHs activity by classifying the target sequence into specific phylotype. Furthermore, the present work disclosed the variation patterns of BSHs among different populations of geographical regions and health/disease cohorts, which is essential to understand the role of BSH in the development and progression of related diseases.
      datePublished:2019-01-23T00:00:00Z
      dateModified:2019-01-23T00:00:00Z
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         Bile salt hydrolase (BSH)
         Gut microbiota
         Taxonomic identification
         Bile acids
         Number of paralogs
         Medical Microbiology
         Bioinformatics
         Microbial Ecology
         Microbiology
         Microbial Genetics and Genomics
         Virology
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               type:PostalAddress
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      name:Jun Liao
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               type:PostalAddress
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      name:Liang Jin
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               name:School of Life Science and Technology, China Pharmaceutical University, Nanjing, China
               type:PostalAddress
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            name:China Pharmaceutical University
            address:
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               type:PostalAddress
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      email:[email protected]
      name:Jing Shang
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            name:China Pharmaceutical University
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               name:School of Life Science and Technology, China Pharmaceutical University, Nanjing, China
               type:PostalAddress
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      url:http://orcid.org/0000-0001-9972-7397
      affiliation:
            name:China Pharmaceutical University
            address:
               name:School of Life Science and Technology, China Pharmaceutical University, Nanjing, China
               type:PostalAddress
            type:Organization
      email:[email protected]
PostalAddress:
      name:School of Life Science and Technology, China Pharmaceutical University, Nanjing, China
      name:School of Life Science and Technology, China Pharmaceutical University, Nanjing, China
      name:State Key Laboratory of Natural Medicines, China Pharmaceutical University, Nanjing, China
      name:School of Life Science and Technology, China Pharmaceutical University, Nanjing, China
      name:School of Life Science and Technology, China Pharmaceutical University, Nanjing, China
      name:School of Life Science and Technology, China Pharmaceutical University, Nanjing, China
      name:School of Life Science and Technology, China Pharmaceutical University, Nanjing, China
      name:School of Life Science and Technology, China Pharmaceutical University, Nanjing, China
      name:State Key Laboratory of Natural Medicines, China Pharmaceutical University, Nanjing, China
      name:School of Life Science and Technology, China Pharmaceutical University, Nanjing, China
      name:State Key Laboratory of Natural Medicines, China Pharmaceutical University, Nanjing, China
      name:School of Life Science and Technology, China Pharmaceutical University, Nanjing, China
      name:State Key Laboratory of Natural Medicines, China Pharmaceutical University, Nanjing, China
      name:School of Life Science and Technology, China Pharmaceutical University, Nanjing, China

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