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Taxonomic profiling and populational patterns of bacterial bile salt hydrolase (BSH) genes based on worldwide human gut microbiome

机译:基于全球人体肠微生物微生物微生物组的分类分类分析和种群模式的细菌胆汁盐水解酶(BSH)基因

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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.
机译:胆汁盐水解酶在胆汁酸介导的信号通路中起着重要作用,其调节脂质吸收,葡萄糖代谢和能量稳态。一些报告表明,在许多因缺陷引起的许多疾病中发现了胆汁酸组合物的变化。在这里,我们介绍人微生物群中胆汁盐水解酶(BSH)的分类鉴定,并阐明了来自六大洲的11种不同种群的各种细菌Bsh的丰富和活性差异。我们首次揭示胆汁盐水解酶蛋白序列(BSH)分布在171个肠道细菌菌株中,在117人中的117个属的肠道细菌菌群中分布,以及含有BSH副葡萄球菌的27.52%的这些细菌菌株。在不同群体中的BSH分布模式中观察到显着变化。基于系统发育分析,我们将这些BSH重新分类为八个这样的文学型,并研究了不同群体之间这些种植型的丰度模式。从不同BSH文型中的酶活性检查,BSH-T3显示出最高的酶活性,仅在乳杆菌中发现。 BSH-T5和BSH-T6的文型主要来自具有高百分比的靶菌具有不同的酶活性和欺诈活动。此外,我们发现,健康个体和患有动脉粥样硬化和糖尿病的患者之间存在显着差异,但在BSH的某些文学中,虽然相关性是抗脂病。本研究揭示了人肠道微生物组中BSH的分类和丰度分析,并提供了一种基于系统发育的系统来评估BSHS活性,通过将靶序列分类为特异性的农场型来评估BSHS活性。此外,本作者披露了地理区域和健康/疾病队列的不同群体中BSH的变化模式,这对于了解BSH在相关疾病发展和进展中的作用至关重要。

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