全球微生物组中二级胆汁酸产生基因的系统鉴定。

IF 5 2区 生物学 Q1 MICROBIOLOGY mSystems Pub Date : 2025-01-21 Epub Date: 2024-12-17 DOI:10.1128/msystems.00817-24
Yuwei Yang, Wenxing Gao, Ruixin Zhu, Liwen Tao, Wanning Chen, Xinyue Zhu, Mengping Shen, Tingjun Xu, Tingting Zhao, Xiaobai Zhang, Lixin Zhu, Na Jiao
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引用次数: 0

摘要

胆汁酸(BA)的微生物代谢对维持脊椎动物宿主和环境的平衡至关重要。尽管参与胆汁酸代谢的某些生物已被确定,但对微生物、代谢酶和胆汁酸的全面、综合阐释仍未完成。为了弥补这一差距,我们采用隐马尔可夫模型在一个由 28,813 个 RefSeq 多王国微生物完整基因组组成的大规模高质量搜索库中进行了系统搜索,从而构建了一个次级胆汁酸生产基因目录。该目录大大扩展了次级胆汁酸产生基因在 11 个门(包括细菌、古菌和真菌)中的分布,并扩展到 14 个栖息地,涵盖了宿主和环境背景。此外,我们还强调了次级胆汁酸 (SBA) 与胃肠道和肝脏疾病(包括炎症性肠病 (IBD)、结肠直肠癌 (CRC) 和非酒精性脂肪肝 (NAFLD))之间的关联,进一步阐明了次级胆汁酸产生基因的疾病特异性改变。此外,鉴于猪的次级胆汁酸生成基因组成非常接近,我们建议将猪作为特别适合研究人类次级胆汁酸生成的动物模型。该基因目录为今后研究微生物胆汁酸代谢提供了全面可靠的基础,为了解微生物对健康和疾病的贡献提供了新的视角:胆汁酸代谢是宿主微生物和环境微生物的一项重要功能。现有的功能注释来源单一,对跨栖息地分析造成了限制。我们构建了一个系统的次级胆汁酸生产基因目录,其中包括大量高质量的参考序列,这推动了全球微生物组中胆汁酸代谢的研究,对 "同一健康 "概念具有重要意义。我们进一步强调了微生物群-次级胆汁酸轴作为肝脏和肠道疾病治疗靶点的潜力,以及利用动物模型研究人类胆汁酸代谢的不同可行性。该基因目录为研究人类、动物、植物和环境等不同领域的微生物胆汁酸代谢提供了坚实的基础,揭示了微生物对 "整体健康 "的贡献。
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Systematic identification of secondary bile acid production genes in global microbiome.

Microbial metabolism of bile acids (BAs) is crucial for maintaining homeostasis in vertebrate hosts and environments. Although certain organisms involved in bile acid metabolism have been identified, a global, comprehensive elucidation of the microbes, metabolic enzymes, and bile acid remains incomplete. To bridge this gap, we employed hidden Markov models to systematically search in a large-scale and high-quality search library comprising 28,813 RefSeq multi-kingdom microbial complete genomes, enabling us to construct a secondary bile acid production gene catalog. This catalog greatly expanded the distribution of secondary bile acid production genes across 11 phyla, encompassing bacteria, archaea, and fungi, and extended to 14 habitats spanning hosts and environmental contexts. Furthermore, we highlighted the associations between secondary bile acids (SBAs) and gastrointestinal and hepatic disorders, including inflammatory bowel disease (IBD), colorectal cancer (CRC), and nonalcoholic fatty liver disease (NAFLD), further elucidating disease-specific alterations in secondary bile acid production genes. Additionally, we proposed the pig as a particularly suitable animal model for investigating secondary bile acid production in humans, given its closely aligned secondary bile acid production gene composition. This gene catalog provides a comprehensive and reliable foundation for future studies on microbial bile acid metabolism, offering new insights into the microbial contributions to health and disease.

Importance: Bile acid metabolism is an important function in both host and environmental microorganisms. The existing functional annotations from single source pose limitations on cross-habitat analysis. Our construction of a systematic secondary bile acid production gene catalog encompassing numerous high-quality reference sequences propelled research on bile acid metabolism in the global microbiome, holding significance for the concept of One Health. We further highlighted the potential of the microbiota-secondary bile acid axis as a target for the treatment of hepatic and intestinal diseases, as well as the varying feasibility of using animal models for studying human bile acid metabolism. This gene catalog offers a solid groundwork for investigating microbial bile acid metabolism across different compartments, including humans, animals, plants, and environments, shedding light on the contributions of microorganisms to One Health.

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来源期刊
mSystems
mSystems Biochemistry, Genetics and Molecular Biology-Biochemistry
CiteScore
10.50
自引率
3.10%
发文量
308
审稿时长
13 weeks
期刊介绍: mSystems™ will publish preeminent work that stems from applying technologies for high-throughput analyses to achieve insights into the metabolic and regulatory systems at the scale of both the single cell and microbial communities. The scope of mSystems™ encompasses all important biological and biochemical findings drawn from analyses of large data sets, as well as new computational approaches for deriving these insights. mSystems™ will welcome submissions from researchers who focus on the microbiome, genomics, metagenomics, transcriptomics, metabolomics, proteomics, glycomics, bioinformatics, and computational microbiology. mSystems™ will provide streamlined decisions, while carrying on ASM''s tradition of rigorous peer review.
期刊最新文献
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