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胆酸依赖菌株诱导初级胆汁酸 7-脱羟化。

Strain-dependent induction of primary bile acid 7-dehydroxylation by cholic acid.

机构信息

Environmental Microbiology Laboratory, School of Architecture, Civil and Environmental Engineering, École Polytechnique Fédérale de Lausanne, Lausanne, Switzerland.

Institute for Infectious Diseases, University of Bern, Bern, Switzerland.

出版信息

BMC Microbiol. 2024 Aug 1;24(1):286. doi: 10.1186/s12866-024-03433-y.

Abstract

BACKGROUND

Bile acids (BAs) are steroid-derived molecules with important roles in digestion, the maintenance of host metabolism, and immunomodulation. Primary BAs are synthesized by the host, while secondary BAs are produced by the gut microbiome through transformation of the former. The regulation of microbial production of secondary BAs is not well understood, particularly the production of 7-dehydroxylated BAs, which are the most potent agonists for host BA receptors. The 7-dehydroxylation of cholic acid (CA) is well established and is linked to the expression of a bile acid-inducible (bai) operon responsible for this process. However, little to no 7-dehydroxylation has been reported for other host-derived BAs (e.g., chenodeoxycholic acid, CDCA or ursodeoxycholic acid, UDCA).

RESULTS

Here, we demonstrate that the 7-dehydroxylation of CDCA and UDCA by the human isolate Clostridium scindens is induced when CA is present, suggesting that CA-dependent transcriptional regulation is required for substantial 7-dehydroxylation of these primary BAs. This is supported by the finding that UDCA alone does not promote expression of bai genes. CDCA upregulates expression of the bai genes but the expression is greater when CA is present. In contrast, the murine isolate Extibacter muris exhibits a distinct response; CA did not induce significant 7-dehydroxylation of primary BAs, whereas BA 7-dehydroxylation was promoted upon addition of germ-free mouse cecal content in vitro. However, E. muris was found to 7-dehydroxylate in vivo.

CONCLUSIONS

The distinct expression responses amongst strains indicate that bai genes are regulated differently. CA promoted bai operon gene expression and the 7-dehydroxylating activity in C. scindens strains. Conversely, the in vitro activity of E. muris was promoted only after the addition of cecal content and the isolate did not alter bai gene expression in response to CA. The accessory gene baiJ was only upregulated in the C. scindens ATCC 35704 strain, implying mechanistic differences amongst isolates. Interestingly, the human-derived C. scindens strains were also capable of 7-dehydroxylating murine bile acids (muricholic acids) to a limited extent. This study shows novel 7-dehydroxylation activity in vitro resulting from the presence of CA and suggests distinct bai gene expression across bacterial species.

摘要

背景

胆汁酸(BAs)是甾体衍生分子,在消化、宿主代谢维持和免疫调节中发挥重要作用。初级 BAs 由宿主合成,而次级 BAs 则由肠道微生物群通过转化前者产生。微生物次级 BAs 产生的调控尚不清楚,特别是 7-脱羟基 BAs 的产生,7-脱羟基 BAs 是宿主 BA 受体的最有效激动剂。胆酸(CA)的 7-脱羟基化作用得到了很好的证实,并且与负责该过程的胆汁酸诱导(bai)操纵子的表达有关。然而,其他宿主来源的 BAs(如鹅脱氧胆酸、CDCA 或熊去氧胆酸、UDCA)几乎没有报道过 7-脱羟基化作用。

结果

在这里,我们证明当 CA 存在时,人源分离株 Clostridium scindens 对 CDCA 和 UDCA 的 7-脱羟基化作用是诱导的,这表明 CA 依赖性转录调控对于这些初级 BAs 的大量 7-脱羟基化作用是必需的。这一发现得到了支持,即单独的 UDCA 不会促进 bai 基因的表达。CDCA 上调 bai 基因的表达,但当 CA 存在时表达更大。相比之下,鼠源分离株 Extibacter muris 表现出明显不同的反应;CA 不会诱导初级 BAs 的显著 7-脱羟基化作用,而 BA 7-脱羟基化作用在体外添加无菌鼠盲肠内容物后得到促进。然而,发现 E. muris 在体内进行 7-脱羟基化。

结论

不同菌株之间的表达反应表明 bai 基因受到不同的调控。CA 促进了 C. scindens 菌株 bai 操纵子基因的表达和 7-脱羟基化活性。相反,E. muris 的体外活性仅在添加盲肠内容物后才得到促进,并且该分离株没有响应 CA 改变 bai 基因的表达。辅助基因 baiJ 仅在 C. scindens ATCC 35704 菌株中上调,暗示了分离株之间的机制差异。有趣的是,人源分离株 C. scindens 也能够在一定程度上 7-脱羟基化鼠胆汁酸(muricholic acids)。本研究表明,在 CA 的存在下,体外产生了新的 7-脱羟基化活性,并表明不同细菌物种之间 bai 基因表达的不同。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eb4b/11293179/fb7f8bab8f70/12866_2024_3433_Fig1_HTML.jpg

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