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黑斑息肉综合征患者黏膜细菌和代谢组学的改变

Altered mucosal bacteria and metabolomics in patients with Peutz-Jeghers syndrome.

作者信息

Wang Sui, Kou Guan-Jun, Zhao Xiao-Han, Huang Gang, Wang Jue-Xin, Tian Lin, Zuo Xiu-Li, Li Yan-Qing, Wang Jia-Yong, Yu Yan-Bo

机构信息

Department of Respiratory Medicine, The Second Hospital of Shandong University, Jinan, 250033, Shandong, People's Republic of China.

Department of Gastroenterology, Qilu Hospital of Shandong University, 107 Wenhuaxi Road, Jinan, 250012, Shandong, People's Republic of China.

出版信息

Gut Pathog. 2024 Apr 27;16(1):25. doi: 10.1186/s13099-024-00617-9.

Abstract

BACKGROUND

Peutz-Jeghers syndrome (PJS) is a rare genetic disorder characterized by the development of pigmented spots, gastrointestinal polyps and increased susceptibility to cancers. Currently, most studies have investigated intestinal microbiota through fecal microbiota, and there are few reports about mucosa-associated microbiota. It remains valuable to search for the key intestinal microbiota or abnormal metabolic pathways linked to PJS.

AIM

This study aimed to assess the structure and composition of mucosa-associated microbiota in patients with PJS and to explore the potential influence of intestinal microbiota disorders and metabolite changes on PJS.

METHODS

The bacterial composition was analyzed in 13 PJS patients and 12 controls using 16S rRNA gene sequencing (Illumina MiSeq) for bacteria. Differential analyses of the intestinal microbiota were performed from the phylum to species level. Liquid chromatography-tandem mass spectrometry (LC‒MS) was used to detect the differentially abundant metabolites of PJS patients and controls to identify different metabolites and metabolic biomarkers of small intestinal mucosa samples.

RESULTS

High-throughput sequencing confirmed the special characteristics and biodiversity of the mucosa microflora in patients with PJS. They had lower bacterial biodiversity than controls. The abundance of intestinal mucosal microflora was significantly lower than that of fecal microflora. In addition, lipid metabolism, amino acid metabolism, carbohydrate metabolism, nucleotide metabolism and other pathways were significantly different from those of controls, which were associated with the development of the enteric nervous system, intestinal inflammation and development of tumors.

CONCLUSION

This is the first report on the mucosa-associated microbiota and metabolite profile of subjects with PJS, which may be meaningful to provide a structural basis for further research on intestinal microecology in PJS.

摘要

背景

黑斑息肉综合征(PJS)是一种罕见的遗传性疾病,其特征为色素沉着斑、胃肠道息肉以及患癌易感性增加。目前,大多数研究通过粪便微生物群来研究肠道微生物群,关于黏膜相关微生物群的报道较少。寻找与PJS相关的关键肠道微生物群或异常代谢途径仍然具有重要价值。

目的

本研究旨在评估PJS患者黏膜相关微生物群的结构和组成,并探讨肠道微生物群紊乱和代谢物变化对PJS的潜在影响。

方法

使用16S rRNA基因测序(Illumina MiSeq)分析13例PJS患者和12例对照的细菌组成。从门到种水平对肠道微生物群进行差异分析。采用液相色谱 - 串联质谱(LC - MS)检测PJS患者和对照的差异丰富代谢物,以鉴定小肠黏膜样本的不同代谢物和代谢生物标志物。

结果

高通量测序证实了PJS患者黏膜微生物群的特殊特征和生物多样性。他们的细菌生物多样性低于对照组。肠道黏膜微生物群的丰度明显低于粪便微生物群。此外,脂质代谢、氨基酸代谢、碳水化合物代谢、核苷酸代谢等途径与对照组有显著差异,这些差异与肠神经系统的发育、肠道炎症和肿瘤的发生发展有关。

结论

这是关于PJS患者黏膜相关微生物群和代谢物谱的首次报道,可能为进一步研究PJS肠道微生态提供结构基础,具有重要意义。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/575d/11056063/6b0872be1aac/13099_2024_617_Fig1_HTML.jpg

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