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系统性红斑狼疮患者肠道病毒组的改变。

Alterations of the gut virome in patients with systemic lupus erythematosus.

机构信息

Department of Rheumatology and Immunology, The Second Affiliated Hospital of Guizhou University of Traditional Chinese Medicine, Guiyang, China.

Department of Microbiology, College of Basic Medical Sciences, Dalian Medical University, Dalian, China.

出版信息

Front Immunol. 2023 Jan 11;13:1050895. doi: 10.3389/fimmu.2022.1050895. eCollection 2022.

Abstract

BACKGROUND

Systemic lupus erythematosus (SLE) is a systemic autoimmune disease that has been linked to the dysbiosis of the gut microbiome and virome. However, the potential characterization of the gut virome in SLE patients needs to be explored more extensively.

METHODS

Herein, we analyzed the gut viral community of 16 SLE patients and 31 healthy controls using both bulk and virus-like particle (VLP)-based metagenomic sequencing of their fecal samples. A total of 15,999 non-redundant viral operational taxonomic units (vOTUs) were identified from the metagenomic assembled contigs and used for gut virome profiling.

RESULTS

SLE patients exhibited a significant decrease in gut viral diversity in the bulk metagenome dataset, but this change was not significant in the VLP metagenome dataset. Also, considerable alterations of the overall gut virome composition and remarkable changes in the viral family compositions were observed in SLE patients compared with healthy controls, as observed in both two technologies. We identified 408 vOTUs (177 SLE-enriched and 231 control-enriched) with significantly different relative abundances between patients and controls in the bulk virome, and 18 vOTUs (17 SLE-enriched in 1 control-enriched) in the VLP virome. The SLE-enriched vOTUs included numerous , , and viruses and were frequently predicted to infect , , and , while the control-enriched contained numerous members of and and were predicted to infect and . We explored the correlations between gut viruses and bacteria and found that some and phages may play key roles in the virus-bacterium network. Furthermore, we explored the gut viral signatures for disease discrimination and achieved an area under the receiver operator characteristic curve (AUC) of above 0.95, suggesting the potential of the gut virome in the prediction of SLE.

CONCLUSION

Our findings demonstrated the alterations in viral diversity and taxonomic composition of the gut virome of SLE patients. Further research into the etiology of SLE and the gut viral community will open up new avenues for treating and preventing SLE and other autoimmune diseases.

摘要

背景

系统性红斑狼疮(SLE)是一种全身性自身免疫性疾病,与肠道微生物组和病毒组的失调有关。然而,需要更广泛地探索 SLE 患者肠道病毒组的潜在特征。

方法

在此,我们通过对粪便样本进行大容量和病毒样颗粒(VLP)为基础的宏基因组测序,分析了 16 名 SLE 患者和 31 名健康对照者的肠道病毒群落。从宏基因组组装的连续体中鉴定出 15999 个非冗余病毒操作分类单位(vOTU),用于肠道病毒组谱分析。

结果

SLE 患者在大容量宏基因组数据集的肠道病毒多样性显著下降,但在 VLP 宏基因组数据集中这种变化并不显著。此外,与健康对照组相比,SLE 患者的整体肠道病毒群落组成发生了相当大的改变,病毒家族组成也发生了显著的变化,这两种技术都观察到了这种变化。我们在大容量病毒组中鉴定出 408 个 vOTU(177 个 SLE 富集和 231 个对照富集),在 VLP 病毒组中鉴定出 18 个 vOTU(17 个 SLE 富集和 1 个对照富集),这些 vOTU 在患者和对照组之间的相对丰度存在显著差异。SLE 富集的 vOTU 包括许多、和病毒,并且经常预测感染、和,而对照富集的 vOTU 则包含许多和病毒,并且预测感染和。我们探讨了肠道病毒与细菌之间的相关性,发现一些和噬菌体可能在病毒-细菌网络中发挥关键作用。此外,我们探讨了肠道病毒特征用于疾病鉴别,并获得了大于 0.95 的接收器操作特性曲线(AUC)下面积,这表明肠道病毒组在 SLE 预测中的潜力。

结论

我们的研究结果表明 SLE 患者肠道病毒组的多样性和分类组成发生了改变。进一步研究 SLE 的病因和肠道病毒群落将为治疗和预防 SLE 和其他自身免疫性疾病开辟新的途径。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5cb4/9874095/6c6e4e7e9f1b/fimmu-13-1050895-g001.jpg

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