探讨CpG低聚脱氧核苷酸治疗ova诱导哮喘小鼠模型中肺和肠道微生物群的变化。

IF 4.2 2区 医学 Q2 IMMUNOLOGY Journal of Inflammation Research Pub Date : 2025-01-11 eCollection Date: 2025-01-01 DOI:10.2147/JIR.S487916
Qingqing Wang, Jingjing Ji, Shuaijun Xiao, Jiong Wang, Xuebo Yan, Lei Fang
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引用次数: 0

摘要

目的:我们试图研究CpG寡脱氧核苷酸(CpG- odn)给药对哮喘小鼠肺和肠道微生物群的影响,特别关注其组成、多样性和丰度的变化,并阐明CpG- odn治疗效果的微生物机制,并鉴定其疗效的潜在有益菌。方法:采用HE染色法对大鼠肺、结肠、小肠组织炎症进行分析。采用靶向16S rRNA的高通量测序技术,分析对照组、模型组和CpG-ODN给药组肺、结肠和小肠微生物组的组成、多样性和相关性。结果:(1)组织病理学上,哮喘小鼠肺和肠组织均表现出明显的结构损伤和炎症反应,而CpG-ODN治疗后肺和肠组织结构均接近正常水平,炎症反应明显改善。(2)在特定菌群组成分析中,哮喘小鼠观察到细菌生态失调,伴有Proteobacteria的富集,引起肺和肠上皮损伤和炎症反应。施用CpG-ODN后,细菌生态失调得到改善,有益菌显著富集,提示出现了一种新的微生态。同时,还鉴定出了CpG-ODN治疗的两种生物标志物——示波螺旋体和梭状芽孢杆菌。(3)热图分析显示,肺、小肠和结肠微生物群之间存在显著相关性。结论:CpG-ODN治疗可改善ova诱导的小鼠哮喘。一方面,保持肺和肠的结构完整,保护粘膜物理屏障,另一方面,改善哮喘小鼠肺和肠道微生物群的失调。有益菌及其代谢物发挥微生态优势,调节免疫细胞,参与粘膜免疫反应,保护免疫屏障。同时,Oscillospira和Clostridium作为CpG-ODN治疗的生物标志物,对于探索粪便微生物群移植治疗哮喘的精准治疗具有参考意义。
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Explore Alteration of Lung and Gut Microbiota in a Murine Model of OVA-Induced Asthma Treated by CpG Oligodeoxynucleotides.

Aim: We sought to investigate the impact of CpG oligodeoxynucleotides (CpG-ODN) administration on the lung and gut microbiota in asthmatic mice, specifically focusing on changes in composition, diversity, and abundance, and to elucidate the microbial mechanisms underlying the therapeutic effects of CpG-ODN and identify potential beneficial bacteria indicative of its efficacy.

Methods: HE staining were used to analyze inflammation in lung, colon and small intestine tissues. High-throughput sequencing technology targeting 16S rRNA was employed to analyze the composition, diversity, and correlation of microbiome in the lung, colon and small intestine of control, model and CpG-ODN administration groups.

Results: (1) Histopathologically, both lung and intestinal tissue in asthmatic mice exhibited significant structural damage and inflammatory response, whereas the structure of both lung and intestinal tissue approached normal levels, accompanied by a notable improvement in the inflammatory response after CpG-ODN treatment. (2) In the specific microbiota composition analysis, bacterial dysbiosis observed in the asthmatic mice, accompanied by enrichment of Proteobacteria found to cause lung and intestinal epithelial damage and inflammatory reaction. After CpG-ODN administration, bacterial dysbiosis was improved, and a notable enrichment of beneficial bacteria, indicating a novel microecology. Meanwhile Oscillospira and Clostridium were identified as two biomarkers of the CpG-ODN treatment. (3) Heatmap analysis revealed significant correlations among lung, small intestine, and colon microbiota.

Conclusion: CpG-ODN treatment can ameliorate OVA-induced asthma in mice. One side, preserving the structural integrity of the lung and intestine, safeguarding the mucosal physical barrier, the other side, improving the dysbiosis of lung and gut microbiota in asthmatic mice. Beneficial bacteria and metabolites take up microecological advantages, regulate immune cells and participate in the mucosal immune response to protect the immune barrier. Meanwhile, Oscillospira and Clostridium as biomarkers for CpG-ODN treatment, has reference significance for exploring precise Fecal microbiota transplantation treatment for asthma.

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来源期刊
Journal of Inflammation Research
Journal of Inflammation Research Immunology and Microbiology-Immunology
CiteScore
6.10
自引率
2.20%
发文量
658
审稿时长
16 weeks
期刊介绍: An international, peer-reviewed, open access, online journal that welcomes laboratory and clinical findings on the molecular basis, cell biology and pharmacology of inflammation.
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