粪拟杆菌IM01抗哮喘功能的临床前研究

Pre-clinical study of anti-asthma function of Bacteroides caccae IM01

  • 摘要:
    目的 利用优化的小鼠过敏性哮喘模型,体内评价一株粪拟杆菌IM01的抗哮喘功能及对肠道菌群的影响。
    方法 对比不同激发方式优化卵清蛋白(OVA)诱导的哮喘小鼠模型。 将雌性BALB/c小鼠随机分为磷酸盐缓冲溶液、OVA模型组和IM01干预组。 IM01干预组经口给予1×109菌落形成单位/只IM01活菌,连续21 d,第22天采集肺部组织。 检测血清OVA特异性免疫球蛋白E(IgE)及肺白细胞介素(IL)-4、IL-5、IL-13水平,并进行肺组织苏木精–伊红染色和粪便16S rRNA基因测序分析。
    结果 OVA雾化激发方式建模更优;口服IM01显著降低哮喘小鼠血清IgE及肺部IL-4、IL-5、IL-13水平,减轻肺病理炎性细胞浸润; IM01调节肠道菌群结构(增高有益菌/降低有害菌丰度)。
    结论 IM01经口干预可缓解哮喘小鼠肺部炎症及病理损伤,并调节肠道菌群组成。

     

    Abstract:
    Objective  To evaluate the anti-asthma function of Bacteroides caccae IM01 and its effect on the gut microbiota using the optimized mouse model of allergic asthma.
    Methods An ovalbumin (OVA)-induced asthmatic mouse model was optimized by comparing different challenge protocols. Female BALB/c mice were randomly divided into phosphate-buffered saline control group, OVA model group, and IM01 intervention group. The IM01 group received daily oral administration of 1×109 colony-forming unit/mouse live IM01 for 21 days. Lung tissues of the mice were collected on day 22 for the detections of serum OVA-specific immunoglobulin E (IgE) level, lung Interleukin (IL)-4, IL-5, and IL-13 concentrations, and H&E staining of lung histopathology and 16S rRNA sequencing of fecal microbiota were conducted.
    Results The OVA aerosol challenge protocol demonstrated superior model establishment. Oral administration of IM01 significantly reduced serum IgE and lung IL-4/IL-5/IL-13 levels in asthmatic mice, while alleviating pathological inflammatory cell infiltration; IM01 modulated gut microbiota composition (increasing beneficial bacteria and decreasing pathogenic bacteria).
    Conclusion Oral administration of IM01 alleviates lung inflammation and pathological damage in asthmatic mice while regulating gut microbiota profiles

     

/

返回文章
返回