Ma Qianzi, Wang Nan, Zheng Xingyue, Liu Junjie, Che Yanlu, Wang Jingting
Department of Otorhinolaryngology-Head and Neck Surgery, The Second Affiliated Hospital, Harbin Medical University, Harbin, People's Republic of China.
Department of Otorhinolaryngology of The Sixth Affiliated Hospital, School of Medicine, South China University of Technology, Foshan, People's Republic of China.
J Inflamm Res. 2025 Jul 26;18:9919-9934. doi: 10.2147/JIR.S526181. eCollection 2025.
The aim of this study was to investigate the correlation between nasal microbiome, metabolites, and their potential contribution to the pathogenesis of allergic rhinitis (AR), a widespread chronic inflammatory disorder that poses a considerable healthcare burden worldwide. Immune dysregulation and environmental factors are key in the development of allergic responses, but the importance of host-microbiota interactions in influencing these responses is gaining recognition.
32 AR patients and 20 healthy controls underwent 16S rDNA sequencing and untargeted metabolomics analysis. Microbial diversity, composition, and functional pathways were compared between groups. Metabolomic alterations were evaluated using LC-MS/MS, and correlations between microbiota and metabolites were analyzed.
While α-diversity did not differ significantly between groups, β-diversity analysis revealed distinct microbial community shifts in AR patients. Specifically, Actinobacteria and Bacteroidetes abundances were increased, and genera Vibrio and Aeromonas were significantly enriched. Metabolomic profiling identified 528 differential metabolites, including altered levels of LPC, and pathway analysis highlighted disrupted linoleic acid metabolism, arachidonic acid metabolism, and tryptophan metabolism. Correlation analysis revealed significant associations between specific microbial taxa (eg, Aeromonas, Vibrio) and metabolites (eg, LPC, arachidonic acid), suggesting a potential link between microbiota-derived metabolic shifts and inflammatory responses in AR.
The perturbation of nasal microbiota-metabolite interactions may play a role in the pathogenesis of AR, emphasizing the need for future investigations into potential pathophysiological mechanisms.
本研究旨在调查鼻腔微生物群、代谢物之间的相关性,以及它们对变应性鼻炎(AR)发病机制的潜在影响。AR是一种广泛存在的慢性炎症性疾病,在全球范围内造成了相当大的医疗负担。免疫失调和环境因素是过敏反应发生发展的关键,但宿主-微生物群相互作用在影响这些反应中的重要性正日益受到认可。
32例AR患者和20名健康对照者接受了16S rDNA测序和非靶向代谢组学分析。比较了各组之间的微生物多样性、组成和功能途径。使用液相色谱-串联质谱法评估代谢组学改变,并分析微生物群与代谢物之间的相关性。
虽然各组之间的α多样性没有显著差异,但β多样性分析显示AR患者的微生物群落发生了明显变化。具体而言,放线菌和拟杆菌的丰度增加,弧菌属和气单胞菌属显著富集。代谢组学分析确定了528种差异代谢物,包括LPC水平的改变,通路分析突出了亚油酸代谢、花生四烯酸代谢和色氨酸代谢的紊乱。相关性分析显示特定微生物类群(如气单胞菌、弧菌)与代谢物(如LPC、花生四烯酸)之间存在显著关联,表明微生物群衍生的代谢变化与AR中的炎症反应之间可能存在联系。
鼻腔微生物群-代谢物相互作用的紊乱可能在AR的发病机制中起作用,这强调了未来对潜在病理生理机制进行研究的必要性。