Salivary microbiota and metabolic phenotype of patients with recurrent aphthous ulcers

被引:4
作者
Dong, Yunmei [1 ]
Lou, Fangzhi [1 ]
Yan, Li [1 ]
Luo, Shihong [1 ]
Zhang, Yingying [1 ]
Liu, Yang [1 ]
Lv, Shiping [1 ]
Xu, Jingyi [1 ]
Kang, Ning [1 ]
Luo, Zhuoyan [1 ]
Liu, Yiyun [2 ]
Pu, Juncai [2 ]
Ji, Ping [1 ]
Jin, Xin [1 ]
机构
[1] Chongqing Med Univ, Coll Stomatol, Chongqing Key Lab Oral Dis & Biomed Sci, Chongqing, Peoples R China
[2] Chongqing Med Univ, NHC Key Lab Diag & Treatment Brain Funct Dis, Affiliated Hosp 1, Chongqing, Peoples R China
关键词
16S rRNA sequencing; liquid chromatography-mass spectrometry; recurrent aphthous ulcers; salivary metabolites; salivary microbiota; STOMATITIS; STREPTOCOCCUS; ANTIGENS; DISEASE;
D O I
10.1111/odi.14852
中图分类号
R78 [口腔科学];
学科分类号
1003 ;
摘要
ObjectivesRecurrent aphthous ulcer (RAU) is a prevalent oral mucosal disease, affecting around 20% of the global population. It can greatly impair the quality of life for affected individuals. However, the exact etiology of RAU remains unknown. Subjects and Methods16S rRNA sequencing (16S rRNA-seq) and non-targeted liquid chromatography-mass spectrometry (LC-MS) were employed to investigate the salivary microbiota and metabolic phenotype between RAU patients (N=61) and healthy controls (HCs) (N=105). ResultsFindings from 16S rRNA -seq indicated reduced oral microbial diversity in RAU patients compared to HCs, but increased interactions. Clinical variables did not show any significant association with the overall diversity of oral microbiota in RAU patients. However, significant correlations were observed between specific microorganisms and clinical variables. LC-MS results revealed dysregulation of amino acid, lipid, nucleotide, and caffeine metabolism in RAU patients. Furthermore, correlation analysis of 16S rRNA-seq and LC-MS data revealed a significant association between salivary microbiota and metabolites in RAU patients. ConclusionsOur study revealed notable differences in salivary microbiota and metabolic profiles between RAU patients and HCs, indicating a strong link between oral microbiota dysbiosis, metabolic disturbances, and the onset and progression of RAU.
引用
收藏
页码:4412 / 4425
页数:14
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