Chen Jian, Liu Kaikai, Sun Xiaona, Shi Xuanxuan, Zhao Guanghui, Yang Zhongjun
Department of Stomatology, Qilu Hospital (Qingdao), Cheeloo College of Medicine, Shandong University, Qingdao, China.
School and Hospital of Stomatology, Cheeloo College of Medicine, Shandong University, Jinan, China.
Front Microbiol. 2022 Oct 20;13:992065. doi: 10.3389/fmicb.2022.992065. eCollection 2022.
The pathogenesis of oral lichen planus (OLP) remains unclear, and microbial dysbiosis has been proposed to play a role in the pathogenesis of OLP. Oral mucosal swabs from 77 OLP patients and 76 healthy subjects were collected. The bacterial community among the OLP lesion, the adjacent normal mucosal, and the oral mucosal surface in healthy people were analyzed by 16S sequencing. The factor of gender and age that may affect the flora distribution of OLP patients were explored. Results indicate no significant difference in microbiota between OLP and the adjacent group. Compared with the healthy group, Neisseria, Haemophilus, Fusobacterium, Porphyromonas, Rothia, Actinomyces, and Capnocytophaga significantly increased in the OLP group. Actinomyces increased in male OLP patients, and the other six bacteria increased in female OLP patients. In female OLP patients, Lautropia and Dialister were positively correlated with age. While in male OLP patients, Moraxella, Porphyromonas, and Fusobacterium were positively correlated with age. Functional enrichment analysis suggested that abnormal energy metabolism related to ATP synthases, abnormal transport and metabolism of glycans, amino acids, and vitamins, and disorders of the local immune microenvironment might exist in OLP lesion.
口腔扁平苔藓(OLP)的发病机制尚不清楚,有研究提出微生物群落失调在OLP发病机制中起作用。收集了77例OLP患者和76例健康受试者的口腔黏膜拭子。通过16S测序分析了OLP病变组织、相邻正常黏膜组织以及健康人口腔黏膜表面的细菌群落。探讨了可能影响OLP患者菌群分布的性别和年龄因素。结果表明,OLP组与其相邻组之间的微生物群无显著差异。与健康组相比,OLP组中的奈瑟菌属、嗜血杆菌属、梭杆菌属、卟啉单胞菌属、罗氏菌属、放线菌属和二氧化碳嗜纤维菌属显著增加。男性OLP患者中放线菌属增加,而女性OLP患者中其他六种细菌增加。在女性OLP患者中,劳特罗普菌属和戴阿利斯特菌属与年龄呈正相关。而在男性OLP患者中,莫拉菌属、卟啉单胞菌属和梭杆菌属与年龄呈正相关。功能富集分析表明,OLP病变组织中可能存在与ATP合酶相关的能量代谢异常、聚糖、氨基酸和维生素的转运与代谢异常以及局部免疫微环境紊乱。