Oral microbial dysbiosis in patients with periodontitis and chronic obstructive pulmonary disease

牙周炎 慢性牙周炎 失调 慢性阻塞性肺病 生物 牙密螺旋体 小桶 维管菌 微生物学 肠道菌群 医学 牙龈卟啉单胞菌 免疫学 内科学 链球菌 遗传学 细菌 基因 转录组 基因表达
作者
Siqin Liu,Guofang Xie,Meifeng Chen,Yukun He,Wenyi Yu,Xiaobo Chen,Weigang Mao,Nanxia Liu,Yuanjie Zhang,Qin Chang,Yingying Qiao,Xinqian Ma,Jianbo Xue,Mengtong Jin,Shuming Guo,Yudong Hou,Zhancheng Gao
出处
期刊:Frontiers in Cellular and Infection Microbiology [Frontiers Media]
卷期号:13: 1121399-1121399 被引量:35
标识
DOI:10.3389/fcimb.2023.1121399
摘要

Background Oral microbiota is closely related to the homeostasis of the oral cavity and lungs. To provide potential information for the prediction, screening, and treatment strategies of individuals, this study compared and investigated the bacterial signatures in periodontitis and chronic obstructive pulmonary disease (COPD). Materials and methods We collected subgingival plaque and gingival crevicular fluid samples from 112 individuals (31 healthy controls, 24 patients with periodontitis, 28 patients with COPD, and 29 patients with both periodontitis and COPD). The oral microbiota was analyzed using 16S rRNA gene sequencing and diversity and functional prediction analysis were performed. Results We observed higher bacterial richness in individuals with periodontitis in both types of oral samples. Using LEfSe and DESeq2 analyses, we found differentially abundant genera that may be potential biomarkers for each group. Mogibacterium is the predominant genus in COPD. Ten genera, including Desulfovibrio , Filifactor , Fretibacterium, Moraxella, Odoribacter, Pseudoramibacter Pyramidobacter, Scardovia, Shuttleworthia and Treponema were predominant in periodontitis. Bergeyella, Lautropia, Rothia, Propionibacterium and Cardiobacterium were the signature of the healthy controls. The significantly different pathways in the Kyoto Encyclopedia of Genes and Genomes (KEGG) between healthy controls and other groups were concentrated in genetic information processing, translation, replication and repair, and metabolism of cofactors and vitamins. Conclusions We found the significant differences in the bacterial community and functional characterization of oral microbiota in periodontitis, COPD and comorbid diseases. Compared to gingival crevicular fluid, subgingival plaque may be more appropriate for reflecting the difference of subgingival microbiota in periodontitis patients with COPD. These results may provide potentials for predicting, screening, and treatment strategies for individuals with periodontitis and COPD.
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