Frontiers in Cellular and Infection Microbiology (Feb 2023)

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

  • 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

DOI
https://doi.org/10.3389/fcimb.2023.1121399
Journal volume & issue
Vol. 13

Abstract

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BackgroundOral 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 methodsWe 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.ResultsWe 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.ConclusionsWe 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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