Comparative analysis of the microbiota in gingival crevicular fluid from peri-implantitis and periodontitis using 16 S ribosomal RNA gene amplicon sequencing: a cross-sectional study

利用16S核糖体RNA基因扩增子测序对种植体周围炎和牙周炎患者龈沟液中的微生物群进行比较分析:一项横断面研究

阅读:1

Abstract

OBJECTIVE: This study aimed to investigate the diversity, composition, and functional characteristics of the gingival crevicular fluid (GCF) microbiota in individuals with periodontitis, peri-implantitis, and healthy controls (Groups P, PI, and H, respectively), and to identify potential biomarkers specific to PI. MATERIALS AND METHODS: GCF samples were collected from nine participants diagnosed with periodontitis, peri-implantitis, or classified as healthy. Microbial communities were analyzed using 16 S ribosomal RNA (rRNA) gene amplicon sequencing to profile the plaque microbiota. RESULTS: Groups P and PI showed significantly higher species richness than Group H. Principal coordinates analysis revealed that the microbial composition of Group PI was more similar to Group P than Group H. Firmicutes were enriched in Group PI at the phylum level, whereas Neisseria, Veillonella, Streptococcus, Haemophilus, and Prevotella were dominant at the genus level. Linear discriminant analysis effect size analysis identified Proteobacteria, Prevotella, Prevotella_7, Actinobacillus, and Lachnoanaerobaculum as significantly enriched in Group PI. Functional prediction showed associations with energy metabolism, cell wall synthesis, and amino acid synthesis. BugBase analysis revealed distinct phenotypic microbiota profiles in Group PI. Spearman correlation analysis indicated strong positive associations between PI-enriched genera and periodontitis-associated pathogens such as Fusobacterium. CONCLUSION: The microbiota of Group PI exhibits unique taxonomic and functional profiles. Prevotella and other taxa may serve as potential candidate biomarkers associated with PI. Their diagnostic efficacy and clinical applicability require further clarification through large-sample, multi-center validation studies. Functional enrichment in energy metabolism, cell wall synthesis, and amino acid synthesis pathways suggests a role in disease progression.

特别声明

1、本页面内容包含部分的内容是基于公开信息的合理引用;引用内容仅为补充信息,不代表本站立场。

2、若认为本页面引用内容涉及侵权,请及时与本站联系,我们将第一时间处理。

3、其他媒体/个人如需使用本页面原创内容,需注明“来源:[生知库]”并获得授权;使用引用内容的,需自行联系原作者获得许可。

4、投稿及合作请联系:info@biocloudy.com。