Periodontal Inflammation and Dysbiosis Relate to Microbial Changes in the Gut

Author:

Kamer Angela R.1,Pushalkar Smruti2ORCID,Hamidi Babak1,Janal Malvin N.3ORCID,Tang Vera1,Annam Kumar Raghava Chowdary1,Palomo Leena1,Gulivindala Deepthi1,Glodzik Lidia4,Saxena Deepak5

Affiliation:

1. Department of Periodontology and Implant Dentistry, College of Dentistry, New York University, 345 East 24th Street, New York, NY 10010, USA

2. Center for Genomics and Systems Biology, New York University, 12 Waverly Place, New York, NY 10003, USA

3. Department of Epidemiology and Health Promotion, College of Dentistry, New York University, 345 East 24th Street, New York, NY 10010, USA

4. Department of Radiology, Weill Cornell Medicine, Brain Health Imaging Institute Cornell University, New York, NY 10021, USA

5. Department of Basic Sciences and Craniofacial Biology, College of Dentistry, New York University, 345 East 24th Street, New York, NY 10010, USA

Abstract

Periodontal disease (PerioD) is a chronic inflammatory disease of dysbiotic etiology. Animal models and few human data showed a relationship between oral bacteria and gut dysbiosis. However, the effect of periodontal inflammation and subgingival dysbiosis on the gut is unknown. We hypothesized that periodontal inflammation and its associated subgingival dysbiosis contribute to gut dysbiosis even in subjects free of known gut disorders. We evaluated and compared elderly subjects with Low and High periodontal inflammation (assessed by Periodontal Inflamed Surface Area (PISA)) for stool and subgingival derived bacteria (assayed by 16S rRNA sequencing). The associations between PISA/subgingival dysbiosis and gut dysbiosis and bacteria known to produce short-chain fatty acid (SCFA) were assessed. LEfSe analysis showed that, in Low PISA, species belonging to Lactobacillus, Roseburia, and Ruminococcus taxa and Lactobacillus zeae were enriched, while species belonging to Coprococcus, Clostridiales, and Atopobium were enriched in High PISA. Regression analyses showed that PISA associated with indicators of dysbiosis in the gut mainly reduced abundance of SCFA producing bacteria (Radj = −0.38, p = 0.03). Subgingival bacterial dysbiosis also associated with reduced levels of gut SCFA producing bacteria (Radj = −0.58, p = 0.002). These results suggest that periodontal inflammation and subgingival microbiota contribute to gut bacterial changes.

Funder

NIH

Alzheimer’s Association

Publisher

MDPI AG

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