Journal Article

The mediating roles of the oral microbiome in saliva and subgingival sites between e-cigarette smoking and gingival inflammation

Patatanian, Michael, Meinert, Jill, Zhao, Ni, Koh, Hyunwook, Park, Bongsoo, Biswal, Shyam, Leinbach, Leah I., Reyes-Caballero, Hermes, Holbrook, Janet T.

2023

Overview

Background Electronic cigarettes (ECs) have been widely used by young individuals in the U.S. while being considered less harmful than conventional tobacco cigarettes. However, ECs have increasingly been regarded as a health risk, producing detrimental chemicals that may cause, combined with poor oral hygiene, substantial inflammation in gingival and subgingival sites. In this paper, we first report that EC smoking significantly increases the odds of gingival inflammation. Then, through mediation analysis, we seek to identify and explain the mechanism that underlies the relationship between EC smoking and gingival inflammation via the oral microbiome. Methods We collected saliva and subgingival samples from 75 EC users and 75 non-users between 18 and 34 years in age and profiled their microbial compositions via 16S rRNA amplicon sequencing. We conducted raw sequence data processing, denoising and taxonomic annotations using QIIME2 based on the expanded human oral microbiome database (eHOMD). We then created functional annotations (i.e., KEGG pathways) using PICRUSt2. Results We found significant increases in α-diversity for EC users and disparities in β-diversity between EC users and non-users. We also found significant disparities between EC users and non-users in the relative abundance of 36 microbial taxa in the saliva site and 71 microbial taxa in the subgingival site. Finally, we found that 1 microbial taxon in the saliva site and 18 microbial taxa in the subgingival site significantly mediated the effects of EC smoking on gingival inflammation. The mediators on the genus level, for example, include Actinomyces , Rothia, Neisseria, and Enterococcus in the subgingival site. In addition, we report significant disparities between EC users and non-users in the relative abundance of 71 KEGG pathways in the subgingival site. Conclusions These findings reveal that continued EC use can further increase microbial dysbiosis that may lead to periodontal disease. Our findings also suggest that continued surveillance for the effect of ECs on the oral microbiome and its transmission to oral diseases is needed.

• Publisher: BioMed Central,BioMed Central Ltd,Springer Nature B.V,BMC
• Subject: Abundance / Age / Analysis / Annotations / Bacteria / Biological diversity / Biological Microscopy / Biomedical and Life Sciences / Cigarette Smoking / Cigarettes / Complications and side effects / Cytokines / Data processing / Dental caries / Development and progression / Disease / Disease transmission / Dysbacteriosis / Dysbiosis / Electronic cigarette / Electronic cigarettes / Electronic Nicotine Delivery Systems / Gender / Gingiva / Gingival inflammation / Gingivitis / Gum disease / Gums / Health aspects / Health risks / Humans / Hygiene / Inflammation / Life Sciences / Mediation / Microbiology / Microbiomes / Microbiota / Microbiota (Symbiotic organisms) / Microorganisms / Mycology / Nicotine / Oral hygiene / Oral microbiome / Oral mucosa / Parasitology / Periodontal disease / Periodontal diseases / Relative abundance / Risk factors / RNA / RNA, Ribosomal, 16S - genetics / rRNA 16S / Saliva / Saliva microbiome / Secondary school students / Secondary schools / Smoking / Subgingival microbiome / Taxa / Taxonomy / Teenagers / Teeth / Tobacco / Tobacco Products / Toiletries industry / Vaping / Virology