Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2025 Oct 6.
doi: 10.1002/acn3.70212. Online ahead of print.

Relapsing-Remitting Multiple Sclerosis Is Associated With a Dysbiotic Oral Microbiome

Affiliations
Free article

Relapsing-Remitting Multiple Sclerosis Is Associated With a Dysbiotic Oral Microbiome

Sukirth M Ganesan et al. Ann Clin Transl Neurol. .
Free article

Abstract

Objective: Multiple sclerosis (MS) is a chronic autoimmune disorder characterized by inflammation, demyelination, and neurological impairment. While the gut microbiota's role in MS is extensively studied, the association between the oral microbiota and MS remains underexplored, particularly in North American cohorts. This study aimed to investigate the microbiota (bacterial) composition as well as functional pathways and immune profiles of the oral cavity in 60 patients with relapsing-remitting MS (RRMS), stratified by treatment status, compared to 44 healthy controls (HC).

Methods: Unstimulated saliva was collected for genomic DNA extraction and salivary cytokine quantification. Oral bacterial composition and diversity were analyzed using 16S rRNA sequencing, with functional pathways inferred using PICRUSt2. Salivary cytokine levels were measured via multiplex immunoassays. LEfSe and random forest models identified key discriminatory taxa, and correlations between microbiota and cytokines were assessed using Spearman's rank analysis.

Results: RRMS patients exhibited distinct microbial communities compared to HC and a higher Bacteroidota to Firmicutes ratio. Key taxa such as Campylobacter, Lachnoanaerobaculum, and Porphyromonas were enriched in RRMS. Functional profiling revealed 49 differentially abundant pathways, including the enrichment of lipopolysaccharide biosynthesis in MS. Elevated levels of IFN-γ, IL-6, and other cytokines correlated with the altered microbiome. IL-21, elevated in HC, correlated with anti-inflammatory pathways, suggesting a protective role in immune homeostasis.

Interpretation: This study provides, for the first time, insights into oral microbiome-host interactions in North American RRMS patients, underscoring the interplay between microbial dysbiosis, functional pathways, and immune dysregulation. The oral microbiome shows potential as a biomarker for MS-related immune alterations.

Keywords: cytokines; dysbiosis; inflammation; multiple sclerosis; oral microbiome.

PubMed Disclaimer

References

    1. H. Lassmann, “Multiple Sclerosis Pathology,” Cold Spring Harbor Perspectives in Medicine 8 (2018): a028936.
    1. M. Sospedra and R. Martin, “Immunology of Multiple Sclerosis,” Annual Review of Immunology 23 (2005): 683–747.
    1. E. Huisman, K. Papadimitropoulou, J. Jarrett, et al., “Systematic Literature Review and Network Meta‐Analysis in Highly Active Relapsing–Remitting Multiple Sclerosis and Rapidly Evolving Severe Multiple Sclerosis,” BMJ Open 7 (2017): e013430.
    1. K. Berer, L. A. Gerdes, E. Cekanaviciute, et al., “Gut Microbiota From Multiple Sclerosis Patients Enables Spontaneous Autoimmune Encephalomyelitis in Mice,” Proceedings of the National Academy of Sciences of the United States of America 114 (2017): 10719–10724.
    1. E. Cekanaviciute, B. B. Yoo, T. F. Runia, et al., “Gut Bacteria From Multiple Sclerosis Patients Modulate Human T Cells and Exacerbate Symptoms in Mouse Models,” Proceedings of the National Academy of Sciences of the United States of America 114 (2017): 10713–10718.

LinkOut - more resources