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Investigating the metabolite signature of an altered oral microbiota as a discriminant factor for multiple sclerosis: a pilot study
by
Morille, Jérémy
, Stürner, Klarissa H.
, Boussamet, Léo
, Nicot, Arnaud B.
, Laplaud, David-Axel
, Shah, Sita
, Bang, Corinna
, Vince, Nicolas
, Mathé, Camille
, Gourdel, Mathilde
, Dugast, Emilie
, Feinstein, Douglas L.
, Montassier, Emmanuel
, Berthelot, Laureline
, Wiertlewski, Sandrine
, Masson, Damien
, Garcia, Alexandra
in
631/250
/ 631/326
/ 692/420
/ Antigens
/ Autoimmune diseases
/ Bacteria
/ Bacteria - genetics
/ Diversity indices
/ Feces
/ Gut
/ Humanities and Social Sciences
/ Humans
/ Inflammation
/ Intestinal microflora
/ Life Sciences
/ Metabolism
/ Metabolites
/ Microbiomes
/ Microbiota
/ Microbiota - genetics
/ Microorganisms
/ multidisciplinary
/ Multiple Sclerosis
/ Pilot Projects
/ Rheumatoid arthritis
/ RNA, Ribosomal, 16S - analysis
/ RNA, Ribosomal, 16S - genetics
/ rRNA 16S
/ Saliva
/ Science
/ Science (multidisciplinary)
/ Surface antigens
2024
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Investigating the metabolite signature of an altered oral microbiota as a discriminant factor for multiple sclerosis: a pilot study
by
Morille, Jérémy
, Stürner, Klarissa H.
, Boussamet, Léo
, Nicot, Arnaud B.
, Laplaud, David-Axel
, Shah, Sita
, Bang, Corinna
, Vince, Nicolas
, Mathé, Camille
, Gourdel, Mathilde
, Dugast, Emilie
, Feinstein, Douglas L.
, Montassier, Emmanuel
, Berthelot, Laureline
, Wiertlewski, Sandrine
, Masson, Damien
, Garcia, Alexandra
in
631/250
/ 631/326
/ 692/420
/ Antigens
/ Autoimmune diseases
/ Bacteria
/ Bacteria - genetics
/ Diversity indices
/ Feces
/ Gut
/ Humanities and Social Sciences
/ Humans
/ Inflammation
/ Intestinal microflora
/ Life Sciences
/ Metabolism
/ Metabolites
/ Microbiomes
/ Microbiota
/ Microbiota - genetics
/ Microorganisms
/ multidisciplinary
/ Multiple Sclerosis
/ Pilot Projects
/ Rheumatoid arthritis
/ RNA, Ribosomal, 16S - analysis
/ RNA, Ribosomal, 16S - genetics
/ rRNA 16S
/ Saliva
/ Science
/ Science (multidisciplinary)
/ Surface antigens
2024
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While trying to remove the title from your shelf something went wrong :( Kindly try again later!
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Investigating the metabolite signature of an altered oral microbiota as a discriminant factor for multiple sclerosis: a pilot study
by
Morille, Jérémy
, Stürner, Klarissa H.
, Boussamet, Léo
, Nicot, Arnaud B.
, Laplaud, David-Axel
, Shah, Sita
, Bang, Corinna
, Vince, Nicolas
, Mathé, Camille
, Gourdel, Mathilde
, Dugast, Emilie
, Feinstein, Douglas L.
, Montassier, Emmanuel
, Berthelot, Laureline
, Wiertlewski, Sandrine
, Masson, Damien
, Garcia, Alexandra
in
631/250
/ 631/326
/ 692/420
/ Antigens
/ Autoimmune diseases
/ Bacteria
/ Bacteria - genetics
/ Diversity indices
/ Feces
/ Gut
/ Humanities and Social Sciences
/ Humans
/ Inflammation
/ Intestinal microflora
/ Life Sciences
/ Metabolism
/ Metabolites
/ Microbiomes
/ Microbiota
/ Microbiota - genetics
/ Microorganisms
/ multidisciplinary
/ Multiple Sclerosis
/ Pilot Projects
/ Rheumatoid arthritis
/ RNA, Ribosomal, 16S - analysis
/ RNA, Ribosomal, 16S - genetics
/ rRNA 16S
/ Saliva
/ Science
/ Science (multidisciplinary)
/ Surface antigens
2024
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Investigating the metabolite signature of an altered oral microbiota as a discriminant factor for multiple sclerosis: a pilot study
Journal Article
Investigating the metabolite signature of an altered oral microbiota as a discriminant factor for multiple sclerosis: a pilot study
2024
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Overview
In multiple sclerosis (MS), alterations of the gut microbiota lead to inflammation. However, the role of other microbiomes in the body in MS has not been fully elucidated. In a pilot case-controlled study, we carried out simultaneous characterization of faecal and oral microbiota and conducted an in-depth analysis of bacterial alterations associated with MS. Using 16S rRNA sequencing and metabolic inference tools, we compared the oral/faecal microbiota and bacterial metabolism pathways in French MS patients (n = 14) and healthy volunteers (HV, n = 21). A classification model based on metabolite flux balance was established and validated in an independent German cohort (MS n = 12, HV n = 38). Our analysis revealed decreases in diversity indices and oral/faecal compartmentalization, the depletion of commensal bacteria (
Aggregatibacter
and
Streptococcus
in saliva and
Coprobacter
and
Roseburia
in faeces) and enrichment of inflammation-associated bacteria in MS patients (
Leptotrichia
and
Fusobacterium
in saliva and Enterobacteriaceae and
Actinomyces
in faeces). Several microbial pathways were also altered (the polyamine pathway and remodelling of bacterial surface antigens and energetic metabolism) while flux balance analysis revealed associated alterations in metabolite production in MS (nitrogen and nucleoside). Based on this analysis, we identified a specific oral metabolite signature in MS patients, that could discriminate MS patients from HV and rheumatoid arthritis patients. This signature allowed us to create and validate a discrimination model on an independent cohort, which reached a specificity of 92%. Overall, the oral and faecal microbiomes were altered in MS patients. This pilot study highlights the need to study the oral microbiota and oral health implications in patients with autoimmune diseases on a larger scale and suggests that knowledge of the salivary microbiome could help guide the identification of new pathogenic mechanisms associated with the microbiota in MS patients.
Publisher
Nature Publishing Group UK,Nature Publishing Group,Nature Portfolio
Subject
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