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SAL_22219 details
Primary information
SALIDSAL_22219
Biomarker nameFusobacteria Fusobacterium
Biomarker TypeNA
Sampling MethodAnalyzed the composition of salivary microbiota of 35 IBD patients by 454 Pyrosequencing of the bacterial 16S rRNA gene and compared it with that of 24 healthy controls (HCs).
Collection MethodUnstimulated saliva collected from subjects was immediately frozen by liquid nitrogen and stored in -80degreeC until use.
Analysis MethodPyrosequencing of the bacterial 16S rRNA gene
Collection SiteUnstimulated Saliva
Disease CategoryHealthy
Disease/ConditionNA
Disease SubtypeNA
Fold Change/ ConcentrationNA
Up/DownregulatedNA
ExosomalNA
OrganismHomo sapiens
PMID24013298
Year of Publication2014
Biomarker ID203490
Biomarker CategoryMicrobe
SequenceNC_004974.1
Title of studyDysbiosis of salivary microbiota in inflammatory bowel disease and its association with oral immunological biomarkers
Abstract of studyAnalysis of microbiota in various biological and environmental samples under a variety of conditions has recently become more practical due to remarkable advances in next-generation sequencing. Changes leading to specific biological states including some of the more complex diseases can now be characterized with relative ease. It is known that gut microbiota is involved in the pathogenesis of inflammatory bowel disease (IBD), mainly Crohn's disease and ulcerative colitis, exhibiting symptoms in the gastrointestinal tract. Recent studies also showed increased frequency of oral manifestations among IBD patients, indicating aberrations in the oral microbiota. Based on these observations, we analyzed the composition of salivary microbiota of 35 IBD patients by 454 pyrosequencing of the bacterial 16S rRNA gene and compared it with that of 24 healthy controls (HCs). The results showed that Bacteroidetes was significantly increased with a concurrent decrease in Proteobacteria in the salivary microbiota of IBD patients. The dominant genera, Streptococcus, Prevotella, Neisseria, Haemophilus, Veillonella, and Gemella, were found to largely contribute to dysbiosis (dysbacteriosis) observed in the salivary microbiota of IBD patients. Analysis of immunological biomarkers in the saliva of IBD patients showed elevated levels of many inflammatory cytokines and immunoglobulin A, and a lower lysozyme level. A strong correlation was shown between lysozyme and IL-1β levels and the relative abundance of Streptococcus, Prevotella, Haemophilus and Veillonella. Our data demonstrate that dysbiosis of salivary microbiota is associated with inflammatory responses in IBD patients, suggesting that it is possibly linked to dysbiosis of their gut microbiota.