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dc.contributor.authorFrid, Paula
dc.contributor.authorBaraniya, Divyashri
dc.contributor.authorHalbig, Josefine Mareile
dc.contributor.authorRypdal, Veronika Gjertsen
dc.contributor.authorSongstad, Nils Thomas
dc.contributor.authorRosén, Annika
dc.contributor.authorBerstad, Johanna Elisabeth Rykke
dc.contributor.authorFlatø, Berit
dc.contributor.authorAlakwaa, Fadhl
dc.contributor.authorGil, Elisabeth Grut
dc.contributor.authorCetrelli, Lena Elisabet
dc.contributor.authorChen, Tsute
dc.contributor.authorAl-hebshi, Nezar Noor
dc.contributor.authorNordal, Ellen Berit
dc.contributor.authorAl-Haroni, Mohammed
dc.date.accessioned2021-05-04T13:52:19Z
dc.date.available2021-05-04T13:52:19Z
dc.date.created2020-12-03T12:45:54Z
dc.date.issued2020
dc.PublishedFrontiers in Cellular and Infection Microbiology. 2020, 10 1-13.
dc.identifier.issn2235-2988
dc.identifier.urihttps://hdl.handle.net/11250/2753550
dc.description.abstractBackground: The oral microbiota has been connected to the pathogenesis of rheumatoid arthritis through activation of mucosal immunity. The objective of this study was to characterize the salivary oral microbiome associated with juvenile idiopathic arthritis (JIA), and correlate it with the disease activity including gingival inflammation. Methods: Fifty-nine patients with JIA (mean age, 12.6 ± 2.7 years) and 34 healthy controls (HC; mean age 12.3 ± 3.0 years) were consecutively recruited in this Norwegian cross-sectional study. Information about demographics, disease activity, medication history, frequency of tooth brushing and a modified version of the gingival bleeding index (GBI) and the simplified oral hygiene index (OHI-S) was obtained. Microbiome profiling of saliva samples was performed by sequencing of the V1-V3 region of the 16S rRNA gene, coupled with a species-level taxonomy assignment algorithm; QIIME, LEfSe and R-package for Spearman correlation matrix were used for downstream analysis. Results: There were no significant differences between JIA and HC in alpha- and beta-diversity. However, differential abundance analysis revealed several taxa to be associated with JIA: TM7-G1, Solobacterium and Mogibacterium at the genus level; and Leptotrichia oral taxon 417, TM7-G1 oral taxon 352 and Capnocytophaga oral taxon 864 among others, at the species level. Haemophilus species, Leptotrichia oral taxon 223, and Bacillus subtilis, were associated with healthy controls. Gemella morbillorum, Leptotrichia sp. oral taxon 498 and Alloprevotella oral taxon 914 correlated positively with the composite juvenile arthritis 10-joint disease activity score (JADAS10), while Campylobacter oral taxon 44 among others, correlated with the number of active joints. Of all microbial markers identified, only Bacillus subtilis and Campylobacter oral taxon 44 maintained false discovery rate (FDR) < 0.1. Conclusions: In this exploratory study of salivary oral microbiome we found similar alpha- and beta-diversity among children with JIA and healthy. Several taxa associated with chronic inflammation were found to be associated with JIA and disease activity, which warrants further investigation.en_US
dc.language.isoengen_US
dc.publisherFrontiersen_US
dc.rightsNavngivelse 4.0 Internasjonal*
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/deed.no*
dc.titleSalivary Oral Microbiome of Children With Juvenile Idiopathic Arthritis: A Norwegian Cross-Sectional Studyen_US
dc.typeJournal articleen_US
dc.typePeer revieweden_US
dc.description.versionpublishedVersionen_US
dc.rights.holderCopyright 2020 Frid, Baraniya, Halbig, Rypdal, Songstad, Rosèn, Berstad, Flatø, Alakwaa, Gil, Cetrelli, Chen, Al-Hebshi, Nordal and Al-Haroni.en_US
dc.source.articlenumber602239en_US
cristin.ispublishedtrue
cristin.fulltextoriginal
cristin.qualitycode1
dc.identifier.doi10.3389/fcimb.2020.602239
dc.identifier.cristin1855791
dc.source.journalFrontiers in Cellular and Infection Microbiologyen_US
dc.source.4010
dc.identifier.citationFrontiers in Cellular and Infection Microbiology. 2020, 10, 602239en_US
dc.source.volume10en_US


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