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dc.contributor.authorKalanzi, Dunstan
dc.contributor.authorMayanja-Kizza, Harriet
dc.contributor.authorNakanjako, Damalie
dc.contributor.authorSemitala, Fred
dc.contributor.authorMboowa, Gerald
dc.contributor.authorMbabali, Muhammad
dc.contributor.authorKigozi, Edgar
dc.contributor.authorKatabazi, Fred Ashaba
dc.contributor.authorSserwadda, Ivan
dc.contributor.authorKateete, David P.
dc.contributor.authorAchan, Beatrice
dc.contributor.authorSewankambo, Nelson K.
dc.contributor.authorMuwonge, Adrian
dc.date.accessioned2023-08-03T12:06:04Z
dc.date.available2023-08-03T12:06:04Z
dc.date.issued2022
dc.identifier.uri10.3389/froh.2022.1004930
dc.identifier.urihttp://hdl.handle.net/10570/12069
dc.description.abstractBackground: Dental caries is a multifactorial disease that affects many people. Even though microorganisms play a crucial role in causing dental caries, diagnosis is routinely macroscopic. In order to improve early detection especially in HIV patients who are disproportionately affected, there is need to reconcile the macroscopic and microscopic characteristics of dental caries. Therefore, the aim of this study was to characterize the oral microbiota profile along the decayed, missing, filled teeth (DMFT) index using amplicon sequencing data. Methods: Amplicon sequencing of the V6-V8 region of the 16S rRNA gene was done on DNA recovered from whole unstimulated saliva of 59 HIV positive and 29 HIV negative individuals. The microbial structure, composition and co-occurrence networks were characterized using QIIME-2, Phyloseq, Microbiome-1.9.2 and Metacoder in R. Results: We characterized the oral microbiota into 2,093 operational taxonomic units (OTUs), 21 phyla and 239 genera from 2.6 million high quality sequence reads. While oral microbiota did not cluster participants into distinct groups that track with the DMFT index, we observed the following: (a) The proportion of accessory microbiota was highest in the high DMFT category while the core size (∼50% of richness) remained relatively stable across all categories. (b) The abundance of core genera such as Stomatobaculum, Peptostreptococcus and Campylobacter was high at onset of dental caries, (c) A general difference in oral microbial biomass. (d) The onset of dental caries (low DMFT) was associated with significantly lower oral microbial entropy. Conclusions: Although oral microbial shifts along the DMFT index were not distinct, we demonstrated the potential utility of microbiota dynamics to characterize oral disease. Therefore, we propose a microbial framework using the DMFT index to better understand dental caries among HIV positive people in resource limited settings.en_US
dc.description.sponsorshipNational Institutes of Health (OD), National Institute of Dental & Craniofacial Research (NIDCR), National Institute of Neurological Disorders and Stroke (NINDS), National Heart, Lung, And Blood Institute (NHLBI), Fogarty International Center (FIC), National Institute on Minority Health and Health Disparities (NIMHD), Wellcome Trusten_US
dc.language.isoenen_US
dc.subjectDMFT indexen_US
dc.subjectDental cariesen_US
dc.subjectHIV/AIDSen_US
dc.subjectMicrobial co-occurrence networksen_US
dc.subjectOral microbiotaen_US
dc.titleMicrobial characteristics of dental caries in HIV positive individualsen_US
dc.typeArticleen_US


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