Enrichment of sulphate-reducers and depletion of butyrate-producers may be hyperglycaemia signatures in the diabetic oral microbiome
This study aimed to investigate oral microbial signatures associated with hyperglycaemia, by correlating the oral microbiome with three glycaemic markers. Potential association between clinical parameters and oral bacterial taxa that could be modulating the hyperglycaemic microbiome was also explore...
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Veröffentlicht in: | Journal of oral microbiology 2022-12, Vol.14 (1), p.2082727-2082727 |
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creator | Vieira Lima, Camilla Pedrosa Grisi, Daniela Corrêa Guimarães, Maria Do Carmo Machado Salles, Loise Pedrosa Kruly, Paula de Castro Do, Thuy Dos Anjos Borges, Luiz Gustavo Dame-Teixeira, Naile |
description | This study aimed to investigate oral microbial signatures associated with hyperglycaemia, by correlating the oral microbiome with three glycaemic markers. Potential association between clinical parameters and oral bacterial taxa that could be modulating the hyperglycaemic microbiome was also explored.
Twenty-three individuals diagnosed with type 2 Diabetes Mellitus (T2D) and presenting periodontitis were included, as well as 25 systemically and periodontally healthy ones. Fasting blood glucose, glycated haemoglobin, salivary glucose, periodontitis classification, caries experience and activity and salivary pH were evaluated. The V4 region of the 16S rRNA gene was amplified from total salivary DNA, and amplicons were sequenced (Illumina MiSeq).
Hyperglycaemia was correlated with proportions of Treponema, Desulfobulbus, Phocaiecola and Saccharimonadaceae. Desulfobulbus was ubiquitous and the most enriched organism in T2D individuals (log2FC = 4). The Firmicutes/Bacteroidetes ratio was higher at alkali salivary pH than acidic pH. In the network analysis, Desulfobulbus was clustered in a negative association with caries-associated and butyrate-producing bacteria.
The salivary microbiome is shaped by systemic hyperglycaemia, as well as changes in the salivary pH, which may be linked to local hyperglycaemia. The enrichment of predictive biomarkers of gut dysbiosis in the salivary microbiome can reflect its capacity for impairment of hyperglycaemia. |
doi_str_mv | 10.1080/20002297.2022.2082727 |
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Twenty-three individuals diagnosed with type 2 Diabetes Mellitus (T2D) and presenting periodontitis were included, as well as 25 systemically and periodontally healthy ones. Fasting blood glucose, glycated haemoglobin, salivary glucose, periodontitis classification, caries experience and activity and salivary pH were evaluated. The V4 region of the 16S rRNA gene was amplified from total salivary DNA, and amplicons were sequenced (Illumina MiSeq).
Hyperglycaemia was correlated with proportions of Treponema, Desulfobulbus, Phocaiecola and Saccharimonadaceae. Desulfobulbus was ubiquitous and the most enriched organism in T2D individuals (log2FC = 4). The Firmicutes/Bacteroidetes ratio was higher at alkali salivary pH than acidic pH. In the network analysis, Desulfobulbus was clustered in a negative association with caries-associated and butyrate-producing bacteria.
The salivary microbiome is shaped by systemic hyperglycaemia, as well as changes in the salivary pH, which may be linked to local hyperglycaemia. The enrichment of predictive biomarkers of gut dysbiosis in the salivary microbiome can reflect its capacity for impairment of hyperglycaemia.</description><identifier>ISSN: 2000-2297</identifier><identifier>EISSN: 2000-2297</identifier><identifier>DOI: 10.1080/20002297.2022.2082727</identifier><identifier>PMID: 35694216</identifier><language>eng</language><publisher>United States: Taylor & Francis</publisher><subject>16S rRNA sequencing ; blood glucose ; diabetes mellitus ; hyperglycaemia ; Oral microbiome ; Original ; periodontitis ; salivary glucose ; salivary pH</subject><ispartof>Journal of oral microbiology, 2022-12, Vol.14 (1), p.2082727-2082727</ispartof><rights>2022 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group. 2022</rights><rights>2022 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group.</rights><rights>2022 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group. 2022 The Author(s)</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c534t-8cca8f1a5f35d34f8f8d7932eeed72dbfe0b0356ca2eb449e0a1aea2765caea3</citedby><cites>FETCH-LOGICAL-c534t-8cca8f1a5f35d34f8f8d7932eeed72dbfe0b0356ca2eb449e0a1aea2765caea3</cites><orcidid>0000-0002-0490-0036</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC9176348/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC9176348/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,860,881,2095,27481,27903,27904,53769,53771,59119,59120</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/35694216$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Vieira Lima, Camilla Pedrosa</creatorcontrib><creatorcontrib>Grisi, Daniela Corrêa</creatorcontrib><creatorcontrib>Guimarães, Maria Do Carmo Machado</creatorcontrib><creatorcontrib>Salles, Loise Pedrosa</creatorcontrib><creatorcontrib>Kruly, Paula de Castro</creatorcontrib><creatorcontrib>Do, Thuy</creatorcontrib><creatorcontrib>Dos Anjos Borges, Luiz Gustavo</creatorcontrib><creatorcontrib>Dame-Teixeira, Naile</creatorcontrib><title>Enrichment of sulphate-reducers and depletion of butyrate-producers may be hyperglycaemia signatures in the diabetic oral microbiome</title><title>Journal of oral microbiology</title><addtitle>J Oral Microbiol</addtitle><description>This study aimed to investigate oral microbial signatures associated with hyperglycaemia, by correlating the oral microbiome with three glycaemic markers. Potential association between clinical parameters and oral bacterial taxa that could be modulating the hyperglycaemic microbiome was also explored.
Twenty-three individuals diagnosed with type 2 Diabetes Mellitus (T2D) and presenting periodontitis were included, as well as 25 systemically and periodontally healthy ones. Fasting blood glucose, glycated haemoglobin, salivary glucose, periodontitis classification, caries experience and activity and salivary pH were evaluated. The V4 region of the 16S rRNA gene was amplified from total salivary DNA, and amplicons were sequenced (Illumina MiSeq).
Hyperglycaemia was correlated with proportions of Treponema, Desulfobulbus, Phocaiecola and Saccharimonadaceae. Desulfobulbus was ubiquitous and the most enriched organism in T2D individuals (log2FC = 4). The Firmicutes/Bacteroidetes ratio was higher at alkali salivary pH than acidic pH. In the network analysis, Desulfobulbus was clustered in a negative association with caries-associated and butyrate-producing bacteria.
The salivary microbiome is shaped by systemic hyperglycaemia, as well as changes in the salivary pH, which may be linked to local hyperglycaemia. The enrichment of predictive biomarkers of gut dysbiosis in the salivary microbiome can reflect its capacity for impairment of hyperglycaemia.</description><subject>16S rRNA sequencing</subject><subject>blood glucose</subject><subject>diabetes mellitus</subject><subject>hyperglycaemia</subject><subject>Oral microbiome</subject><subject>Original</subject><subject>periodontitis</subject><subject>salivary glucose</subject><subject>salivary pH</subject><issn>2000-2297</issn><issn>2000-2297</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><sourceid>0YH</sourceid><sourceid>DOA</sourceid><recordid>eNp9kstu1TAQhiNERau2jwDyks0pvuW2QaCqQKVKbLq3Jvb4xFViBzsBZd8Hx-GcVu2GjS_jfz7P2H9RvGf0itGGfuKUUs7b-ornKQ8Nr3n9pjjb4rvt4O2L9WlxmdJD3lHBm0byd8WpKKtWcladFY83Pjrdj-hnEixJyzD1MOMuolk0xkTAG2JwGnB2wW-SbpnXuEmmGI6aEVbSIenXCeN-WDXg6IAkt_cwLxETcZ7MPRLjoMscTUKEgYxOx9C5MOJFcWJhSHh5nM-L-28399c_dnc_v99ef73b6VLIeddoDY1lUFpRGiFtYxtTt4Ijoqm56SzSjubWNHDspGyRAgMEXldlLgnEeXF7wJoAD2qKboS4qgBO_QuEuFcQc3kDKmqY6WopmKlpBmWIZB211AhkzEidWZ8PrGnpRjQ6v1_u6RX09Yl3vdqH36pldSVkkwEfj4AYfi2YZjW6pHEYwGNYkuJVXbZN2XKZpeVBmt8rpYj2-RpG1eYH9eQHtflBHf2Q8z68rPE56-n3s-DLQeC8DXGEPyEORs2wDiHaCF67pMT_7_gLpIPJqA</recordid><startdate>20221231</startdate><enddate>20221231</enddate><creator>Vieira Lima, Camilla Pedrosa</creator><creator>Grisi, Daniela Corrêa</creator><creator>Guimarães, Maria Do Carmo Machado</creator><creator>Salles, Loise Pedrosa</creator><creator>Kruly, Paula de Castro</creator><creator>Do, Thuy</creator><creator>Dos Anjos Borges, Luiz Gustavo</creator><creator>Dame-Teixeira, Naile</creator><general>Taylor & Francis</general><general>Taylor & Francis Group</general><scope>0YH</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope><orcidid>https://orcid.org/0000-0002-0490-0036</orcidid></search><sort><creationdate>20221231</creationdate><title>Enrichment of sulphate-reducers and depletion of butyrate-producers may be hyperglycaemia signatures in the diabetic oral microbiome</title><author>Vieira Lima, Camilla Pedrosa ; Grisi, Daniela Corrêa ; Guimarães, Maria Do Carmo Machado ; Salles, Loise Pedrosa ; Kruly, Paula de Castro ; Do, Thuy ; Dos Anjos Borges, Luiz Gustavo ; Dame-Teixeira, Naile</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c534t-8cca8f1a5f35d34f8f8d7932eeed72dbfe0b0356ca2eb449e0a1aea2765caea3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>16S rRNA sequencing</topic><topic>blood glucose</topic><topic>diabetes mellitus</topic><topic>hyperglycaemia</topic><topic>Oral microbiome</topic><topic>Original</topic><topic>periodontitis</topic><topic>salivary glucose</topic><topic>salivary pH</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Vieira Lima, Camilla Pedrosa</creatorcontrib><creatorcontrib>Grisi, Daniela Corrêa</creatorcontrib><creatorcontrib>Guimarães, Maria Do Carmo Machado</creatorcontrib><creatorcontrib>Salles, Loise Pedrosa</creatorcontrib><creatorcontrib>Kruly, Paula de Castro</creatorcontrib><creatorcontrib>Do, Thuy</creatorcontrib><creatorcontrib>Dos Anjos Borges, Luiz Gustavo</creatorcontrib><creatorcontrib>Dame-Teixeira, Naile</creatorcontrib><collection>Taylor & Francis Open Access</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>Journal of oral microbiology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Vieira Lima, Camilla Pedrosa</au><au>Grisi, Daniela Corrêa</au><au>Guimarães, Maria Do Carmo Machado</au><au>Salles, Loise Pedrosa</au><au>Kruly, Paula de Castro</au><au>Do, Thuy</au><au>Dos Anjos Borges, Luiz Gustavo</au><au>Dame-Teixeira, Naile</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Enrichment of sulphate-reducers and depletion of butyrate-producers may be hyperglycaemia signatures in the diabetic oral microbiome</atitle><jtitle>Journal of oral microbiology</jtitle><addtitle>J Oral Microbiol</addtitle><date>2022-12-31</date><risdate>2022</risdate><volume>14</volume><issue>1</issue><spage>2082727</spage><epage>2082727</epage><pages>2082727-2082727</pages><issn>2000-2297</issn><eissn>2000-2297</eissn><abstract>This study aimed to investigate oral microbial signatures associated with hyperglycaemia, by correlating the oral microbiome with three glycaemic markers. Potential association between clinical parameters and oral bacterial taxa that could be modulating the hyperglycaemic microbiome was also explored.
Twenty-three individuals diagnosed with type 2 Diabetes Mellitus (T2D) and presenting periodontitis were included, as well as 25 systemically and periodontally healthy ones. Fasting blood glucose, glycated haemoglobin, salivary glucose, periodontitis classification, caries experience and activity and salivary pH were evaluated. The V4 region of the 16S rRNA gene was amplified from total salivary DNA, and amplicons were sequenced (Illumina MiSeq).
Hyperglycaemia was correlated with proportions of Treponema, Desulfobulbus, Phocaiecola and Saccharimonadaceae. Desulfobulbus was ubiquitous and the most enriched organism in T2D individuals (log2FC = 4). The Firmicutes/Bacteroidetes ratio was higher at alkali salivary pH than acidic pH. In the network analysis, Desulfobulbus was clustered in a negative association with caries-associated and butyrate-producing bacteria.
The salivary microbiome is shaped by systemic hyperglycaemia, as well as changes in the salivary pH, which may be linked to local hyperglycaemia. The enrichment of predictive biomarkers of gut dysbiosis in the salivary microbiome can reflect its capacity for impairment of hyperglycaemia.</abstract><cop>United States</cop><pub>Taylor & Francis</pub><pmid>35694216</pmid><doi>10.1080/20002297.2022.2082727</doi><tpages>1</tpages><orcidid>https://orcid.org/0000-0002-0490-0036</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | 16S rRNA sequencing blood glucose diabetes mellitus hyperglycaemia Oral microbiome Original periodontitis salivary glucose salivary pH |
title | Enrichment of sulphate-reducers and depletion of butyrate-producers may be hyperglycaemia signatures in the diabetic oral microbiome |
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