Oral microbiomes of patients with infective endocarditis (IE): a comparative pilot study of IE patients, patients at risk for IE and healthy controls
Infective endocarditis (IE) is an uncommon disease with high morbidity and mortality rates, which often develops from oral bacterial species entering circulation. We compared oral microbiome profiles of three groups: IE patients (N 9 patients; n = 27 samples), disease controls at risk for IE (N = 2...
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creator | Mougeot, Jean-Luc C. Beckman, Micaela Paster, Bruce J. Lockhart, Peter B. Bahrani Mougeot, Farah |
description | Infective endocarditis (IE) is an uncommon disease with high morbidity and mortality rates, which often develops from oral bacterial species entering circulation.
We compared oral microbiome profiles of three groups: IE patients (N 9 patients; n = 27 samples), disease controls at risk for IE (N = 28; n = 84), and healthy controls (N = 37; n = 111). Bacterial species in IE patients' blood cultures were identified for comparison with matched oral samples.
Oral microbiome profiles were obtained from buccal mucosa, saliva, and tongue samples for all three groups and from sub- and supra-gingival plaque samples of the IE group (N = 9; n = 16) and disease controls (N = 28; n = 54). Alpha- and beta-diversities were determined based on relative abundance data. Discriminative species were identified by LEfSe, post hoc Mann-Whitney, and ROC analyses. Identity of the bacterial species in IE patients' blood cultures was confirmed by 16S-rRNA gene Sanger sequencing.
Alpha- and beta-diversities differed between groups. Discriminative IE-associated species were identified, e.g. Haemophilus parainfluenzae and Streptococcus sanguinis. Two blood isolates were Staphylococcus aureus, also identified in one matched saliva sample. Streptococcus mutans was present in one patient's plaque samples and blood culture.
Oral microbiomes of IE, non-IE disease controls, and healthy controls differed significantly. A better understanding of IE-related bacterial-host interactions is warranted. |
doi_str_mv | 10.1080/20002297.2022.2144614 |
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We compared oral microbiome profiles of three groups: IE patients (N 9 patients; n = 27 samples), disease controls at risk for IE (N = 28; n = 84), and healthy controls (N = 37; n = 111). Bacterial species in IE patients' blood cultures were identified for comparison with matched oral samples.
Oral microbiome profiles were obtained from buccal mucosa, saliva, and tongue samples for all three groups and from sub- and supra-gingival plaque samples of the IE group (N = 9; n = 16) and disease controls (N = 28; n = 54). Alpha- and beta-diversities were determined based on relative abundance data. Discriminative species were identified by LEfSe, post hoc Mann-Whitney, and ROC analyses. Identity of the bacterial species in IE patients' blood cultures was confirmed by 16S-rRNA gene Sanger sequencing.
Alpha- and beta-diversities differed between groups. Discriminative IE-associated species were identified, e.g. Haemophilus parainfluenzae and Streptococcus sanguinis. Two blood isolates were Staphylococcus aureus, also identified in one matched saliva sample. Streptococcus mutans was present in one patient's plaque samples and blood culture.
Oral microbiomes of IE, non-IE disease controls, and healthy controls differed significantly. A better understanding of IE-related bacterial-host interactions is warranted.</description><identifier>ISSN: 2000-2297</identifier><identifier>EISSN: 2000-2297</identifier><identifier>DOI: 10.1080/20002297.2022.2144614</identifier><identifier>PMID: 36407280</identifier><language>eng</language><publisher>United States: Taylor & Francis</publisher><subject>Associated species ; Bacteria ; bacterial species ; Blood ; Blood culture ; Buccal mucosa ; Disease control ; Endocarditis ; Gene sequencing ; Health risks ; Infective endocarditis ; Microbiomes ; Morbidity ; next-generation sequencing ; oral microbiome ; Original ; Relative abundance ; Risk management ; rRNA 16S ; Saliva ; Species ; Streptococcus infections</subject><ispartof>Journal of oral microbiology, 2023-01, Vol.15 (1), p.2144614-2144614</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. This work is licensed under the Creative Commons Attribution License http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</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-c562t-c8268e1377a621b9b6cf011c719def41f3fa558d6ed016e7592d07326af5ed3b3</citedby><cites>FETCH-LOGICAL-c562t-c8268e1377a621b9b6cf011c719def41f3fa558d6ed016e7592d07326af5ed3b3</cites><orcidid>0000-0002-8903-333X</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/PMC9668282/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC9668282/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,864,885,2102,27502,27924,27925,53791,53793,59143,59144</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/36407280$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Mougeot, Jean-Luc C.</creatorcontrib><creatorcontrib>Beckman, Micaela</creatorcontrib><creatorcontrib>Paster, Bruce J.</creatorcontrib><creatorcontrib>Lockhart, Peter B.</creatorcontrib><creatorcontrib>Bahrani Mougeot, Farah</creatorcontrib><title>Oral microbiomes of patients with infective endocarditis (IE): a comparative pilot study of IE patients, patients at risk for IE and healthy controls</title><title>Journal of oral microbiology</title><addtitle>J Oral Microbiol</addtitle><description>Infective endocarditis (IE) is an uncommon disease with high morbidity and mortality rates, which often develops from oral bacterial species entering circulation.
We compared oral microbiome profiles of three groups: IE patients (N 9 patients; n = 27 samples), disease controls at risk for IE (N = 28; n = 84), and healthy controls (N = 37; n = 111). Bacterial species in IE patients' blood cultures were identified for comparison with matched oral samples.
Oral microbiome profiles were obtained from buccal mucosa, saliva, and tongue samples for all three groups and from sub- and supra-gingival plaque samples of the IE group (N = 9; n = 16) and disease controls (N = 28; n = 54). Alpha- and beta-diversities were determined based on relative abundance data. Discriminative species were identified by LEfSe, post hoc Mann-Whitney, and ROC analyses. Identity of the bacterial species in IE patients' blood cultures was confirmed by 16S-rRNA gene Sanger sequencing.
Alpha- and beta-diversities differed between groups. Discriminative IE-associated species were identified, e.g. Haemophilus parainfluenzae and Streptococcus sanguinis. Two blood isolates were Staphylococcus aureus, also identified in one matched saliva sample. Streptococcus mutans was present in one patient's plaque samples and blood culture.
Oral microbiomes of IE, non-IE disease controls, and healthy controls differed significantly. A better understanding of IE-related bacterial-host interactions is warranted.</description><subject>Associated species</subject><subject>Bacteria</subject><subject>bacterial species</subject><subject>Blood</subject><subject>Blood culture</subject><subject>Buccal mucosa</subject><subject>Disease control</subject><subject>Endocarditis</subject><subject>Gene sequencing</subject><subject>Health risks</subject><subject>Infective endocarditis</subject><subject>Microbiomes</subject><subject>Morbidity</subject><subject>next-generation sequencing</subject><subject>oral microbiome</subject><subject>Original</subject><subject>Relative abundance</subject><subject>Risk management</subject><subject>rRNA 16S</subject><subject>Saliva</subject><subject>Species</subject><subject>Streptococcus infections</subject><issn>2000-2297</issn><issn>2000-2297</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><sourceid>0YH</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><sourceid>DOA</sourceid><recordid>eNp9kstuEzEUhkcIRKvQRwBZYlMkEnwbj82iAlUBIlXqBtaWx5fGYWYcbE-rPAjvi6dJQ8sCb47t85_P9vFfVa8RXCDI4QcMIcRYNAtcwgIjShmiz6rTaX8-JZ4_mp9UZyltygoSzDnFL6sTwihsMIen1e_rqDrQex1D60NvEwgObFX2dsgJ3Pm8Bn5wVmd_a4EdTNAqGp99Auer5buPQAEd-q2K6l6w9V3IIOXR7CbOanlEvf8LVRlEn34CF-KkUIMBa6u6vN4V1pBj6NKr6oVTXbJnhzirfnxZfr_8Nr-6_rq6_Hw11zXDea45Ztwi0jSKYdSKlmkHEdINEsY6ihxxqq65YdZAxGxTC2xgQzBTrraGtGRWrfZcE9RGbqPvVdzJoLy83wjxRqqYve6stMyZWhCkNeOUOCi0IQpBQU1LcDmwsC72rO3Y9tbo8tbS2ifQp5nBr-VNuJWCMY45LoDzAyCGX6NNWfY-adt1arBhTBI3hFPBSBmz6u0_0k0Y41BaJTEXlEAh6HSjeq8qn5tStO54GQTl5CP54CM5-UgefFTq3jx-ybHqwTVF8GkvKNYIsVd3IXZGZrXrQnRRDdonSf5_xh-_gdgD</recordid><startdate>20230101</startdate><enddate>20230101</enddate><creator>Mougeot, Jean-Luc C.</creator><creator>Beckman, Micaela</creator><creator>Paster, Bruce J.</creator><creator>Lockhart, Peter B.</creator><creator>Bahrani Mougeot, Farah</creator><general>Taylor & Francis</general><general>Taylor & Francis Ltd</general><general>Taylor & Francis Group</general><scope>0YH</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7QP</scope><scope>7T7</scope><scope>7X7</scope><scope>7XB</scope><scope>8FD</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>C1K</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M7P</scope><scope>P64</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope><orcidid>https://orcid.org/0000-0002-8903-333X</orcidid></search><sort><creationdate>20230101</creationdate><title>Oral microbiomes of patients with infective endocarditis (IE): a comparative pilot study of IE patients, patients at risk for IE and healthy controls</title><author>Mougeot, Jean-Luc C. ; 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We compared oral microbiome profiles of three groups: IE patients (N 9 patients; n = 27 samples), disease controls at risk for IE (N = 28; n = 84), and healthy controls (N = 37; n = 111). Bacterial species in IE patients' blood cultures were identified for comparison with matched oral samples.
Oral microbiome profiles were obtained from buccal mucosa, saliva, and tongue samples for all three groups and from sub- and supra-gingival plaque samples of the IE group (N = 9; n = 16) and disease controls (N = 28; n = 54). Alpha- and beta-diversities were determined based on relative abundance data. Discriminative species were identified by LEfSe, post hoc Mann-Whitney, and ROC analyses. Identity of the bacterial species in IE patients' blood cultures was confirmed by 16S-rRNA gene Sanger sequencing.
Alpha- and beta-diversities differed between groups. Discriminative IE-associated species were identified, e.g. Haemophilus parainfluenzae and Streptococcus sanguinis. Two blood isolates were Staphylococcus aureus, also identified in one matched saliva sample. Streptococcus mutans was present in one patient's plaque samples and blood culture.
Oral microbiomes of IE, non-IE disease controls, and healthy controls differed significantly. A better understanding of IE-related bacterial-host interactions is warranted.</abstract><cop>United States</cop><pub>Taylor & Francis</pub><pmid>36407280</pmid><doi>10.1080/20002297.2022.2144614</doi><tpages>1</tpages><orcidid>https://orcid.org/0000-0002-8903-333X</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Associated species Bacteria bacterial species Blood Blood culture Buccal mucosa Disease control Endocarditis Gene sequencing Health risks Infective endocarditis Microbiomes Morbidity next-generation sequencing oral microbiome Original Relative abundance Risk management rRNA 16S Saliva Species Streptococcus infections |
title | Oral microbiomes of patients with infective endocarditis (IE): a comparative pilot study of IE patients, patients at risk for IE and healthy controls |
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