Julien Santi-Rocca, David F. Martín-García, Iván Lorca-Alonso, Sandra la González-de la Fuente, Begoña Aguado, Mark Bonner, Véronique Amard, Pierre Amiot, Charlotte Bar, Vincent Berbon, Nefissa Berkani, Alix Burke, Ivonne Cartagena, Jean-Michel Chatard, Céline Coutayar, Guillaume Depraz, Isabel Morales, Narcisa Popa, Stéphane Regniers, Thomas Rissoan, Catherine Robert, Arnaud Tremoureux, Marion Verdy, Manuel Fresno Escudero, Núria Gironès Pujol
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Martín-García, Iván Lorca-Alonso, Sandra la González-de la Fuente, Begoña Aguado, Mark Bonner, Véronique Amard, Pierre Amiot, Charlotte Bar, Vincent Berbon, Nefissa Berkani, Alix Burke, Ivonne Cartagena, Jean-Michel Chatard, Céline Coutayar, Guillaume Depraz, Isabel Morales, Narcisa Popa, Stéphane Regniers, Thomas Rissoan, Catherine Robert, Arnaud Tremoureux, Marion Verdy, Manuel Fresno Escudero, Núria Gironès Pujol","doi":"10.1111/jcpe.14138","DOIUrl":null,"url":null,"abstract":"<div>\n \n \n <section>\n \n <h3> Aim</h3>\n \n <p>To leverage technological advances to propose a more accurate representation of subgingival microbiota diversity and dynamics across health and disease, 25 years after the seminal and still authoritative contribution of Socransky and his colleagues.</p>\n </section>\n \n <section>\n \n <h3> Materials and Methods</h3>\n \n <p>Subgingival plaque from 135 patients (41 healthy, 47 gingivitis, 47 periodontitis) was analysed by V3–V4 16S rRNA sequencing. Sequences were probabilistically assigned to unambiguous taxon groups (UTGs) using advanced bioinformatics. Beyond univariate analyses across health groups, samples were re-classified into microbiota patterns using unsupervised clustering. Bacterial community ordination was performed via correlation analysis.</p>\n </section>\n \n <section>\n \n <h3> Results</h3>\n \n <p>In total, 394 fully characterized UTGs were detected with a confidence level of at least 98% in all samples, with an average of 157 in each sample and 162 representing more than 95% of the bacteriome. Hierarchical clustering identified 10 UTG complexes, with 1 particularly associated with health (Complex 6) and 1 with disease (Complex 10). Complex 10 corresponded to 29 taxa, among which the three species from Socransky's red complex and additional 8 <i>Treponema</i> UTGs, as well as species from the orange complex. Complex 6 comprised species from Socransky's green, yellow and purple complexes. While gingivitis appeared as an intermediate state between health and periodontitis, k-clustering revealed five microbiota patterns related to disease progression, and with specific contributions of bacterial complexes, evidencing alternative pathophysiological routes.</p>\n </section>\n \n <section>\n \n <h3> Conclusion</h3>\n \n <p>These 10 new complexes offer an entry point to understanding plaque ecology, beyond the complexity of microbial dynamics in the periodontal microenvironments revealed by the variability within these groups and the existence of ‘boundary taxa’ linking them. These microbial complexes co-exist in specific microenvironments, and shifts in their relative abundance mark the transition from a healthy microbiota to a diseased microbiota, with intermediary patterns in between. We propose to use these patterns as indicators for the classification of periodontal diseases along a microbial risk scale to complement the current staging and grading system.</p>\n </section>\n </div>","PeriodicalId":15380,"journal":{"name":"Journal of Clinical Periodontology","volume":"52 7","pages":"983-998"},"PeriodicalIF":5.8000,"publicationDate":"2025-06-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Microbial Complexes in Subgingival Plaque: A Bacterial Meta-Taxonomic Study\",\"authors\":\"Julien Santi-Rocca, David F. Martín-García, Iván Lorca-Alonso, Sandra la González-de la Fuente, Begoña Aguado, Mark Bonner, Véronique Amard, Pierre Amiot, Charlotte Bar, Vincent Berbon, Nefissa Berkani, Alix Burke, Ivonne Cartagena, Jean-Michel Chatard, Céline Coutayar, Guillaume Depraz, Isabel Morales, Narcisa Popa, Stéphane Regniers, Thomas Rissoan, Catherine Robert, Arnaud Tremoureux, Marion Verdy, Manuel Fresno Escudero, Núria Gironès Pujol\",\"doi\":\"10.1111/jcpe.14138\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div>\\n \\n \\n <section>\\n \\n <h3> Aim</h3>\\n \\n <p>To leverage technological advances to propose a more accurate representation of subgingival microbiota diversity and dynamics across health and disease, 25 years after the seminal and still authoritative contribution of Socransky and his colleagues.</p>\\n </section>\\n \\n <section>\\n \\n <h3> Materials and Methods</h3>\\n \\n <p>Subgingival plaque from 135 patients (41 healthy, 47 gingivitis, 47 periodontitis) was analysed by V3–V4 16S rRNA sequencing. Sequences were probabilistically assigned to unambiguous taxon groups (UTGs) using advanced bioinformatics. Beyond univariate analyses across health groups, samples were re-classified into microbiota patterns using unsupervised clustering. Bacterial community ordination was performed via correlation analysis.</p>\\n </section>\\n \\n <section>\\n \\n <h3> Results</h3>\\n \\n <p>In total, 394 fully characterized UTGs were detected with a confidence level of at least 98% in all samples, with an average of 157 in each sample and 162 representing more than 95% of the bacteriome. Hierarchical clustering identified 10 UTG complexes, with 1 particularly associated with health (Complex 6) and 1 with disease (Complex 10). Complex 10 corresponded to 29 taxa, among which the three species from Socransky's red complex and additional 8 <i>Treponema</i> UTGs, as well as species from the orange complex. Complex 6 comprised species from Socransky's green, yellow and purple complexes. While gingivitis appeared as an intermediate state between health and periodontitis, k-clustering revealed five microbiota patterns related to disease progression, and with specific contributions of bacterial complexes, evidencing alternative pathophysiological routes.</p>\\n </section>\\n \\n <section>\\n \\n <h3> Conclusion</h3>\\n \\n <p>These 10 new complexes offer an entry point to understanding plaque ecology, beyond the complexity of microbial dynamics in the periodontal microenvironments revealed by the variability within these groups and the existence of ‘boundary taxa’ linking them. These microbial complexes co-exist in specific microenvironments, and shifts in their relative abundance mark the transition from a healthy microbiota to a diseased microbiota, with intermediary patterns in between. We propose to use these patterns as indicators for the classification of periodontal diseases along a microbial risk scale to complement the current staging and grading system.</p>\\n </section>\\n </div>\",\"PeriodicalId\":15380,\"journal\":{\"name\":\"Journal of Clinical Periodontology\",\"volume\":\"52 7\",\"pages\":\"983-998\"},\"PeriodicalIF\":5.8000,\"publicationDate\":\"2025-06-04\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of Clinical Periodontology\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://onlinelibrary.wiley.com/doi/10.1111/jcpe.14138\",\"RegionNum\":1,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"DENTISTRY, ORAL SURGERY & MEDICINE\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Clinical Periodontology","FirstCategoryId":"3","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1111/jcpe.14138","RegionNum":1,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"DENTISTRY, ORAL SURGERY & MEDICINE","Score":null,"Total":0}
Microbial Complexes in Subgingival Plaque: A Bacterial Meta-Taxonomic Study
Aim
To leverage technological advances to propose a more accurate representation of subgingival microbiota diversity and dynamics across health and disease, 25 years after the seminal and still authoritative contribution of Socransky and his colleagues.
Materials and Methods
Subgingival plaque from 135 patients (41 healthy, 47 gingivitis, 47 periodontitis) was analysed by V3–V4 16S rRNA sequencing. Sequences were probabilistically assigned to unambiguous taxon groups (UTGs) using advanced bioinformatics. Beyond univariate analyses across health groups, samples were re-classified into microbiota patterns using unsupervised clustering. Bacterial community ordination was performed via correlation analysis.
Results
In total, 394 fully characterized UTGs were detected with a confidence level of at least 98% in all samples, with an average of 157 in each sample and 162 representing more than 95% of the bacteriome. Hierarchical clustering identified 10 UTG complexes, with 1 particularly associated with health (Complex 6) and 1 with disease (Complex 10). Complex 10 corresponded to 29 taxa, among which the three species from Socransky's red complex and additional 8 Treponema UTGs, as well as species from the orange complex. Complex 6 comprised species from Socransky's green, yellow and purple complexes. While gingivitis appeared as an intermediate state between health and periodontitis, k-clustering revealed five microbiota patterns related to disease progression, and with specific contributions of bacterial complexes, evidencing alternative pathophysiological routes.
Conclusion
These 10 new complexes offer an entry point to understanding plaque ecology, beyond the complexity of microbial dynamics in the periodontal microenvironments revealed by the variability within these groups and the existence of ‘boundary taxa’ linking them. These microbial complexes co-exist in specific microenvironments, and shifts in their relative abundance mark the transition from a healthy microbiota to a diseased microbiota, with intermediary patterns in between. We propose to use these patterns as indicators for the classification of periodontal diseases along a microbial risk scale to complement the current staging and grading system.
期刊介绍:
Journal of Clinical Periodontology was founded by the British, Dutch, French, German, Scandinavian, and Swiss Societies of Periodontology.
The aim of the Journal of Clinical Periodontology is to provide the platform for exchange of scientific and clinical progress in the field of Periodontology and allied disciplines, and to do so at the highest possible level. The Journal also aims to facilitate the application of new scientific knowledge to the daily practice of the concerned disciplines and addresses both practicing clinicians and academics. The Journal is the official publication of the European Federation of Periodontology but wishes to retain its international scope.
The Journal publishes original contributions of high scientific merit in the fields of periodontology and implant dentistry. Its scope encompasses the physiology and pathology of the periodontium, the tissue integration of dental implants, the biology and the modulation of periodontal and alveolar bone healing and regeneration, diagnosis, epidemiology, prevention and therapy of periodontal disease, the clinical aspects of tooth replacement with dental implants, and the comprehensive rehabilitation of the periodontal patient. Review articles by experts on new developments in basic and applied periodontal science and associated dental disciplines, advances in periodontal or implant techniques and procedures, and case reports which illustrate important new information are also welcome.