Microbiome in paired root apices and periapical lesions and its association with clinical signs in persistent apical periodontitis using next‐generation sequencing
Aim To assess and compare the microbiome of paired root apices and periapical lesions from cases with failed endodontic treatment and to associate the microbiome and bacterial metabolic pathways in both sites with asymptomatic apical periodontitis (AAP) and symptomatic apical periodontitis (SAP), us...
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Veröffentlicht in: | International endodontic journal 2023-05, Vol.56 (5), p.622-636 |
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creator | Pérez‐Carrasco, Virginia Uroz‐Torres, David Soriano, Miguel Solana, Carmen Ruiz‐Linares, Matilde Garcia‐Salcedo, Jose Antonio Arias‐Moliz, Maria Teresa |
description | Aim
To assess and compare the microbiome of paired root apices and periapical lesions from cases with failed endodontic treatment and to associate the microbiome and bacterial metabolic pathways in both sites with asymptomatic apical periodontitis (AAP) and symptomatic apical periodontitis (SAP), using next‐generation sequencing (NGS).
Methodology
Matched root apices and periapical lesions of patients with failed root canal treatments were surgically extracted. Specimens were cryopulverized, bacterial DNA was extracted and the V3–V4 hypervariable regions of the 16 S rRNA gene were amplified and sequenced using the Illumina Miseq platform. Diversity and community composition were studied in the paired samples, as well as in AAP and SAP cases. Diversity indices were compared in each case by means of the Wilcoxon matched‐pairs signed rank and Mann–Whitney U tests. Differences in the community composition were explored with multivariate statistical analysis and Linear discriminant analysis Effect Size (LEfSe). Bacterial functional study was performed through the Phylogenetic Investigation of Communities by Reconstruction of Unobserved States (PICRUSt) analysis.
Results
Twenty‐one paired apices and lesions were successfully sequenced and analysed, identifying a total of 21 phyla and 600 genera. A higher alpha‐diversity was observed in the periapical lesions, although no global differences in the community composition between the two sites were found (p = .87), the most prevalent genera being Fusobacterium, Porphyromonas and Streptococcus. Prevotella, Clostridiales_vadinBB60_group, Bosea, Phreatobacter, Afipia and Xanthobacteriaceae_unclassified were enriched in SAP samples, while Pseudopropionibacterium, Campylobacter and Peptoniphilus were significantly more abundant in AAP cases (p |
doi_str_mv | 10.1111/iej.13893 |
format | Article |
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To assess and compare the microbiome of paired root apices and periapical lesions from cases with failed endodontic treatment and to associate the microbiome and bacterial metabolic pathways in both sites with asymptomatic apical periodontitis (AAP) and symptomatic apical periodontitis (SAP), using next‐generation sequencing (NGS).
Methodology
Matched root apices and periapical lesions of patients with failed root canal treatments were surgically extracted. Specimens were cryopulverized, bacterial DNA was extracted and the V3–V4 hypervariable regions of the 16 S rRNA gene were amplified and sequenced using the Illumina Miseq platform. Diversity and community composition were studied in the paired samples, as well as in AAP and SAP cases. Diversity indices were compared in each case by means of the Wilcoxon matched‐pairs signed rank and Mann–Whitney U tests. Differences in the community composition were explored with multivariate statistical analysis and Linear discriminant analysis Effect Size (LEfSe). Bacterial functional study was performed through the Phylogenetic Investigation of Communities by Reconstruction of Unobserved States (PICRUSt) analysis.
Results
Twenty‐one paired apices and lesions were successfully sequenced and analysed, identifying a total of 21 phyla and 600 genera. A higher alpha‐diversity was observed in the periapical lesions, although no global differences in the community composition between the two sites were found (p = .87), the most prevalent genera being Fusobacterium, Porphyromonas and Streptococcus. Prevotella, Clostridiales_vadinBB60_group, Bosea, Phreatobacter, Afipia and Xanthobacteriaceae_unclassified were enriched in SAP samples, while Pseudopropionibacterium, Campylobacter and Peptoniphilus were significantly more abundant in AAP cases (p < .05). Metabolic pathways involved in the amino acid metabolism or degradation and flagellum assembly were more abundant in SAP samples, whereas glucose metabolism‐related pathways were associated with AAP.
Conclusions
The bacterial community composition was similar in the apices and periapical lesions. The microbiome was different in AAP and SAP samples, gram‐negative bacteria showing higher relative abundances in SAP cases. An association was observed between amino acid degradation and flagellum assembly pathways, and the development of tenderness to percussion or palpation.</description><identifier>ISSN: 0143-2885</identifier><identifier>EISSN: 1365-2591</identifier><identifier>DOI: 10.1111/iej.13893</identifier><identifier>PMID: 36689323</identifier><language>eng</language><publisher>England: Wiley Subscription Services, Inc</publisher><subject>Amino acids ; Amino Acids - genetics ; apices ; Bacteria ; Bacteria - genetics ; Community composition ; Dental Pulp Cavity - microbiology ; Discriminant analysis ; Diversity indices ; Flagella ; Glucose metabolism ; Gram-negative bacteria ; Gum disease ; High-Throughput Nucleotide Sequencing ; Humans ; Lesions ; Metabolic pathways ; Metabolism ; microbiome ; Microbiomes ; Microbiota - genetics ; next‐generation sequencing ; periapical lesions ; Periapical Periodontitis - microbiology ; Periodontitis ; persistent apical periodontitis ; Phylogeny ; Root canals ; rRNA ; Statistical analysis ; symptoms</subject><ispartof>International endodontic journal, 2023-05, Vol.56 (5), p.622-636</ispartof><rights>2023 The Authors. published by John Wiley & Sons Ltd on behalf of British Endodontic Society.</rights><rights>2023 The Authors. International Endodontic Journal published by John Wiley & Sons Ltd on behalf of British Endodontic Society.</rights><rights>2023. This article is published under http://creativecommons.org/licenses/by-nc-nd/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3883-5b5565c81179da843df4e6103ec88e3b5a3e09e403fba1fa68951b3fa103d0c83</citedby><cites>FETCH-LOGICAL-c3883-5b5565c81179da843df4e6103ec88e3b5a3e09e403fba1fa68951b3fa103d0c83</cites><orcidid>0000-0002-1358-6616 ; 0000-0003-0559-2159</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1111%2Fiej.13893$$EPDF$$P50$$Gwiley$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2Fiej.13893$$EHTML$$P50$$Gwiley$$Hfree_for_read</linktohtml><link.rule.ids>314,776,780,1411,27901,27902,45550,45551</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/36689323$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Pérez‐Carrasco, Virginia</creatorcontrib><creatorcontrib>Uroz‐Torres, David</creatorcontrib><creatorcontrib>Soriano, Miguel</creatorcontrib><creatorcontrib>Solana, Carmen</creatorcontrib><creatorcontrib>Ruiz‐Linares, Matilde</creatorcontrib><creatorcontrib>Garcia‐Salcedo, Jose Antonio</creatorcontrib><creatorcontrib>Arias‐Moliz, Maria Teresa</creatorcontrib><title>Microbiome in paired root apices and periapical lesions and its association with clinical signs in persistent apical periodontitis using next‐generation sequencing</title><title>International endodontic journal</title><addtitle>Int Endod J</addtitle><description>Aim
To assess and compare the microbiome of paired root apices and periapical lesions from cases with failed endodontic treatment and to associate the microbiome and bacterial metabolic pathways in both sites with asymptomatic apical periodontitis (AAP) and symptomatic apical periodontitis (SAP), using next‐generation sequencing (NGS).
Methodology
Matched root apices and periapical lesions of patients with failed root canal treatments were surgically extracted. Specimens were cryopulverized, bacterial DNA was extracted and the V3–V4 hypervariable regions of the 16 S rRNA gene were amplified and sequenced using the Illumina Miseq platform. Diversity and community composition were studied in the paired samples, as well as in AAP and SAP cases. Diversity indices were compared in each case by means of the Wilcoxon matched‐pairs signed rank and Mann–Whitney U tests. Differences in the community composition were explored with multivariate statistical analysis and Linear discriminant analysis Effect Size (LEfSe). Bacterial functional study was performed through the Phylogenetic Investigation of Communities by Reconstruction of Unobserved States (PICRUSt) analysis.
Results
Twenty‐one paired apices and lesions were successfully sequenced and analysed, identifying a total of 21 phyla and 600 genera. A higher alpha‐diversity was observed in the periapical lesions, although no global differences in the community composition between the two sites were found (p = .87), the most prevalent genera being Fusobacterium, Porphyromonas and Streptococcus. Prevotella, Clostridiales_vadinBB60_group, Bosea, Phreatobacter, Afipia and Xanthobacteriaceae_unclassified were enriched in SAP samples, while Pseudopropionibacterium, Campylobacter and Peptoniphilus were significantly more abundant in AAP cases (p < .05). Metabolic pathways involved in the amino acid metabolism or degradation and flagellum assembly were more abundant in SAP samples, whereas glucose metabolism‐related pathways were associated with AAP.
Conclusions
The bacterial community composition was similar in the apices and periapical lesions. The microbiome was different in AAP and SAP samples, gram‐negative bacteria showing higher relative abundances in SAP cases. An association was observed between amino acid degradation and flagellum assembly pathways, and the development of tenderness to percussion or palpation.</description><subject>Amino acids</subject><subject>Amino Acids - genetics</subject><subject>apices</subject><subject>Bacteria</subject><subject>Bacteria - genetics</subject><subject>Community composition</subject><subject>Dental Pulp Cavity - microbiology</subject><subject>Discriminant analysis</subject><subject>Diversity indices</subject><subject>Flagella</subject><subject>Glucose metabolism</subject><subject>Gram-negative bacteria</subject><subject>Gum disease</subject><subject>High-Throughput Nucleotide Sequencing</subject><subject>Humans</subject><subject>Lesions</subject><subject>Metabolic pathways</subject><subject>Metabolism</subject><subject>microbiome</subject><subject>Microbiomes</subject><subject>Microbiota - genetics</subject><subject>next‐generation sequencing</subject><subject>periapical lesions</subject><subject>Periapical Periodontitis - microbiology</subject><subject>Periodontitis</subject><subject>persistent apical periodontitis</subject><subject>Phylogeny</subject><subject>Root canals</subject><subject>rRNA</subject><subject>Statistical analysis</subject><subject>symptoms</subject><issn>0143-2885</issn><issn>1365-2591</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><sourceid>24P</sourceid><sourceid>EIF</sourceid><recordid>eNp1kUFu1TAQhi1ERR-FBRdAltjAIq0dx6mzRFUpRa3YwDpynMljnvLs4HHUdscRuEQvxklwmsICCW9Gnvn02ZqfsVdSHMt8ThB2x1KZRj1hG6lqXZS6kU_ZRshKFaUx-pA9J9oJIbRQ8hk7VHWd6VJt2P01uhg6DHvg6PlkMULPYwiJ2wkdELe-5xNEXK525CMQBr-2MeVKFBzalJv8BtM37kb0DyThNnOLFCIhJfCrM48WX-iDT5iQ-Ezot9zDbfr14-cWPMRVR_B9Bu_y8AU7GOxI8PKxHrGvH86_nH0srj5fXJ69vyqcMkYVutO61s5Iedr01lSqHyqopVDgjAHVaatANFAJNXRWDjYvQctODTYjvXBGHbG3q3eKIb9Nqd0jORhH6yHM1JantTGyrKTO6Jt_0F2Yo8-_y1RTKylqsVDvViovmSjC0E4R9zbetVK0S3Ztzq59yC6zrx-Nc7eH_i_5J6wMnKzADY5w939Te3n-aVX-BgS0p8g</recordid><startdate>202305</startdate><enddate>202305</enddate><creator>Pérez‐Carrasco, Virginia</creator><creator>Uroz‐Torres, David</creator><creator>Soriano, Miguel</creator><creator>Solana, Carmen</creator><creator>Ruiz‐Linares, Matilde</creator><creator>Garcia‐Salcedo, Jose Antonio</creator><creator>Arias‐Moliz, Maria Teresa</creator><general>Wiley Subscription Services, Inc</general><scope>24P</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QP</scope><scope>K9.</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0002-1358-6616</orcidid><orcidid>https://orcid.org/0000-0003-0559-2159</orcidid></search><sort><creationdate>202305</creationdate><title>Microbiome in paired root apices and periapical lesions and its association with clinical signs in persistent apical periodontitis using next‐generation sequencing</title><author>Pérez‐Carrasco, Virginia ; Uroz‐Torres, David ; Soriano, Miguel ; Solana, Carmen ; Ruiz‐Linares, Matilde ; Garcia‐Salcedo, Jose Antonio ; Arias‐Moliz, Maria Teresa</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3883-5b5565c81179da843df4e6103ec88e3b5a3e09e403fba1fa68951b3fa103d0c83</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>Amino acids</topic><topic>Amino Acids - genetics</topic><topic>apices</topic><topic>Bacteria</topic><topic>Bacteria - genetics</topic><topic>Community composition</topic><topic>Dental Pulp Cavity - microbiology</topic><topic>Discriminant analysis</topic><topic>Diversity indices</topic><topic>Flagella</topic><topic>Glucose metabolism</topic><topic>Gram-negative bacteria</topic><topic>Gum disease</topic><topic>High-Throughput Nucleotide Sequencing</topic><topic>Humans</topic><topic>Lesions</topic><topic>Metabolic pathways</topic><topic>Metabolism</topic><topic>microbiome</topic><topic>Microbiomes</topic><topic>Microbiota - genetics</topic><topic>next‐generation sequencing</topic><topic>periapical lesions</topic><topic>Periapical Periodontitis - microbiology</topic><topic>Periodontitis</topic><topic>persistent apical periodontitis</topic><topic>Phylogeny</topic><topic>Root canals</topic><topic>rRNA</topic><topic>Statistical analysis</topic><topic>symptoms</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Pérez‐Carrasco, Virginia</creatorcontrib><creatorcontrib>Uroz‐Torres, David</creatorcontrib><creatorcontrib>Soriano, Miguel</creatorcontrib><creatorcontrib>Solana, Carmen</creatorcontrib><creatorcontrib>Ruiz‐Linares, Matilde</creatorcontrib><creatorcontrib>Garcia‐Salcedo, Jose Antonio</creatorcontrib><creatorcontrib>Arias‐Moliz, Maria Teresa</creatorcontrib><collection>Wiley Online Library Open Access</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>MEDLINE - Academic</collection><jtitle>International endodontic journal</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Pérez‐Carrasco, Virginia</au><au>Uroz‐Torres, David</au><au>Soriano, Miguel</au><au>Solana, Carmen</au><au>Ruiz‐Linares, Matilde</au><au>Garcia‐Salcedo, Jose Antonio</au><au>Arias‐Moliz, Maria Teresa</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Microbiome in paired root apices and periapical lesions and its association with clinical signs in persistent apical periodontitis using next‐generation sequencing</atitle><jtitle>International endodontic journal</jtitle><addtitle>Int Endod J</addtitle><date>2023-05</date><risdate>2023</risdate><volume>56</volume><issue>5</issue><spage>622</spage><epage>636</epage><pages>622-636</pages><issn>0143-2885</issn><eissn>1365-2591</eissn><abstract>Aim
To assess and compare the microbiome of paired root apices and periapical lesions from cases with failed endodontic treatment and to associate the microbiome and bacterial metabolic pathways in both sites with asymptomatic apical periodontitis (AAP) and symptomatic apical periodontitis (SAP), using next‐generation sequencing (NGS).
Methodology
Matched root apices and periapical lesions of patients with failed root canal treatments were surgically extracted. Specimens were cryopulverized, bacterial DNA was extracted and the V3–V4 hypervariable regions of the 16 S rRNA gene were amplified and sequenced using the Illumina Miseq platform. Diversity and community composition were studied in the paired samples, as well as in AAP and SAP cases. Diversity indices were compared in each case by means of the Wilcoxon matched‐pairs signed rank and Mann–Whitney U tests. Differences in the community composition were explored with multivariate statistical analysis and Linear discriminant analysis Effect Size (LEfSe). Bacterial functional study was performed through the Phylogenetic Investigation of Communities by Reconstruction of Unobserved States (PICRUSt) analysis.
Results
Twenty‐one paired apices and lesions were successfully sequenced and analysed, identifying a total of 21 phyla and 600 genera. A higher alpha‐diversity was observed in the periapical lesions, although no global differences in the community composition between the two sites were found (p = .87), the most prevalent genera being Fusobacterium, Porphyromonas and Streptococcus. Prevotella, Clostridiales_vadinBB60_group, Bosea, Phreatobacter, Afipia and Xanthobacteriaceae_unclassified were enriched in SAP samples, while Pseudopropionibacterium, Campylobacter and Peptoniphilus were significantly more abundant in AAP cases (p < .05). Metabolic pathways involved in the amino acid metabolism or degradation and flagellum assembly were more abundant in SAP samples, whereas glucose metabolism‐related pathways were associated with AAP.
Conclusions
The bacterial community composition was similar in the apices and periapical lesions. The microbiome was different in AAP and SAP samples, gram‐negative bacteria showing higher relative abundances in SAP cases. An association was observed between amino acid degradation and flagellum assembly pathways, and the development of tenderness to percussion or palpation.</abstract><cop>England</cop><pub>Wiley Subscription Services, Inc</pub><pmid>36689323</pmid><doi>10.1111/iej.13893</doi><tpages>15</tpages><orcidid>https://orcid.org/0000-0002-1358-6616</orcidid><orcidid>https://orcid.org/0000-0003-0559-2159</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Amino acids Amino Acids - genetics apices Bacteria Bacteria - genetics Community composition Dental Pulp Cavity - microbiology Discriminant analysis Diversity indices Flagella Glucose metabolism Gram-negative bacteria Gum disease High-Throughput Nucleotide Sequencing Humans Lesions Metabolic pathways Metabolism microbiome Microbiomes Microbiota - genetics next‐generation sequencing periapical lesions Periapical Periodontitis - microbiology Periodontitis persistent apical periodontitis Phylogeny Root canals rRNA Statistical analysis symptoms |
title | Microbiome in paired root apices and periapical lesions and its association with clinical signs in persistent apical periodontitis using next‐generation sequencing |
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