Antibiotic effects on bacterial profile in osteonecrosis of the jaw
Identifieur interne : 006534 ( Istex/Corpus ); précédent : 006533; suivant : 006535Antibiotic effects on bacterial profile in osteonecrosis of the jaw
Auteurs : X. Ji ; S. Pushalkar ; Y. Li ; R. Glickman ; K. Fleisher ; D. SaxenaSource :
- Oral Diseases [ 1354-523X ] ; 2012-01.
English descriptors
- KwdEn :
- Actinomyces, Antibiotic, Antibiotic cohort, Antibiotic therapy, Atcc, Bacterial diversity, Bacterial species, Bacterial species phylotypes, Bisphosphonate, Bisphosphonate therapy, Bisphosphonaterelated osteonecrosis, Bisphosphonates, Bronj, Bronj lesion, Bronj tissue samples, Bronj tissues, Cancer patients, Clin, Clin microbiol, Clone, Cohort, Deepak saxena, Denaturing, Denaturing gradient, Dent, Dgge, Doxycycline, Estimator, Eubacterium, Firmicutes, Genus, Kumar, Lactobacillus, Maxillofac, Microbial, Microbiol, Multiple myeloma, Nucleatum, Oral diseases, Oral maxillofac surg, Oral microbiota, Oral pathol, Oral taxon, Osteomyelitis, Osteonecrosis, Osteoporosis, Parvimonas, Parvimonas micra, Phylotypes, Phylum, Pushalkar, Radiol endod, Rdna, Risk factors, Rrna, Ruggiero, Sample groups, Sequencing, Smruti pushalkar, Soft tissues, Species diversity, Species phylotypes, Species richness, Streptococcus, Surg, Taxon, Tetracycline, Tissue samples, Total number, Uncultured, Veillonella, York university college.
- Teeft :
- Actinomyces, Antibiotic, Antibiotic cohort, Antibiotic therapy, Atcc, Bacterial diversity, Bacterial species, Bacterial species phylotypes, Bisphosphonate, Bisphosphonate therapy, Bisphosphonaterelated osteonecrosis, Bisphosphonates, Bronj, Bronj lesion, Bronj tissue samples, Bronj tissues, Cancer patients, Clin, Clin microbiol, Clone, Cohort, Deepak saxena, Denaturing, Denaturing gradient, Dent, Dgge, Doxycycline, Estimator, Eubacterium, Firmicutes, Genus, Kumar, Lactobacillus, Maxillofac, Microbial, Microbiol, Multiple myeloma, Nucleatum, Oral diseases, Oral maxillofac surg, Oral microbiota, Oral pathol, Oral taxon, Osteomyelitis, Osteonecrosis, Osteoporosis, Parvimonas, Parvimonas micra, Phylotypes, Phylum, Pushalkar, Radiol endod, Rdna, Risk factors, Rrna, Ruggiero, Sample groups, Sequencing, Smruti pushalkar, Soft tissues, Species diversity, Species phylotypes, Species richness, Streptococcus, Surg, Taxon, Tetracycline, Tissue samples, Total number, Uncultured, Veillonella, York university college.
Abstract
Oral Diseases (2011) 18, 85–95
Url:
DOI: 10.1111/j.1601-0825.2011.01848.x
Links to Exploration step
ISTEX:CBADEA6DED66F8338E3496F6C8CC50FCED8ABD2CLe document en format XML
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Diseases</title><language><json:string>unknown</json:string></language><doi><json:string>10.1111/(ISSN)1601-0825</json:string></doi><issn><json:string>1354-523X</json:string></issn><eissn><json:string>1601-0825</json:string></eissn><publisherId><json:string>ODI</json:string></publisherId><volume>18</volume><issue>1</issue><pages><first>85</first><last>95</last><total>11</total></pages><genre><json:string>journal</json:string></genre><subject><json:item><value>ORIGINAL ARTICLE</value></json:item></subject></host><namedEntities><unitex><date><json:string>2012</json:string><json:string>16S</json:string></date><geogName></geogName><orgName><json:string>Polytechnic Institute of New York University</json:string><json:string>Institutional Review Board of New York University</json:string><json:string>Department of Basic Sciences</json:string><json:string>Alpha Innotech Corporation</json:string><json:string>Department of Oral and Maxillofacial Surgery</json:string><json:string>NanoDrop 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profile in BRONJ</title><author xml:id="author-0000"><persName><forename type="first">X</forename><surname>Ji</surname></persName><affiliation>Department of Chemical and Biological Sciences, Polytechnic Institute of New York University<address><country key="US"></country></address></affiliation></author><author xml:id="author-0001"><persName><forename type="first">S</forename><surname>Pushalkar</surname></persName><affiliation>Department of Basic Sciences and Craniofacial Biology, New York University College of Dentistry<address><country key="US"></country></address></affiliation></author><author xml:id="author-0002"><persName><forename type="first">Y</forename><surname>Li</surname></persName><affiliation>Department of Basic Sciences and Craniofacial Biology, New York University College of Dentistry<address><country key="US"></country></address></affiliation></author><author xml:id="author-0003"><persName><forename type="first">R</forename><surname>Glickman</surname></persName><affiliation>Department of Oral and Maxillofacial Surgery, New York University College of Dentistry, New York, NY, USA<address><country key="US"></country></address></affiliation></author><author xml:id="author-0004"><persName><forename type="first">K</forename><surname>Fleisher</surname></persName><affiliation>Department of Oral and Maxillofacial Surgery, New York University College of Dentistry, New York, NY, USA<address><country key="US"></country></address></affiliation></author><author xml:id="author-0005"><persName><forename type="first">D</forename><surname>Saxena</surname></persName><affiliation>Department of Basic Sciences and Craniofacial Biology, New York University College of Dentistry<address><country key="US"></country></address></affiliation></author><idno type="istex">CBADEA6DED66F8338E3496F6C8CC50FCED8ABD2C</idno><idno type="ark">ark:/67375/WNG-XQD73D3B-6</idno><idno type="DOI">10.1111/j.1601-0825.2011.01848.x</idno><idno type="unit">ODI1848</idno><idno type="toTypesetVersion">file:ODI.ODI1848.pdf</idno></analytic><monogr><title level="j" type="main">Oral Diseases</title><title level="j" type="alt">ORAL DISEASES</title><idno type="pISSN">1354-523X</idno><idno type="eISSN">1601-0825</idno><idno type="book-DOI">10.1111/(ISSN)1601-0825</idno><idno type="book-part-DOI">10.1111/odi.2011.18.issue-1</idno><idno type="product">ODI</idno><idno type="publisherDivision">ST</idno><imprint><biblScope unit="vol">18</biblScope><biblScope unit="issue">1</biblScope><biblScope unit="page" from="85">85</biblScope><biblScope unit="page" to="95">95</biblScope><biblScope unit="page-count">11</biblScope><publisher>Blackwell Publishing Ltd</publisher><pubPlace>Oxford, UK</pubPlace><date type="published" when="2012-01"></date></imprint></monogr></biblStruct></sourceDesc></fileDesc><profileDesc><abstract xml:lang="en" style="main"><p><hi rend="italic">Oral Diseases</hi> (2011) <hi rend="bold">18</hi>, 85–95</p><p><hi rend="bold">Objective: </hi> Oral infection is considered to play a critical role in the pathogenesis of bisphosphonate‐related osteonecrosis of the jaw (BRONJ), and antibiotic therapy has become a mainstay of BRONJ therapy. This study was aimed to investigate the effect of antibiotics on bacterial diversity in BRONJ tissues.</p><p><hi rend="bold">Materials and methods: </hi> The bacterial profile from soft tissues associated with the BRONJ lesion was determined using 16S rRNA‐based denaturing gradient gel electrophoresis (DGGE) and sequencing. Twenty BRONJ subjects classified as stage 0–2 were enrolled in this study, and patient groups were divided into an antibiotic cohort (n = 10) treated with systemic antibiotic and a non‐antibiotic cohort (n = 10) with no prior antibiotic therapy.</p><p><hi rend="bold">Results: </hi> The DGGE fingerprints indicated no significant differences in bacterial diversity of BRONJ tissue samples. Patients on antibiotics had higher relative abundance of phylum Firmicutes with bacterial species, Streptococcus intermedius, Lactobacillus gasseri, Mogibacterium timidum, and Solobacterium moorei, whereas patients without antibiotics had greater amounts of Parvimonas micra and Streptococcus anginosus. Thirty percent of bacterial populations were uncultured (yet‐to be cultured) phylotypes.</p><p><hi rend="bold">Conclusion: </hi> This study using limited sample size indicated that oral antibiotic therapy may have a limited efficacy on the bacterial population associated with BRONJ lesions.</p></abstract><textClass><keywords xml:lang="en"><term xml:id="k1">BRONJ</term><term xml:id="k2">antibiotics</term><term xml:id="k3">DGGE</term><term xml:id="k4">microbial diversity</term></keywords><keywords rend="tocHeading1"><term>Original Articles</term></keywords><keywords rend="articleCategory"><term>ORIGINAL ARTICLE</term></keywords></textClass><langUsage><language ident="en"></language></langUsage></profileDesc></teiHeader></istex:fulltextTEI><json:item><extension>txt</extension><original>false</original><mimetype>text/plain</mimetype><uri>https://api.istex.fr/document/CBADEA6DED66F8338E3496F6C8CC50FCED8ABD2C/fulltext/txt</uri></json:item></fulltext><metadata><istex:metadataXml wicri:clean="Wiley, elements deleted: body"><istex:xmlDeclaration>version="1.0" encoding="UTF-8" standalone="yes"</istex:xmlDeclaration><istex:document><component version="2.0" type="serialArticle" xml:lang="en"><header><publicationMeta level="product"><publisherInfo><publisherName>Blackwell Publishing Ltd</publisherName><publisherLoc>Oxford, UK</publisherLoc></publisherInfo><doi origin="wiley" registered="yes">10.1111/(ISSN)1601-0825</doi><issn type="print">1354-523X</issn><issn type="electronic">1601-0825</issn><idGroup><id type="product" value="ODI"></id><id type="publisherDivision" value="ST"></id></idGroup><titleGroup><title type="main" sort="ORAL DISEASES">Oral Diseases</title></titleGroup></publicationMeta><publicationMeta level="part" position="01101"><doi origin="wiley">10.1111/odi.2011.18.issue-1</doi><numberingGroup><numbering type="journalVolume" number="18">18</numbering><numbering type="journalIssue" number="1">1</numbering></numberingGroup><coverDate startDate="2012-01">January 2012</coverDate></publicationMeta><publicationMeta level="unit" type="article" position="10" status="forIssue"><doi origin="wiley">10.1111/j.1601-0825.2011.01848.x</doi><idGroup><id type="unit" value="ODI1848"></id></idGroup><countGroup><count type="pageTotal" number="11"></count></countGroup><titleGroup><title type="tocHeading1">Original Articles</title><title type="articleCategory">ORIGINAL ARTICLE</title></titleGroup><copyright>© 2011 John Wiley & Sons A/S</copyright><eventGroup><event type="xmlConverted" agent="Converter:BPG_TO_WML3G version:3.0.1 mode:FullText" date="2011-12-20"></event><event type="publishedOnlineAccepted" date="2011-08-04"></event><event type="publishedOnlineEarlyUnpaginated" date="2011-08-29"></event><event type="firstOnline" date="2011-08-29"></event><event type="publishedOnlineFinalForm" date="2011-12-20"></event><event type="xmlConverted" agent="Converter:WILEY_ML3G_TO_WILEY_ML3GV2 version:3.8.8" date="2014-02-06"></event><event type="xmlConverted" agent="Converter:WML3G_To_WML3G version:4.3.4 mode:FullText" date="2015-02-25"></event></eventGroup><numberingGroup><numbering type="pageFirst" number="85">85</numbering><numbering type="pageLast" number="95">95</numbering></numberingGroup><correspondenceTo>Deepak Saxena, Ph.D, Department of Basic Sciences and Craniofacial Biology, New York University College of Dentistry, 345 East 24th Street, 921‐B, New York, NY 10010‐4086. Tel: +1 212 998 9256, Fax: +1 212 995 4087, E‐mail: <email>ds100@nyu.edu</email></correspondenceTo><linkGroup><link type="toTypesetVersion" href="file:ODI.ODI1848.pdf"></link></linkGroup></publicationMeta><contentMeta><unparsedEditorialHistory>Received 25 February 2011; revised 22 June 2011; accepted 24 July 2011</unparsedEditorialHistory><countGroup><count type="figureTotal" number="6"></count><count type="tableTotal" number="3"></count></countGroup><titleGroup><title type="main">Antibiotic effects on bacterial profile in osteonecrosis of the jaw</title><title type="shortAuthors">X Ji <i>et al</i></title><title type="short"><b>Bacterial profile in BRONJ</b></title></titleGroup><creators><creator creatorRole="author" xml:id="cr1" affiliationRef="#a1"><personName><givenNames>X</givenNames><familyName>Ji</familyName></personName></creator><creator creatorRole="author" xml:id="cr2" affiliationRef="#a2"><personName><givenNames>S</givenNames><familyName>Pushalkar</familyName></personName></creator><creator creatorRole="author" xml:id="cr3" affiliationRef="#a2"><personName><givenNames>Y</givenNames><familyName>Li</familyName></personName></creator><creator creatorRole="author" xml:id="cr4" affiliationRef="#a3"><personName><givenNames>R</givenNames><familyName>Glickman</familyName></personName></creator><creator creatorRole="author" xml:id="cr5" affiliationRef="#a3"><personName><givenNames>K</givenNames><familyName>Fleisher</familyName></personName></creator><creator creatorRole="author" xml:id="cr6" affiliationRef="#a2"><personName><givenNames>D</givenNames><familyName>Saxena</familyName></personName></creator></creators><affiliationGroup><affiliation xml:id="a1" countryCode="US"><unparsedAffiliation>Department of Chemical and Biological Sciences, Polytechnic Institute of New York University</unparsedAffiliation></affiliation><affiliation xml:id="a2" countryCode="US"><unparsedAffiliation>Department of Basic Sciences and Craniofacial Biology, New York University College of Dentistry</unparsedAffiliation></affiliation><affiliation xml:id="a3" countryCode="US"><unparsedAffiliation>Department of Oral and Maxillofacial Surgery, New York University College of Dentistry, New York, NY, USA</unparsedAffiliation></affiliation></affiliationGroup><keywordGroup xml:lang="en"><keyword xml:id="k1">BRONJ</keyword><keyword xml:id="k2">antibiotics</keyword><keyword xml:id="k3">DGGE</keyword><keyword xml:id="k4">microbial diversity</keyword></keywordGroup><abstractGroup><abstract type="main" xml:lang="en"><p><i>Oral Diseases</i> (2011) <b>18</b>, 85–95</p><p><b>Objective: </b> Oral infection is considered to play a critical role in the pathogenesis of bisphosphonate‐related osteonecrosis of the jaw (BRONJ), and antibiotic therapy has become a mainstay of BRONJ therapy. This study was aimed to investigate the effect of antibiotics on bacterial diversity in BRONJ tissues.</p><p><b>Materials and methods: </b> The bacterial profile from soft tissues associated with the BRONJ lesion was determined using 16S rRNA‐based denaturing gradient gel electrophoresis (DGGE) and sequencing. Twenty BRONJ subjects classified as stage 0–2 were enrolled in this study, and patient groups were divided into an antibiotic cohort (n = 10) treated with systemic antibiotic and a non‐antibiotic cohort (n = 10) with no prior antibiotic therapy.</p><p><b>Results: </b> The DGGE fingerprints indicated no significant differences in bacterial diversity of BRONJ tissue samples. Patients on antibiotics had higher relative abundance of phylum Firmicutes with bacterial species, Streptococcus intermedius, Lactobacillus gasseri, Mogibacterium timidum, and Solobacterium moorei, whereas patients without antibiotics had greater amounts of Parvimonas micra and Streptococcus anginosus. Thirty percent of bacterial populations were uncultured (yet‐to be cultured) phylotypes.</p><p><b>Conclusion: </b> This study using limited sample size indicated that oral antibiotic therapy may have a limited efficacy on the bacterial population associated with BRONJ lesions.</p></abstract></abstractGroup></contentMeta></header></component></istex:document></istex:metadataXml><mods version="3.6"><titleInfo lang="en"><title>Antibiotic effects on bacterial profile in osteonecrosis of the jaw</title></titleInfo><titleInfo type="abbreviated" lang="en"><title>Bacterial profile in BRONJ</title></titleInfo><titleInfo type="alternative" contentType="CDATA" lang="en"><title>Antibiotic effects on bacterial profile in osteonecrosis of the jaw</title></titleInfo><name type="personal"><namePart type="given">X</namePart><namePart type="family">Ji</namePart><affiliation>Department of Chemical and Biological Sciences, Polytechnic Institute of New York University</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">S</namePart><namePart type="family">Pushalkar</namePart><affiliation>Department of Basic Sciences and Craniofacial Biology, New York University College of Dentistry</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">Y</namePart><namePart type="family">Li</namePart><affiliation>Department of Basic Sciences and Craniofacial Biology, New York University College of Dentistry</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">R</namePart><namePart type="family">Glickman</namePart><affiliation>Department of Oral and Maxillofacial Surgery, New York University College of Dentistry, New York, NY, USA</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">K</namePart><namePart type="family">Fleisher</namePart><affiliation>Department of Oral and Maxillofacial Surgery, New York University College of Dentistry, New York, NY, USA</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">D</namePart><namePart type="family">Saxena</namePart><affiliation>Department of Basic Sciences and Craniofacial Biology, New York University College of Dentistry</affiliation><role><roleTerm type="text">author</roleTerm></role></name><typeOfResource>text</typeOfResource><genre type="article" displayLabel="article" authority="ISTEX" authorityURI="https://content-type.data.istex.fr" valueURI="https://content-type.data.istex.fr/ark:/67375/XTP-6N5SZHKN-D">article</genre><originInfo><publisher>Blackwell Publishing Ltd</publisher><place><placeTerm type="text">Oxford, UK</placeTerm></place><dateIssued encoding="w3cdtf">2012-01</dateIssued><edition>Received 25 February 2011; revised 22 June 2011; accepted 24 July 2011</edition><copyrightDate encoding="w3cdtf">2012</copyrightDate></originInfo><language><languageTerm type="code" authority="rfc3066">en</languageTerm><languageTerm type="code" authority="iso639-2b">eng</languageTerm></language><physicalDescription><extent unit="figures">6</extent><extent unit="tables">3</extent></physicalDescription><abstract>Oral Diseases (2011) 18, 85–95</abstract><abstract>Objective: Oral infection is considered to play a critical role in the pathogenesis of bisphosphonate‐related osteonecrosis of the jaw (BRONJ), and antibiotic therapy has become a mainstay of BRONJ therapy. This study was aimed to investigate the effect of antibiotics on bacterial diversity in BRONJ tissues.</abstract><abstract>Materials and methods: The bacterial profile from soft tissues associated with the BRONJ lesion was determined using 16S rRNA‐based denaturing gradient gel electrophoresis (DGGE) and sequencing. Twenty BRONJ subjects classified as stage 0–2 were enrolled in this study, and patient groups were divided into an antibiotic cohort (n = 10) treated with systemic antibiotic and a non‐antibiotic cohort (n = 10) with no prior antibiotic therapy.</abstract><abstract>Results: The DGGE fingerprints indicated no significant differences in bacterial diversity of BRONJ tissue samples. Patients on antibiotics had higher relative abundance of phylum Firmicutes with bacterial species, Streptococcus intermedius, Lactobacillus gasseri, Mogibacterium timidum, and Solobacterium moorei, whereas patients without antibiotics had greater amounts of Parvimonas micra and Streptococcus anginosus. Thirty percent of bacterial populations were uncultured (yet‐to be cultured) phylotypes.</abstract><abstract>Conclusion: This study using limited sample size indicated that oral antibiotic therapy may have a limited efficacy on the bacterial population associated with BRONJ lesions.</abstract><subject lang="en"><genre>keywords</genre><topic>BRONJ</topic><topic>antibiotics</topic><topic>DGGE</topic><topic>microbial diversity</topic></subject><relatedItem type="host"><titleInfo><title>Oral Diseases</title></titleInfo><genre type="journal" authority="ISTEX" authorityURI="https://publication-type.data.istex.fr" valueURI="https://publication-type.data.istex.fr/ark:/67375/JMC-0GLKJH51-B">journal</genre><subject><genre>article-category</genre><topic>ORIGINAL ARTICLE</topic></subject><identifier type="ISSN">1354-523X</identifier><identifier type="eISSN">1601-0825</identifier><identifier type="DOI">10.1111/(ISSN)1601-0825</identifier><identifier type="PublisherID">ODI</identifier><part><date>2012</date><detail type="volume"><caption>vol.</caption><number>18</number></detail><detail type="issue"><caption>no.</caption><number>1</number></detail><extent unit="pages"><start>85</start><end>95</end><total>11</total></extent></part></relatedItem><identifier type="istex">CBADEA6DED66F8338E3496F6C8CC50FCED8ABD2C</identifier><identifier type="ark">ark:/67375/WNG-XQD73D3B-6</identifier><identifier type="DOI">10.1111/j.1601-0825.2011.01848.x</identifier><identifier type="ArticleID">ODI1848</identifier><accessCondition type="use and reproduction" contentType="copyright">© 2011 John Wiley & Sons A/S</accessCondition><recordInfo><recordContentSource authority="ISTEX" authorityURI="https://loaded-corpus.data.istex.fr" valueURI="https://loaded-corpus.data.istex.fr/ark:/67375/XBH-L0C46X92-X">wiley</recordContentSource><recordOrigin>Blackwell Publishing Ltd</recordOrigin></recordInfo></mods><json:item><extension>json</extension><original>false</original><mimetype>application/json</mimetype><uri>https://api.istex.fr/document/CBADEA6DED66F8338E3496F6C8CC50FCED8ABD2C/metadata/json</uri></json:item></metadata><serie></serie></istex></record>Pour manipuler ce document sous Unix (Dilib)
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