Prevalence of β-lactamase-producing bacteria in human periodontitis

Background and Objective Beta‐lactam antibiotics prescribed in periodontal therapy are vulnerable to degradation by bacterial β‐lactamases. This study evaluated the occurrence of β‐lactamase‐positive subgingival bacteria in chronic periodontitis subjects of USA origin, and assessed their in vitro re...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Journal of periodontal research 2013-08, Vol.48 (4), p.493-499
Hauptverfasser: Rams, T. E., Degener, J. E., van Winkelhoff, A. J.
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 499
container_issue 4
container_start_page 493
container_title Journal of periodontal research
container_volume 48
creator Rams, T. E.
Degener, J. E.
van Winkelhoff, A. J.
description Background and Objective Beta‐lactam antibiotics prescribed in periodontal therapy are vulnerable to degradation by bacterial β‐lactamases. This study evaluated the occurrence of β‐lactamase‐positive subgingival bacteria in chronic periodontitis subjects of USA origin, and assessed their in vitro resistance to metronidazole at a breakpoint concentration of 4 μg/mL. Material and Methods Subgingival plaque specimens from deep periodontal pockets with bleeding on probing were removed from 564 adults with severe chronic periodontitis before treatment. The samples were transported in VMGA III and then plated onto: (i) nonselective enriched Brucella blood agar (EBBA) and incubated anaerobically for 7 d; and (ii) selective trypticase soy‐bacitracin‐vancomycin (TSBV) and incubated for 3 d in air + 5% CO2. At the end of the incubation periods, the bacterial test species were identified and quantified. Specimen dilutions were also plated onto EBBA plates supplemented with 2 μg/mL of amoxicillin, a combination of 2 μg/mL of amoxicillin plus 2 μg/mL of the β‐lactamase inhibitor clavulanic acid, or 4 μg/mL of metronidazole, followed by anaerobic incubation for 7 d. Bacterial test species presumptively positive for β‐lactamase production were identified by growth on EBBA primary isolation plates supplemented with amoxicillin alone and no growth on EBBA primary isolation plates containing both amoxicillin plus clavulanic acid. A subset of such isolates was subjected to nitrocefin‐based chromogenic disk testing to confirm the presence of β‐lactamase activity. In vitro resistance to 4 μg/mL of metronidazole was noted when growth of test species occurred on metronidazole‐supplemented EBBA culture plates. Results Two‐hundred and ninety‐four (52.1%) of the study subjects yielded β‐lactamase‐producing subgingival bacterial test species, with Prevotella intermedia/nigrescens, Fusobacterium nucleatum and other Prevotella species most frequently identified as β‐lactamase‐producing organisms. Of the β‐lactamase‐producing bacterial test species strains recovered, 98.9% were susceptible in vitro to metronidazole at 4 μg/mL. Conclusion The occurrence of β‐lactamase‐positive subgingival bacterial species in more than half of the subjects with severe chronic periodontitis raises questions about the therapeutic potential of single‐drug regimens with β‐lactam antibiotics in periodontal therapy. The in vitro effectiveness of metronidazole against nearly all recovered β‐lactamase‐producing
doi_str_mv 10.1111/jre.12031
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_1412501603</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>1412501603</sourcerecordid><originalsourceid>FETCH-LOGICAL-c3111-205d83ed84865a85d6375c936944af5573f4f66e193ff7591eef4b172eb220173</originalsourceid><addsrcrecordid>eNqFkMtO3DAUhi1UBAPtghdAWZZFwPaJ7WRZce0wKtVoqpHYWJ7kGAy5DHbC5bX6IDwTpgPsKryxztF3fv36CNlhdJ_Fd3DjcZ9xCmyNjJikNKVKii9kRCnnKWR5tkm2QrihcZaq2CCbHJiCXPEROfrt8d7U2JaYdDZ5_pvWpuxNYwKmS99VQ-naq2QRd-idSVybXA-NaZNlHLuqa3vXu_CVrFtTB_z29m-TPyfHs8OzdHJx-vPwxyQtIdZMORVVDljlWS6FyUUlQYmyAFlkmbFCKLCZlRJZAdYqUTBEmy2Y4rjgnMbG2-T7Kjc2uxsw9LpxocS6Ni12Q9AsY1zQaAA-R0FRCQDyFd1boaXvQvBo9dK7xvgnzah-9aujX_3Pb2R332KHRYPVB_kuNAIHK-DB1fj0_yQ9nh6_R6arCxd6fPy4MP5WSxUF6fmvUw1TNR-Pzy_1DF4AdRKSVQ</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1370633363</pqid></control><display><type>article</type><title>Prevalence of β-lactamase-producing bacteria in human periodontitis</title><source>MEDLINE</source><source>Wiley Online Library All Journals</source><creator>Rams, T. E. ; Degener, J. E. ; van Winkelhoff, A. J.</creator><creatorcontrib>Rams, T. E. ; Degener, J. E. ; van Winkelhoff, A. J.</creatorcontrib><description>Background and Objective Beta‐lactam antibiotics prescribed in periodontal therapy are vulnerable to degradation by bacterial β‐lactamases. This study evaluated the occurrence of β‐lactamase‐positive subgingival bacteria in chronic periodontitis subjects of USA origin, and assessed their in vitro resistance to metronidazole at a breakpoint concentration of 4 μg/mL. Material and Methods Subgingival plaque specimens from deep periodontal pockets with bleeding on probing were removed from 564 adults with severe chronic periodontitis before treatment. The samples were transported in VMGA III and then plated onto: (i) nonselective enriched Brucella blood agar (EBBA) and incubated anaerobically for 7 d; and (ii) selective trypticase soy‐bacitracin‐vancomycin (TSBV) and incubated for 3 d in air + 5% CO2. At the end of the incubation periods, the bacterial test species were identified and quantified. Specimen dilutions were also plated onto EBBA plates supplemented with 2 μg/mL of amoxicillin, a combination of 2 μg/mL of amoxicillin plus 2 μg/mL of the β‐lactamase inhibitor clavulanic acid, or 4 μg/mL of metronidazole, followed by anaerobic incubation for 7 d. Bacterial test species presumptively positive for β‐lactamase production were identified by growth on EBBA primary isolation plates supplemented with amoxicillin alone and no growth on EBBA primary isolation plates containing both amoxicillin plus clavulanic acid. A subset of such isolates was subjected to nitrocefin‐based chromogenic disk testing to confirm the presence of β‐lactamase activity. In vitro resistance to 4 μg/mL of metronidazole was noted when growth of test species occurred on metronidazole‐supplemented EBBA culture plates. Results Two‐hundred and ninety‐four (52.1%) of the study subjects yielded β‐lactamase‐producing subgingival bacterial test species, with Prevotella intermedia/nigrescens, Fusobacterium nucleatum and other Prevotella species most frequently identified as β‐lactamase‐producing organisms. Of the β‐lactamase‐producing bacterial test species strains recovered, 98.9% were susceptible in vitro to metronidazole at 4 μg/mL. Conclusion The occurrence of β‐lactamase‐positive subgingival bacterial species in more than half of the subjects with severe chronic periodontitis raises questions about the therapeutic potential of single‐drug regimens with β‐lactam antibiotics in periodontal therapy. The in vitro effectiveness of metronidazole against nearly all recovered β‐lactamase‐producing subgingival bacterial species further supports clinical periodontitis treatment strategies involving the combination of systemic amoxicillin plus metronidazole.</description><identifier>ISSN: 0022-3484</identifier><identifier>EISSN: 1600-0765</identifier><identifier>DOI: 10.1111/jre.12031</identifier><identifier>PMID: 23173872</identifier><language>eng</language><publisher>United States: Blackwell Publishing Ltd</publisher><subject>Adult ; Aged ; Aged, 80 and over ; Amoxicillin - pharmacology ; Amoxicillin-Potassium Clavulanate Combination - pharmacology ; Anti-Bacterial Agents - pharmacology ; Anti-Infective Agents - pharmacology ; Bacteriological Techniques ; beta-lactamase ; beta-Lactamase Inhibitors ; beta-Lactamases - biosynthesis ; Brucella ; Chronic Periodontitis - microbiology ; Dental Plaque - microbiology ; Dentistry ; Drug Resistance, Bacterial ; Enzyme Inhibitors - pharmacology ; Female ; Fusobacterium nucleatum ; Fusobacterium nucleatum - drug effects ; Fusobacterium nucleatum - enzymology ; Fusobacterium nucleatum - isolation &amp; purification ; Gingiva - microbiology ; Gram-Negative Bacteria - drug effects ; Gram-Negative Bacteria - enzymology ; Gram-Negative Bacteria - isolation &amp; purification ; Humans ; in vitro ; Male ; Metronidazole - pharmacology ; Middle Aged ; Periodontal Pocket - microbiology ; periodontitis ; Prevotella ; Prevotella - classification ; Prevotella - drug effects ; Prevotella - enzymology ; Prevotella intermedia ; Prevotella intermedia - drug effects ; Prevotella intermedia - enzymology ; Prevotella intermedia - isolation &amp; purification ; Prevotella nigrescens - drug effects ; Prevotella nigrescens - enzymology ; Prevotella nigrescens - isolation &amp; purification ; subgingival microbiota</subject><ispartof>Journal of periodontal research, 2013-08, Vol.48 (4), p.493-499</ispartof><rights>2012 John Wiley &amp; Sons A/S. Published by John Wiley &amp; Sons Ltd</rights><rights>2012 John Wiley &amp; Sons A/S. Published by John Wiley &amp; Sons Ltd.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3111-205d83ed84865a85d6375c936944af5573f4f66e193ff7591eef4b172eb220173</citedby><cites>FETCH-LOGICAL-c3111-205d83ed84865a85d6375c936944af5573f4f66e193ff7591eef4b172eb220173</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1111%2Fjre.12031$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2Fjre.12031$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,780,784,1417,27924,27925,45574,45575</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/23173872$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Rams, T. E.</creatorcontrib><creatorcontrib>Degener, J. E.</creatorcontrib><creatorcontrib>van Winkelhoff, A. J.</creatorcontrib><title>Prevalence of β-lactamase-producing bacteria in human periodontitis</title><title>Journal of periodontal research</title><addtitle>J Periodontal Res</addtitle><description>Background and Objective Beta‐lactam antibiotics prescribed in periodontal therapy are vulnerable to degradation by bacterial β‐lactamases. This study evaluated the occurrence of β‐lactamase‐positive subgingival bacteria in chronic periodontitis subjects of USA origin, and assessed their in vitro resistance to metronidazole at a breakpoint concentration of 4 μg/mL. Material and Methods Subgingival plaque specimens from deep periodontal pockets with bleeding on probing were removed from 564 adults with severe chronic periodontitis before treatment. The samples were transported in VMGA III and then plated onto: (i) nonselective enriched Brucella blood agar (EBBA) and incubated anaerobically for 7 d; and (ii) selective trypticase soy‐bacitracin‐vancomycin (TSBV) and incubated for 3 d in air + 5% CO2. At the end of the incubation periods, the bacterial test species were identified and quantified. Specimen dilutions were also plated onto EBBA plates supplemented with 2 μg/mL of amoxicillin, a combination of 2 μg/mL of amoxicillin plus 2 μg/mL of the β‐lactamase inhibitor clavulanic acid, or 4 μg/mL of metronidazole, followed by anaerobic incubation for 7 d. Bacterial test species presumptively positive for β‐lactamase production were identified by growth on EBBA primary isolation plates supplemented with amoxicillin alone and no growth on EBBA primary isolation plates containing both amoxicillin plus clavulanic acid. A subset of such isolates was subjected to nitrocefin‐based chromogenic disk testing to confirm the presence of β‐lactamase activity. In vitro resistance to 4 μg/mL of metronidazole was noted when growth of test species occurred on metronidazole‐supplemented EBBA culture plates. Results Two‐hundred and ninety‐four (52.1%) of the study subjects yielded β‐lactamase‐producing subgingival bacterial test species, with Prevotella intermedia/nigrescens, Fusobacterium nucleatum and other Prevotella species most frequently identified as β‐lactamase‐producing organisms. Of the β‐lactamase‐producing bacterial test species strains recovered, 98.9% were susceptible in vitro to metronidazole at 4 μg/mL. Conclusion The occurrence of β‐lactamase‐positive subgingival bacterial species in more than half of the subjects with severe chronic periodontitis raises questions about the therapeutic potential of single‐drug regimens with β‐lactam antibiotics in periodontal therapy. The in vitro effectiveness of metronidazole against nearly all recovered β‐lactamase‐producing subgingival bacterial species further supports clinical periodontitis treatment strategies involving the combination of systemic amoxicillin plus metronidazole.</description><subject>Adult</subject><subject>Aged</subject><subject>Aged, 80 and over</subject><subject>Amoxicillin - pharmacology</subject><subject>Amoxicillin-Potassium Clavulanate Combination - pharmacology</subject><subject>Anti-Bacterial Agents - pharmacology</subject><subject>Anti-Infective Agents - pharmacology</subject><subject>Bacteriological Techniques</subject><subject>beta-lactamase</subject><subject>beta-Lactamase Inhibitors</subject><subject>beta-Lactamases - biosynthesis</subject><subject>Brucella</subject><subject>Chronic Periodontitis - microbiology</subject><subject>Dental Plaque - microbiology</subject><subject>Dentistry</subject><subject>Drug Resistance, Bacterial</subject><subject>Enzyme Inhibitors - pharmacology</subject><subject>Female</subject><subject>Fusobacterium nucleatum</subject><subject>Fusobacterium nucleatum - drug effects</subject><subject>Fusobacterium nucleatum - enzymology</subject><subject>Fusobacterium nucleatum - isolation &amp; purification</subject><subject>Gingiva - microbiology</subject><subject>Gram-Negative Bacteria - drug effects</subject><subject>Gram-Negative Bacteria - enzymology</subject><subject>Gram-Negative Bacteria - isolation &amp; purification</subject><subject>Humans</subject><subject>in vitro</subject><subject>Male</subject><subject>Metronidazole - pharmacology</subject><subject>Middle Aged</subject><subject>Periodontal Pocket - microbiology</subject><subject>periodontitis</subject><subject>Prevotella</subject><subject>Prevotella - classification</subject><subject>Prevotella - drug effects</subject><subject>Prevotella - enzymology</subject><subject>Prevotella intermedia</subject><subject>Prevotella intermedia - drug effects</subject><subject>Prevotella intermedia - enzymology</subject><subject>Prevotella intermedia - isolation &amp; purification</subject><subject>Prevotella nigrescens - drug effects</subject><subject>Prevotella nigrescens - enzymology</subject><subject>Prevotella nigrescens - isolation &amp; purification</subject><subject>subgingival microbiota</subject><issn>0022-3484</issn><issn>1600-0765</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkMtO3DAUhi1UBAPtghdAWZZFwPaJ7WRZce0wKtVoqpHYWJ7kGAy5DHbC5bX6IDwTpgPsKryxztF3fv36CNlhdJ_Fd3DjcZ9xCmyNjJikNKVKii9kRCnnKWR5tkm2QrihcZaq2CCbHJiCXPEROfrt8d7U2JaYdDZ5_pvWpuxNYwKmS99VQ-naq2QRd-idSVybXA-NaZNlHLuqa3vXu_CVrFtTB_z29m-TPyfHs8OzdHJx-vPwxyQtIdZMORVVDljlWS6FyUUlQYmyAFlkmbFCKLCZlRJZAdYqUTBEmy2Y4rjgnMbG2-T7Kjc2uxsw9LpxocS6Ni12Q9AsY1zQaAA-R0FRCQDyFd1boaXvQvBo9dK7xvgnzah-9aujX_3Pb2R332KHRYPVB_kuNAIHK-DB1fj0_yQ9nh6_R6arCxd6fPy4MP5WSxUF6fmvUw1TNR-Pzy_1DF4AdRKSVQ</recordid><startdate>201308</startdate><enddate>201308</enddate><creator>Rams, T. E.</creator><creator>Degener, J. E.</creator><creator>van Winkelhoff, A. J.</creator><general>Blackwell Publishing Ltd</general><scope>BSCLL</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>7X8</scope><scope>7QL</scope><scope>7T7</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>P64</scope></search><sort><creationdate>201308</creationdate><title>Prevalence of β-lactamase-producing bacteria in human periodontitis</title><author>Rams, T. E. ; Degener, J. E. ; van Winkelhoff, A. J.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3111-205d83ed84865a85d6375c936944af5573f4f66e193ff7591eef4b172eb220173</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2013</creationdate><topic>Adult</topic><topic>Aged</topic><topic>Aged, 80 and over</topic><topic>Amoxicillin - pharmacology</topic><topic>Amoxicillin-Potassium Clavulanate Combination - pharmacology</topic><topic>Anti-Bacterial Agents - pharmacology</topic><topic>Anti-Infective Agents - pharmacology</topic><topic>Bacteriological Techniques</topic><topic>beta-lactamase</topic><topic>beta-Lactamase Inhibitors</topic><topic>beta-Lactamases - biosynthesis</topic><topic>Brucella</topic><topic>Chronic Periodontitis - microbiology</topic><topic>Dental Plaque - microbiology</topic><topic>Dentistry</topic><topic>Drug Resistance, Bacterial</topic><topic>Enzyme Inhibitors - pharmacology</topic><topic>Female</topic><topic>Fusobacterium nucleatum</topic><topic>Fusobacterium nucleatum - drug effects</topic><topic>Fusobacterium nucleatum - enzymology</topic><topic>Fusobacterium nucleatum - isolation &amp; purification</topic><topic>Gingiva - microbiology</topic><topic>Gram-Negative Bacteria - drug effects</topic><topic>Gram-Negative Bacteria - enzymology</topic><topic>Gram-Negative Bacteria - isolation &amp; purification</topic><topic>Humans</topic><topic>in vitro</topic><topic>Male</topic><topic>Metronidazole - pharmacology</topic><topic>Middle Aged</topic><topic>Periodontal Pocket - microbiology</topic><topic>periodontitis</topic><topic>Prevotella</topic><topic>Prevotella - classification</topic><topic>Prevotella - drug effects</topic><topic>Prevotella - enzymology</topic><topic>Prevotella intermedia</topic><topic>Prevotella intermedia - drug effects</topic><topic>Prevotella intermedia - enzymology</topic><topic>Prevotella intermedia - isolation &amp; purification</topic><topic>Prevotella nigrescens - drug effects</topic><topic>Prevotella nigrescens - enzymology</topic><topic>Prevotella nigrescens - isolation &amp; purification</topic><topic>subgingival microbiota</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Rams, T. E.</creatorcontrib><creatorcontrib>Degener, J. E.</creatorcontrib><creatorcontrib>van Winkelhoff, A. J.</creatorcontrib><collection>Istex</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Industrial and Applied Microbiology Abstracts (Microbiology A)</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><jtitle>Journal of periodontal research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Rams, T. E.</au><au>Degener, J. E.</au><au>van Winkelhoff, A. J.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Prevalence of β-lactamase-producing bacteria in human periodontitis</atitle><jtitle>Journal of periodontal research</jtitle><addtitle>J Periodontal Res</addtitle><date>2013-08</date><risdate>2013</risdate><volume>48</volume><issue>4</issue><spage>493</spage><epage>499</epage><pages>493-499</pages><issn>0022-3484</issn><eissn>1600-0765</eissn><abstract>Background and Objective Beta‐lactam antibiotics prescribed in periodontal therapy are vulnerable to degradation by bacterial β‐lactamases. This study evaluated the occurrence of β‐lactamase‐positive subgingival bacteria in chronic periodontitis subjects of USA origin, and assessed their in vitro resistance to metronidazole at a breakpoint concentration of 4 μg/mL. Material and Methods Subgingival plaque specimens from deep periodontal pockets with bleeding on probing were removed from 564 adults with severe chronic periodontitis before treatment. The samples were transported in VMGA III and then plated onto: (i) nonselective enriched Brucella blood agar (EBBA) and incubated anaerobically for 7 d; and (ii) selective trypticase soy‐bacitracin‐vancomycin (TSBV) and incubated for 3 d in air + 5% CO2. At the end of the incubation periods, the bacterial test species were identified and quantified. Specimen dilutions were also plated onto EBBA plates supplemented with 2 μg/mL of amoxicillin, a combination of 2 μg/mL of amoxicillin plus 2 μg/mL of the β‐lactamase inhibitor clavulanic acid, or 4 μg/mL of metronidazole, followed by anaerobic incubation for 7 d. Bacterial test species presumptively positive for β‐lactamase production were identified by growth on EBBA primary isolation plates supplemented with amoxicillin alone and no growth on EBBA primary isolation plates containing both amoxicillin plus clavulanic acid. A subset of such isolates was subjected to nitrocefin‐based chromogenic disk testing to confirm the presence of β‐lactamase activity. In vitro resistance to 4 μg/mL of metronidazole was noted when growth of test species occurred on metronidazole‐supplemented EBBA culture plates. Results Two‐hundred and ninety‐four (52.1%) of the study subjects yielded β‐lactamase‐producing subgingival bacterial test species, with Prevotella intermedia/nigrescens, Fusobacterium nucleatum and other Prevotella species most frequently identified as β‐lactamase‐producing organisms. Of the β‐lactamase‐producing bacterial test species strains recovered, 98.9% were susceptible in vitro to metronidazole at 4 μg/mL. Conclusion The occurrence of β‐lactamase‐positive subgingival bacterial species in more than half of the subjects with severe chronic periodontitis raises questions about the therapeutic potential of single‐drug regimens with β‐lactam antibiotics in periodontal therapy. The in vitro effectiveness of metronidazole against nearly all recovered β‐lactamase‐producing subgingival bacterial species further supports clinical periodontitis treatment strategies involving the combination of systemic amoxicillin plus metronidazole.</abstract><cop>United States</cop><pub>Blackwell Publishing Ltd</pub><pmid>23173872</pmid><doi>10.1111/jre.12031</doi><tpages>7</tpages></addata></record>
fulltext fulltext
identifier ISSN: 0022-3484
ispartof Journal of periodontal research, 2013-08, Vol.48 (4), p.493-499
issn 0022-3484
1600-0765
language eng
recordid cdi_proquest_miscellaneous_1412501603
source MEDLINE; Wiley Online Library All Journals
subjects Adult
Aged
Aged, 80 and over
Amoxicillin - pharmacology
Amoxicillin-Potassium Clavulanate Combination - pharmacology
Anti-Bacterial Agents - pharmacology
Anti-Infective Agents - pharmacology
Bacteriological Techniques
beta-lactamase
beta-Lactamase Inhibitors
beta-Lactamases - biosynthesis
Brucella
Chronic Periodontitis - microbiology
Dental Plaque - microbiology
Dentistry
Drug Resistance, Bacterial
Enzyme Inhibitors - pharmacology
Female
Fusobacterium nucleatum
Fusobacterium nucleatum - drug effects
Fusobacterium nucleatum - enzymology
Fusobacterium nucleatum - isolation & purification
Gingiva - microbiology
Gram-Negative Bacteria - drug effects
Gram-Negative Bacteria - enzymology
Gram-Negative Bacteria - isolation & purification
Humans
in vitro
Male
Metronidazole - pharmacology
Middle Aged
Periodontal Pocket - microbiology
periodontitis
Prevotella
Prevotella - classification
Prevotella - drug effects
Prevotella - enzymology
Prevotella intermedia
Prevotella intermedia - drug effects
Prevotella intermedia - enzymology
Prevotella intermedia - isolation & purification
Prevotella nigrescens - drug effects
Prevotella nigrescens - enzymology
Prevotella nigrescens - isolation & purification
subgingival microbiota
title Prevalence of β-lactamase-producing bacteria in human periodontitis
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-05T19%3A55%3A36IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Prevalence%20of%20%CE%B2-lactamase-producing%20bacteria%20in%20human%20periodontitis&rft.jtitle=Journal%20of%20periodontal%20research&rft.au=Rams,%20T.%20E.&rft.date=2013-08&rft.volume=48&rft.issue=4&rft.spage=493&rft.epage=499&rft.pages=493-499&rft.issn=0022-3484&rft.eissn=1600-0765&rft_id=info:doi/10.1111/jre.12031&rft_dat=%3Cproquest_cross%3E1412501603%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=1370633363&rft_id=info:pmid/23173872&rfr_iscdi=true