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...
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Veröffentlicht in: | Journal of periodontal research 2013-08, Vol.48 (4), p.493-499 |
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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 |
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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 & 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</subject><ispartof>Journal of periodontal research, 2013-08, Vol.48 (4), p.493-499</ispartof><rights>2012 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd</rights><rights>2012 John Wiley & Sons A/S. Published by John Wiley & 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 & purification</subject><subject>Gingiva - microbiology</subject><subject>Gram-Negative Bacteria - drug effects</subject><subject>Gram-Negative Bacteria - enzymology</subject><subject>Gram-Negative Bacteria - isolation & 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 & purification</subject><subject>Prevotella nigrescens - drug effects</subject><subject>Prevotella nigrescens - enzymology</subject><subject>Prevotella nigrescens - isolation & 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 & purification</topic><topic>Gingiva - microbiology</topic><topic>Gram-Negative Bacteria - drug effects</topic><topic>Gram-Negative Bacteria - enzymology</topic><topic>Gram-Negative Bacteria - isolation & 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 & purification</topic><topic>Prevotella nigrescens - drug effects</topic><topic>Prevotella nigrescens - enzymology</topic><topic>Prevotella nigrescens - isolation & 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> |
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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 |
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