Porphyromonas gingivalis biofilms persist after chlorhexidine treatment
Chlorhexidine (CHX) gluconate effectively reduces the viability of biofilm‐forming bacteria, such as Porphyromonas gingivalis. However, it is impossible to completely remove biofilms. The goal of the present study was to assess the potential pathogenicity of residual P. gingivalis biofilms in vitro...
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Veröffentlicht in: | European journal of oral sciences 2013-06, Vol.121 (3pt1), p.162-168 |
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creator | Yamaguchi, Mikiyo Noiri, Yuichiro Kuboniwa, Masae Yamamoto, Reiko Asahi, Yoko Maezono, Hazuki Hayashi, Mikako Ebisu, Shigeyuki |
description | Chlorhexidine (CHX) gluconate effectively reduces the viability of biofilm‐forming bacteria, such as Porphyromonas gingivalis. However, it is impossible to completely remove biofilms. The goal of the present study was to assess the potential pathogenicity of residual P. gingivalis biofilms in vitro after treatment with CHX gluconate. Scanning and transmission electron microscopy and confocal laser imaging revealed that treatment with CHX gluconate disrupted individual biofilm‐forming P. gingivalis cells but did not destroy the biofilms. The volumes of the protein and carbohydrate constituents in the residual biofilms were not significantly different from those of the controls. The physical resistance of the residual biofilms to ultrasonication was significantly higher than that of controls. The volume of P. gingivalis adherent to the residual biofilms was higher than that to saliva‐coated wells. These findings suggest that although CHX gluconate caused disruption of biofilm‐forming cells, the constituents derived from disrupted cells were maintained in the biofilms, which sustained their external structures. Moreover, the residual biofilms could serve as a scaffold for the formation of new biofilms. |
doi_str_mv | 10.1111/eos.12050 |
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However, it is impossible to completely remove biofilms. The goal of the present study was to assess the potential pathogenicity of residual P. gingivalis biofilms in vitro after treatment with CHX gluconate. Scanning and transmission electron microscopy and confocal laser imaging revealed that treatment with CHX gluconate disrupted individual biofilm‐forming P. gingivalis cells but did not destroy the biofilms. The volumes of the protein and carbohydrate constituents in the residual biofilms were not significantly different from those of the controls. The physical resistance of the residual biofilms to ultrasonication was significantly higher than that of controls. The volume of P. gingivalis adherent to the residual biofilms was higher than that to saliva‐coated wells. These findings suggest that although CHX gluconate caused disruption of biofilm‐forming cells, the constituents derived from disrupted cells were maintained in the biofilms, which sustained their external structures. Moreover, the residual biofilms could serve as a scaffold for the formation of new biofilms.</description><identifier>ISSN: 0909-8836</identifier><identifier>EISSN: 1600-0722</identifier><identifier>DOI: 10.1111/eos.12050</identifier><identifier>PMID: 23659238</identifier><language>eng</language><publisher>England: Blackwell Publishing Ltd</publisher><subject>Anti-Infective Agents, Local - pharmacology ; antimicrobial agents ; Bacterial Adhesion - drug effects ; Bacterial Proteins - physiology ; biofilms ; Biofilms - drug effects ; chlorhexidine ; Chlorhexidine - pharmacology ; Dentistry ; High-Energy Shock Waves ; Imaging, Three-Dimensional - methods ; Microbial Viability - drug effects ; Polysaccharides, Bacterial - physiology ; Porphyromonas gingivalis ; Porphyromonas gingivalis - chemistry ; Porphyromonas gingivalis - drug effects ; Porphyromonas gingivalis - pathogenicity</subject><ispartof>European journal of oral sciences, 2013-06, Vol.121 (3pt1), p.162-168</ispartof><rights>2013 Eur J Oral Sci</rights><rights>2013 Eur J Oral Sci.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1111%2Feos.12050$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2Feos.12050$$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/23659238$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Yamaguchi, Mikiyo</creatorcontrib><creatorcontrib>Noiri, Yuichiro</creatorcontrib><creatorcontrib>Kuboniwa, Masae</creatorcontrib><creatorcontrib>Yamamoto, Reiko</creatorcontrib><creatorcontrib>Asahi, Yoko</creatorcontrib><creatorcontrib>Maezono, Hazuki</creatorcontrib><creatorcontrib>Hayashi, Mikako</creatorcontrib><creatorcontrib>Ebisu, Shigeyuki</creatorcontrib><title>Porphyromonas gingivalis biofilms persist after chlorhexidine treatment</title><title>European journal of oral sciences</title><addtitle>Eur J Oral Sci</addtitle><description>Chlorhexidine (CHX) gluconate effectively reduces the viability of biofilm‐forming bacteria, such as Porphyromonas gingivalis. However, it is impossible to completely remove biofilms. The goal of the present study was to assess the potential pathogenicity of residual P. gingivalis biofilms in vitro after treatment with CHX gluconate. Scanning and transmission electron microscopy and confocal laser imaging revealed that treatment with CHX gluconate disrupted individual biofilm‐forming P. gingivalis cells but did not destroy the biofilms. The volumes of the protein and carbohydrate constituents in the residual biofilms were not significantly different from those of the controls. The physical resistance of the residual biofilms to ultrasonication was significantly higher than that of controls. The volume of P. gingivalis adherent to the residual biofilms was higher than that to saliva‐coated wells. These findings suggest that although CHX gluconate caused disruption of biofilm‐forming cells, the constituents derived from disrupted cells were maintained in the biofilms, which sustained their external structures. Moreover, the residual biofilms could serve as a scaffold for the formation of new biofilms.</description><subject>Anti-Infective Agents, Local - pharmacology</subject><subject>antimicrobial agents</subject><subject>Bacterial Adhesion - drug effects</subject><subject>Bacterial Proteins - physiology</subject><subject>biofilms</subject><subject>Biofilms - drug effects</subject><subject>chlorhexidine</subject><subject>Chlorhexidine - pharmacology</subject><subject>Dentistry</subject><subject>High-Energy Shock Waves</subject><subject>Imaging, Three-Dimensional - methods</subject><subject>Microbial Viability - drug effects</subject><subject>Polysaccharides, Bacterial - physiology</subject><subject>Porphyromonas gingivalis</subject><subject>Porphyromonas gingivalis - chemistry</subject><subject>Porphyromonas gingivalis - drug effects</subject><subject>Porphyromonas gingivalis - pathogenicity</subject><issn>0909-8836</issn><issn>1600-0722</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkUtPwzAQhC0EgvI48AdQjlxC13YcO0datQWBChKgHi0n2bSGPIqdQvvvCS1wZi-70nyzhxlCzilc0W762PgrykDAHunRGCAEydg-6UECSagUj4_IsfevAJTTRB6SI8ZjkTCuemTy2LjlYuOaqqmND-a2ntsPU1ofpLYpbFn5YInOW98GpmjRBdmibNwC1za3NQatQ9NWWLen5KAwpcezn31CXsaj5-FNeP8wuR1e34eWKwVhUcQ5ZUKmqUoEU7nIUhbnGFMJBiNmqCkAjEqQm6jIperoLAXgMgMjEg78hFzu_i5d875C3-rK-gzL0tTYrLymPJaRUkyyf6ACqIiihHfoxQ-6SivM9dLZyriN_s2pA_o74NOWuPnTKejvAnRXgN4WoEcPT9ujc4Q7Rxcdrv8cxr3pWHIp9Gw60dPZbDC-Gyit-BfvBodN</recordid><startdate>201306</startdate><enddate>201306</enddate><creator>Yamaguchi, Mikiyo</creator><creator>Noiri, Yuichiro</creator><creator>Kuboniwa, Masae</creator><creator>Yamamoto, Reiko</creator><creator>Asahi, Yoko</creator><creator>Maezono, Hazuki</creator><creator>Hayashi, Mikako</creator><creator>Ebisu, Shigeyuki</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>7X8</scope><scope>7QL</scope><scope>C1K</scope></search><sort><creationdate>201306</creationdate><title>Porphyromonas gingivalis biofilms persist after chlorhexidine treatment</title><author>Yamaguchi, Mikiyo ; Noiri, Yuichiro ; Kuboniwa, Masae ; Yamamoto, Reiko ; Asahi, Yoko ; Maezono, Hazuki ; Hayashi, Mikako ; Ebisu, Shigeyuki</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-i3880-ff6d1257bb89528d5cb26de6170ae42a1af00a89e3a4fd786d1cb0037c0a59303</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2013</creationdate><topic>Anti-Infective Agents, Local - pharmacology</topic><topic>antimicrobial agents</topic><topic>Bacterial Adhesion - drug effects</topic><topic>Bacterial Proteins - physiology</topic><topic>biofilms</topic><topic>Biofilms - drug effects</topic><topic>chlorhexidine</topic><topic>Chlorhexidine - pharmacology</topic><topic>Dentistry</topic><topic>High-Energy Shock Waves</topic><topic>Imaging, Three-Dimensional - methods</topic><topic>Microbial Viability - drug effects</topic><topic>Polysaccharides, Bacterial - physiology</topic><topic>Porphyromonas gingivalis</topic><topic>Porphyromonas gingivalis - chemistry</topic><topic>Porphyromonas gingivalis - drug effects</topic><topic>Porphyromonas gingivalis - pathogenicity</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Yamaguchi, Mikiyo</creatorcontrib><creatorcontrib>Noiri, Yuichiro</creatorcontrib><creatorcontrib>Kuboniwa, Masae</creatorcontrib><creatorcontrib>Yamamoto, Reiko</creatorcontrib><creatorcontrib>Asahi, Yoko</creatorcontrib><creatorcontrib>Maezono, Hazuki</creatorcontrib><creatorcontrib>Hayashi, Mikako</creatorcontrib><creatorcontrib>Ebisu, Shigeyuki</creatorcontrib><collection>Istex</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>MEDLINE - Academic</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Environmental Sciences and Pollution Management</collection><jtitle>European journal of oral sciences</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Yamaguchi, Mikiyo</au><au>Noiri, Yuichiro</au><au>Kuboniwa, Masae</au><au>Yamamoto, Reiko</au><au>Asahi, Yoko</au><au>Maezono, Hazuki</au><au>Hayashi, Mikako</au><au>Ebisu, Shigeyuki</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Porphyromonas gingivalis biofilms persist after chlorhexidine treatment</atitle><jtitle>European journal of oral sciences</jtitle><addtitle>Eur J Oral Sci</addtitle><date>2013-06</date><risdate>2013</risdate><volume>121</volume><issue>3pt1</issue><spage>162</spage><epage>168</epage><pages>162-168</pages><issn>0909-8836</issn><eissn>1600-0722</eissn><abstract>Chlorhexidine (CHX) gluconate effectively reduces the viability of biofilm‐forming bacteria, such as Porphyromonas gingivalis. However, it is impossible to completely remove biofilms. The goal of the present study was to assess the potential pathogenicity of residual P. gingivalis biofilms in vitro after treatment with CHX gluconate. Scanning and transmission electron microscopy and confocal laser imaging revealed that treatment with CHX gluconate disrupted individual biofilm‐forming P. gingivalis cells but did not destroy the biofilms. The volumes of the protein and carbohydrate constituents in the residual biofilms were not significantly different from those of the controls. The physical resistance of the residual biofilms to ultrasonication was significantly higher than that of controls. The volume of P. gingivalis adherent to the residual biofilms was higher than that to saliva‐coated wells. These findings suggest that although CHX gluconate caused disruption of biofilm‐forming cells, the constituents derived from disrupted cells were maintained in the biofilms, which sustained their external structures. Moreover, the residual biofilms could serve as a scaffold for the formation of new biofilms.</abstract><cop>England</cop><pub>Blackwell Publishing Ltd</pub><pmid>23659238</pmid><doi>10.1111/eos.12050</doi><tpages>7</tpages></addata></record> |
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subjects | Anti-Infective Agents, Local - pharmacology antimicrobial agents Bacterial Adhesion - drug effects Bacterial Proteins - physiology biofilms Biofilms - drug effects chlorhexidine Chlorhexidine - pharmacology Dentistry High-Energy Shock Waves Imaging, Three-Dimensional - methods Microbial Viability - drug effects Polysaccharides, Bacterial - physiology Porphyromonas gingivalis Porphyromonas gingivalis - chemistry Porphyromonas gingivalis - drug effects Porphyromonas gingivalis - pathogenicity |
title | Porphyromonas gingivalis biofilms persist after chlorhexidine treatment |
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