Proteins, pathogens, and failure at the composite-tooth interface.
Identifieur interne : 000212 ( Main/Exploration ); précédent : 000211; suivant : 000213Proteins, pathogens, and failure at the composite-tooth interface.
Auteurs : P. Spencer [États-Unis] ; Q. Ye ; A. Misra [États-Unis] ; S E P. Goncalves [Brésil] ; J S Laurence [États-Unis]Source :
- Journal of dental research [ 1544-0591 ] ; 2014.
Descripteurs français
- KwdFr :
- Adhérence bactérienne (physiologie), Biofilms (MeSH), Collage dentaire (MeSH), Dent (microbiologie), Dent (métabolisme), Déminéralisation dentaire (microbiologie), Humains (MeSH), Matériaux dentaires (composition chimique), Pellicule salivaire (microbiologie), Protéines et peptides salivaires (pharmacocinétique), Résines composites (composition chimique), Streptococcus mutans (physiologie), Échec de restauration dentaire (MeSH).
- MESH :
- composition chimique : Matériaux dentaires, Résines composites.
- microbiologie : Dent, Déminéralisation dentaire, Pellicule salivaire.
- métabolisme : Dent.
- pharmacocinétique : Protéines et peptides salivaires.
- physiologie : Adhérence bactérienne, Streptococcus mutans.
- Biofilms, Collage dentaire, Humains, Échec de restauration dentaire.
English descriptors
- KwdEn :
- Bacterial Adhesion (physiology), Biofilms (MeSH), Composite Resins (chemistry), Dental Bonding (MeSH), Dental Materials (chemistry), Dental Pellicle (microbiology), Dental Restoration Failure (MeSH), Humans (MeSH), Salivary Proteins and Peptides (pharmacokinetics), Streptococcus mutans (physiology), Tooth (metabolism), Tooth (microbiology), Tooth Demineralization (microbiology).
- MESH :
- chemical , chemistry : Composite Resins, Dental Materials.
- metabolism : Tooth.
- microbiology : Dental Pellicle, Tooth, Tooth Demineralization.
- chemical , pharmacokinetics : Salivary Proteins and Peptides.
- physiology : Bacterial Adhesion, Streptococcus mutans.
- Biofilms, Dental Bonding, Dental Restoration Failure, Humans.
Abstract
In the United States, composites accounted for nearly 70% of the 173.2 million composite and amalgam restorations placed in 2006 (Kingman et al., 2012), and it is likely that the use of composite will continue to increase as dentists phase out dental amalgam. This trend is not, however, without consequences. The failure rate of composite restorations is double that of amalgam (Ferracane, 2013). Composite restorations accumulate more biofilm, experience more secondary decay, and require more frequent replacement. In vivo biodegradation of the adhesive bond at the composite-tooth interface is a major contributor to the cascade of events leading to restoration failure. Binding by proteins, particularly gp340, from the salivary pellicle leads to biofilm attachment, which accelerates degradation of the interfacial bond and demineralization of the tooth by recruiting the pioneer bacterium Streptococcus mutans to the surface. Bacterial production of lactic acid lowers the pH of the oral microenvironment, erodes hydroxyapatite in enamel and dentin, and promotes hydrolysis of the adhesive. Secreted esterases further hydrolyze the adhesive polymer, exposing the soft underlying collagenous dentinal matrix and allowing further infiltration by the pathogenic biofilm. Manifold approaches are being pursued to increase the longevity of composite dental restorations based on the major contributing factors responsible for degradation. The key material and biological components and the interactions involved in the destructive processes, including recent advances in understanding the structural and molecular basis of biofilm recruitment, are described in this review. Innovative strategies to mitigate these pathogenic effects and slow deterioration are discussed.
DOI: 10.1177/0022034514550039
PubMed: 25190266
PubMed Central: PMC4237635
Affiliations:
Links toward previous steps (curation, corpus...)
Le document en format XML
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Spencer</name><affiliation wicri:level="1"><nlm:affiliation>Department of Mechanical Engineering Bioengineering Research Center pspencer@ku.edu.</nlm:affiliation><country wicri:rule="url">États-Unis</country></affiliation></author><author><name sortKey="Ye, Q" sort="Ye, Q" uniqKey="Ye Q" first="Q" last="Ye">Q. Ye</name><affiliation><nlm:affiliation>Bioengineering Research Center.</nlm:affiliation><wicri:noCountry code="no comma">Bioengineering Research Center.</wicri:noCountry><wicri:noCountry code="no comma">Bioengineering Research Center.</wicri:noCountry></affiliation></author><author><name sortKey="Misra, A" sort="Misra, A" uniqKey="Misra A" first="A" last="Misra">A. Misra</name><affiliation wicri:level="4"><nlm:affiliation>Bioengineering Research Center Department of Civil Engineering, University of Kansas, Lawrence, KS, USA.</nlm:affiliation><country xml:lang="fr">États-Unis</country><wicri:regionArea>Bioengineering Research Center Department of Civil Engineering, University of Kansas, Lawrence, KS</wicri:regionArea><placeName><region type="state">Kansas</region><settlement type="city">Lawrence (Kansas)</settlement></placeName><orgName type="university">Université du Kansas</orgName></affiliation></author><author><name sortKey="Goncalves, S E P" sort="Goncalves, S E P" uniqKey="Goncalves S" first="S E P" last="Goncalves">S E P. Goncalves</name><affiliation wicri:level="2"><nlm:affiliation>School of Dentistry of São José dos Campos, UNESP, Univ Estadual Paulista, São José dos Campos, SP, Brazil.</nlm:affiliation><country xml:lang="fr">Brésil</country><wicri:regionArea>School of Dentistry of São José dos Campos, UNESP, Univ Estadual Paulista, São José dos Campos, SP</wicri:regionArea><placeName><region type="state">État de São Paulo</region></placeName></affiliation></author><author><name sortKey="Laurence, J S" sort="Laurence, J S" uniqKey="Laurence J" first="J S" last="Laurence">J S Laurence</name><affiliation wicri:level="4"><nlm:affiliation>Department of Pharmaceutical Chemistry, University of Kansas, Lawrence, KS, USA.</nlm:affiliation><country xml:lang="fr">États-Unis</country><wicri:regionArea>Department of Pharmaceutical Chemistry, University of Kansas, Lawrence, KS</wicri:regionArea><placeName><region type="state">Kansas</region><settlement type="city">Lawrence (Kansas)</settlement></placeName><orgName type="university">Université du Kansas</orgName></affiliation></author></analytic><series><title level="j">Journal of dental research</title><idno type="eISSN">1544-0591</idno><imprint><date when="2014" type="published">2014</date></imprint></series></biblStruct></sourceDesc></fileDesc><profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Bacterial Adhesion (physiology)</term><term>Biofilms (MeSH)</term><term>Composite Resins (chemistry)</term><term>Dental Bonding (MeSH)</term><term>Dental Materials (chemistry)</term><term>Dental Pellicle (microbiology)</term><term>Dental Restoration Failure (MeSH)</term><term>Humans (MeSH)</term><term>Salivary Proteins and Peptides (pharmacokinetics)</term><term>Streptococcus mutans (physiology)</term><term>Tooth (metabolism)</term><term>Tooth (microbiology)</term><term>Tooth Demineralization (microbiology)</term></keywords><keywords scheme="KwdFr" xml:lang="fr"><term>Adhérence bactérienne (physiologie)</term><term>Biofilms (MeSH)</term><term>Collage dentaire (MeSH)</term><term>Dent (microbiologie)</term><term>Dent (métabolisme)</term><term>Déminéralisation dentaire (microbiologie)</term><term>Humains (MeSH)</term><term>Matériaux dentaires (composition chimique)</term><term>Pellicule salivaire (microbiologie)</term><term>Protéines et peptides salivaires (pharmacocinétique)</term><term>Résines composites (composition chimique)</term><term>Streptococcus mutans (physiologie)</term><term>Échec de restauration dentaire (MeSH)</term></keywords><keywords scheme="MESH" type="chemical" qualifier="chemistry" xml:lang="en"><term>Composite Resins</term><term>Dental Materials</term></keywords><keywords scheme="MESH" qualifier="composition chimique" xml:lang="fr"><term>Matériaux dentaires</term><term>Résines composites</term></keywords><keywords scheme="MESH" qualifier="metabolism" xml:lang="en"><term>Tooth</term></keywords><keywords scheme="MESH" qualifier="microbiologie" xml:lang="fr"><term>Dent</term><term>Déminéralisation dentaire</term><term>Pellicule salivaire</term></keywords><keywords scheme="MESH" qualifier="microbiology" xml:lang="en"><term>Dental Pellicle</term><term>Tooth</term><term>Tooth Demineralization</term></keywords><keywords scheme="MESH" qualifier="métabolisme" xml:lang="fr"><term>Dent</term></keywords><keywords scheme="MESH" qualifier="pharmacocinétique" xml:lang="fr"><term>Protéines et peptides salivaires</term></keywords><keywords scheme="MESH" type="chemical" qualifier="pharmacokinetics" xml:lang="en"><term>Salivary Proteins and Peptides</term></keywords><keywords scheme="MESH" qualifier="physiologie" xml:lang="fr"><term>Adhérence bactérienne</term><term>Streptococcus mutans</term></keywords><keywords scheme="MESH" qualifier="physiology" xml:lang="en"><term>Bacterial Adhesion</term><term>Streptococcus mutans</term></keywords><keywords scheme="MESH" xml:lang="en"><term>Biofilms</term><term>Dental Bonding</term><term>Dental Restoration Failure</term><term>Humans</term></keywords><keywords scheme="MESH" xml:lang="fr"><term>Biofilms</term><term>Collage dentaire</term><term>Humains</term><term>Échec de restauration dentaire</term></keywords></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">In the United States, composites accounted for nearly 70% of the 173.2 million composite and amalgam restorations placed in 2006 (Kingman et al., 2012), and it is likely that the use of composite will continue to increase as dentists phase out dental amalgam. This trend is not, however, without consequences. The failure rate of composite restorations is double that of amalgam (Ferracane, 2013). Composite restorations accumulate more biofilm, experience more secondary decay, and require more frequent replacement. In vivo biodegradation of the adhesive bond at the composite-tooth interface is a major contributor to the cascade of events leading to restoration failure. Binding by proteins, particularly gp340, from the salivary pellicle leads to biofilm attachment, which accelerates degradation of the interfacial bond and demineralization of the tooth by recruiting the pioneer bacterium Streptococcus mutans to the surface. Bacterial production of lactic acid lowers the pH of the oral microenvironment, erodes hydroxyapatite in enamel and dentin, and promotes hydrolysis of the adhesive. Secreted esterases further hydrolyze the adhesive polymer, exposing the soft underlying collagenous dentinal matrix and allowing further infiltration by the pathogenic biofilm. Manifold approaches are being pursued to increase the longevity of composite dental restorations based on the major contributing factors responsible for degradation. The key material and biological components and the interactions involved in the destructive processes, including recent advances in understanding the structural and molecular basis of biofilm recruitment, are described in this review. Innovative strategies to mitigate these pathogenic effects and slow deterioration are discussed. </div></front></TEI><pubmed><MedlineCitation Status="MEDLINE" Owner="NLM"><PMID Version="1">25190266</PMID><DateCompleted><Year>2015</Year><Month>01</Month><Day>22</Day></DateCompleted><DateRevised><Year>2018</Year><Month>11</Month><Day>13</Day></DateRevised><Article PubModel="Print-Electronic"><Journal><ISSN IssnType="Electronic">1544-0591</ISSN><JournalIssue CitedMedium="Internet"><Volume>93</Volume><Issue>12</Issue><PubDate><Year>2014</Year><Month>Dec</Month></PubDate></JournalIssue><Title>Journal of dental research</Title><ISOAbbreviation>J Dent Res</ISOAbbreviation></Journal><ArticleTitle>Proteins, pathogens, and failure at the composite-tooth interface.</ArticleTitle><Pagination><MedlinePgn>1243-9</MedlinePgn></Pagination><ELocationID EIdType="doi" ValidYN="Y">10.1177/0022034514550039</ELocationID><Abstract><AbstractText>In the United States, composites accounted for nearly 70% of the 173.2 million composite and amalgam restorations placed in 2006 (Kingman et al., 2012), and it is likely that the use of composite will continue to increase as dentists phase out dental amalgam. This trend is not, however, without consequences. The failure rate of composite restorations is double that of amalgam (Ferracane, 2013). Composite restorations accumulate more biofilm, experience more secondary decay, and require more frequent replacement. In vivo biodegradation of the adhesive bond at the composite-tooth interface is a major contributor to the cascade of events leading to restoration failure. Binding by proteins, particularly gp340, from the salivary pellicle leads to biofilm attachment, which accelerates degradation of the interfacial bond and demineralization of the tooth by recruiting the pioneer bacterium Streptococcus mutans to the surface. Bacterial production of lactic acid lowers the pH of the oral microenvironment, erodes hydroxyapatite in enamel and dentin, and promotes hydrolysis of the adhesive. Secreted esterases further hydrolyze the adhesive polymer, exposing the soft underlying collagenous dentinal matrix and allowing further infiltration by the pathogenic biofilm. Manifold approaches are being pursued to increase the longevity of composite dental restorations based on the major contributing factors responsible for degradation. The key material and biological components and the interactions involved in the destructive processes, including recent advances in understanding the structural and molecular basis of biofilm recruitment, are described in this review. Innovative strategies to mitigate these pathogenic effects and slow deterioration are discussed. </AbstractText><CopyrightInformation>© International & American Associations for Dental Research.</CopyrightInformation></Abstract><AuthorList CompleteYN="Y"><Author ValidYN="Y"><LastName>Spencer</LastName><ForeName>P</ForeName><Initials>P</Initials><AffiliationInfo><Affiliation>Department of Mechanical Engineering Bioengineering Research Center pspencer@ku.edu.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Ye</LastName><ForeName>Q</ForeName><Initials>Q</Initials><AffiliationInfo><Affiliation>Bioengineering Research Center.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Misra</LastName><ForeName>A</ForeName><Initials>A</Initials><AffiliationInfo><Affiliation>Bioengineering Research Center Department of Civil Engineering, University of Kansas, Lawrence, KS, USA.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Goncalves</LastName><ForeName>S E P</ForeName><Initials>SE</Initials><AffiliationInfo><Affiliation>School of Dentistry of São José dos Campos, UNESP, Univ Estadual Paulista, São José dos Campos, SP, Brazil.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Laurence</LastName><ForeName>J S</ForeName><Initials>JS</Initials><AffiliationInfo><Affiliation>Department of Pharmaceutical Chemistry, University of Kansas, Lawrence, KS, USA.</Affiliation></AffiliationInfo></Author></AuthorList><Language>eng</Language><GrantList CompleteYN="Y"><Grant><GrantID>R01 DE014392</GrantID><Acronym>DE</Acronym><Agency>NIDCR NIH HHS</Agency><Country>United States</Country></Grant><Grant><GrantID>R01DE14392-08S1</GrantID><Acronym>DE</Acronym><Agency>NIDCR NIH HHS</Agency><Country>United States</Country></Grant><Grant><GrantID>R01DE14392</GrantID><Acronym>DE</Acronym><Agency>NIDCR NIH HHS</Agency><Country>United States</Country></Grant><Grant><GrantID>R01DE022054</GrantID><Acronym>DE</Acronym><Agency>NIDCR NIH HHS</Agency><Country>United States</Country></Grant><Grant><GrantID>R01 DE022054</GrantID><Acronym>DE</Acronym><Agency>NIDCR NIH HHS</Agency><Country>United States</Country></Grant></GrantList><PublicationTypeList><PublicationType UI="D016428">Journal Article</PublicationType><PublicationType UI="D052061">Research Support, N.I.H., Extramural</PublicationType><PublicationType UI="D016454">Review</PublicationType></PublicationTypeList><ArticleDate DateType="Electronic"><Year>2014</Year><Month>09</Month><Day>04</Day></ArticleDate></Article><MedlineJournalInfo><Country>United States</Country><MedlineTA>J Dent Res</MedlineTA><NlmUniqueID>0354343</NlmUniqueID><ISSNLinking>0022-0345</ISSNLinking></MedlineJournalInfo><ChemicalList><Chemical><RegistryNumber>0</RegistryNumber><NameOfSubstance UI="D003188">Composite Resins</NameOfSubstance></Chemical><Chemical><RegistryNumber>0</RegistryNumber><NameOfSubstance UI="D003764">Dental Materials</NameOfSubstance></Chemical><Chemical><RegistryNumber>0</RegistryNumber><NameOfSubstance UI="D012471">Salivary Proteins and Peptides</NameOfSubstance></Chemical></ChemicalList><CitationSubset>D</CitationSubset><CitationSubset>IM</CitationSubset><MeshHeadingList><MeshHeading><DescriptorName UI="D001422" MajorTopicYN="N">Bacterial Adhesion</DescriptorName><QualifierName UI="Q000502" MajorTopicYN="N">physiology</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D018441" MajorTopicYN="Y">Biofilms</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D003188" MajorTopicYN="N">Composite Resins</DescriptorName><QualifierName UI="Q000737" MajorTopicYN="Y">chemistry</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D001840" MajorTopicYN="N">Dental Bonding</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D003764" MajorTopicYN="N">Dental Materials</DescriptorName><QualifierName UI="Q000737" MajorTopicYN="Y">chemistry</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D044622" MajorTopicYN="N">Dental Pellicle</DescriptorName><QualifierName UI="Q000382" MajorTopicYN="N">microbiology</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D019232" MajorTopicYN="Y">Dental Restoration Failure</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D006801" MajorTopicYN="N">Humans</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D012471" MajorTopicYN="N">Salivary Proteins and Peptides</DescriptorName><QualifierName UI="Q000493" MajorTopicYN="Y">pharmacokinetics</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D013295" MajorTopicYN="N">Streptococcus mutans</DescriptorName><QualifierName UI="Q000502" MajorTopicYN="Y">physiology</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D014070" MajorTopicYN="N">Tooth</DescriptorName><QualifierName 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