The effect of iron on Streptococcus mutans biofilm and on enamel demineralization

Detalhes bibliográficos
Autor(a) principal: Ribeiro,Cecília Cláudia Costa
Data de Publicação: 2012
Outros Autores: Ccahuana-Vásquez,Renzo Alberto, Carmo,Cadidja Dayane Sousa do, Alves,Cláudia Maria Coêlho, Leitão,Tarcísio Jorge, Vidotti,Lisandra Rocha, Cury,Jaime Aparecido
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Brazilian Oral Research
Texto Completo: http://old.scielo.br/scielo.php?script=sci_arttext&pid=S1806-83242012000400003
Resumo: Iron (Fe) may have an anticaries effect by specific inhibition of glycosyltransferase (GTF) enzymes of Streptococcus mutans, but this hypothesis has not yet been clarified. In this study, S. mutans biofilms were formed on blocks of bovine dental enamel of a predetermined surface hardness (SH). These biofilms were exposed eight times/day to 10% sucrose, and two times/day they were subjected to one of the following treatments: G1, 0.9% NaCl as a negative control; G2, 0.12% chlorhexidine digluconate (CHX) as a positive antibacterial control; G3, 0.05% NaF (225 ppm F) as a positive anticaries control; G4, G5, and G6, ferrous sulfate (Fe2+) at concentrations of 1.0, 10.0, and 100.0 µg Fe/mL, respectively. The experiment was performed in triplicate and was repeated three times (n = 9). The pH of the culture medium was determined every 24 h as an indicator of the biofilm's acidogenicity. The biofilm formed on each block was collected for determination of the viable bacteria and concentration of extracellular polysaccharides (EPS). Enamel SH was again determined and the percentage of SH loss (%SHL) was calculated as an indicator of demineralization. Iron treatment reduced the number of viable bacteria formed in the S. mutans biofilm (p = 0.04), in a dose-dependent manner, and also reduced the enamel's %SHL (p = 0.005). At 100 µg/mL, Fe reduced enamel demineralization as effectively as CHX and NaF (p < 0.05), but it did not inhibit EPS production. In conclusion, the data suggest that the anticaries mechanism of action of Fe may not involve the oxidative inhibition of GTFs.
id SBPQO-1_7a363e9ba6f8632ab12c5068d8b031b3
oai_identifier_str oai:scielo:S1806-83242012000400003
network_acronym_str SBPQO-1
network_name_str Brazilian Oral Research
repository_id_str
spelling The effect of iron on Streptococcus mutans biofilm and on enamel demineralizationIronBiofilmsDental EnamelDemineralizationIron (Fe) may have an anticaries effect by specific inhibition of glycosyltransferase (GTF) enzymes of Streptococcus mutans, but this hypothesis has not yet been clarified. In this study, S. mutans biofilms were formed on blocks of bovine dental enamel of a predetermined surface hardness (SH). These biofilms were exposed eight times/day to 10% sucrose, and two times/day they were subjected to one of the following treatments: G1, 0.9% NaCl as a negative control; G2, 0.12% chlorhexidine digluconate (CHX) as a positive antibacterial control; G3, 0.05% NaF (225 ppm F) as a positive anticaries control; G4, G5, and G6, ferrous sulfate (Fe2+) at concentrations of 1.0, 10.0, and 100.0 µg Fe/mL, respectively. The experiment was performed in triplicate and was repeated three times (n = 9). The pH of the culture medium was determined every 24 h as an indicator of the biofilm's acidogenicity. The biofilm formed on each block was collected for determination of the viable bacteria and concentration of extracellular polysaccharides (EPS). Enamel SH was again determined and the percentage of SH loss (%SHL) was calculated as an indicator of demineralization. Iron treatment reduced the number of viable bacteria formed in the S. mutans biofilm (p = 0.04), in a dose-dependent manner, and also reduced the enamel's %SHL (p = 0.005). At 100 µg/mL, Fe reduced enamel demineralization as effectively as CHX and NaF (p < 0.05), but it did not inhibit EPS production. In conclusion, the data suggest that the anticaries mechanism of action of Fe may not involve the oxidative inhibition of GTFs.Sociedade Brasileira de Pesquisa Odontológica - SBPqO2012-08-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersiontext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S1806-83242012000400003Brazilian Oral Research v.26 n.4 2012reponame:Brazilian Oral Researchinstname:Sociedade Brasileira de Pesquisa Odontológica (SBPqO)instacron:SBPQO10.1590/S1806-83242012000400003info:eu-repo/semantics/openAccessRibeiro,Cecília Cláudia CostaCcahuana-Vásquez,Renzo AlbertoCarmo,Cadidja Dayane Sousa doAlves,Cláudia Maria CoêlhoLeitão,Tarcísio JorgeVidotti,Lisandra RochaCury,Jaime Aparecidoeng2012-07-10T00:00:00Zoai:scielo:S1806-83242012000400003Revistahttps://www.scielo.br/j/bor/https://old.scielo.br/oai/scielo-oai.phppob@edu.usp.br||bor@sbpqo.org.br1807-31071806-8324opendoar:2012-07-10T00:00Brazilian Oral Research - Sociedade Brasileira de Pesquisa Odontológica (SBPqO)false
dc.title.none.fl_str_mv The effect of iron on Streptococcus mutans biofilm and on enamel demineralization
title The effect of iron on Streptococcus mutans biofilm and on enamel demineralization
spellingShingle The effect of iron on Streptococcus mutans biofilm and on enamel demineralization
Ribeiro,Cecília Cláudia Costa
Iron
Biofilms
Dental Enamel
Demineralization
title_short The effect of iron on Streptococcus mutans biofilm and on enamel demineralization
title_full The effect of iron on Streptococcus mutans biofilm and on enamel demineralization
title_fullStr The effect of iron on Streptococcus mutans biofilm and on enamel demineralization
title_full_unstemmed The effect of iron on Streptococcus mutans biofilm and on enamel demineralization
title_sort The effect of iron on Streptococcus mutans biofilm and on enamel demineralization
author Ribeiro,Cecília Cláudia Costa
author_facet Ribeiro,Cecília Cláudia Costa
Ccahuana-Vásquez,Renzo Alberto
Carmo,Cadidja Dayane Sousa do
Alves,Cláudia Maria Coêlho
Leitão,Tarcísio Jorge
Vidotti,Lisandra Rocha
Cury,Jaime Aparecido
author_role author
author2 Ccahuana-Vásquez,Renzo Alberto
Carmo,Cadidja Dayane Sousa do
Alves,Cláudia Maria Coêlho
Leitão,Tarcísio Jorge
Vidotti,Lisandra Rocha
Cury,Jaime Aparecido
author2_role author
author
author
author
author
author
dc.contributor.author.fl_str_mv Ribeiro,Cecília Cláudia Costa
Ccahuana-Vásquez,Renzo Alberto
Carmo,Cadidja Dayane Sousa do
Alves,Cláudia Maria Coêlho
Leitão,Tarcísio Jorge
Vidotti,Lisandra Rocha
Cury,Jaime Aparecido
dc.subject.por.fl_str_mv Iron
Biofilms
Dental Enamel
Demineralization
topic Iron
Biofilms
Dental Enamel
Demineralization
description Iron (Fe) may have an anticaries effect by specific inhibition of glycosyltransferase (GTF) enzymes of Streptococcus mutans, but this hypothesis has not yet been clarified. In this study, S. mutans biofilms were formed on blocks of bovine dental enamel of a predetermined surface hardness (SH). These biofilms were exposed eight times/day to 10% sucrose, and two times/day they were subjected to one of the following treatments: G1, 0.9% NaCl as a negative control; G2, 0.12% chlorhexidine digluconate (CHX) as a positive antibacterial control; G3, 0.05% NaF (225 ppm F) as a positive anticaries control; G4, G5, and G6, ferrous sulfate (Fe2+) at concentrations of 1.0, 10.0, and 100.0 µg Fe/mL, respectively. The experiment was performed in triplicate and was repeated three times (n = 9). The pH of the culture medium was determined every 24 h as an indicator of the biofilm's acidogenicity. The biofilm formed on each block was collected for determination of the viable bacteria and concentration of extracellular polysaccharides (EPS). Enamel SH was again determined and the percentage of SH loss (%SHL) was calculated as an indicator of demineralization. Iron treatment reduced the number of viable bacteria formed in the S. mutans biofilm (p = 0.04), in a dose-dependent manner, and also reduced the enamel's %SHL (p = 0.005). At 100 µg/mL, Fe reduced enamel demineralization as effectively as CHX and NaF (p < 0.05), but it did not inhibit EPS production. In conclusion, the data suggest that the anticaries mechanism of action of Fe may not involve the oxidative inhibition of GTFs.
publishDate 2012
dc.date.none.fl_str_mv 2012-08-01
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://old.scielo.br/scielo.php?script=sci_arttext&pid=S1806-83242012000400003
url http://old.scielo.br/scielo.php?script=sci_arttext&pid=S1806-83242012000400003
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv 10.1590/S1806-83242012000400003
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv text/html
dc.publisher.none.fl_str_mv Sociedade Brasileira de Pesquisa Odontológica - SBPqO
publisher.none.fl_str_mv Sociedade Brasileira de Pesquisa Odontológica - SBPqO
dc.source.none.fl_str_mv Brazilian Oral Research v.26 n.4 2012
reponame:Brazilian Oral Research
instname:Sociedade Brasileira de Pesquisa Odontológica (SBPqO)
instacron:SBPQO
instname_str Sociedade Brasileira de Pesquisa Odontológica (SBPqO)
instacron_str SBPQO
institution SBPQO
reponame_str Brazilian Oral Research
collection Brazilian Oral Research
repository.name.fl_str_mv Brazilian Oral Research - Sociedade Brasileira de Pesquisa Odontológica (SBPqO)
repository.mail.fl_str_mv pob@edu.usp.br||bor@sbpqo.org.br
_version_ 1750318322886377472