Presence of Streptococcus dentisani in the dental plaque of children from different Colombian cities

Streptococcus dentisani has been identified as an oral cavity probiotic due to its beneficial characteristics. One of its beneficial features is the production of bacteriocins, which inhibit the growth of cariogenic bacteria, and another is its buffering capacity through the production of ammonium f...

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Autores:
Universidad Cooperativa de Colombia
Angarita Díaz, María del Pilar
Díaz, Jaime
Tupaz Erira, Herlinto Alveiro
López López, Arantxa
Forero Escobar, Diana
Mira Obrador, Alex
Dávila Narváez, Fernando
Cerón Bastidas, Ximena Andrea
Ochoa Acosta, Emilia María
Goméz, Olga
González Banoy, Gladys
Tipo de recurso:
Article of journal
Fecha de publicación:
2019
Institución:
Universidad Cooperativa de Colombia
Repositorio:
Repositorio UCC
Idioma:
OAI Identifier:
oai:repository.ucc.edu.co:20.500.12494/16131
Acceso en línea:
https://hdl.handle.net/20.500.12494/16131
Palabra clave:
Bacteria
Niño
Caries dental
Probióticos
PCR
Bacteria
Bhild
Dental caries
Probiotics
Real‐time PCR
Rights
openAccess
License
Atribución – No comercial – Sin Derivar
id COOPER2_fe20a98cc01323afea789747b597603d
oai_identifier_str oai:repository.ucc.edu.co:20.500.12494/16131
network_acronym_str COOPER2
network_name_str Repositorio UCC
repository_id_str
dc.title.spa.fl_str_mv Presence of Streptococcus dentisani in the dental plaque of children from different Colombian cities
title Presence of Streptococcus dentisani in the dental plaque of children from different Colombian cities
spellingShingle Presence of Streptococcus dentisani in the dental plaque of children from different Colombian cities
Bacteria
Niño
Caries dental
Probióticos
PCR
Bacteria
Bhild
Dental caries
Probiotics
Real‐time PCR
title_short Presence of Streptococcus dentisani in the dental plaque of children from different Colombian cities
title_full Presence of Streptococcus dentisani in the dental plaque of children from different Colombian cities
title_fullStr Presence of Streptococcus dentisani in the dental plaque of children from different Colombian cities
title_full_unstemmed Presence of Streptococcus dentisani in the dental plaque of children from different Colombian cities
title_sort Presence of Streptococcus dentisani in the dental plaque of children from different Colombian cities
dc.creator.fl_str_mv Universidad Cooperativa de Colombia
Angarita Díaz, María del Pilar
Díaz, Jaime
Tupaz Erira, Herlinto Alveiro
López López, Arantxa
Forero Escobar, Diana
Mira Obrador, Alex
Dávila Narváez, Fernando
Cerón Bastidas, Ximena Andrea
Ochoa Acosta, Emilia María
Goméz, Olga
González Banoy, Gladys
dc.contributor.advisor.none.fl_str_mv Jokstad, Asbjørn
dc.contributor.author.none.fl_str_mv Universidad Cooperativa de Colombia
Angarita Díaz, María del Pilar
Díaz, Jaime
Tupaz Erira, Herlinto Alveiro
López López, Arantxa
Forero Escobar, Diana
Mira Obrador, Alex
Dávila Narváez, Fernando
Cerón Bastidas, Ximena Andrea
Ochoa Acosta, Emilia María
Goméz, Olga
González Banoy, Gladys
dc.subject.spa.fl_str_mv Bacteria
Niño
Caries dental
Probióticos
PCR
topic Bacteria
Niño
Caries dental
Probióticos
PCR
Bacteria
Bhild
Dental caries
Probiotics
Real‐time PCR
dc.subject.other.spa.fl_str_mv Bacteria
Bhild
Dental caries
Probiotics
Real‐time PCR
description Streptococcus dentisani has been identified as an oral cavity probiotic due to its beneficial characteristics. One of its beneficial features is the production of bacteriocins, which inhibit the growth of cariogenic bacteria, and another is its buffering capacity through the production of ammonium from arginine. The purpose of this study was to determine the presence of S. dentisani in the dental plaque of Colombian children and whether the presence of this bacterium is related to oral health and other conditions. Dental plaque and information on diet and oral hygiene habits were collected from children between 6 and 12 years of age from four Colombian cities, divided into caries‐free children (International Caries Detection and Assessment System [ICDAS] 0, Decayed Missing Filled Teeth index [DMFT] 0), children with ICDAS 1 and 2, and children with ICDAS >3. Plaque DNA was extracted and quantified, and real‐time polymerase chain reaction was performed using specific primers. This bacterium was identified in all samples, with a median of 0.46 cells/ng DNA (interquartile range [IQR] 0.13–1.02), without finding significant differences between the groups (P > 0.05). In caries‐free children, a median of 0.45 cells/ng DNA (IQR 0.14–1.23) was found. In children with ICDAS 1 and 2, the median was 0.49 cells/ng DNA (IQR 0.11–0.97), and in children with ICDAS >3, the median was 0.35 cells/ng DNA (IQR 0.12–1.07). However, statistically significant differences were found in the origin of children (P < 0.01), the use of fluoride‐containing products (P < 0.01), and the frequency of food intake (P < 0.05). In conclusion, the presence of S. dentisani was quantified in children from four Colombian cities, without finding significant differences in oral health status. Nevertheless, three conditions showed a possible relationship with S. dentisani.
publishDate 2019
dc.date.issued.none.fl_str_mv 2019-05-09
dc.date.accessioned.none.fl_str_mv 2020-01-20T19:31:24Z
dc.date.available.none.fl_str_mv 2020-01-20T19:31:24Z
dc.type.none.fl_str_mv Artículo
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dc.identifier.bibliographicCitation.spa.fl_str_mv Angarita‐Díaz, M.P., Díaz, J.A., Tupaz, H.A., López-López, A., Forero Escobar, D., Mira Obrador, A., Dávila Narvaezet F., Cerón Bastidas, X.A., Ochoa-Acosta, E.M., Goméz, O.L. y Gonzalez Banoy, G. (2018) Presence of Streptococcus dentisani in the dental plaque of children from different Colombian cities. Clin Exp Dent Res. 5,184–190. DOI: 10.1002/cre2.158. Recuperado de: https://onlinelibrary.wiley.com/doi/full/10.1002/cre2.158
identifier_str_mv 2057-4347
Angarita‐Díaz, M.P., Díaz, J.A., Tupaz, H.A., López-López, A., Forero Escobar, D., Mira Obrador, A., Dávila Narvaezet F., Cerón Bastidas, X.A., Ochoa-Acosta, E.M., Goméz, O.L. y Gonzalez Banoy, G. (2018) Presence of Streptococcus dentisani in the dental plaque of children from different Colombian cities. Clin Exp Dent Res. 5,184–190. DOI: 10.1002/cre2.158. Recuperado de: https://onlinelibrary.wiley.com/doi/full/10.1002/cre2.158
url https://hdl.handle.net/20.500.12494/16131
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dc.relation.ispartofjournal.spa.fl_str_mv Clinical and Experimental Dental Research
dc.relation.references.spa.fl_str_mv Becker, M. R., Paster, B. J., Leys, E. J., Moeschberger, M. L., Kenyon, S. G., Galvin, J. L., … Griffen, A. L. (2002). Molecular analysis of bacterial species associated with childhood caries. Journal of Clinical Microbiology, 40, 1001–1009. https://doi.org/10.1128/JCM.40.3.1001‐1009.2002
Benítez‐Páez, A., Belda‐Ferre, P., Simón‐Soro, A., & Mira, A. (2014). Microbiota diversity and gene expression dynamics in human oral biofilms. BMC Genomics, 15, 311. https://doi.org/10.1186/1471‐2164‐15‐311
Benn, A. M. L., Heng, N. C. K., Broadbent, J. M., & Thomson, W. M. (2018). Studying the human oral microbiome: Challenges and the evolution of solutions. Australian Dental Journal, 63, 14–24. https://doi.org/ 10.1111/adj.12565
Burton, J. P., Drummond, B. K., Chilcott, C. N., Tagg, J. R., Thomson, W. M., Hale, J. D. F., & Wescombe, P. A. (2013). Influence of the probiotic Streptococcus salivarius strain M18 on indices of dental health in children: A randomized double‐blind, placebo‐controlled trial. Journal of Medical Microbiology, 62, 875–884. https://doi.org/10.1099/jmm.0.056663‐0
Camelo‐Castillo, A., Benítez‐Páez, A., Belda‐Ferre, P., Cabrera‐Rubio, R., & Mira, A. (2014). Streptococcus dentisani sp. nov., a novel member of the mitis group. International Journal of Systematic and Evolutionary Microbiology, 64, 60–65. https://doi.org/10.1099/ijs.0.054098‐0
Huang, X., Palmer, S. R., Ahn, S. J., Richards, V. P., Williams, M. L., Nascimento, M. M., & Burne, R. A. (2016). A highly arginolytic Streptococcus species that potently antagonizes Streptococcus mutans. Applied and Environmental Microbiology, 82, 2187–2201. https://doi.org/ 10.1128/AEM.03887‐15
Jiang, S., Gao, X., Jin, L., & Lo, E. C. (2016). Salivary microbiome diversity in caries‐free and caries‐affected children. International Journal of Molecular Sciences, 17, E1978.
Kato, I., Vasquez, A., & Moyerbrailean, G. (2017). Nutritional correlates of human oral microbiome. Journal of the American College of Nutrition, 36, 88–98. https://doi.org/10.1080/07315724.2016.1185386
Kilian, M., Chapple, I. L. C., Hannig, M., Marsh, P. D., Meuric, V., Pedersen, A. M. L., … Zaura, E. (2016). The oral microbiome—An update for oral healthcare professionals. British Dental Journal, 221, 657–666. https://doi.org/10.1038/sj.bdj.2016.865
Kralik, P., & Ricchi, M. (2017). A basic guide to real time PCR in microbial diagnostics: Definitions, parameters, and everything. Frontiers in Microbiology, 8, 108.
Kressirer, C. A., Smith, D. J., King, W. F., Dobeck, J. M., Starr, J. R., & Tanner, A. C. R. (2017). Scardovia wiggsiae and its potential role as a caries pathogen. Journal of Oral Biosciences, 59, 135–141. https://doi.org/ 10.1016/j.job.2017.05.002
Kreth, J., Merritt, J., & Qi, F. (2009). Bacterial and host interactions of oral streptococci. DNA and Cell Biology, 28, 397–403. https://doi.org/ 10.1089/dna.2009.0868
Lee, P. P., Mak, W. Y., & Newsome, P. (2004). The aetiology and treatment of oral halitosis: An update. Hong Kong Medical Journal, 10, 414–418.
López‐López, A., Camelo‐Castillo, A., Ferrer, M. D., Simon‐Soro, A., & Mira, A. (2017). Health‐associated niche inhabitants as oral probiotics: The case of Streptococcus dentisani. Frontiers in Microbiology, 8, 379.
Loskill, P., Zeitz, C., Grandthyll, S., Thewes, N., Müller, F., Bischoff, M., … Jacobs, K. (2013). Reduced adhesion of oral bacteria on hydroxyapatite by fluoride treatment. Langmuir, 29, 5528–5533. https://doi.org/10.1021/la4008558
Mineoka, T., Awano, S., Rikimaru, T., Kurata, H., Yoshida, A., Ansai, T., & Takehara, T. (2008). Site‐specific development of periodontal disease is associated with increased levels of Porphyromonas gingivalis, Treponema denticola, and Tannerella forsythia in subgingival plaque. Journal of Periodontology, 79, 670–676. https://doi.org/10.1902/jop.2008.070398
Mombelli, A., Van Oosten, M. A. C., Schürch, E., & Lang, N. P. (1987). The microbiota associated with successful or failing osseointegrated titanium implants. Oral Microbiology and Immunology, 2, 145–151.
Moynihan, P. J. (2005). The role of diet and nutrition in the etiology and prevention of oral diseases. Bulletin of the World Health Organization, 83, 694–699.
Nascimiento, M. M., Gordan, V. V., Garvan, C. W., Browngardt, C. M., & Burne, R. A. (2009). Correlations of oral bacterial arginine and urea catabolism with caries experience. Oral Microbiology and Immunology, 24, 89–95. https://doi.org/10.1111/j.1399‐302X.2008.00477.x
Nasidze, I., Li, J., Schroeder, R., Creasey, J. L., Li, M., & Stoneking, M. (2011). High diversity of the saliva microbiome in Batwa Pygmies. PLoS One, 6, 23352.
Rosier, B. T., Marsh, P. D., & Mira, A. (2018). Resilience of the oral microbiota in health: Mechanisms that prevent dysbiosis. Journal of Dental Research, 97, 371–380. https://doi.org/10.1177/0022034517742139
Sampaio‐Maia, B., & Monteiro‐Silva, F. (2014). Acquisition and maturation of oral microbiome throughout childhood: An update. Dental Research Journal, 11, 291–301.
Simón‐Soro, A., Guillen‐Navarro, M., & Mira, A. (2014). Metatranscriptomics reveals overall active bacterial composition in caries lesions. Journal of Oral Microbiology, 6, 25443. https://doi.org/ 10.3402/jom.v6.25443
Simón‐Soro, A., & Mira, A. (2015). Solving the etiology of dental caries. Trends in Microbiology, 23, 76–82. https://doi.org/10.1016/j. tim.2014.10.010
Wake, N., Asahi, Y., Noiri, Y., et al. (2016). Temporal dynamics of bacterial microbiota in the human oral cavity determined using an in situ model of dental biofilms. NPJ Biofilms Microbiomes, 10, 16018.
Yasuda, K., Hsu, T., Gallini, C. A., et al. (2017). Fluoride depletes acidogenic taxa in oral but not gut microbial communities in mice. mSystems, 2, e00047–e00017.
Zaura, E., Nicu, E. A., Krom, B. P., & Keijser, B. J. F. (2014). Acquiring and maintaining a normal oral microbiome: Current perspective. Frontiers in Cellular and Infection Microbiology, 4, 85.
Zhang, Y., Zhen, M., Zhan, Y., Song, Y., Zhang, Q., & Wang, J. (2017). Population‐ genomic insights into variation in Prevotella intermedia and Prevotella nigrescens isolates and its association with periodontal disease. Frontiers in Cellular and Infection Microbiology, 7, 409. https:// doi.org/10.3389/fcimb.2017.00409
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Universidad Cooperativa de Colombia, Facultad de Ciencias de la Salud, Programa de Odontología, Villavicencio
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institution Universidad Cooperativa de Colombia
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spelling Jokstad, AsbjørnUniversidad Cooperativa de ColombiaAngarita Díaz, María del PilarDíaz, JaimeTupaz Erira, Herlinto AlveiroLópez López, ArantxaForero Escobar, DianaMira Obrador, AlexDávila Narváez, FernandoCerón Bastidas, Ximena AndreaOchoa Acosta, Emilia MaríaGoméz, OlgaGonzález Banoy, Gladys52020-01-20T19:31:24Z2020-01-20T19:31:24Z2019-05-092057-4347https://hdl.handle.net/20.500.12494/16131Angarita‐Díaz, M.P., Díaz, J.A., Tupaz, H.A., López-López, A., Forero Escobar, D., Mira Obrador, A., Dávila Narvaezet F., Cerón Bastidas, X.A., Ochoa-Acosta, E.M., Goméz, O.L. y Gonzalez Banoy, G. (2018) Presence of Streptococcus dentisani in the dental plaque of children from different Colombian cities. Clin Exp Dent Res. 5,184–190. DOI: 10.1002/cre2.158. Recuperado de: https://onlinelibrary.wiley.com/doi/full/10.1002/cre2.158Streptococcus dentisani has been identified as an oral cavity probiotic due to its beneficial characteristics. One of its beneficial features is the production of bacteriocins, which inhibit the growth of cariogenic bacteria, and another is its buffering capacity through the production of ammonium from arginine. The purpose of this study was to determine the presence of S. dentisani in the dental plaque of Colombian children and whether the presence of this bacterium is related to oral health and other conditions. Dental plaque and information on diet and oral hygiene habits were collected from children between 6 and 12 years of age from four Colombian cities, divided into caries‐free children (International Caries Detection and Assessment System [ICDAS] 0, Decayed Missing Filled Teeth index [DMFT] 0), children with ICDAS 1 and 2, and children with ICDAS >3. Plaque DNA was extracted and quantified, and real‐time polymerase chain reaction was performed using specific primers. This bacterium was identified in all samples, with a median of 0.46 cells/ng DNA (interquartile range [IQR] 0.13–1.02), without finding significant differences between the groups (P > 0.05). In caries‐free children, a median of 0.45 cells/ng DNA (IQR 0.14–1.23) was found. In children with ICDAS 1 and 2, the median was 0.49 cells/ng DNA (IQR 0.11–0.97), and in children with ICDAS >3, the median was 0.35 cells/ng DNA (IQR 0.12–1.07). However, statistically significant differences were found in the origin of children (P < 0.01), the use of fluoride‐containing products (P < 0.01), and the frequency of food intake (P < 0.05). In conclusion, the presence of S. dentisani was quantified in children from four Colombian cities, without finding significant differences in oral health status. Nevertheless, three conditions showed a possible relationship with S. dentisani.http://scienti.colciencias.gov.co:8081/cvlac/visualizador/generarCurriculoCv.do?cod_rh=0001561382https://orcid.org/0000-0002-5435-3456GIOMETGIODGIOMODONTOPOSGRADOSmaria.angaritad@campusucc.edu.cojaime.diazg@campusucc.edu.coalveiro.erira@campusucc.edu.colopez_aralop@gva.esdiana.foreroe@ucc.edu.comira_ale@gva.esfernando.davila@ucc.edu.coximena.ceron@campusucc.edu.coemilia.ochoa@campusucc.edu.coolga.gomez@javeriana.edu.cogladys.gonzalezb@campusucc.edu.co6Asbjørn JokstadUniversidad Cooperativa de Colombia, Facultad de Ciencias de la Salud, Programa de Odontología, VillavicencioOdontologíaVillavicenciohttps://onlinelibrary.wiley.com/doi/full/10.1002/cre2.158Clinical and Experimental Dental ResearchBecker, M. R., Paster, B. J., Leys, E. J., Moeschberger, M. L., Kenyon, S. G., Galvin, J. L., … Griffen, A. L. (2002). Molecular analysis of bacterial species associated with childhood caries. Journal of Clinical Microbiology, 40, 1001–1009. https://doi.org/10.1128/JCM.40.3.1001‐1009.2002Benítez‐Páez, A., Belda‐Ferre, P., Simón‐Soro, A., & Mira, A. (2014). Microbiota diversity and gene expression dynamics in human oral biofilms. BMC Genomics, 15, 311. https://doi.org/10.1186/1471‐2164‐15‐311Benn, A. M. L., Heng, N. C. K., Broadbent, J. M., & Thomson, W. M. (2018). Studying the human oral microbiome: Challenges and the evolution of solutions. Australian Dental Journal, 63, 14–24. https://doi.org/ 10.1111/adj.12565Burton, J. P., Drummond, B. K., Chilcott, C. N., Tagg, J. R., Thomson, W. M., Hale, J. D. F., & Wescombe, P. A. (2013). Influence of the probiotic Streptococcus salivarius strain M18 on indices of dental health in children: A randomized double‐blind, placebo‐controlled trial. Journal of Medical Microbiology, 62, 875–884. https://doi.org/10.1099/jmm.0.056663‐0Camelo‐Castillo, A., Benítez‐Páez, A., Belda‐Ferre, P., Cabrera‐Rubio, R., & Mira, A. (2014). Streptococcus dentisani sp. nov., a novel member of the mitis group. International Journal of Systematic and Evolutionary Microbiology, 64, 60–65. https://doi.org/10.1099/ijs.0.054098‐0Huang, X., Palmer, S. R., Ahn, S. J., Richards, V. P., Williams, M. L., Nascimento, M. M., & Burne, R. A. (2016). A highly arginolytic Streptococcus species that potently antagonizes Streptococcus mutans. Applied and Environmental Microbiology, 82, 2187–2201. https://doi.org/ 10.1128/AEM.03887‐15Jiang, S., Gao, X., Jin, L., & Lo, E. C. (2016). Salivary microbiome diversity in caries‐free and caries‐affected children. International Journal of Molecular Sciences, 17, E1978.Kato, I., Vasquez, A., & Moyerbrailean, G. (2017). Nutritional correlates of human oral microbiome. Journal of the American College of Nutrition, 36, 88–98. https://doi.org/10.1080/07315724.2016.1185386Kilian, M., Chapple, I. L. C., Hannig, M., Marsh, P. D., Meuric, V., Pedersen, A. M. L., … Zaura, E. (2016). The oral microbiome—An update for oral healthcare professionals. British Dental Journal, 221, 657–666. https://doi.org/10.1038/sj.bdj.2016.865Kralik, P., & Ricchi, M. (2017). A basic guide to real time PCR in microbial diagnostics: Definitions, parameters, and everything. Frontiers in Microbiology, 8, 108.Kressirer, C. A., Smith, D. J., King, W. F., Dobeck, J. M., Starr, J. R., & Tanner, A. C. R. (2017). Scardovia wiggsiae and its potential role as a caries pathogen. Journal of Oral Biosciences, 59, 135–141. https://doi.org/ 10.1016/j.job.2017.05.002Kreth, J., Merritt, J., & Qi, F. (2009). Bacterial and host interactions of oral streptococci. DNA and Cell Biology, 28, 397–403. https://doi.org/ 10.1089/dna.2009.0868Lee, P. P., Mak, W. Y., & Newsome, P. (2004). The aetiology and treatment of oral halitosis: An update. Hong Kong Medical Journal, 10, 414–418.López‐López, A., Camelo‐Castillo, A., Ferrer, M. D., Simon‐Soro, A., & Mira, A. (2017). Health‐associated niche inhabitants as oral probiotics: The case of Streptococcus dentisani. Frontiers in Microbiology, 8, 379.Loskill, P., Zeitz, C., Grandthyll, S., Thewes, N., Müller, F., Bischoff, M., … Jacobs, K. (2013). Reduced adhesion of oral bacteria on hydroxyapatite by fluoride treatment. Langmuir, 29, 5528–5533. https://doi.org/10.1021/la4008558Mineoka, T., Awano, S., Rikimaru, T., Kurata, H., Yoshida, A., Ansai, T., & Takehara, T. (2008). Site‐specific development of periodontal disease is associated with increased levels of Porphyromonas gingivalis, Treponema denticola, and Tannerella forsythia in subgingival plaque. Journal of Periodontology, 79, 670–676. https://doi.org/10.1902/jop.2008.070398Mombelli, A., Van Oosten, M. A. C., Schürch, E., & Lang, N. P. (1987). The microbiota associated with successful or failing osseointegrated titanium implants. Oral Microbiology and Immunology, 2, 145–151.Moynihan, P. J. (2005). The role of diet and nutrition in the etiology and prevention of oral diseases. Bulletin of the World Health Organization, 83, 694–699.Nascimiento, M. M., Gordan, V. V., Garvan, C. W., Browngardt, C. M., & Burne, R. A. (2009). Correlations of oral bacterial arginine and urea catabolism with caries experience. Oral Microbiology and Immunology, 24, 89–95. https://doi.org/10.1111/j.1399‐302X.2008.00477.xNasidze, I., Li, J., Schroeder, R., Creasey, J. L., Li, M., & Stoneking, M. (2011). High diversity of the saliva microbiome in Batwa Pygmies. PLoS One, 6, 23352.Rosier, B. T., Marsh, P. D., & Mira, A. (2018). Resilience of the oral microbiota in health: Mechanisms that prevent dysbiosis. Journal of Dental Research, 97, 371–380. https://doi.org/10.1177/0022034517742139Sampaio‐Maia, B., & Monteiro‐Silva, F. (2014). Acquisition and maturation of oral microbiome throughout childhood: An update. Dental Research Journal, 11, 291–301.Simón‐Soro, A., Guillen‐Navarro, M., & Mira, A. (2014). 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