Probiotic effect of Streptococcus dentisani on oral pathogens: an in vitro study

Eng: Probiotics, including Streptococcus dentisani, have been proposed as an alternative to reestablish the ecology of the oral cavity and inhibit the formation of pathogenic biofilms. The main objective of this work was to assess the probiotic ability of S. dentisani against Streptococcus mutans, S...

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Autores:: Arango Santander, Santiago
Bedoya Correa Claudia María
Betancur Giraldo, Santiago
Franco Aguirre, John Querubín

Tipo de recurso:: Article of journal

Fecha de publicación:: 2024

Institución:: Universidad Cooperativa de Colombia

Repositorio:: Repositorio UCC

Idioma:: eng

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repository_id_str
dc.title.eng.fl_str_mv	Probiotic effect of Streptococcus dentisani on oral pathogens: an in vitro study
title	Probiotic effect of Streptococcus dentisani on oral pathogens: an in vitro study
spellingShingle	Probiotic effect of Streptococcus dentisani on oral pathogens: an in vitro study
title_short	Probiotic effect of Streptococcus dentisani on oral pathogens: an in vitro study
title_full	Probiotic effect of Streptococcus dentisani on oral pathogens: an in vitro study
title_fullStr	Probiotic effect of Streptococcus dentisani on oral pathogens: an in vitro study
title_full_unstemmed	Probiotic effect of Streptococcus dentisani on oral pathogens: an in vitro study
title_sort	Probiotic effect of Streptococcus dentisani on oral pathogens: an in vitro study
dc.creator.fl_str_mv	Arango Santander, Santiago Bedoya Correa Claudia María Betancur Giraldo, Santiago Franco Aguirre, John Querubín
dc.contributor.author.none.fl_str_mv	Arango Santander, Santiago Bedoya Correa Claudia María Betancur Giraldo, Santiago Franco Aguirre, John Querubín
dc.contributor.researchgroup.none.fl_str_mv	GIOM
description	Eng: Probiotics, including Streptococcus dentisani, have been proposed as an alternative to reestablish the ecology of the oral cavity and inhibit the formation of pathogenic biofilms. The main objective of this work was to assess the probiotic ability of S. dentisani against Streptococcus mutans, Streptococcus mitis, and Candida albicans biofilms. The ability of the strains to form a monospecies biofilm and the probiotic potential of S. dentisani using the competition, exclusion, and displacement strategies were determined. All strains were moderate biofilm producers. The ability of S. dentisani to compete with and exclude S. mutans and S. mitis during biofilm formation was not significant. However, S. dentisani significantly reduced pathologic streptococcal biofilms using the displacement strategy. Also S. dentisani reduced the formation of the C. albicans biofilm mainly through competition and displacement. In vitro, S. dentisani exhibited probiotic potential to reduce the formation of potentially pathogenic biofilms. Further investigation is required to understand the biofilm-inhibiting mechanisms exhibited by this probiotic strain.
publishDate	2024
dc.date.accessioned.none.fl_str_mv	2024-05-27T20:26:48Z
dc.date.available.none.fl_str_mv	2024-05-27T20:26:48Z
dc.date.issued.none.fl_str_mv	2024-04-24
dc.type.none.fl_str_mv	Artículo
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dc.identifier.citation.none.fl_str_mv	Bedoya-Correa, C.M.; Betancur-Giraldo, S.; Franco, J.; Arango-Santander, S. Probiotic Effect of Streptococcus dentisani on Oral Pathogens: An In Vitro Study. Pathogens 2024, 13, 351.https://hdl.handle.net/20.500.12494/55660
dc.identifier.issn.none.fl_str_mv	2076-0817
dc.identifier.uri.none.fl_str_mv	https://hdl.handle.net/20.500.12494/55660
dc.identifier.doi.none.fl_str_mv	https://doi.org/10.3390/pathogens13050351
identifier_str_mv	Bedoya-Correa, C.M.; Betancur-Giraldo, S.; Franco, J.; Arango-Santander, S. Probiotic Effect of Streptococcus dentisani on Oral Pathogens: An In Vitro Study. Pathogens 2024, 13, 351.https://hdl.handle.net/20.500.12494/55660 2076-0817
url	https://hdl.handle.net/20.500.12494/55660 https://doi.org/10.3390/pathogens13050351
dc.language.iso.none.fl_str_mv	eng
language	eng
dc.relation.citationissue.none.fl_str_mv	351
dc.relation.citationvolume.none.fl_str_mv	13
dc.relation.ispartofjournal.none.fl_str_mv	Pathogens
dc.relation.references.none.fl_str_mv	Baker, J.L.; Mark Welch, J.L.; Kauffman, K.M.; McLean, J.S.; He, X. The oral microbiome: Diversity, biogeography and human health. Nat. Rev. Microbiol. 2024, 22, 89–104 Dewhirst, F.E.; Chen, T.; Izard, J.; Paster, B.J.; Tanner, A.C.R.; Yu, W.-H.; Lakshmanan, A.; Wade, W.G. The human oral microbiome. J. Bacteriol. 2010, 192, 5002–5017 Deo, P.N.; Deshmukh, R. Oral microbiome: Unveiling the fundamentals. J. Oral Maxillofac. Pathol. 2019, 23, 122–128 Willis, J.R.; Gabaldón, T. The human oral microbiome in health and disease: From sequences to ecosystems. Microorganisms 2020, 8, 308 Carvalho, F.M.; Teixeira-Santos, R.; Mergulhão, F.J.M.; Gomes, L.C. Targeting Biofilms in Medical Devices using Probiotic Cells: A systematic review. AIMS Mater Sci. 2021, 8, 501–523. Costerton, J.W.; Stewart, P.S.; Greenberg, E.P. Bacterial biofilms: A common cause of persistent infections. Science 1999, 284, 1318–1322. Berger, D.; Rakhamimova, A.; Pollack, A.; Loewy, Z. Oral Biofilms: Development, Control, and Analysis. High Throughput 2018, 7, 3. Hancock, V.; Dahl, M.; Klemm, P. Probiotic Escherichia coli strain Nissle 1917 outcompetes intestinal pathogens during biofilm formation. J. Med. Microbiol. 2010, 59, 392–399 Walker, T.S.; Tomlin, K.L.; Worthen, G.S.; Poch, K.R.; Lieber, J.G.; Saavedra, M.T.; Fessler, M.B.; Malcolm, K.C.; Vasil, M.L.; Nick, J.A. Enhanced Pseudomonas aeruginosa biofilm development mediated by human neutrophils. Infect. Immun. 2005, 73, 3693– 3701 Colombo, A.P.V.; do Souto, R.M.; da Silva-Boghossian, C.M.; Miranda, R.; Lourenço, T.G.B. Microbiology of Oral Biofilm-Dependent Diseases: Have We Made Significant Progress to Understand and Treat These Diseases? Curr. Oral Health Rep. 2015, 2, 37–47 Castro-Rodríguez, Y. Ciencias clínicas y patológicas artículo de revisión La higiene oral y los efectos de la terapia periodontal mecánica. Rev. Habanera Cienc. Med. 2021, 20, e3127 Haque, M.; Sartelli, M.; Haque, S.Z. Dental infection and resistance-global health consequences. Dent. J. 2019, 7, 22 Allaker, R.P.; Stephen, A.S. Use of Probiotics and Oral Health. Curr. Oral Health Rep. 2017, 4, 309–318 Seminario-Amez, M.; López-López, J.; Estrugo-Devesa, A.; Ayuso-Montero, R.; Jané-Salas, E. Probiotics and oral health: A systematic review. Med. Oral Patol. Oral Cir. Bucal 2017, 22, e282–e288 Food and Agriculture Organization of the United Nations; World Health Organization. Probiotics in Food: Health and Nutritional Properties and Guidelines for Evaluation; Food and Agriculture Organization of the United Nations: Rome, Italy, 2006; 50p. Amargianitakis, M.; Antoniadou, M.; Rahiotis, C.; Varzakas, T. Probiotics, prebiotics, synbiotics and dental caries. New perspectives, suggestions, and patient coaching approach for a cavity-free mouth. Appl. Sci. 2021, 11, 5472 Luo, S.C.; Wei, S.M.; Luo, X.T.; Yang, Q.Q.; Wong, K.H.; Cheung, P.C.K.; Zhang, B.B. How probiotics, prebiotics, synbiotics, and postbiotics prevent dental caries: An oral microbiota perspective. NPJ Biofilms Microbiomes 2024, 10, 14 Camelo-Castillo, A.; Benítez-Páez, A.; Belda-Ferre, P.; Cabrera-Rubio, R.; Mira, A. Streptococcus dentisani sp. nov., a novel member of the mitis group. Int. J. Syst. Evol. Microbiol. 2014, 64, 60–65 López-López, A.; Camelo-Castillo, A.; Ferrer, M.D.; Simon-Soro, A.; Mira, A. Health-associated niche inhabitants as oral probiotics: The case of Streptococcus dentisani. Front. Microbiol. 2017, 8, 379 Llena, C.; Almarche, A.; Mira, A.; López, M.A. Antimicrobial efficacy of the supernatant of streptococcus dentisani against microorganisms implicated in root canal infections. J. Oral Sci. 2019, 61, 184–194 Esteban-Fernández, A.; Zorraquín-Peña, I.; Ferrer, M.D.; Mira, A.; Bartolomé, B.; González de Llano, D.; Moreno-Arribas, M.V. Inhibition of oral pathogens adhesion to human gingival fibroblasts by wine polyphenols alone and in combination with an oral probiotic. J. Agric. Food Chem. 2018, 66, 2071–2082 Huang, X.; Palmer, S.R.; Ahn, S.; Richards, V.P.; Williams, M.L.; Nascimento, M.M.; Burne, R.A. A Highly Arginolytic Streptococcus Species That Potently Antagonizes Streptococcus mutans. Appl. Environ. Microbiol. 2016, 82, 2187–2201 Poorni, S.; Srinivasan, M.R.; Nivedhitha, M.S. Probiotic Streptococcus strains in caries prevention: A systematic review. J. Conserv. Dent. 2019, 22, 123–128 Tagg, J.R.; Harold, L.K.; Jain, R.; Hale, J.D.F. Beneficial modulation of human health in the oral cavity and beyond using bacteriocin- like inhibitory substance-producing streptococcal probiotics. Front. Microbiol. 2023, 14, 1161155 Elexson, N.; Sabrina, H.; Dalene, L.; Eddy, B.; Nurul, F.R.; Nasra, P.; Grace, B.; Nick, L.; Amirah, Z.J.; Nur, D.Z.; et al. Assessment of Pseudomonas aeruginosa biofilm-forming capacities from drinking water in water vending machine. Food Res. 2022, 6, 76–83 Kırmusaoğlu, S. The Methods for detection of biofilm and screening antibiofilm activity of agents. In Antimicrobials, Antibiotic Resistance, Antibiofilm Strategies and Activity Methods; IntechOpen: London, UK, 2019 Woo, J.; Ahn, J. Probiotic-mediated competition, exclusion and displacement in biofilm formation by food-borne pathogens. Le. Appl. Microbiol. 2013, 56, 307–313 Schwendicke, F.; Korte, F.; Dörfer, C.E.; Kneist, S.; Fawzy El-Sayed, K.; Paris, S. Inhibition of Streptococcus mutans growth and biofilm formation by probiotics in vitro. Caries Res. 2017, 51, 87–95 Ruiz, M.J.; García, M.D.; Padola, N.L.; Etcheverría, A.I. Capacidad de Lactiplantibacillus plantarum de reducir biofilms de bacterias patógenas transmitidas por alimentos. Rev. Vet. 2022, 33, 48–52 Bernabè, G.; Pauleo, A.; Zamuner, A.; Cassari, L.; Castagliuolo, I.; Brun, P.; Dein, M. Exploiting conserved quorum sensing signals in Streptococcus mutans and Streptococcus pneumoniae. Microorganisms 2022, 10, 12 Metwalli, K.H.; Khan, S.A.; Krom, B.P.; Jabra-Rizk, M.A. Streptococcus mutans, Candida albicans, and the human mouth: A sticky situation. PLoS Pathog. 2013, 9, 10 Marcinkiewicz, J.; Strus, M.; Pasich, E. Antibiotic resistance: A «dark side» of biofilm-associated chronic infections. Pol. Arch. Med. Wewn. 2013, 123, 309–313 Whitmore, S.E.; Lamont, R.J. The pathogenic persona of community-associated oral streptococci. Mol. Microbiol. 2011, 81, 305– 314 Li, Y.H.; Hanna, M.N.; Svensäter, G.; Ellen, R.P.; Cvitkovitch, D.G. Cell density modulates acid adaptation in Streptococcus mutans: Implications for survival in biofilms. J. Bacteriol. 2001, 183, 6875–6884 Zayed, S.M.; Aboulwafa, M.M.; Hashem, A.M.; Saleh, S.E. Biofilm formation by Streptococcus mutans and its inhibition by green tea extracts. AMB Express. 2021, 11, 73 Denapaite, D.; Brückner, R.; Nuhn, M.; Reichmann, P.; Henrich, B.; Maurer, P.; Schähle, Y.; Selbmann, P.; Zimmermann, W.; Wambu, R.; et al. The genome of Streptococcus mitis B6--what is a commensal? PLoS ONE 2010, 5, e9426 Palmieri, C.; Magi, G.; Orsini, G.; Putignano, A.; Facinelli, B. Antibiofilm activity of zinc-carbonate hydroxyapatite nanocrystals against Streptococcus mutans and mitis group streptococci. Curr. Microbiol. 2013, 67, 679–681 Mitchell, J. Streptococcus mitis: Walking the line between commensalism and pathogenesis. Mol. Oral Microbiol. 2011, 26, 89–98 Watanabe, A.; Kawada-Matsuo, M.; Le, M.N.; Hisatsune, J.; Oogai, Y.; Nakano, Y.; Nakata, M.; Miyawaki, S.; Sugai, M.; Komatsuzawa, H. Comprehensive analysis of bacteriocins in Streptococcus mutans. Sci. Rep. 2021, 11, 12963 Junges, R.; Sturød, K.; Salvadori, G.; Åmdal, H.A.; Chen, T.; Petersen, F.C. Characterization of a signaling system in Streptococcus mitis that mediates interspecies communication with Streptococcus pneumoniae. Appl. Environ. Microbiol. 2019, 85, e02297-18 Senadheera, D.; Cvitkovitch, D.G. Quorum sensing and biofilm formation by Streptococcus mutans. Adv. Exp. Med. Biol. 2008, 631, 178–188 Cvitkovitch, D.G.; Li, Y.H.; Ellen, R.P. Quorum sensing and biofilm formation in Streptococcal infections. J. Clin. Investig. 2003, 112, 1626–1632 Conrads, G.; Westenberger, J.; Lürkens, M.; Abdelbary, M.M.H. Isolation and bacteriocin-related typing of Streptococcus dentisani. Front. Cell Infect. Microbiol. 2019, 9, 110 Matsubara, V.H.; Wang, Y.; Bandara, H.M.H.N.; Mayer, M.P.A.; Samaranayake, L.P. Probiotic lactobacilli inhibit early stages of Candida albicans biofilm development by reducing their growth, cell adhesion, and filamentation. Appl. Microbiol. Biotechnol. 2016, 100, 6415–6426 Banas, J.A.; Zhu, M.; Dawson, D.V.; Blanchee, D.R.; Drake, D.R.; Gu, H.; Frost, R.; McCaulley, G.; Levy, S.M. Acidogenicity and acid tolerance of Streptococcus oralis and Streptococcus mitis isolated from plaque of healthy and incipient caries teeth. J. Oral Microbiol. 2016, 8, 1
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spelling	Arango Santander, SantiagoBedoya Correa Claudia MaríaBetancur Giraldo, SantiagoFranco Aguirre, John Querubín GIOM2024-05-27T20:26:48Z2024-05-27T20:26:48Z2024-04-24Bedoya-Correa, C.M.; Betancur-Giraldo, S.; Franco, J.; Arango-Santander, S. Probiotic Effect of Streptococcus dentisani on Oral Pathogens: An In Vitro Study. Pathogens 2024, 13, 351.https://hdl.handle.net/20.500.12494/556602076-0817https://hdl.handle.net/20.500.12494/55660https://doi.org/10.3390/pathogens13050351Eng: Probiotics, including Streptococcus dentisani, have been proposed as an alternative to reestablish the ecology of the oral cavity and inhibit the formation of pathogenic biofilms. The main objective of this work was to assess the probiotic ability of S. dentisani against Streptococcus mutans, Streptococcus mitis, and Candida albicans biofilms. The ability of the strains to form a monospecies biofilm and the probiotic potential of S. dentisani using the competition, exclusion, and displacement strategies were determined. All strains were moderate biofilm producers. The ability of S. dentisani to compete with and exclude S. mutans and S. mitis during biofilm formation was not significant. However, S. dentisani significantly reduced pathologic streptococcal biofilms using the displacement strategy. Also S. dentisani reduced the formation of the C. albicans biofilm mainly through competition and displacement. In vitro, S. dentisani exhibited probiotic potential to reduce the formation of potentially pathogenic biofilms. Further investigation is required to understand the biofilm-inhibiting mechanisms exhibited by this probiotic strain.14application/pdfengUniversidad Cooperativa de Colombia, Facultad de Ciencias de la Salud, Especialización en Ortodoncia, Medellín y EnvigadoMedellínhttps://creativecommons.org/licenses/by/4.0/info:eu-repo/semantics/openAccessAttribution 4.0 Internationalhttp://purl.org/coar/access_right/c_abf2https://www.mdpi.com/2076-0817/13/5/351Probiotic effect of Streptococcus dentisani on oral pathogens: an in vitro studyArtículohttp://purl.org/coar/resource_type/c_6501http://purl.org/coar/resource_type/c_2df8fbb1http://purl.org/coar/version/c_970fb48d4fbd8a85info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersion35113PathogensBaker, J.L.; Mark Welch, J.L.; Kauffman, K.M.; McLean, J.S.; He, X. The oral microbiome: Diversity, biogeography and human health. Nat. Rev. Microbiol. 2024, 22, 89–104Dewhirst, F.E.; Chen, T.; Izard, J.; Paster, B.J.; Tanner, A.C.R.; Yu, W.-H.; Lakshmanan, A.; Wade, W.G. The human oral microbiome. J. Bacteriol. 2010, 192, 5002–5017Deo, P.N.; Deshmukh, R. Oral microbiome: Unveiling the fundamentals. J. Oral Maxillofac. Pathol. 2019, 23, 122–128Willis, J.R.; Gabaldón, T. The human oral microbiome in health and disease: From sequences to ecosystems. Microorganisms 2020, 8, 308Carvalho, F.M.; Teixeira-Santos, R.; Mergulhão, F.J.M.; Gomes, L.C. Targeting Biofilms in Medical Devices using Probiotic Cells: A systematic review. AIMS Mater Sci. 2021, 8, 501–523.Costerton, J.W.; Stewart, P.S.; Greenberg, E.P. Bacterial biofilms: A common cause of persistent infections. Science 1999, 284, 1318–1322.Berger, D.; Rakhamimova, A.; Pollack, A.; Loewy, Z. Oral Biofilms: Development, Control, and Analysis. High Throughput 2018, 7, 3.Hancock, V.; Dahl, M.; Klemm, P. Probiotic Escherichia coli strain Nissle 1917 outcompetes intestinal pathogens during biofilm formation. J. Med. Microbiol. 2010, 59, 392–399Walker, T.S.; Tomlin, K.L.; Worthen, G.S.; Poch, K.R.; Lieber, J.G.; Saavedra, M.T.; Fessler, M.B.; Malcolm, K.C.; Vasil, M.L.; Nick, J.A. Enhanced Pseudomonas aeruginosa biofilm development mediated by human neutrophils. Infect. Immun. 2005, 73, 3693– 3701Colombo, A.P.V.; do Souto, R.M.; da Silva-Boghossian, C.M.; Miranda, R.; Lourenço, T.G.B. Microbiology of Oral Biofilm-Dependent Diseases: Have We Made Significant Progress to Understand and Treat These Diseases? Curr. Oral Health Rep. 2015, 2, 37–47Castro-Rodríguez, Y. Ciencias clínicas y patológicas artículo de revisión La higiene oral y los efectos de la terapia periodontal mecánica. Rev. Habanera Cienc. Med. 2021, 20, e3127Haque, M.; Sartelli, M.; Haque, S.Z. Dental infection and resistance-global health consequences. Dent. J. 2019, 7, 22Allaker, R.P.; Stephen, A.S. Use of Probiotics and Oral Health. Curr. Oral Health Rep. 2017, 4, 309–318Seminario-Amez, M.; López-López, J.; Estrugo-Devesa, A.; Ayuso-Montero, R.; Jané-Salas, E. Probiotics and oral health: A systematic review. Med. Oral Patol. Oral Cir. Bucal 2017, 22, e282–e288Food and Agriculture Organization of the United Nations; World Health Organization. Probiotics in Food: Health and Nutritional Properties and Guidelines for Evaluation; Food and Agriculture Organization of the United Nations: Rome, Italy, 2006; 50p.Amargianitakis, M.; Antoniadou, M.; Rahiotis, C.; Varzakas, T. Probiotics, prebiotics, synbiotics and dental caries. New perspectives, suggestions, and patient coaching approach for a cavity-free mouth. Appl. Sci. 2021, 11, 5472Luo, S.C.; Wei, S.M.; Luo, X.T.; Yang, Q.Q.; Wong, K.H.; Cheung, P.C.K.; Zhang, B.B. How probiotics, prebiotics, synbiotics, and postbiotics prevent dental caries: An oral microbiota perspective. NPJ Biofilms Microbiomes 2024, 10, 14Camelo-Castillo, A.; Benítez-Páez, A.; Belda-Ferre, P.; Cabrera-Rubio, R.; Mira, A. Streptococcus dentisani sp. nov., a novel member of the mitis group. Int. J. Syst. Evol. Microbiol. 2014, 64, 60–65López-López, A.; Camelo-Castillo, A.; Ferrer, M.D.; Simon-Soro, A.; Mira, A. Health-associated niche inhabitants as oral probiotics: The case of Streptococcus dentisani. Front. Microbiol. 2017, 8, 379Llena, C.; Almarche, A.; Mira, A.; López, M.A. Antimicrobial efficacy of the supernatant of streptococcus dentisani against microorganisms implicated in root canal infections. J. Oral Sci. 2019, 61, 184–194Esteban-Fernández, A.; Zorraquín-Peña, I.; Ferrer, M.D.; Mira, A.; Bartolomé, B.; González de Llano, D.; Moreno-Arribas, M.V. Inhibition of oral pathogens adhesion to human gingival fibroblasts by wine polyphenols alone and in combination with an oral probiotic. J. Agric. Food Chem. 2018, 66, 2071–2082Huang, X.; Palmer, S.R.; Ahn, S.; Richards, V.P.; Williams, M.L.; Nascimento, M.M.; Burne, R.A. A Highly Arginolytic Streptococcus Species That Potently Antagonizes Streptococcus mutans. Appl. Environ. Microbiol. 2016, 82, 2187–2201Poorni, S.; Srinivasan, M.R.; Nivedhitha, M.S. Probiotic Streptococcus strains in caries prevention: A systematic review. J. Conserv. Dent. 2019, 22, 123–128Tagg, J.R.; Harold, L.K.; Jain, R.; Hale, J.D.F. Beneficial modulation of human health in the oral cavity and beyond using bacteriocin- like inhibitory substance-producing streptococcal probiotics. Front. Microbiol. 2023, 14, 1161155Elexson, N.; Sabrina, H.; Dalene, L.; Eddy, B.; Nurul, F.R.; Nasra, P.; Grace, B.; Nick, L.; Amirah, Z.J.; Nur, D.Z.; et al. Assessment of Pseudomonas aeruginosa biofilm-forming capacities from drinking water in water vending machine. Food Res. 2022, 6, 76–83Kırmusaoğlu, S. The Methods for detection of biofilm and screening antibiofilm activity of agents. In Antimicrobials, Antibiotic Resistance, Antibiofilm Strategies and Activity Methods; IntechOpen: London, UK, 2019Woo, J.; Ahn, J. Probiotic-mediated competition, exclusion and displacement in biofilm formation by food-borne pathogens. Le. Appl. Microbiol. 2013, 56, 307–313Schwendicke, F.; Korte, F.; Dörfer, C.E.; Kneist, S.; Fawzy El-Sayed, K.; Paris, S. Inhibition of Streptococcus mutans growth and biofilm formation by probiotics in vitro. Caries Res. 2017, 51, 87–95Ruiz, M.J.; García, M.D.; Padola, N.L.; Etcheverría, A.I. Capacidad de Lactiplantibacillus plantarum de reducir biofilms de bacterias patógenas transmitidas por alimentos. Rev. Vet. 2022, 33, 48–52Bernabè, G.; Pauleo, A.; Zamuner, A.; Cassari, L.; Castagliuolo, I.; Brun, P.; Dein, M. Exploiting conserved quorum sensing signals in Streptococcus mutans and Streptococcus pneumoniae. Microorganisms 2022, 10, 12Metwalli, K.H.; Khan, S.A.; Krom, B.P.; Jabra-Rizk, M.A. Streptococcus mutans, Candida albicans, and the human mouth: A sticky situation. PLoS Pathog. 2013, 9, 10Marcinkiewicz, J.; Strus, M.; Pasich, E. Antibiotic resistance: A «dark side» of biofilm-associated chronic infections. Pol. Arch. Med. Wewn. 2013, 123, 309–313Whitmore, S.E.; Lamont, R.J. The pathogenic persona of community-associated oral streptococci. Mol. Microbiol. 2011, 81, 305– 314Li, Y.H.; Hanna, M.N.; Svensäter, G.; Ellen, R.P.; Cvitkovitch, D.G. Cell density modulates acid adaptation in Streptococcus mutans: Implications for survival in biofilms. J. Bacteriol. 2001, 183, 6875–6884Zayed, S.M.; Aboulwafa, M.M.; Hashem, A.M.; Saleh, S.E. Biofilm formation by Streptococcus mutans and its inhibition by green tea extracts. AMB Express. 2021, 11, 73Denapaite, D.; Brückner, R.; Nuhn, M.; Reichmann, P.; Henrich, B.; Maurer, P.; Schähle, Y.; Selbmann, P.; Zimmermann, W.; Wambu, R.; et al. 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Probiotic effect of Streptococcus dentisani on oral pathogens: an in vitro study

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