Interactions between Oral Bacteria: Inhibition of Streptococcus mutans Bacteriocin Production by Streptococcus gordonii

Bacteriocins of gram-positive bacteria

Jack, R. W., Tagg, J. R., & Ray, B. (1995) · Microbiological Reviews · doi:10.1128/mr.59.2.171-200.1995 · Cited by 2,711 · see citing works

How bacteria talk to each other: regulation of gene expression by quorum sensing

Bassler, B. L. (1999) · Current Opinion in Microbiology · doi:10.1016/s1369-5274(99)00025-9 · Cited by 1,034 · see citing works

AiiA, an enzyme that inactivates the acylhomoserine lactone quorum-sensing signal and attenuates the virulence of Erwinia carotovora

Dong, Y.-H., Xu, J., Li, X., & Zhang, L. (2000) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.97.7.3526 · Cited by 803 · see citing works

Quorum sensing by peptide pheromones and two‐component signal‐transduction systems in Gram‐positive bacteria

Kleerebezem, M., Quadri, L. E. N., Kuipers, O. P., & de Vos, W. M. (1997) · Molecular Microbiology · doi:10.1046/j.1365-2958.1997.4251782.x · Cited by 791 · see citing works

AiiA, an enzyme that inactivates the acylhomoserine lactone quorum-sensing signal and attenuates the virulence of Erwinia carotovora

Dong, Y. (2000) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.060023897 · Cited by 783 · see citing works

An unmodified heptadecapeptide pheromone induces competence for genetic transformation in Streptococcus pneumoniae.

Håvarstein, L. S., Coomaraswamy, G., & Morrison, D. A. (1995) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.92.24.11140 · Cited by 737 · see citing works

Natural Genetic Transformation of Streptococcus mutans Growing in Biofilms

Li, Y.-H., Lau, P. C. Y., Lee, J. H., Ellen, R. P., & Cvitkovitch, D. G. (2001) · Journal of Bacteriology · doi:10.1128/jb.183.3.897-908.2001 · Cited by 526 · see citing works

A Quorum-Sensing Signaling System Essential for Genetic Competence in Streptococcus mutans Is Involved in Biofilm Formation

Li, Y.-H., Tang, N., Aspiras, M., Lau, P. C. Y., Lee, J. H., Ellen, R. P., & Cvitkovitch, D. G. (2002) · Journal of Bacteriology · doi:10.1128/jb.184.10.2699-2708.2002 · Cited by 480 · see citing works

Bacteriocins of gram-positive bacteria

Tagg, J. R., Dajani, A. S., & Wannamaker, L. W. (1976) · Bacteriological Reviews · doi:10.1128/br.40.3.722-756.1976 · Cited by 480 · see citing works

CELL-CELL COMMUNICATION IN GRAM-POSITIVE BACTERIA

Dunny, G. M., & Buttaro, B. A. (1997) · Annual Review of Microbiology · doi:10.1146/annurev.micro.51.1.527 · Cited by 454 · see citing works

Quorum sensing and biofilm formation in Streptococcal infections

Cvitkovitch, D. G., Li, Y.-H., & Ellen, R. P. (2003) · Journal of Clinical Investigation · doi:10.1172/jci200320430 · Cited by 358 · see citing works

Self perception in bacteria: quorum sensing with acylated homoserine lactones

Fuqua, C., & Greenberg, E. P. (1998) · Current Opinion in Microbiology · doi:10.1016/s1369-5274(98)80009-x · Cited by 302 · see citing works

FUNCTIONS OF SECONDARY METABOLITES

Vining, L. C. (1990) · Annual Review of Microbiology · doi:10.1146/annurev.mi.44.100190.002143 · Cited by 291 · see citing works

Quorum sensing and biofilm formation in Streptococcal infections

Cvitkovitch, D. G., Li, Y.-H., & Ellen, R. P. (2003) · Journal of Clinical Investigation · doi:10.1172/jci20430 · Cited by 289 · see citing works

Cloning of a Streptococcus mutans glucosyltransferase gene coding for insoluble glucan synthesis

Aoki, H., Shiroza, T., Hayakawa, M., Sato, S., & Kuramitsu, H. K. (1986) · Infection and Immunity · doi:10.1128/iai.53.3.587-594.1986 · Cited by 273 · see citing works

Cell Density Modulates Acid Adaptation in Streptococcus mutans : Implications for Survival in Biofilms

Li, Y.-H., Hanna, M. N., Svensäter, G., Ellen, R. P., & Cvitkovitch, D. G. (2001) · Journal of Bacteriology · doi:10.1128/jb.183.23.6875-6884.2001 · Cited by 239 · see citing works

Novel Two-Component Regulatory System Involved in Biofilm Formation and Acid Resistance inStreptococcus mutans

Li, Y.-H., Lau, P. C. Y., Tang, N., Svensäter, G., Ellen, R. P., & Cvitkovitch, D. G. (2002) · Journal of Bacteriology · doi:10.1128/jb.184.22.6333-6342.2002 · Cited by 211 · see citing works

The Group I Strain of Streptococcus mutans , UA140, Produces Both the Lantibiotic Mutacin I and a Nonlantibiotic Bacteriocin, Mutacin IV

Qi, F., Chen, P., & Caufield, P. W. (2001) · Applied and Environmental Microbiology · doi:10.1128/aem.67.1.15-21.2001 · Cited by 204 · see citing works

Peptide pheromone-dependent regulation of antimicrobial peptide production in Gram-positive bacteria: a case of multicellular behavior

Kleerebezem, M., & Quadri, L. E. N. (2001) · Peptides · doi:10.1016/s0196-9781(01)00493-4 · Cited by 202 · see citing works

Pheromone Cross-Inhibition between Staphylococcus aureus and Staphylococcus epidermidis

Otto, M. J., Echner, H., Voelter, W., & Götz, F. (2001) · Infection and Immunity · doi:10.1128/iai.69.3.1957-1960.2001 · Cited by 202 · see citing works

Multiple Streptococcus mutans Genes Are Involved in Biofilm Formation

Yoshida, A., & Kuramitsu, H. K. (2002) · Applied and Environmental Microbiology · doi:10.1128/aem.68.12.6283-6291.2002 · Cited by 194 · see citing works

Sequence analysis of the gtfC gene from Streptococcus mutans GS-5

Ueda, S., Shiroza, T., & Kuramitsu, H. K. (1988) · Gene · doi:10.1016/0378-1119(88)90382-4 · Cited by 156 · see citing works

Sequence analysis of the Streptococcus mutans fructosyltransferase gene and flanking regions

Shiroza, T., & Kuramitsu, H. K. (1988) · Journal of Bacteriology · doi:10.1128/jb.170.2.810-816.1988 · Cited by 120 · see citing works

Purification of Mutacin III from Group III Streptococcus mutans UA787 and Genetic Analyses of Mutacin III Biosynthesis Genes

Qi, F., Chen, P., & Caufield, P. W. (1999) · Applied and Environmental Microbiology · doi:10.1128/aem.65.9.3880-3887.1999 · Cited by 117 · see citing works

Streptococcal Competence for Genetic Transformation: Regulation by Peptide Pheromones

Morrison, D. A. (1997) · Microbial Drug Resistance · doi:10.1089/mdr.1997.3.27 · Cited by 80 · see citing works

The Specific Genes for Lantibiotic Mutacin II Biosynthesis in Streptococcus mutans T8 Are Clustered and Can Be Transferred En Bloc

Chen, P., Qi, F., Novák, J., & Caufield, P. W. (1999) · Applied and Environmental Microbiology · doi:10.1128/aem.65.3.1356-1360.1999 · Cited by 64 · see citing works

Production and properties of an extracellular bacteriocin from Streptococcus mutans bacteriocidal for group A and other streptococci

Paul, D., & Slade, H. D. (1975) · Infection and Immunity · doi:10.1128/iai.12.6.1375-1385.1975 · Cited by 52 · see citing works

Molecular basis for the spontaneous generation of colonization‐defective mutants of Streptococcus mutans

Ueda, S., & Kuramitsu, H. K. (1988) · Molecular Microbiology · doi:10.1111/j.1365-2958.1988.tb00014.x · Cited by 51 · see citing works

Bacteriocins as Factors in the In Vitro Interaction Between Oral Streptococci in Plaque

Weerkamp, A. H., Bongaerts-Larik, L., & Vogels, G. D. (1977) · Infection and Immunity · doi:10.1128/iai.16.3.773-780.1977 · Cited by 47 · see citing works

Effect of the Medium on Bacteriocin Production Among Strains of Streptococcus mutans

Rogers, A. H. (1972) · Applied Microbiology · doi:10.1128/am.24.2.294-295.1972 · Cited by 46 · see citing works

Cloning of a locus involved in Streptococcus mutans intracellular polysaccharide accumulation and virulence testing of an intracellular polysaccharide-deficient mutant

Harris, G. S., Michalek, S. M., & Curtiss, R. (1992) · Infection and Immunity · doi:10.1128/iai.60.8.3175-3185.1992 · Cited by 37 · see citing works

Genetic Exchange Between Oral Streptococci During Mixed Growth

Kuramitsu, H. K., & Trapa, V. (1984) · Microbiology · doi:10.1099/00221287-130-10-2497 · Cited by 34 · see citing works

Purification and characterization of a protease from Porphyromonas gingivalis capable of degrading salt-solubilized collagen

Sojar, H. T., Lee, J. Y., Bedi, G. S., & Genco, R. J. (1993) · Infection and Immunity · doi:10.1128/iai.61.6.2369-2376.1993 · Cited by 30 · see citing works

Production of bacteriocin-like substances by human oral streptococci.

Fabio, U., Bondi, M., Manicardi, G. C., Messi, P., & Neglia, R. G. (1987) · PubMed · Cited by 25 · see citing works

Plasmid-mediated transformation of Streptococcus mutans

Kuramitsu, H. K., & Long, C.-F. (1982) · Infection and Immunity · doi:10.1128/iai.36.1.435-436.1982 · Cited by 11 · see citing works

Bacterial competition: surviving and thriving in the microbial jungle

Hibbing, M. E., Fuqua, C., Parsek, M. R., & Peterson, S. B. (2009) · Nature Reviews Microbiology · doi:10.1038/nrmicro2259 · Cited by 2,658 · see citing works

Bacteriocins: Developing innate immunity for food

Cotter, P. D., Hill, C., & Ross, R. P. (2005) · Nature Reviews Microbiology · doi:10.1038/nrmicro1273 · Cited by 2,380 · see citing works

Oral multispecies biofilm development and the key role of cell–cell distance

Kolenbrander, P. E., Palmer, R. J., Periasamy, S., & Jakubovics, N. S. (2010) · Nature Reviews Microbiology · doi:10.1038/nrmicro2381 · Cited by 1,309 · see citing works

The oral microbiome: Role of key organisms and complex networks in oral health and disease

Sedghi, L., DiMassa, V., Harrington, A., Lynch, S. V., & Kapila, Y. L. (2021) · Periodontology 2000 · doi:10.1111/prd.12393 · Cited by 755 · see citing works

Biosynthesis and Mode of Action of Lantibiotics

Chatterjee, C., Paul, M., Xie, L., & van der Donk, W. A. (2005) · Chemical Reviews · doi:10.1021/cr030105v · Cited by 727 · see citing works

<i>Streptococcus</i> Adherence and Colonization

Nobbs, A. H., Lamont, R. J., & Jenkinson, H. F. (2009) · Microbiology and Molecular Biology Reviews · doi:10.1128/mmbr.00014-09 · Cited by 657 · see citing works

Lantibiotics: Peptides of Diverse Structure and Function

Willey, J. M., & van der Donk, W. A. (2007) · Annual Review of Microbiology · doi:10.1146/annurev.micro.61.080706.093501 · Cited by 621 · see citing works

Interspecies Interactions within Oral Microbial Communities

Kuramitsu, H. K., He, X., Lux, R., Anderson, M. H., & Shi, W. (2007) · Microbiology and Molecular Biology Reviews · doi:10.1128/mmbr.00024-07 · Cited by 595 · see citing works

Ecology and evolution of metabolic cross-feeding interactions in bacteria

D’Souza, G. G., Shitut, S., Preußger, D., Yousif, G., Waschina, S., & Kost, C. (2018) · Natural Product Reports · doi:10.1039/c8np00009c · Cited by 556 · see citing works

Biology of Oral Streptococci

Abranches, J., Zeng, L., Kajfasz, J. K., Palmer, S. R., Chakraborty, B., Wen, Z. T., Richards, V. P., Brady, L. J., & Lemos, J. A. C. (2018) · Microbiology Spectrum · doi:10.1128/microbiolspec.gpp3-0042-2018 · Cited by 558 · see citing works

Beyond Streptococcus mutans: Dental Caries Onset Linked to Multiple Species by 16S rRNA Community Analysis

Gross, E. L., Beall, C. J., Kutsch, S. R., Firestone, N. D., Leys, E. J., & Griffen, A. L. (2012) · PLoS ONE · doi:10.1371/journal.pone.0047722 · Cited by 508 · see citing works

The dental plaque biofilm matrix

Jakubovics, N. S., Goodman, S. D., Mashburn‐Warren, L., Stafford, G. P., & Cieplik, F. (2021) · Periodontology 2000 · doi:10.1111/prd.12361 · Cited by 488 · see citing works

Bacterial 16S Sequence Analysis of Severe Caries in Young Permanent Teeth

Gross, E. L., Leys, E. J., Gasparovich, S. R., Firestone, N. D., Schwartzbaum, J., Janies, D. A., Asnani, K. M., & Griffen, A. L. (2010) · Journal of Clinical Microbiology · doi:10.1128/jcm.01232-10 · Cited by 351 · see citing works

High prevalence of biofilm synergy among bacterial soil isolates in cocultures indicates bacterial interspecific cooperation

Ren, D., Madsen, J. S., Sørensen, S. J., & Burmølle, M. (2014) · The ISME Journal · doi:10.1038/ismej.2014.96 · Cited by 334 · see citing works

The Genotypic View of Social Interactions in Microbial Communities

Mitri, S., & Foster, K. R. (2013) · Annual Review of Genetics · doi:10.1146/annurev-genet-111212-133307 · Cited by 291 · see citing works

Impact of Oral Microbiome in Periodontal Health and Periodontitis: A Critical Review on Prevention and Treatment

Di Stefano, M., Polizzi, A., Santonocito, S., Romano, A., Lombardi, T., & Isola, G. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms23095142 · Cited by 292 · see citing works

Bacterial and Host Interactions of Oral Streptococci

Kreth, J., Merritt, J. L., & Qi, F. (2009) · DNA and Cell Biology · doi:10.1089/dna.2009.0868 · Cited by 241 · see citing works

Regulation of Bacteriocin Production in Streptococcus mutans by the Quorum-Sensing System Required for Development of Genetic Competence

van der Ploeg, J. R. (2005) · Journal of Bacteriology · doi:10.1128/jb.187.12.3980-3989.2005 · Cited by 237 · see citing works

Streptococcus Sanguinis Biofilm Formation & Interaction with Oral Pathogens

Zhu, B., Macleod, L. C., Kitten, T. O., & Xu, P. (2018) · Future Microbiology · doi:10.2217/fmb-2018-0043 · Cited by 228 · see citing works

Bacterial interactions in biofilms

Moons, P., Michiels, C. W., & Aertsen, A. (2009) · Critical Reviews in Microbiology · doi:10.1080/10408410902809431 · Cited by 210 · see citing works

Correlations of oral bacterial arginine and urea catabolism with caries experience

Nascimento, M. M., Gordan, V. V., Garvan, C. W., Browngardt, C. M., & Burne, R. A. (2009) · Oral Microbiology and Immunology · doi:10.1111/j.1399-302x.2008.00477.x · Cited by 196 · see citing works

Microbial interactions in building of communities

Wright, C. J., Burns, L. H., Jack, A. A., Back, C. R., Dutton, L. C., Nobbs, A. H., Lamont, R. J., & Jenkinson, H. F. (2013) · Molecular Oral Microbiology · doi:10.1111/omi.12012 · Cited by 185 · see citing works

Bacteriocins : ecology and evolution

Riley, M. A., & Chavan, M. A. (2007) · doi:10.1007/978-3-540-36604-1 · Cited by 137 · see citing works

A Highly Arginolytic Streptococcus Species That Potently Antagonizes Streptococcus mutans

Huang, X., Palmer, S. R., Ahn, S.-J., Richards, V. P., Williams, M. L., Nascimento, M. M., & Burne, R. A. (2016) · Applied and Environmental Microbiology · doi:10.1128/aem.03887-15 · Cited by 127 · see citing works

Competence in Streptococcus pneumoniae and Close Commensal Relatives: Mechanisms and Implications

Salvadori, G., Junges, R., Morrison, D. A., & Petersen, F. C. (2019) · Frontiers in Cellular and Infection Microbiology · doi:10.3389/fcimb.2019.00094 · Cited by 118 · see citing works

Community Interactions of Oral Streptococci

Jakubovics, N. S., Yassin, S. A., & Rickard, A. H. (2014) · Advances in Applied Microbiology · doi:10.1016/b978-0-12-800261-2.00002-5 · Cited by 107 · see citing works

Antimicrobial effects of commensal oral species are regulated by environmental factors

Herrero, E. R., Slomka, V., Bernaerts, K., Boon, N., Hernandez‐Sanabria, E., Passoni, B. B., Quirynen, M., & Teughels, W. (2016) · Journal of Dentistry · doi:10.1016/j.jdent.2016.02.007 · Cited by 105 · see citing works

RNA-Seq Reveals Enhanced Sugar Metabolism in Streptococcus mutans Co-cultured with Candida albicans within Mixed-Species Biofilms

He, J., Kim, D., Zhou, X., Ahn, S., Burne, R. A., Richards, V. P., & Koo, H. (2017) · Frontiers in Microbiology · doi:10.3389/fmicb.2017.01036 · Cited by 100 · see citing works

Association between the gut and oral microbiome with obesity

Benahmed, A. G., Gasmi, A., Doşa, A., Chirumbolo, S., Mujawdiya, P. K., Aaseth, J., Dadar, M., & Bjørklund, G. (2020) · Anaerobe · doi:10.1016/j.anaerobe.2020.102248 · Cited by 102 · see citing works

Cariogenic microbiome and microbiota of the early primary dentition: A contemporary overview

Fakhruddin, K. S., Ngo, H. C., & Samaranayake, L. P. (2018) · Oral Diseases · doi:10.1111/odi.12932 · Cited by 95 · see citing works

An Extracelluar Protease, SepM, Generates Functional Competence-Stimulating Peptide in Streptococcus mutans UA159

Hossain, M. S., & Biswas, I. (2012) · Journal of Bacteriology · doi:10.1128/jb.01381-12 · Cited by 93 · see citing works

Inhibition of Streptococcus mutans Biofilm Formation by Streptococcus salivarius FruA

Ogawa, A., Furukawa, S., Fujita, S., Mitobe, J., Kawarai, T., Narisawa, N., Sekizuka, T., Kuroda, M., Ochiai, K., Ogihara, H., et al. (2011) · Applied and Environmental Microbiology · doi:10.1128/aem.02066-10 · Cited by 85 · see citing works

The road less traveled – defining molecular commensalism with Streptococcus sanguinis

Kreth, J., Giacaman, R. A., Raghavan, R., & Merritt, J. L. (2016) · Molecular Oral Microbiology · doi:10.1111/omi.12170 · Cited by 83 · see citing works

Interspecies Communication among Commensal and Pathogenic Streptococci

Cook, L. C., LaSarre, B., & Federle, M. J. (2013) · mBio · doi:10.1128/mbio.00382-13 · Cited by 81 · see citing works

Inhibiting effects of Streptococcus salivarius on competence‐stimulating peptide‐dependent biofilm formation by Streptococcus mutans

TAMURA, S., Yonezawa, H., Motegi, M., Nakao, R., Yoneda, S., Watanabe, H., Yamazaki, T., & Senpuku, H. (2009) · Oral Microbiology and Immunology · doi:10.1111/j.1399-302x.2008.00489.x · Cited by 78 · see citing works

Intercellular communications in multispecies oral microbial communities

Guo, L., He, X., & Shi, W. (2014) · Frontiers in Microbiology · doi:10.3389/fmicb.2014.00328 · Cited by 77 · see citing works

Effects of Arginine on Streptococcus mutans Growth, Virulence Gene Expression, and Stress Tolerance

Chakraborty, B., & Burne, R. A. (2017) · Applied and Environmental Microbiology · doi:10.1128/aem.00496-17 · Cited by 76 · see citing works

Streptococcus mutans et les streptocoques buccaux dans la plaque dentaire

Nicolas, G. G., & Lavoie, M. C. (2011) · Canadian Journal of Microbiology · doi:10.1139/w10-095 · Cited by 74 · see citing works

Identification of a signalling molecule involved in bacterial intergeneric communication

Xie, H., Lin, X., Wang, B.-Y., Wu, J., & Lamont, R. J. (2007) · Microbiology · doi:10.1099/mic.0.2007/009050-0 · Cited by 73 · see citing works

Talk of the town: interspecies communication in oral biofilms

Jakubovics, N. S. (2010) · Molecular Oral Microbiology · doi:10.1111/j.2041-1014.2009.00563.x · Cited by 72 · see citing works

Studying bacterial infections through culture-independent approaches

Rogers, G. B., Carroll, M. P., & Bruce, K. D. (2009) · Journal of Medical Microbiology · doi:10.1099/jmm.0.013334-0 · Cited by 72 · see citing works

Differential response of Streptococcus mutans towards friend and foe in mixed-species cultures

Liu, J., Wu, C., Huang, I., Merritt, J. L., & Qi, F. (2011) · Microbiology · doi:10.1099/mic.0.048314-0 · Cited by 69 · see citing works

Antibiotic discovery through microbial interactions

Zhang, C., & Straight, P. D. (2019) · Current Opinion in Microbiology · doi:10.1016/j.mib.2019.06.006 · Cited by 57 · see citing works

Inhibition of Oral Streptococci Growth Induced by the Complementary Action of Berberine Chloride and Antibacterial Compounds

Dziedzic, A. M., Wojtyczka, R. D., & Kubina, R. (2015) · Molecules · doi:10.3390/molecules200813705 · Cited by 56 · see citing works

Competence-Dependent Bacteriocin Production by Streptococcus gordonii DL1 (Challis)

Heng, N. C. K., Tagg, J. R., & Tompkins, G. R. (2007) · Journal of Bacteriology · doi:10.1128/jb.01174-06 · Cited by 52 · see citing works

Identification of novel LPXTG-linked surface proteins from Streptococcus gordonii

Davies, J. R., Svensäter, G., & Herzberg, M. C. (2009) · Microbiology · doi:10.1099/mic.0.027854-0 · Cited by 50 · see citing works

Abrogation of Neuraminidase Reduces Biofilm Formation, Capsule Biosynthesis, and Virulence of Porphyromonas gingivalis

Li, C., Kurniyati, Hu, B., Bian, J., Sun, J., Zhang, W., Liu, J., Pan, Y., & Li, C. (2011) · Infection and Immunity · doi:10.1128/iai.05773-11 · Cited by 49 · see citing works

The Major Autolysin of Streptococcus gordonii Is Subject to Complex Regulation and Modulates Stress Tolerance, Biofilm Formation, and Extracellular-DNA Release

Liu, Y., & Burne, R. A. (2011) · Journal of Bacteriology · doi:10.1128/jb.00056-11 · Cited by 49 · see citing works

Virulence properties of cariogenic bacteria

Kuramitsu, H. K., & Wang, B. (2006) · BMC Oral Health · doi:10.1186/1472-6831-6-s1-s11 · Cited by 44 · see citing works

Enhancing the utility of existing antibiotics by targeting bacterial behaviour?

Rogers, G. B., Carroll, M. P., & Bruce, K. D. (2012) · British Journal of Pharmacology · doi:10.1111/j.1476-5381.2011.01643.x · Cited by 42 · see citing works

A Reciprocal Link between Oral, Gut Microbiota during Periodontitis: The Potential Role of Probiotics in Reducing Dysbiosis-Induced Inflammation

Stefano, M. D., Santonocito, S., Polizzi, A., Mauceri, R., Troiano, G., Giudice, A. L., Romano, A., Mascitti, M., & Isola, G. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms24021084 · Cited by 44 · see citing works

Role of VltAB, an ABC Transporter Complex, in Viologen Tolerance in Streptococcus mutans

Biswas, S., & Biswas, I. (2011) · Antimicrobial Agents and Chemotherapy · doi:10.1128/aac.01094-10 · Cited by 39 · see citing works

Biofilm ecology associated with dental caries: understanding of microbial interactions in oral communities leads to development of therapeutic strategies targeting cariogenic biofilms

Cai, J.-N., & Kim, D. (2023) · Advances in applied microbiology · doi:10.1016/bs.aambs.2023.02.001 · Cited by 41 · see citing works

Amino Sugars Modify Antagonistic Interactions between Commensal Oral Streptococci and Streptococcus mutans

Chen, L., Chakraborty, B., Zou, J., Burne, R. A., & Zeng, L. (2019) · Applied and Environmental Microbiology · doi:10.1128/aem.00370-19 · Cited by 37 · see citing works

Proteases of an Early Colonizer Can Hinder Streptococcus mutans Colonization in vitro

Wang, B.-Y., Deutch, A., Hong, J., & Kuramitsu, H. K. (2010) · Journal of Dental Research · doi:10.1177/0022034510388808 · Cited by 36 · see citing works

Microbial cell surface proteins and secreted metabolites involved in multispecies biofilms.

Demuyser, L., Jabra-Rizk, M., & van Dijck, P. (2014) · Pathogens and Disease · doi:10.1111/2049-632x.12123 · Cited by 37 · see citing works

Engineering chemical interactions in microbial communities

Kenny, D. J., & Balskus, E. P. (2017) · Chemical Society Reviews · doi:10.1039/c7cs00664k · Cited by 37 · see citing works

Guardian genes ensuring subsistence of oral Streptococcus mutans

Shanmugam, K., Sarveswari, H. B., Udayashankar, A., Swamy, S. S., Pudipeddi, A., Shanmugam, T., Solomon, A. P., & Neelakantan, P. (2020) · Critical Reviews in Microbiology · doi:10.1080/1040841x.2020.1796579 · Cited by 35 · see citing works

Novel Probiotic Mechanisms of the Oral Bacterium Streptococcus sp. A12 as Explored with Functional Genomics

Lee, K., Walker, A. R., Chakraborty, B., Kaspar, J. R., Nascimento, M. M., & Burne, R. A. (2019) · Applied and Environmental Microbiology · doi:10.1128/aem.01335-19 · Cited by 31 · see citing works

Direct interactions with commensal streptococci modify intercellular communication behaviors of Streptococcus mutans

Kaspar, J. R., Lee, K., Richard, B., Walker, A. R., & Burne, R. A. (2020) · The ISME Journal · doi:10.1038/s41396-020-00789-7 · Cited by 31 · see citing works

Casein phosphopeptide–amorphous calcium phosphate fluoride treatment enriches the symbiotic dental plaque microbiome in children

Widyarman, A. S., Udawatte, N. S., Theodorea, C. F., Apriani, A., Richi, M., Astoeti, T. E., & Seneviratne, C. J. (2021) · Journal of Dentistry · doi:10.1016/j.jdent.2021.103582 · Cited by 31 · see citing works

The whole is greater than the sum of its parts: dental plaque bacterial interactions can affect the virulence properties of cariogenic Streptococcus mutans.

Kuramitsu, H. K., & Wang, B. (2011) · PubMed · Cited by 31 · see citing works

Getting to Know “The Known Unknowns”: Heterogeneity in the Oral Microbiome

Burne, R. A. (2018) · Advances in Dental Research · doi:10.1177/0022034517735293 · Cited by 30 · see citing works

The rest of the story: the microbiome and gastrointestinal infections

Leslie, J. L., & Young, V. B. (2014) · Current Opinion in Microbiology · doi:10.1016/j.mib.2014.11.010 · Cited by 30 · see citing works

Biology of Oral Streptococci

Abranches, J., Zeng, L., Kajfasz, J. K., Palmer, S. R., Chakraborty, B., Wen, Z. T., Richards, V. P., Brady, L. J., & Lemos, J. A. C. (2019) · ASM Press eBooks · doi:10.1128/9781683670131.ch26 · Cited by 27 · see citing works

Anticariogenic potentials of clove, tobacco and bitter kola

Dibua, E. U., & Nnamani, P. O. (2011) · Asian Pacific Journal of Tropical Medicine · doi:10.1016/s1995-7645(11)60200-9 · Cited by 24 · see citing works

Streptococcus mutans membrane vesicles inhibit the biofilm formation of Streptococcus gordonii and Streptococcus sanguinis

Cui, G., Li, P., Wu, R., & Lin, H. (2022) · AMB Express · doi:10.1186/s13568-022-01499-3 · Cited by 24 · see citing works

Host-Derived Pentapeptide Affecting Adhesion, Proliferation, and Local pH in Biofilm Communities Composed of Streptococcus and Actinomyces Species

Drobni, M., Li, T., Krüger, C., Loimaranta, V., Kilian, M., Hammarström, L. L. G., Jörnvall, H., Bergman, T., & Strömberg, N. (2006) · Infection and Immunity · doi:10.1128/iai.00068-06 · Cited by 24 · see citing works

Role of Streptococcus mutans eukaryotic-type serine/threonine protein kinase in interspecies interactions with Streptococcus sanguinis

Zhu, L., & Kreth, J. (2010) · Archives of Oral Biology · doi:10.1016/j.archoralbio.2010.03.012 · Cited by 23 · see citing works

A Method for Structure–Activity Analysis of Quorum-Sensing Signaling Peptides from Naturally Transformable Streptococci

Tian, X., Syvitski, R. T., Liu, T., Livingstone, N., Jakeman, D. L., & Li, Y.-H. (2009) · Biological Procedures Online · doi:10.1007/s12575-009-9009-9 · Cited by 22 · see citing works

Characterization of Streptococcus gordonii prophage PH15: complete genome sequence and functional analysis of phage-encoded integrase and endolysin

van der Ploeg, J. R. (2008) · Microbiology · doi:10.1099/mic.0.2008/018739-0 · Cited by 22 · see citing works

Periodontal pathogens interfere with quorum-sensing-dependent virulence properties in Streptococcus mutans

Wang, B., Alvarez, P., Hong, J., & Kuramitsu, H. K. (2010) · Journal of Periodontal Research · doi:10.1111/j.1600-0765.2010.01319.x · Cited by 22 · see citing works

Effects of Oral Commensal Streptococci on Porphyromonas gingivalis Invasion into Oral Epithelial Cells

Hanel, A., Herzog, H. M., James, M. G., & Cuadra, G. A. (2020) · Dentistry Journal · doi:10.3390/dj8020039 · Cited by 20 · see citing works

Biosynthesis and Mode of Action of Lantibiotics

Cooper, L. E., Ли, Б., & van der Donk, W. A. (2010) · Elsevier eBooks · doi:10.1016/b978-008045382-8.00116-7 · Cited by 20 · see citing works

Proteome Analysis Identifies the Dpr Protein of Streptococcus mutans as an Important Factor in the Presence of Early Streptococcal Colonizers of Tooth Surfaces

Yoshida, A., Niki, M., Yamamoto, Y., Yasunaga, A., & Ansai, T. (2015) · PLoS ONE · doi:10.1371/journal.pone.0121176 · Cited by 19 · see citing works

Amino Sugars Reshape Interactions between Streptococcus mutans and Streptococcus gordonii

Chen, L., Walker, A. R., Burne, R. A., & Zeng, L. (2020) · Applied and Environmental Microbiology · doi:10.1128/aem.01459-20 · Cited by 19 · see citing works

Influence of oral bacteria on adhesion of Streptococcus mutans and Streptococcus sanguinis to dental materials

Nabert‐Georgi, C., Rodloff, A. C., Jentsch, H. F. R., Reissmann, D. R., Schaumann, R., & Stîngu, C. S. (2018) · Clinical and Experimental Dental Research · doi:10.1002/cre2.107 · Cited by 18 · see citing works

Streptococcus gordonii Challisin protease is required for sensing cell--cell contact with Actinomyces oris

Mohammed, W. K., Krasnogor, N., & Jakubovics, N. S. (2018) · FEMS Microbiology Ecology · doi:10.1093/femsec/fiy043 · Cited by 17 · see citing works

Milk Protein Fragments Induce the Biosynthesis of Macedocin, the Lantibiotic Produced by Streptococcus macedonicus ACA-DC 198

Georgalaki, M. D., Papadelli, M., Chassioti, E., Anastasiou, R., Aktypis, A., Vuyst, L. D., Driessche, G. V., Devreese, B. V., & Tsakalidou, E. (2009) · Applied and Environmental Microbiology · doi:10.1128/aem.00151-09 · Cited by 16 · see citing works

Specific chemiluminescent protocol for dual-site recognition of Streptococcus mutans utilizing strong affinity between teicoplanin and Gram-positive bacteria

Su, X., Wang, M., Wu, Y., He, Y. Q., & Fu, Z. (2017) · Talanta · doi:10.1016/j.talanta.2017.11.004 · Cited by 15 · see citing works

The impact of research and development on the prevention of oral diseases in children and adolescents: an industry perspective.

Cummins, D. (2006) · PubMed · Cited by 14 · see citing works

In Situ Raman Analysis of Biofilm Exopolysaccharides Formed in Streptococcus mutans and Streptococcus sanguinis Commensal Cultures

Pezzotti, G., Ofuji, S., Imamura, H., Adachi, T., Yamamoto, T., Kanamura, N., Ohgitani, E., Marin, E., Zhu, W., Mazda, O., et al. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms24076694 · Cited by 14 · see citing works

Streptococcus pneumoniae, S. mitis, and S. oralis Produce a Phosphatidylglycerol-Dependent, ltaS -Independent Glycerophosphate-Linked Glycolipid

Wei, Y., Joyce, L. R., Wall, A. M., Guan, Z., & Palmer, K. L. (2021) · mSphere · doi:10.1128/msphere.01099-20 · Cited by 14 · see citing works

Conserved Pheromone Production, Response and Degradation by Streptococcus mutans

Ricomini-Filho, A. P., Khan, R. S., Åmdal, H. A., & Petersen, F. C. (2019) · Frontiers in Microbiology · doi:10.3389/fmicb.2019.02140 · Cited by 14 · see citing works

Bacteriocins' Role in Bacterial Communication

Gillor, O. (2006) · Springer eBooks · doi:10.1007/978-3-540-36604-1_7 · Cited by 14 · see citing works

Mutation of the Streptococcus gordonii Thiol-Disulfide Oxidoreductase SdbA Leads to Enhanced Biofilm Formation Mediated by the CiaRH Two-Component Signaling System

Davey, L. E., Halperin, S. A., & Lee, S. F. (2016) · PLoS ONE · doi:10.1371/journal.pone.0166656 · Cited by 13 · see citing works

Interactions between probiotic and oral pathogenic strains

Horváth-Gönczi, N. N., Strang, O., Bagi, Z., Rákhely, G., & Kovács, K. L. (2021) · Biologia Futura · doi:10.1007/s42977-021-00091-3 · Cited by 12 · see citing works

Three Distinct Proteases Are Responsible for Overall Cell Surface Proteolysis in Streptococcus thermophilus

Boulay, M., Metton, C., Mézange, C., Correia, L. O., Meylheuc, T., Monnet, V., Gardan, R., & Juillard, V. (2021) · Applied and Environmental Microbiology · doi:10.1128/aem.01292-21 · Cited by 12 · see citing works

Streptococcus mutans dexA affects exopolysaccharides production and biofilm homeostasis

Yang, Y. L., Hailun, H., Fenghui, Y., Liu, P., Lei, L., Zhili, Z., & Hu, T. (2022) · Molecular Oral Microbiology · doi:10.1111/omi.12395 · Cited by 10 · see citing works

The Influence of Streptococcus mutans Biofilm Formation in a Polymicrobial Environment (Streptococcus gordonii & Porphyromonas gingivalis)

Kriswandini, I. L., Sidarningsih, S., Hermanto, A. C., Tyas, P. R., & Aljunaid, M. (2024) · European Journal of Dentistry · doi:10.1055/s-0044-1782215 · Cited by 10 · see citing works

The human microbiome: opportunities and challenges for clinical care

Rogers, G. B. (2014) · Internal Medicine Journal · doi:10.1111/imj.12650 · Cited by 10 · see citing works

Development and characterisation of a novel antimicrobial peptide GA-C16G2 targeting Streptococcus mutans

Fu, Y., Cannon, R. D., Li, K. C., Ekambaram, M., Cooper, P. R., & Mei, M. L. (2025) · Journal of Dentistry · doi:10.1016/j.jdent.2025.105927 · Cited by 8 · see citing works

Conserved and divergent functions of RcrRPQ inStreptococcus gordoniiandS. mutans

Shields, R. C., & Burne, R. A. (2015) · FEMS Microbiology Letters · doi:10.1093/femsle/fnv119 · Cited by 8 · see citing works

Antagonistic, Synergistic, and Counteroffensive Strategies for Streptococcal Interspecies Interactions

Kreth, J., Merritt, J. L., Qi, F., Dong, X., & Shi, W. (2011) · doi:10.1128/9781555817107.ch22 · Cited by 8 · see citing works

Nattokinase, a Subtilisin-like Alkaline-Serine Protease, Reduces Mutacin Activity by Inactivating the Competence-Stimulating Peptide in Streptococcus mutans

Kimijima, M., Narisawa, N., Hori, E., Mandokoro, K., Ito, T., Ota, Y., Sashida, M., Kawai, Y., & TAKENAGA, F. (2024) · Pathogens · doi:10.3390/pathogens13040286 · Cited by 7 · see citing works

Synthesis, Microbiology, and Biophysical Characterization of Mutanofactins from the Human Oral Microbiome

Lüthy, L., Thies, L. G. S., Beitl, K. N., Hansen, M., McManus, J., Afzal, M., Schrangl, L., Bloch, S., Subbiahdoss, G., Reimhult, E., et al. (2025) · ACS Central Science · doi:10.1021/acscentsci.4c02184 · Cited by 7 · see citing works

Evaluation of antimicrobial activity of bacterial symbionts isolated from wild field cockroach Blattella vaga from Saudi Arabia

Alkhalifah, D. H. M. (2021) · Saudi Journal of Biological Sciences · doi:10.1016/j.sjbs.2021.06.092 · Cited by 7 · see citing works

Dishonest Signaling in Microbial Conflicts

Hashem, I., & van Impe, J. F. M. (2022) · Frontiers in Microbiology · doi:10.3389/fmicb.2022.812763 · Cited by 7 · see citing works

Carboxypeptidase activity common to viridans group streptococci cleaves angiotensin I to angiotensin II: an activity homologous to angiotensin-converting enzyme (ACE)

Harty, D. W. S., & Hunter, N. (2011) · Microbiology · doi:10.1099/mic.0.048710-0 · Cited by 7 · see citing works

Mutation of the Thiol-Disulfide Oxidoreductase SdbA Activates the CiaRH Two-Component System, Leading to Bacteriocin Expression Shutdown in Streptococcus gordonii

Davey, L. E., Halperin, S. A., & Lee, S. F. (2015) · Journal of Bacteriology · doi:10.1128/jb.00800-15 · Cited by 7 · see citing works

Interaction between oral bacteria: inhibition of Streptococcus mutans bacteriocin production by Streptococcus gordonii

Wang, B.-Y., & Kuramitsu, H. K. (2005)

The MutRS quorum-sensing system controls lantibiotic mutacin production in the human pathogen Streptococcus mutans

Wyllie, R. M., & Jensen, P. A. (2025) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2421164122 · Cited by 11 · see citing works

The elimination of bacteriocin production in the oral bacterium Streptococcus mutans

Fukushima, H., Tsuboi, Y., FUKUSHIMA, S., & Sagawa, H. (1980) · Archives of Oral Biology · doi:10.1016/0003-9969(80)90132-6 · Cited by 6 · see citing works

Production of bacteriocin-like substances by human oral streptococci.

Fabio, U., Bondi, M., Manicardi, G. C., Messi, P., & Neglia, R. G. (1987) · PubMed · Cited by 25 · see citing works

Quorum Sensing in Streptococcus mutans Regulates Production of Tryglysin, a Novel RaS-RiPP Antimicrobial Compound

Rued, B. E., Covington, B. C., Bushin, L. B., Szewczyk, G., Laczkovich, I., Seyedsayamdost, M. R., & Federle, M. J. (2021) · mBio · doi:10.1128/mbio.02688-20 · Cited by 40 · see citing works