Bacterial interactions in dental biofilm

References

• Dobell C. The rst observations on entozoic protozoa and bacteria. Antony Van Leeuwenhoek and His ‘Little Animals’ 1958; New York Russell and Russell, Inc 236 - 256
   Google Scholar
• Marsh PD. Dental plaque: biological signicance of a biolm and community life-style. Journal of Clinical Periodontology 2005; 32:7 - 15
   PubMed Web of Science ®Google Scholar
• Madigan MT, Martinko JM. Brock Biology of microorganisms 2006; 617:Upper Saddle River Prentice Hall, Inc 618
   Google Scholar
• Kolenbrander PE, Palmer RJ Jr, Rickard AH, Jakubovics NS, Chalmers NI, Diaz PI. Bacterial interactions and successions during plaque development. Periodontol 2000; 42:47 - 79
   Web of Science ®Google Scholar
• Hojo K, Nagaoka S, Ohshima T, Maeda N. Bacterial interactions in dental biofilm development. J Dent Res 2009; 88:982 - 990
   PubMed Web of Science ®Google Scholar
• Geesey GG, Lewandowski Z, Flemming HC. Biofouling and Biocorrosion in Industrial Water Systems 1994; Ann Arbor Lewis Publishers
   Google Scholar
• Klausen M, Aaes-Jorgensen A, Molin S, Tolker-Nielsen T. Involvement of bacterial migration in the development of complex multicellular structures in Pseudomonas aeruginosa biofilms. Mol Microbiol 2003; 50:61 - 68
   PubMed Web of Science ®Google Scholar
• Kenneth J, Ryan C, Ray G. Sherris' medical microbiology [M] 2004; 4:New York McGraw Hill Medical Pub Division 141 - 149
   Google Scholar
• Hyman RW, Fukushima M, Diamond L, Kumm J, Giudice LC, Davis RW. Microbes on the human vaginal epithelium. Proc Natl Acad Sci USA 2005; 102:7952 - 7957
   PubMed Web of Science ®Google Scholar
• Paster BJ, Olsen I, Aas JA, Dewhirst FE. The breadth of bacterial diversity in the human periodontal pocket and other oral sites. Periodontol 2000 2006; 42:80 - 87
   PubMed Web of Science ®Google Scholar
• Roberts FA, Darveau RP. Beneficial bacteria of the periodontium. Periodontol 2002; 30:40 - 50
   Web of Science ®Google Scholar
• Hannig C, Hannig M. The oral cavity—a key system to understand substratum-dependent bioadhesion on solid surfaces in man. Clinical Oral Investigations 2009; 13:123 - 139
   PubMed Web of Science ®Google Scholar
• Gray JJ. The interaction of proteins with solid surfaces. Current Opinion in Structural Biololy 2004; 14:110 - 115
   PubMed Web of Science ®Google Scholar
• Characklis WG, Marshall KC. Biofilms 1990; New York John Wiley & Sons, Inc
   Google Scholar
• Handley PS. Structure, composition and functions of surface structures on oral bacteria. Biofouling 1990; 2:239 - 264
   Google Scholar
• Ritz HL. Microbial population shifts in developing human dental plaque. Archives of Oral Biologh 1967; 12:1561 - 1568
   PubMed Web of Science ®Google Scholar
• Foster JS, Kolenbrander PE. Development of a multi-species oral bacterial community in a saliva-conditioned flow cell. Appl Environ Microbiol 2004; 70:4340 - 4348
   PubMed Web of Science ®Google Scholar
• Dige I, Nyengaard JR, Kilian M, Nyvad B. Application of stereological principles for quantification of bacteria in intact dental biofilms. Oral Microbiol Immunol 2009; 24:69 - 75
   PubMedGoogle Scholar
• Kreth J, Merritt J, Shi W, Qi F. Competition and coexistence between Streptococcus mutans and Streptococcus sanguinis in the dental biofilm. J Bacteriol 2005; 187:7193 - 7203
   PubMed Web of Science ®Google Scholar
• Kolenbrander PE, Andersen RN, Blehert DS, Egland PG, Foster JS, Palmer RJ. Communication among oral bacteria. Microbiology and Molecular Biology Reviews 2002; 66:486 - 505
   PubMed Web of Science ®Google Scholar
• Kolenbrander PE, London J. Ecological signicance of coaggregation among oral bacteria. Advances in Microbial Ecology 1992; 12:183 - 217
   Web of Science ®Google Scholar
• McIntire FC, Vatter AE, Baros J, Arnold J. Mechanism of coaggregation between Actinomyces viscosus T14V and Streptococcus sanguis 34. Infection and Immunity 1978; 21:978 - 988
   PubMed Web of Science ®Google Scholar
• Kaplan JB. Biofilm dispersal: mechanisms, clinical implications and potential therapeutic uses. J Dent Res 2010; 89:205 - 218
   PubMed Web of Science ®Google Scholar
• Sanui T, Gregory RL. Analysis of Streptococcus mutans biofilm proteins recognized by salivary immunoglobulin A. Oral Microbiol Immunol 2009; 24:361 - 368
   PubMedGoogle Scholar
• Roberts SK, Bass C, Brading M, Lappin-Scott H, Stoodley P. New-man HN, Wilson M. Biolm information and structure: what's new?. Dental plaque revisited 1999; Cardiff Bioline 15 - 35
   Google Scholar
• Kolenbrander PE, Andersen RN, Moore LV. Coaggregation of Fusobacterium nucleatum, Selenomonas flueggei, Selenomonas infelix, Selenomonas noxia and Selenomonas sputigena with strains from 11 genera of oral bacteria. Infect Immun 1989; 57:3194 - 3203
   PubMed Web of Science ®Google Scholar
• Metzger Z, Blasbalg J, Dotan M, Weiss EI. Enhanced attachment of Porphyromonas gingivalis to human fibroblasts mediated by Fusobacterium nucleatum. J Endod 2009; 35:82 - 85
   PubMed Web of Science ®Google Scholar
• Bradshaw DJ, Marsh PD, Watson GK, Allison C. Role of Fusobacterium nucleatum and coaggregation in anaerobe survival in planktonic and biofilm oral microbial communities during aeration. Infect Immun 1998; 66:4729 - 4732
   PubMed Web of Science ®Google Scholar
• Takahashi N. Acid-neutralizing activity during amino acid fermentation by Porphyromonas gingivalis, Prevotella intermedia and Fusobacterium nucleatum. Oral Microbiol Immunol 2003; 18:109 - 113
   PubMedGoogle Scholar
• Stewart PS. Mechanisms of antibiotic resistance in bacterial biofilms. Int J Med Microbiol 2002; 292:107 - 113
   PubMed Web of Science ®Google Scholar
• McCann KS. The diversity-stability debate. Nature 2000; 405:228 - 233
   PubMed Web of Science ®Google Scholar
• Costerton JW. Introduction to biolm. International Journal of Antimicrobial Agents 1999; 11:217 - 221
   PubMed Web of Science ®Google Scholar
• Levy SB. The challenge of antibiotic resistance. Scientific American 1998; 278:46 - 53
   PubMed Web of Science ®Google Scholar
• Erickson PR, Herzberg MC. Emergence of antibiotic resistant Streptococcus sanguis in dental plaque of children after frequent antibiotic therapy. Pediatric Dentistry 1999; 21:181 - 185
   PubMedGoogle Scholar
• Sedlacek MJ, Walker C. Antibiotic resistance in an in vitro subgingival biofilm model. Oral Microbiol Immunol 2007; 22:333 - 339
   PubMedGoogle Scholar
• Kuramitsu HK, He X, Lux R, Anderson MH, Shi W. Interspecies interactions within oral microbial communities. Microbiol Mol Biol Rev 2007; 71:653 - 670
   PubMed Web of Science ®Google Scholar
• Senadheera D, Cvitkovitch DG. Quorum sensing and biofilm formation by Streptococcus mutans. Adv Exp Med Biol 2008; 631:178 - 188
   PubMed Web of Science ®Google Scholar
• Chatterjee C, Paul M, Xie L, Wilfred A, Donk WA. Biosynthesis and mode of action of lantibiotics. Chem Rev 2005; 105:633 - 684
   PubMed Web of Science ®Google Scholar
• Nes IF, Diep DB, Holo H. Bacteriocin diversity in Streptococcus and Enterococcus. J Bacteriol 2007; 189:1189 - 1198
   PubMed Web of Science ®Google Scholar
• Kreth J, Zhang Y, Herzberg MC. Streptococcal antagonism in oral biofilms: Streptococcus sanguinis and Streptococcus gordonii interference with Streptococcus mutans. J Bacteriol 2008; 190:4632 - 4640
   PubMed Web of Science ®Google Scholar
• Wescombe PA, Upton M, Dierksen KP, Ragland NL, Sivabalan S, Wirawan RE, et al. Production of the lantibiotic salivaricin A and its variants by oral streptococci and use of a specific induction assay to detect their presence in human saliva. Appl Environ Microbiol 2006; 72:1459 - 1466
   PubMed Web of Science ®Google Scholar
• Perry JA, Jones MB, Peterson SN, Cvitkovitch DG, Levesque CM. Peptide alarmone signalling triggers an auto-active bacteriocin necessary for genetic competence. Mol Microbiol 2009; 72:905 - 917
   PubMed Web of Science ®Google Scholar
• Reading NC, Sperandio V. Quorum sensing: the many languages of bacteria. FEMS Microbiol Lett 2006; 254:1 - 11
   PubMed Web of Science ®Google Scholar
• Zhang K, Ou M, Wang W, Ling J. Effects of quorum sensing on cell viability in Streptococcus mutans biofilm formation. Biochem Biophys Res Commun 2009; 379:933 - 938
   PubMed Web of Science ®Google Scholar
• Nadell CD, Xavier JB, Levin SA, Foster KR. The evolution of quorum sensing in bacterial biofilms. PLoS Biol 2008; 6:171 - 179
   Web of Science ®Google Scholar
• Sifri CD. Healthcare epidemiology: quorum sensing: bacteria talk sense. Clin Infect Dis 2008; 47:1070 - 1076
   PubMed Web of Science ®Google Scholar
• Kolenbrander PE. Oral microbial communities: biofilms, interactions and genetic systems. Annu Rev Microbiol 2000; 54:413 - 437
   PubMed Web of Science ®Google Scholar
• Henke JM, Bassler BL. Three parallel quorum-sensing systems regulate gene expression in Vibrio harveyi. J Bacteriol 2004; 186:6902 - 6914
   PubMed Web of Science ®Google Scholar
• Jayaraman A, Wood TK. Bacterial quorum sensing: signals, circuits and implications for biofilms and disease. Annu Rev Biomed Eng 2008; 10:145 - 167
   PubMed Web of Science ®Google Scholar
• Karatan E, Watnick P. Signals, regulatory networks and materials that build and break bacterial biofilms. Microbiol Mol Biol Rev 2009; 73:310 - 347
   PubMed Web of Science ®Google Scholar
• Novick RP, Geisinger E. Quorum sensing in staphylococci. Annu Rev Genet 2008; 42:541 - 564
   PubMed Web of Science ®Google Scholar
• Pottathil M, Lazazzera BA. The extracellular Phr peptide-Rap phosphatase signaling circuit of Bacillus subtilis. Front Biosci 2003; 8:32 - 45
   Web of Science ®Google Scholar
• Henke JM, Bassler BL. Bacterial social engagements. Trends Cell Biol 2004; 14:648 - 656
   PubMed Web of Science ®Google Scholar
• Fuqua WC, Winans SC, Greenberg EP. Quorum sensing in bacteria: the LuxR-LuxI family of cell density-responsive transcriptional regulators. J Bacteriol 1994; 176:269 - 275
   PubMed Web of Science ®Google Scholar
• Bassler BL. Small talk: Cell-to-cell communication in bacteria. Cell 2002; 109:421 - 424
   PubMed Web of Science ®Google Scholar
• Xie H, Lin X, Wang BYWJ, Lamont RJ. Identification of a signalling molecule involved in bacterial intergeneric communication. Microbiology 2007; 153:3228 - 3234
   PubMed Web of Science ®Google Scholar
• James CE, Hasegawa Y, Park Y, Yeung V, Tribble GD, Kuboniwa M, et al. LuxS involvement in the regulation of genes coding for hemin and iron acquisition systems in Porphyromonas gingivalis. Infect Immun 2006; 74:3834 - 3844
   PubMed Web of Science ®Google Scholar
• Rickard AH Jr, Palmer RJ, Blehert DS, Campagna SR, Semmelhack MF, Egland PG, et al. Autoinducer 2: a concentration-dependent signal for mutualistic bacterial biofilm growth. Mol Microbiol 2006; 60:1446 - 1456
   PubMed Web of Science ®Google Scholar
• Li Y, Hanna MN, Svensater G, Ellen RP, Cvitkovitch DG. Cell density modulates acid adaptation in Streptococcus mutans: implications for survival in biofilms. J Bacteriol 2001; 183:6875 - 6884
   PubMed Web of Science ®Google Scholar
• Li Y, Lau PC, Lee JH, Ellen RP, Cvitkovitch DG. Natural genetic transformation of Streptococcus mutans growing in biofilms. J Bacteriol 2001; 183:897 - 908
   PubMed Web of Science ®Google Scholar
• Li Y, Tang N, Aspiras MB, Lau PCY, Lee JH, Ellen RP, Cvitkovitch DG. A quorum-sensing signaling system essential for genetic competence in Streptococcus mutans is involved in biofilm formation. J Bacteriol 2002; 184:2699 - 2708
   PubMed Web of Science ®Google Scholar
• Petersen FC, Pecharki D, Scheie AA. Biofilm mode of growth of Streptococcus intermedius favored by a competence-stimulating signaling peptide. J Bacteriol 2004; 186:6327 - 6331
   PubMed Web of Science ®Google Scholar
• Jarosz LM, Deng D, van der Mei Henny C, Crielarrd W, Krom BP. Streptococcus mutans Competence-Stimulating Peptide Inhibits Candida albicans Hypha Formation. Eukaryotic Cell 2009; 8:1658 - 1664
   PubMed Web of Science ®Google Scholar
• Petersen FC, Scheie AA. Genetic transformation in Streptococcus mutans requires a peptide secretion-like apparatus. Oral Microbiol Immunol 2000; 15:329 - 334
   PubMedGoogle Scholar
• Kreth J, Merritt J, Shi W, Qi F. Coordinated bacteriocin production and competence development: a possible mechanism for taking up DNA from neighboring species. Mol Microbiol 2005; 57:392 - 404
   PubMed Web of Science ®Google Scholar
• Eckert R, He J, Yarbrough DK, Qi F, Anderson MH, Shi W. Targeted killing of Streptococcus mutans by a pheromone-guided “smart” antimicrobial peptide. Antimicrob Agents Chemother 2006; 50:3651 - 3657
   PubMed Web of Science ®Google Scholar
• Balakrishnan M, Simmonds RS, Tagg JR. Dental caries is a preventable infectious disease. Australian Dental Journal 2000; 45:235 - 245
   PubMed Web of Science ®Google Scholar
• Marsh PD. Are dental diseases examples of ecological catastrophes?. Microbiology 2003; 149:279 - 294
   PubMed Web of Science ®Google Scholar
• Kemp CW, Robrish SA, Curtis MA, Sharer SA, Bowen WH. Application of a competition model to the growth of Streptococcus mutans and Streptococcus sanguis in binary continuous culture. Appl Environ Microbiol 1983; 45:1277 - 1282
   PubMed Web of Science ®Google Scholar
• Becker MR, Paster BJ, Leys EJ, Moeschberger ML, Kenyon SG, Galvin JL, et al. Molecular analysis of bacterial species associated with childhood caries. J Clin Microbiol 2002; 40:1001 - 1009
   PubMed Web of Science ®Google Scholar
• Komiyama K, Kleinberg I. Comparison of glucose utilization and acid formation by Streptococcus mutans and Streptococcus sanguis at different pH. J dent Res 1974; 53:241
   Web of Science ®Google Scholar
• Iwami Y, Yamada T. Rate-limiting steps of the glycolytic pathway in the oral bacteria Streptococcus mutans and Streptococcus sanguis and the influence of acidic pH on the glucose metabolism. Arch Oral Biol 1980; 25:163 - 169
   PubMed Web of Science ®Google Scholar
• Tong H, Chen W, Shi W, Qi F, Dong X. SO-LAAO, a novel L-amino acid oxidase that enables Streptococcus oligofermentans to outcompete Streptococcus mutans by generating H2O2 from peptone. J Bacteriol 2008; 190:4716 - 4721
   PubMed Web of Science ®Google Scholar
• Stinson MW, Alder S, Kumar S. Invasion and killing of human endothelial cells by viridans group streptococci. Infect Immun 2003; 71:2365 - 2372
   PubMed Web of Science ®Google Scholar
• Merritt J, Kreth J, Shi W, Qi F. LuxS controls bacteriocin production in Streptococcus mutans through a novel regulatory component. Mol Microbiol 2005; 57:960 - 969
   PubMed Web of Science ®Google Scholar
• Baldeck JD, Marquis RE. Targets for hydrogen-peroxide-induced damage to suspension and biolm cells of Streptococcus mutans. Can J Microbiol 2008; 54:868 - 875
   PubMed Web of Science ®Google Scholar
• Skaar EP, Tobiason DM, Quick J, Judd RC, Weissbach H, Etienne F, et al. The outer membrane localization of the Neisseria gonorrhoeae MsrA/B is involved in survival against reactive oxygen species. Proc Natl Acad Sci USA 2002; 99:10108 - 10113
   PubMed Web of Science ®Google Scholar
• Zhu L, Kreth J. Role of Streptococcus mutans eukaryotic-type serine/threonine protein kinase in interspecies interactions with Streptococcus sanguinis. Arch Oral Biol 2010; 55:385 - 390
   PubMed Web of Science ®Google Scholar
• Wen ZT, Yates D, Ahn SJ, Burne RA. Biofilm formation and virulence expression by Streptococcus mutans are altered when grown in dual-species model. BMC Microbiol 2010; 10:111
   PubMed Web of Science ®Google Scholar
• Gregory RL, Lloyd DR. Enhancement of Streptococcus sanguis immunoglobulin A1 protease activity by Streptococcus mutans. Immunol Infect Dis 1993; 3:309 - 315
   Google Scholar
• Periasamy S, Kolenbrander PE. Mutualistic biofilm communities develop with Porphyromonas gingivalis and initial, early and late colonizers of enamel. J Bacteriol 2009; 191:6804 - 6811
   PubMed Web of Science ®Google Scholar
• Lev M. Sphingolipid biosynthesis and vitamin K metabolism in Bacteroides melaninogenicus. Am J Clin Nutr 1979; 32:179 - 186
   PubMed Web of Science ®Google Scholar
• Grenier D. Nutritional interactions between two suspected periodontopathogens, Treponema denticola and Porphyromonas gingivalis. Infect Immun 1992; 60:5298 - 5301
   PubMed Web of Science ®Google Scholar
• Kolenbrander PE, London J. Adhere today, here tomorrow: oral bacterial adherence. J Bacteriol 1993; 175:3247 - 3252
   PubMed Web of Science ®Google Scholar
• Rosen G, Sela MN. Coaggregation of Porphyromonas gingivalis and Fusobacterium nucleatum PK 1594 is mediated by capsular polysaccharide and lipopolysaccharide. FEMS Microbiol Lett 2006; 256:304 - 310
   PubMed Web of Science ®Google Scholar
• Kang MS, Na HS, Oh JS. Coaggregation ability of Weissella cibaria isolates with Fusobacterium nucleatum and their adhesiveness to epithelial cells. FEMS Microbiol Lett 2005; 253:323 - 329
   PubMed Web of Science ®Google Scholar
• Nagaoka S, Hojo K, Murata S, Mori T, Ohshima T, Maeda N. Interactions between salivary Bifidobacterium adolescentis and other oral bacteria: in vitro coaggregation and coadhesion assays. FEMS Microbiol Lett 2008; 281:183 - 189
   PubMed Web of Science ®Google Scholar
• Periasamy S, Chalmers NI, Du-Thumm L, Kolenbrander PE. Fusobacterium nucleatum ATCC 10953 requires Actinomyces naeslundii ATCC 43146 for growth on saliva in a three-species community that includes Streptococcus oralis 34. Appl Environ Microbiol 2009; 75:3250 - 3257
   PubMed Web of Science ®Google Scholar
• Diaz PI, Zilm PS, Rogers AH. Fusobacterium nucleatum supports the growth of Porphyromonas gingivalis in oxygenated and carbondioxide-depleted environments. Microbiology 2002; 148:467 - 472
   PubMed Web of Science ®Google Scholar
• Pangsomboon K, Kaewnopparat S, Pitakpornpreecha T, Srichana T. Antibacterial activity of a bacteriocin from Lactobacillus paracasei HL32 against Porphyromonas gingivalis. Arch Oral Biol 2006; 51:784 - 793
   PubMed Web of Science ®Google Scholar
• Pangsomboon K, Bansal S, Martin GP, Suntinanalert P, Kaewnopparat S, Srichana T. Further characterization of a bacteriocin produced by Lactobacillus paracasei HL32. J Appl Microbiol 2009; 106:1928 - 1940
   PubMed Web of Science ®Google Scholar
• Stadtman ER, Levine RL. Free radical-mediated oxidation of free amino acids and amino acid residues in proteins. Amino Acids 2003; 25:207 - 218
   PubMed Web of Science ®Google Scholar
• Jakubovics NS, Gill SR, Iobst SE, Vickerman MM, Kolenbrander PE. Regulation of gene expression in a mixed-genus community: stabilized arginine biosynthesis in Streptococcus gordonii by coaggregation with Actinomyces naeslundii. J Bacteriol 2008; 190:3646 - 3657
   PubMed Web of Science ®Google Scholar
• Jakubovics NS, Gill SR, Vickerman MM, Kolenbrander PE. Role of hydrogen peroxide in competition and cooperation between Streptococcus gordonii and Actinomyces naeslundii. FEMS Microbiol Ecol 2008; 66:637 - 644
   PubMed Web of Science ®Google Scholar
• Marcotte H, Lavoie MC. Oral microbial ecology and the role of salivary immunoglobulin A. Microbiol Mol Biol Rev 1998; 62:71 - 109
   PubMed Web of Science ®Google Scholar