2016, Number 3
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Rev Mex Periodontol 2016; 7 (3)
Antimicrobial effect of ozone therapy against Streptococcus sanguis as a preventive treatment of periodontal disease: In vitro study
Peralta ER, Vázquez GFJ, Portilla RJ, Carrasco MN, Donohué CA, Cuevas GJC, Tovar CK, Espinosa CLF, Arroyo MMA
Language: Spanish
References: 41
Page: 84-92
PDF size: 402.83 Kb.
ABSTRACT
The periodontal disease is one of the most prevalent oral diseases in worldwide that includes a bacterial etiology. The
Streptococcus sanguis (
S. sanguis) is a microorganism that has been strongly associated with the development of periodontal disease. Notwithstanding that there are acceptable treatments, it is necessary to an evaluate alternative antimicrobial agents for the treatment of periodontal disease. The objective of this study was to evaluate variations of the ozone administration and its antimicrobial effect against
S. sanguis. Tubes with brain-heart infusion broth were exposed to gaseous ozone to obtain aqueous ozone in several concentrations (0.0042-0.0493 mg/mL) in different times (10-900 s) using various accessories for ozone administration (conventional and modified needle respectively). Antimicrobial assay was made using spread microbiologic tests with blood agar plates. Results indicated that aqueous ozone with modified needle inhibited more significantly the
S. sanguis growth using low concentrations and shorter times of exposition compared to conventional ozonized technique, indicating a mechanism dose-time dependent. The ozone therapy could be used as an alternative antimicrobial agent for bacterial growth inhibition of
S. sanguis.
REFERENCES
Marsh PD. Dental plaque as a biofilm and a microbial community-implications for health and disease. BMC Oral Health. 2006; 6 (Suppl 1): S14.
Alcaide F, Liñares J, Pallares R, Carratala J, Benitez MA, Gudiol F et al. In vitro activities of 22 beta-lactam antibiotics against penicillin-resistant and penicillin-susceptible viridans group streptococci isolated from blood. Antimicrob Agents Chemother. 1995; 39 (10): 2243-2247.
Alcaide F, Carratala J, Liñares J, Gudiol F, Martin R. In vitro activities of eight macrolide antibiotics and RP-59500 (quinupristin-dalfopristin) against viridans group streptococci isolated from blood of neutropenic cancer patients. Antimicrob Agents Chemother. 1996; 40 (9): 2117-2120.
Kadowaki M, Hashimoto M, Nakashima M, Fukata M, Odashiro K, Uchida Y et al. Radial mycotic aneurysm complicated with infective endocarditis caused by Streptococcus sanguinis. Intern Med. 2013; 52 (20): 2361-2365.
Kongwattanakul K, Tribuddharat S, Prathanee S, Pachirat O. Postcaesarean open-heart surgery for Streptococcus sanguinis infective endocarditis. BMJ Case Rep. 2013; pii: bcr2013010103.
Crump KE, Bainbridge B, Brusko S, Turner LS, Ge X, Stone V et al. The relationship of the lipoprotein SsaB, manganese and superoxide dismutase in Streptococcus sanguinis virulence for endocarditis. Mol Microbiol. 2014; 92 (6): 1243-1259.
Mulita A, Ajayi T. Streptococcus viridians bacteraemia and colonic adenocarcinoma. BMJ Case Rep. 2014; pii: bcr2014203695.
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 (21): 7193-7203.
Lee SH. Antagonistic effect of peptidoglycan of Streptococcus sanguinis on lipopolysaccharide of major periodontal pathogens. J Microbiol. 2015; 53 (8): 553-560.
Stingu CS, Eschrich K, Rodloff AC, Schaumann R, Jentsch H. Periodontitis is associated with a loss of colonization by Streptococcus sanguinis. J Med Microbiol. 2008; 57 (Pt 4): 495-499.
Ashour AZ, Belov VG, Parfenov YA, Parfenov SA, Ershov EV, Tuchin IA et al. The effectiveness of the combined use of energomonitor antioxidant and cognitive psychotherapy in the treatment of generalized periodontitis in elderly patients. Stomatologiia (Mosk). 2016; 95 (2): 14-17.
Haas AN, Silva-Boghossian CM, Colombo AP, Albandar J, Oppermann RV, Rösing CK et al. Predictors of clinical outcomes after periodontal treatment of aggressive periodontitis: 12-month randomized trial. Braz Oral Res. 2016; 30 (1): e41.
Izuora KE, Ezeanolue EE, Neubauer MF, Gewelber CL, Allenback GL, Shan G et al. Changes in inflammatory and bone turnover markers after periodontal disease treatment in patients with diabetes. Am J Med Sci. 2016; 351 (6): 589-594.
Chapple IL, Van der Weijden F, Doerfer C, Herrera D, Shapira L, Polak D et al. Primary prevention of periodontitis: managing gingivitis. J Clin Periodontol. 2015; 42 (Suppl 16): S71-76.
Oppermann RV, Haas AN, Rösing CK, Susin C. Epidemiology of periodontal diseases in adults from Latin America. Periodontol 2000. 2015; 67 (1): 13-33.
Velano HE, do Nascimento LC, de Barros LM, Panzeri H. In vitro assessment of antibacterial activity of ozonized water against Staphylococcus aureus. Pesqui Odontol Bras. 2001; 15 (1): 18-22.
Martínez-Sánchez G, Al-Dalain SM, Menéndez S, Re L, Giuliani A, Candelario-Jalil E et al. Therapeutic efficacy of ozone in patients with diabetic foot. Eur J Pharmacol. 2005; 523 (1-3): 151-161.
Farac RV, Pizzolitto AC, Tanomaru JM, Morgental RD, Lima RK, Bonetti-Filho I. Ex-vivo effect of intracanal medications based on ozone and calcium hydroxide in root canals contaminated with Enterococcus faecalis. Braz Dent J. 2013; 24 (2): 103-106.
Kollmuss M, Kist S, Obermeier K, Pelka AK, Hickel R, Huth KC. Antimicrobial effect of gaseous and aqueous ozone on caries pathogen microorganisms grown in biofilms. Am J Dent. 2014; 27 (3): 134-138.
Banach JL, Sampers I, Van Haute S, van der Fels-Klerx HJ. Effect of disinfectants on preventing the cross-contamination of pathogens in fresh produce washing water. Int J Environ Res Public Health. 2015; 12 (8): 8658-8677.
Khatri I, Moger G, Kumar NA. Evaluation of effect of topical ozone therapy on salivary Candidal carriage in oral candidiasis. Indian J Dent Res. 2015; 26 (2): 158-162.
Bocci V. Ozone as Janus: this controversial gas can be either toxic or medically useful. Mediators Inflamm. 2004; 13 (1): 3-11.
Stone JR, Collins T. The role of hydrogen peroxide in endothelial proliferative responses. Endothelium. 2002; 9 (4): 231-238.
Boch T, Tennert C, Vach K, Al-Ahmad A, Hellwig E, Polydorou O. Effect of gaseous ozone on Enterococcus faecalis biofilm-an in vitro study. Clin Oral Investig. 2016; 20 (7): 1733-1739.
Zhang K, Wang S, Zhou X, Xu HH, Weir MD, Ge Y et al. Effect of antibacterial dental adhesive on multispecies biofilms formation. J Dent Res. 2015; 94 (4): 622-629.
Cury JA, Tenuta LM. Evidence-based recommendation on toothpaste use. Braz Oral Res. 2014; 28 Spec No: 1-7.
Tahmassebi JF, Drogkari E, Wood SR. A study of the control of oral plaque biofilms via antibacterial photodynamic therapy. Eur Arch Paediatr Dent. 2015; 16 (6): 433-440.
Hauser-Gerspach I, Vadaszan J, Deronjic I, Gass C, Meyer J, Dard M et al. Influence of gaseous ozone in peri-implantitis: bactericidal efficacy and cellular response. An in vitro study using titanium and zirconia. Clin Oral Investig. 2012; 16 (4): 1049-1059.
Bezirtzoglou E, Cretoiu SM, Moldoveanu M, Alexopoulos A, Lazar V, Nakou M. A quantitative approach to the effectiveness of ozone against microbiota organisms colonizing toothbrushes. J Dent. 2008; 36 (8): 600-605.
Zhao H, Zheng D, Hong L. The disinfection efficiency comparison of different treatments on dental impression and gypsum casts. Hua Xi Kou Qiang Yi Xue Za Zhi. 2000; 18 (5): 332-335.
Hauser-Gerspach I, Kulik EM, Weiger R, Decker EM, Von Ohle C, Meyer J. Adhesion of Streptococcus sanguinis to dental implant and restorative materials in vitro. Dent Mater J. 2007; 26 (3): 361-366.
Teughels W, Van Assche N, Sliepen I, Quirynen M. Effect of material characteristics and/or surface topography on biofilm development. Clin Oral Implants Res. 2006; 17 Suppl 2: 68-81.
Orellana M, Menchaca E, Nava JF, Nava N, Orellana J, Ponce S. El ozono como una alternativa para esterilizar piezas de mano y fresas en odontología. Revista Latinoamericana de Ortodoncia y Odontopediatria “Ortodoncia.ws” edición electrónica junio 2010. Disponible en: www.ortodoncia.ws. Consultada,3/Junio/2016.
Eick S, Tigan M, Sculean A. Effect of ozone on periodontopathogenic species--an in vitro study. Clin Oral Investig. 2012; 16 (2): 537-544.
Zan R, Hubbezoglu I, Sümer Z, Tunç T, Tanalp J. Antibacterial effects of two different types of laser and aqueous ozone against Enterococcus faecalis in root canals. Photomed Laser Surg. 2013; 31 (4): 150-154.
Tuncay Ö, Dinçer AN, Kuştarcı A, Er Ö, Dinç G, Demirbuga S. Effects of ozone and photo-activated disinfection against Enterococcus faecalis biofilms in vitro. Niger J Clin Pract. 2015; 18 (6): 814-818.
Fontes B, Cattani Heimbecker AM, de Souza Brito G, Costa SF, van der Heijden IM, Levin AS et al. Effect of low-dose gaseous ozone on pathogenic bacteria. BMC Infect Dis. 2012; 12: 358.
Nagayoshi M, Fukuizumi T, Kitamura C, Yano J, Terashita M, Nishihara T. Efficacy of ozone on survival and permeability of oral microorganisms. Oral Microbiol Immunol. 2004; 19 (4): 240-246.
Millar BJ, Hodson N. Assessment of the safety of two ozone delivery devices. J Dent. 2007; 35 (3): 195-200.
Baysan A, Lynch E. The use of ozone in dentistry and medicine Part 2: ozone and root caries. Primary Dental Care. 2006; 13: 37-41.
Baysan A, Lynch E. The use of ozone in dentistry and medicine. Primary Dental Care. 2005; 12: 47-52.