Keywords : East Java propolis extract, Minimum Biofilm Eradication Concentration, E faecalis

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MINIMUM BACTERICIDAL CONCENTRATION OF EAST JAVA PROPOLIS EXTRACT TO BIOFILM OF Enterococcus faecalis Tamara Yuanita 1, James Hutagalung 1, Ira Widjiastuti 1, M Rulianto 2, Latief Mooduto 2 1 Institute of Tropical Disease Airlangga University, Surabaya-Indonesia 2 Faculty of Dentistry Airlangga University, Surabaya-Indonesia. ABSTRACT Background. Endodontic root canal treatment is a treatment that can be performed in inflammation pulp or dental pulp necrosis. Enterococcus faecalis (E faecalis) bacteria identified 89,6% in root canal treatment failure. Sterilization and irrigation of the root canal are the bacteria elimination stages of root canal treatment, but materials that used do not killing E faecalis specially the bacterial biofilm, so E faecalis can survive to cause periapical disease after root canal treatment. Propolis contain apigenin and tt-farnesol that have mechanisms for inhibiting growth and development of bacterial biofilm. Purpose. To measured Minimum Bactericidal Concentration of East Java Propolis Extract to Biofilm of E faecalis. Methods. This research was laboratory experimental study. Propolis extract used is East Java propolis extracted by maceration method, and dilution into several concentrations using aquadest. Biofilm formation was observed using the microtitter plate method then continued reading of Optical Density (OD) using ELISA reader to determine Minimum Biofilm Eradication Concentration (MBEC) of East Java propolis extract to E faecalis biofilm. Result. East Java Propolis extract had MBEC at concentration of 11,45% against E faecalis biofilm. Conclusion. East Java Propolis extract concentration 11,45% is MBEC to E faecalis biofilm in-vitro. Keywords : East Java propolis extract, Minimum Biofilm Eradication Concentration, E faecalis INTRODUCTION Enterococcus faecalis (E faecalis) are the most species of bacteria found in root canal treatment failure. Sometimes treatment failure without clinical symptoms so that radiographic picture is the only way to see the presence of a periapical lesion known as Chronic apical periodontitis. Chronic apical periodontitis is an asymptomatic condition that originates in the dental pulp is infected by bacteria,it was associated with inflammation and periapical tissue destruction (Cohen,2011). Failed root canal treatment can be seen in the presence of periapical radiolucency. The prevalence of periapical radiolucency high at 36 % of the 28,881 treated teeth root canal treatment (Pak et al,2012).

E faecalis is a facultative anaerobic Gram-positive cocci that are often found in the root canal that has been treated with a prevalence of 30 % to 90 % of cases. E faecalis can survive in root canals that have been treated, including resistance to intracanal medicaments premises the ability to form biofilm, invasion into the dentinal tubules and survive in the long term in nutrient limitation (Fouad,2009). Biofilms are microbial populations containing organic or inorganic substrates coated with extracellular microbial products that form the matrix intermikrobial. On microbial biofilms are more resistant to microbial agents than planktonic cells form. Biofilm formation is a complex process that involves attachment and immobilitation, interactions between cells, the formation of microcolonies, confluent biofilm formation after the formation of threedimensional structure of the biofilm. Biofilm production is regulated by Ouorum sensing system. There is quorum sensing in several pathogenic bacteria to regulate bacterial gene in response to population density of microorganisms obtained through the production of extracellular signaling molecules known as autoinducers (Mohamed and Huang, 2007). Biofilm formation on root canal probably started after the entry of Oral planktonic microorganisms into the root canal. The necrotic pulp tissue would be a favorable environment for the proliferation of microorganisms because of the organic residue that serves as a nutrient medium substrate bacteria (Usha et al, 2010). Propolis is a sticky resin, colored brown and is thermoplastic. A natural product that is a mixture of beeswax and resin collected from the flowers especially important plant and leaf buds by honey bees (Apis and Trigona melifera Sp). Some studies revealed that propolis has anti-oxidant properties, anti-bacterial, anti- fungal, anti-viral and anti-inflammatory (Surendra et al, 2012). Components of propolis depends on the season and the source where the resin exudate was collected by bees. Bees use propolis to protect the hive against intruders from outside factors such as insects, beetles and mice, as an adhesive gap contained in the honeycomb and bee larvae to protect from disease and bacteria. Komposis chemistry of propolis, color and aroma according to geographical places. The composition of propolis is also very varied and close relationship with propolis plant species where it originates. The main components of propolis are flavonoids, which is one of the largest class of natural phenols. Inhibition effect on microorganisms propolis depends on the synergy of many components (Ozen et al, 2010). Anti-microbial power possessed by propolis extracts is influenced by the presence of the active compounds in the extract are flavonoids, polyphenols, terpenoids, galangin, quercetine, myrecetine, robinetin, epighalocathecin, licochalcones AB, caffeic acid, tannins and essential

oils. Each active ingredient has its own mechanism in its activity as an anti- microbial (Fokt et al,2010). Propolis also contains terpenoids or tt - farnesol which is a sesquiterpene alcohol found in the essential oils of various plant extracts that can affect the growth of many bacteria (Gomes et al, 2011). Indonesia is also the world community and especially East Java, now is beginning to prioritize the use of drugs from natural materials (back to nature). The use of herbal medicine began to become the people's choice because in addition to reducing the use of chemicals and synthetic substances that are harmful, low price and can increase the potential use of natural materials that are easy to obtain. In East Java, Apis melifera propolis collected from bee hives located in Lawang area located on the plateau which is dominated by the silk cotton tree (Ceiba pelandra L). Objective in this study was to determine the Minimum Bacterial Concentration of East Java Propolis Extract to biofilms of Enterococcus faecalis to determine Minimum Biofilm Eradication Concentration ( MBEC ). MATERIALS AND METHODS Raw propolis Lawang macerated with 70 % ethanol in a sealed container and then shaken using a shaker with a speed of 80 rpm. After 7 days maceration stopped and filtered. Maceration for 24 hours for 7 days repeated again so that total maceration time was 14 days to obtain a stock solution of propolis (Victorio et al, 2009). E faecalis culture in trypticase soy broth (TSB) diluted to 1:100 for 24 hours and then 0.1 ml concentration of 1 x10 6 E faecalis bacteria / ml loaded on a 96 well-plate bottomed plastic tissue culture plate. Propolis extract was applied into each microtiter concentration of 11.45%, 5.75%, 2.86%, 1.43%, 0.715%, 0.38%, 0.19%, 0.10% and 0% as a positive control. Painting done biofilm microorganisms attached to the well using crystal violet. To quantitatively analyze biofilm formation isopropanolol added 0.2 ml of each well then measured Optical Density (OD) at 570 nm using ELISA reader. Data analysis using oneway ANOVA and LSD at p<0,05. RESULTS AND DATA ANALYSIS Propolis extract with a concentration of 11.45 %, 5.75%, 2.86%, 1.43%, 0.715%, 0.38%, 0.19%, 0.10% and 0% as a positive control to E faecalis biofilm were calculated by ELISA Reader with a wavelength of 570 nm can be seen in Table 1 and Picture 1.

Table 1. Extract Concentration, Mean OD, Percentage OD to E. faecalis biofilm Extract Concentration n Mean OD OD Concentration 0% 5 3,542 100% 0,10% 5 1,458 41,17% 0,19% 5 1,304 36,83% 0,38% 5 1,050 29,65% 0,715% 5 0,759 21,44% 1,43% 5 0,576 16,28% 2,86% 5 0,363 12,32% 5,75% 5 0,313 8,86% 11,45% 5 0 0 Picture 1. Mean OD graph to E faecalis biofilm From Table 1 and Picture 1, it can be seen that there is a concentration of 11,45% biofilm bacteria is zero, it can be concluded that the concentration is 11.45% is Minimum Biofilm Eradication Concentration (MBEC), that is the lowest concentration of propolis extracts can inhibit the growth of test bacteria 100% of the amount of bacteria that managed to grow in a positive control. One way ANOVA analysis found significant differences between the positive control group 11.45%, 5.75%, 2.86%, 1.43%, 0.715%, 0.38%, 0.19%, 0,10%. (p <0,05). DISCUSSION Biofilm is an aspect of microbial physiology that almost all species of bacteria can form it. Multicellular structure of the biofilm enables the bacteria to perform dormancy and hibernation so that bacteria can survive (Bordi and Bentzmann,2011). E faecalis is a pathogenic bacteria that plays a role in most cases of failure of root canal treatment. The prevalence of E faecalis in the re-treatment of root canals treatment is 89.6% and the primary infection is 67.5% (Fouad,2009).

Propolis honey bee Apis melifera spp is antibacterial that can kill all the germs that enter the hive. Propolis is often referred to as Russian penicillin because of intensive research scientist at the Russian worker bees. Propolis is a natural antibiotic called because of its antibacterial ability (Finstrom and Spivak,2010). Propolis can also stop the formation of bacterial biofilms (Gomes et al,2011). In this study, the concentrations of propolis extracts used 11.45%, 5.75%, 2.86%, 1.43 %, 0.715%, 0.38%, 019%, 0.10% and 0% concentration of the used as a positive control. Subsequently the extract was applied to the plate mictotiter previously established biofilm bacteria E. faecalis, and the the determination biofilm OD using ELISA Reader. The results showed that propolis extract at a concentration of 0.10 % can reduce bacterial growth at a concentration of 5.75 % and there is a number of bacterial colonies that live around 10 % compared to the number of colonies on the control and concentration of 11.45 % has no found bacterial growth, so the concentration is referred as the Minimum Biofilm Eradication concentration (MBEC). East Java propolis extract containing 1,03% tt-farrnesol (terpenoids) and the content 5,12% flavonoids (apigenin), tt - farnesol and apigenin content in propolis is useful to destroy biofilms. This is consistent with research Kao et al (2003) who found that the content of propolis is apigenin and tt-farnesol which led to a decrease in the amount of biofilm polysaccharides. tt-farnesol also have hydrophobic properties that are likely to cause disruption of biofilm membrane, which causes the release of cellular biofilm. This will cause the rupture of the cell (Gomes et al,2011). The results showed that the extract of propolis East Java is able to inhibit biofilm formation of E faecalis. This is because the East Java propolis extract contains apigenin and tt-farnesol which may cause the membrane biofilm and cause a decrease in the number of polysaccharide in biofilms to biofilm cell contents regardless. This is evidenced by an increase in the concentration of protein and polysaccharide outside the cell (Kao et al,2003; Gomes et al,2011). The conclusion of this study is, 11,45% concentrations of East Java propolis extract eradicate biofilm E faecalis bacteria. REFERENCES Cohen S, Hargreaves KM. 2011. Cohen s Pathways of the Pulp, 10 th ed, St Louis Missouri, Mosby Inc, p.529-558.

Pak JG, Fayazi S, White SN. 2012. Prevalence of Periapical Radiolucency and Root Canal Treatment : A Systematic Review of Cross-sectional studies. JOE. 38 (9) : 1170-1176. Fouad AF. 2009. Endodontic Microbiology, 1 st ed. Wiley-Blackwell, Baltimore USA. p.95-149. Mohamed JA, Huang DB. 2007. Biofilm Formation by Enterococci. J of Med Microbiol. 56 : 1581-1588. Usha HL, Kaiwar A, Deepak M. 2010. Biofilm in Endodontics : New Understanding To An Old Problem, IJCD. 1 (3) : 71-76. Surendra NS, Bhusshanam M, Ravikumar H. 2012. Antimicrobial Activity of Propolis of Trigona sp and Apis melifera of Karnataka India. Prime J of Microbiol Research. 2 (2) : 80-85. Ozen T, Kilic A, Bedir O, Koru O,Sorkun K, Tanyuksel M, Kilic S, Gencay O, Yildis O, Baysallar M. 2010. In vitro activity of Turkish samples against anaerobic bacteria causing oral cavity infections. Kafkas Univ Vet Derg. 16 (2) : 293-298. Fokt EA. 2010. How does propolis prevent hive protection? The antimicrobial properties of propolis. Current Research, tech and edu topics in Applied Microbiol and Biotech. Victorio CP, Lage CLS, Kusler RM. 2009. Flavanoid extraction from Alpinia Zerum bet (Pers.) Burtt et Smith leaves using different techniques and solvent. Ecl,Quim, Sao Paulo 34 (1) : 19-24. Bordi C, Bentzmann DS. 2011. Hacking into bacterial biofilms : a new therapeutic challenge. Annals of Intensive Care. 1 : 19-24. Finstrom MS, Spivak M. 2010. Propolis and bee health : the natural history and significance of resin use by honey bees. Apilodogie. 41 : 302-304. Gomes F, Leite B, Teixeira P, Oliveira R. 2011. Strategies to control Staphylococcus epidermitis biofilm, science against microbial pathogens : communicating current research and technological advances. Koo H, Hayacibara MF, Schobel BD, Cury JA, Rosalen PL, Park YK, 2003. Inhibition of Streptococcus mutans biofilm accumulation and polysaccharide production by apigenin. J of Antimicrobial Chemotherapy. 52 (5) : 782-789.