Anti-Biofilm Formation of an Adhesive Containing Calcium Salts of Acidic Monomers against Oral Candida Related to Root Caries

2021 ◽  
Vol 904 ◽  
pp. 282-286
Author(s):  
Sroisiri Thaweboon ◽  
Takashi Saito ◽  
Boonyanit Thaweboon

The proportion of older people within the general population is expanding due to the decline of birth rate and the increase of life expectancy. Increasing elderly populations, which is retaining its teeth longer, leads to oral health problems, for example, root caries. The main etiological factor for the initiation and development of root caries is the appearance of cariogenic biofilm. The acid-producing and acid-tolerant bacteria and oral yeast, such as Candida albicans are the major contributors in root caries formation. A new generation of adhesives is developed with several modifications for the prevention of dental caries by incorporating antimicrobial components. The aim of this study was to investigate the antimicrobial effect of adhesive containing calcium salt of acidic monomers on the biofilm formation of oral Candida related to root caries. In the experiments, the flat-bottom surfaces of 96-well plate were painted with an adhesive containing calcium salts of 4-methacryloxyethyl trimellitic acid (CMET) and 10-methacryloyloxydecyl dihydrogen calcium phosphate (MDCP) (Bio-Coat, CA, Sun Medical, Japan). Then they were LED light-cured and coated with sterile saliva at 37 °C for 60 min. The biofilm formation was made by adding of Candida albicans (ATCC 10238 and two clinical strains) suspensions (107 colony forming unit/mL) and incubated at 37°C for 24 h. The amount of vital biofilm was determined by WST-8 Microbial Cell Counting Kit (Dojindo Molecular Technologies, USA). All experiments were done in triplicate and repeated three times. Statistical analysis was performed using Student’s t-test. The results clearly showed that adhesive could significantly inhibit biofilm formation of all tested Candida compared with a control. This suppressive effect was not different among the strains of Candida. The percentages of vital biofilm reduction were 25% to 40%. The ability of this adhesive to suppress biofilm of oral yeast may be its antimicrobial property of acidic monomer or the effect of calcium ion within the adhesive, which can alter Candida cell morphology, and influence their structures or process of biofilm formation. In conclusion, an adhesive containing calcium salts of acidic monomers could significantly inhibit biofilm formation of C. albicans. This adhesive could be effectively applied to exposed root surfaces to prevent or inhibit the progression of root caries. Further studies are necessary to clarify the effect on multispecies biofilm, on long-term activity, and in vivo conditions.

2020 ◽  
Vol 853 ◽  
pp. 41-45
Author(s):  
Sroisiri Thaweboon ◽  
Takashi Saito ◽  
Keiji Nagano ◽  
Boonyanit Thaweboon

Root caries is a critical dental problem for the elderly people due to increased tooth retention and exposed root surfaces in aged society. The presence of a cariogenic biofilm and fermentable carbohydrates is the main etiologic factors. Streptococcus mutans, lactobacilli and Actinomyces spp. have been demonstrated to be associated with root caries. Currently, dental materials with multifunctional features have been combined into clinical adhesives. Calcium salt of acidic monomer (calcium salt of 4-methacryloxyethyl trimellitic acid or CMET) has been demonstrated to promote a significant remineralization and an adhesive containing CMET has been developed. However, there is no data regarding its antimicrobial potential. This study aimed to evaluate the property of an adhesive containing CMET and 10-methacryloyloxydecyl dihydrogen calcium phosphate (MDCP) on the biofilm formation of bacteria related to root caries. The adhesive was applied onto the flat-bottom surface of 96-well plate and LED light-cured. Then it was coated with sterile saliva at 37 °C for 60 min. The bacterial suspensions of 107 colony forming unit (CFU)/mL (Streptococcus mutans ATCC 25715, Lactobacillus casei ATCC 334 and Actinomyvces viscosus ATCC 19246) were added and incubated at 37°C in 5% CO2 atmosphere for 24 h to allow the biofilm formation. The amount of vital biofilm was determined by WST-8 Microbial Cell Counting Kit (Dojindo Molecular Technologies, USA). All tests were carried out in triplicate and repeated three times. Student’s t-test was employed for the statistical analysis. The significant suppressive effects were clearly noticed on S. mutans compared with a control. The percentage of biofilm reduction was nearly 65%. A 2% biofilm reduction was found on L. casei and A. viscosus, though no statistical significant decreases of biofilm were observed compared with a control. In conclusion, an adhesive containing calcium salt of acidic monomers could significantly inhibit biofilm formation of S. mutans. Using this adhesive can be beneficial for the prevention of root caries on the tooth surface.


2007 ◽  
Vol 6 (6) ◽  
pp. 931-939 ◽  
Author(s):  
Fang Li ◽  
Michael J. Svarovsky ◽  
Amy J. Karlsson ◽  
Joel P. Wagner ◽  
Karen Marchillo ◽  
...  

ABSTRACT Candida albicans is the leading cause of systemic fungal infections in immunocompromised humans. The ability to form biofilms on surfaces in the host or on implanted medical devices enhances C. albicans virulence, leading to antimicrobial resistance and providing a reservoir for infection. Biofilm formation is a complex multicellular process consisting of cell adhesion, cell growth, morphogenic switching between yeast form and filamentous states, and quorum sensing. Here we describe the role of the C. albicans EAP1 gene, which encodes a glycosylphosphatidylinositol-anchored, glucan-cross-linked cell wall protein, in adhesion and biofilm formation in vitro and in vivo. Deleting EAP1 reduced cell adhesion to polystyrene and epithelial cells in a gene dosage-dependent manner. Furthermore, EAP1 expression was required for C. albicans biofilm formation in an in vitro parallel plate flow chamber model and in an in vivo rat central venous catheter model. EAP1 expression was upregulated in biofilm-associated cells in vitro and in vivo. Our results illustrate an association between Eap1p-mediated adhesion and biofilm formation in vitro and in vivo.


2020 ◽  
Vol 853 ◽  
pp. 51-55
Author(s):  
Pakpoom Kedcharoen ◽  
Boonyanit Thaweboon ◽  
Natthamet Wongsirichat ◽  
Sroisiri Thaweboon

Self-cure poly-methyl methacrylate (PMMA) resin has been the material commonly used for fabrication of surgical obturator. The appliance is used in the cancer patient after surgical removal of the affected maxillofacial tissues. However, wearing of this resin appliance can enhance a condition for microbial biofilm aggregation and put patients at increased risk of infection. Vanillin-incorporated heat-cure PMMA resin and self-cure PMMA resin have been developed and demonstrated to have antimicrobial activity. This study aimed to evaluate antimicrobial property of vanillin-incorporated self-cure PMMA obturator resin on the biofilm formation of C. albicans and S. aureus. The resin samples (Orthocryl® EQ, Dentaurum, Germany) were prepared with vanillin incorporation (0.1% and 0.5% vanillin). All samples were coated with sterile saliva and incubated at 37 °C for 60 min. The Staphylococcus aureus ATCC 5638 and Candida albicans ATCC 10231 suspensions (107 colony forming unit/mL) were prepared and microbial biofilm formation was done in 96-well plate at 37°C for 24 h. The amount of biofilm was quantified by Cell Counting Kit WST-8 (Dojindo Molecular Technologies, USA) at 450 nm. All tests were performed in triplicate on three separate occasions. One-way ANOVA and Tukey’s test were used for the statistical analysis. It was found that approximately 52% and 48% biofilm reductions were observed in 0.1% and 0.5% vanillin groups against S.aureus compared with 0% vanillin (control group) whereas 46% and 54% biofilm reductions were seen against C. albicans biofilm. In conclusion, the incorporation of vanillin in surgical obturator PMMA resin was demonstrated to have antimicrobial property against biofilm formation of S. aureus and C. albicans. This can help the patient who wears surgical obturator for the prevention of opportunistic infections.


2016 ◽  
Vol 60 (5) ◽  
pp. 3152-3155 ◽  
Author(s):  
Jeniel E. Nett ◽  
Jonathan Cabezas-Olcoz ◽  
Karen Marchillo ◽  
Deane F. Mosher ◽  
David R. Andes

ABSTRACTNew drug targets are of great interest for the treatment of fungal biofilms, which are routinely resistant to antifungal therapies. We theorized that the interaction ofCandida albicanswith matricellular host proteins would provide a novel target. Here, we show that an inhibitory protein (FUD) targetingCandida-fibronectin interactions disrupts biofilm formationin vitroandin vivoin a rat venous catheter model. The peptide appears to act by blocking the surface adhesion ofCandida, halting biofilm formation.


PLoS ONE ◽  
2012 ◽  
Vol 7 (4) ◽  
pp. e35543 ◽  
Author(s):  
Yan Li ◽  
Yukui Ma ◽  
Li Zhang ◽  
Feng Guo ◽  
Lei Ren ◽  
...  

2015 ◽  
Vol 29 (1) ◽  
pp. 1-4
Author(s):  
Nagesh Khurana ◽  
Divya S. Sharma ◽  
Himanshu Sharma ◽  
Apurva K. Pathak

2014 ◽  
Vol 58 (12) ◽  
pp. 7606-7610 ◽  
Author(s):  
Kaat De Cremer ◽  
Nicolas Delattin ◽  
Katrijn De Brucker ◽  
Annelies Peeters ◽  
Soña Kucharíková ◽  
...  

ABSTRACTWe here report on thein vitroactivity of toremifene to inhibit biofilm formation of different fungal and bacterial pathogens, includingCandida albicans,Candida glabrata,Candida dubliniensis,Candida krusei,Pseudomonas aeruginosa,Staphylococcus aureus, andStaphylococcus epidermidis. We validated thein vivoefficacy of orally administered toremifene againstC. albicans and S. aureusbiofilm formation in a rat subcutaneous catheter model. Combined, our results demonstrate the potential of toremifene as a broad-spectrum oral antibiofilm compound.


2021 ◽  
Vol 12 ◽  
Author(s):  
Rui Yuan ◽  
Jie Tu ◽  
Chunquan Sheng ◽  
Xi Chen ◽  
Na Liu

Candida albicans is the most common fungal pathogen. Recently, drug resistance of C. albicans is increasingly severe. Hsp90 is a promising antifungal target to overcome this problem. To evaluate the effects of Hsp90 inhibitor ganetespib on the inhibition of azole-resistant C. albicans, the microdilution checkerboard method was used to measure the in vitro synergistic efficacy of ganetespib. The XTT/menadione reduction assay, microscopic observation, and Rh6G efflux assay were established to investigate the effects of ganetespib on azole-resistant C. albicans biofilm formation, filamentation, and efflux pump. Real-time RT-PCR analysis was employed to clarify the mechanism of antagonizing drug resistance. The in vivo antifungal efficacy of ganetespib was determined by the infectious model of azole-resistant C. albicans. Ganetespib showed an excellent synergistic antifungal activity in vitro and significantly inhibited the fungal biofilm formation, whereas it had no inhibitory effect on fungal hypha formation. Expression of azole-targeting enzyme gene ERG11 and efflux pump genes CDR1, CDR2, and MDR1 was significantly down-regulated when ganetespib was used in combination with FLC. In a mouse model infected with FLC-resistant C. albicans, the combination of ganetespib and FLC effectively reversed the FLC resistance and significantly decreased the kidney fungal load of mouse.


Author(s):  
Alena Kašperová ◽  
Jaroslav Turánek ◽  
Václav Čeřovský ◽  
Milan Raška

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