Antimicrobial and Antibiofilm Activities of Synthetic Lawsone Derivatives Containing N-Substituted 1,2,3-Triazole Against Dental Caries Pathogens

Authors

  • Pichayaporn Ratti Department of Conservative Dentistry, Faculty of Dentistry, Prince of Songkla University, Hat Yai, Songkhla 90110, Thailand.
  • Jutharat Manuschai Department of Conservative Dentistry, Faculty of Dentistry, Prince of Songkla University, Hat Yai, Songkhla 90110, Thailand.
  • Jiraporn Kara Department of Pharmaceutical Chemistry, Faculty of Pharmaceutical Sciences, Prince of Songkla University, Hat Yai, Songkhla 90110, Thailand. Phytomedicine and Pharmaceutical Biotechnology Excellent Center (PPBEC), Faculty of Pharmaceutical Sciences, Prince of Songkla University, Hat Yai, Songkhla 90110, Thailand.
  • Supawadee Naorungroj Department of Conservative Dentistry, Faculty of Dentistry, Prince of Songkla University, Hat Yai, Songkhla 90110, Thailand.
  • Luelak Lomlim Department of Pharmaceutical Chemistry, Faculty of Pharmaceutical Sciences, Prince of Songkla University, Hat Yai, Songkhla 90110, Thailand. Phytomedicine and Pharmaceutical Biotechnology Excellent Center (PPBEC), Faculty of Pharmaceutical Sciences, Prince of Songkla University, Hat Yai, Songkhla 90110, Thailand.

DOI:

https://doi.org/10.31584/jhsmr.2022906

Keywords:

antibacterial activity, anticaries, dental biofilm, lawsone derivatives, naphthoquinone, triazole

Abstract

Objective: Presently, one of the most common oral diseases is dental caries, which is a biofilm-mediated disease. Lawsone methyl ether (LME) has shown promising antibacterial activity due to its 1,4-napthoquinone structure. Recently, a 1,2,3-triazole scaffold has been used in the structural modification of potential antimicrobial agents. To develop novel anticaries agents, the structure modification of 1,4-napthoquinone with N-substituted 1,2,3-triazole, therefore, may be a candidate.
Material and Methods:
LME was used as a lead compound, and three new lawsone derivatives were prepared by two[1]step reactions. Their antimicrobial effects against three dental caries pathogens; including S. mutans, L. casei, and A. naeslundii were investigated, using the microdilution technique (0.78-100 µg/mL). A growth curve assay was performed to assess the effects of compounds on the growth kinetics of bacteria. Moreover, the effect of synthetic lawsone derivatives on the biofilm formation of S. mutans was also evaluated by crystal violet assay.
Results: Overall, S. mutans was most sensitive to lawsone derivatives (minimum inhibitory concentration (MIC)=1.56- 50 µg/mL), followed by A. naeslundii and L. casei: corresponding to their growth curves. Lawsone derivatives, at the concentration of 1/2 MIC and 1/4 MIC, inhibited 12-hour S. mutans biofilm formation by 86.0-98.0%. The inhibitory effect decreased with decreasing concentrations and increasing incubation times.
Conclusion: Synthetic lawsone derivatives have an inhibitory effect on the growth of three tested cariogenic bacteria, and the biofilm formation of S. mutans. The compounds exhibited anti-cariogenic bacterial strains and satisfying anti-biofilm formation effects on S. mutans.

References

Global Burden of Disease Study 2019 (GBD 2019) [homepage on the Internet]. Washington: Institute for Health Metrics and Evaluation; 2020. [cited 2022 May 29]. Available from: http:// ghdx.healthdata.org/gbd-results-tool.

Yadav K, Prakash S. Dental caries: a microbiological approach. J Clin Infect Dis Pract 2017;02:118.

Tanner ACR, Kressirer CA, Rothmiller S, Johansson I, Chalmers NI. The caries microbiome: implications for reversing dysbiosis. Adv Dent Res 2018;29:78-85.

Jeon JG, Rosalen PL, Falsetta ML, Koo H. Natural products in caries research: current (limited) knowledge, challenges and future perspective. Caries Res 2011;45:243-63.

Howell A, Jr., Jordan HV, Georg LK, Pine L. Odontomyces viscosus, gen. nov., spec. nov., a filamentous microorganism isolated from periodontal plaque in hamsters. Sabouraudia 1965;4:65-8. 6. Caufield PW, Schon CN, Saraithong P, Li Y, Argimon S. Oral lactobacilli and dental caries: a model for niche adaptation in humans. J Dent Res 2015;94 (9 Suppl):110S-8S.

Panichayupakaranant P, Septama AW, Sinviratpong A. Synergistic activity of lawsone methyl ether in combination with some antibiotics and artocarpin against methicillin-resistant Staphylococcus aureus, Candida albicans, and Trychophyton rubrum. Chin Herb Med 2019;11:321-5.

Yang X, Summerhurst DK, Koval SF, Ficker C, Smith ML, Bernards MA. Isolation of an antimicrobial compound from Impatiens balsamina L. using bioassay-guided fractionation. Phytother Res 2001;15:676-80.

Sakunphueak A, Panichayupakaranant P. Comparison of antimicrobial activities of naphthoquinones from Impatiens balsamina. Nat Prod Res 2012;26:1119-24.

Lopez L, López L, Nery-Flores S, Flores N, Yesenia S, Silva Y, et al. Naphthoquinones: biological properties and synthesis of lawsone and derivatives. Vitae 2014;21:248-58.

Aneja B, Azam M, Alam S, Perwez A, Maguire R, Yadava U, et al. Natural product-based 1,2,3-triazole/sulfonate analogues as potential chemotherapeutic agents for bacterial infections. ACS Omega 2018;3:6912-30.

Nural Y, Ozdemir S, Doluca O, Demir B, Yalcin MS, Atabey H, et al. Synthesis, biological properties, and acid dissociation constant of novel naphthoquinone-triazole hybrids. Bioorg Chem 2020;105:104441.

Bunders C, Cavanagh J, Melander C. Flustramine inspired synthesis and biological evaluation of pyrroloindoline triazole amides as novel inhibitors of bacterial biofilms. Org Biomol Chem 2011;9:5476-81.

Minvielle MJ, Bunders CA, Melander C. Indole/triazole conjugates are selective inhibitors and inducers of bacterial biofilms. Med Chem Comm 2013;4:916-9.

Ballard TE, Richards JJ, Wolfe AL, Melander C. Synthesis and antibiofilm activity of a second-generation reverse-amide oroidin library: a structure-activity relationship study. Chemistry 2008;14:10745-61.

Rogers SA, Melander C. Construction and screening of a 2-aminoimidazole library identifies a small molecule capable of inhibiting and dispersing bacterial biofilms across order, class, and phylum. Angew Chem Int Ed Engl 2008;47:5229-31.

Huigens RW, 3rd, Rogers SA, Steinhauer AT, Melander C. Inhibition of Acinetobacter baumannii, Staphylococcus aureus and Pseudomonas aeruginosa biofilm formation with a class of TAGE-triazole conjugates. Org Biomol Chem 2009;7:794-802.

Nagender P, Malla Reddy G, Naresh Kumar R, Poornachandra Y, Ganesh Kumar C, Narsaiah B. Synthesis, cytotoxicity, antimicrobial and anti-biofilm activities of novel pyrazolo[3,4-b] pyridine and pyrimidine functionalized 1,2,3-triazole derivatives. Bioorg Med Chem Lett 2014;24:2905-8.

Linares D, Bottzeck O, Pereira O, Praud-Tabariès A, Blache Y. Designing 2-aminoimidazole alkaloids analogs with anti-biofilm activities: Structure–activities relationships of polysubstituted triazoles. Bioorg Med Chem Lett 2011;21:6751-5.

Praud-Tabaries A, Dombrowsky L, Bottzek O, Briand J-F, Blache Y. Synthesis of a polyprenyl-type library containing 1,4-disubstituted-1,2,3-triazoles with anti-biofilm activities against Pseudoalteromonas sp. Tetrahedron Lett 2009;50:1645- 8.

Anaissi-Afonso L, Oramas-Royo S, Ayra-Plasencia J, Martín Rodríguez P, García-Luis J, Lorenzo-Castrillejo I, et al. Lawsone, juglone, and β-lapachone derivatives with enhanced mitochondrial-based toxicity. ACS Chem Biol 2018;13:1950-7.

Petrat W, Wattanapiromsakul C, Nualnoi T, Sabri NH, Lee VS, Lomlim L. Cholinesterase inhibitory activity, kinetic and molecular docking studies of N-(1-substituted-1H-1,2,3- triazole-4-yl)-aralkylamide derivatives. Walailak J Sci Technol 2016;14:687-701.

Daina A, Michielin O, Zoete V. SwissADME: a free web tool to evaluate pharmacokinetics, drug-likeness and medicinal chemistry friendliness of small molecules. Sci Rep 2017;7:42717.

Potts RO, Guy RH. Predicting skin permeability. Pharm Res 1992;9:663-9.

Brookes ZLS, Bescos R, Belfield LA, Ali K, Roberts A. Current uses of chlorhexidine for management of oral disease: a narrative review. J Dent 2020;103:103497.

Wilkins JC, Homer KA, Beighton D. Analysis of streptococcus mutans proteins modulated by culture under acidic conditions. Appl Environ Microbiol 2002;68:2382-90.

Dieterle ME, Fina Martin J, Durán R, et al. Characterization of prophages containing “evolved” Dit/Tal modules in the genome of Lactobacillus casei BL23. Appl Microbiol Biotechnol 2016;100:9201-15.

Kawashima J, Nakajo K, Washio J, Mayanagi G, Shimauchi H, Takahashi N. Fluoride-sensitivity of growth and acid production of oral actinomyces: comparison with oral streptococcus. Microbiol Immunol 2013;57:797-804.

Jiang X, Hao X, Jing L, Wu G, Kang D, Liu X, et al. Recent applications of click chemistry in drug discovery. Expert Opin Drug Discov 2019;14:779-89.

Xu Z, Zhao SJ, Liu Y. 1,2,3-Triazole-containing hybrids as potential anticancer agents: current developments, action mechanisms and structure-activity relationships. Eur J Med Chem 2019;183:111700.

Kolb HC, Finn MG, Sharpless KB. Click chemistry: diverse chemical function from a few good reactions. Angew Chem Int Ed Engl 2001;40:2004-21.

Zotta T, Parente E, Ricciardi A. Aerobic metabolism in the genus lactobacillus: impact on stress response and potential applications in the food industry. J Appl Microbiol 2017;122:857- 69.

Ahn SJ, Wen ZT, Burne RA. Effects of oxygen on virulence traits of streptococcus mutans. J Bacteriol 2007;189:8519-27.

van der Hoeven JS, van den Kieboom CWA. Oxygen-dependent lactate utilization by Actinomyces viscosus and Actinomyces naeslundii. Oral Microbiol Immunol 1990;5:223-5.

He Z, Huang Z, Jiang W, Zhou W. Antimicrobial activity of cinnamaldehyde on streptococcus mutans biofilms. Front Microbiol 2019;10:2241.

Hasan S, Danishuddin M, Khan AU. Inhibitory effect of zingiber officinale towards Streptococcus mutans virulence and caries development: in vitro and in vivo studies. BMC Microbiol 2015;15:1.

Ratti P, Manuschai J, Kara J, Lomlim L, Naorungroj S. Effects of synthetic lawsone derivatives on streptococcus mutans biofilm formation. poster presented at: 35th annual scientific meeting, IADR-SEA Division; 2021 Dec 8-9; Hong Kong, China.

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Published

2023-04-21

How to Cite

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Ratti P, Manuschai J, Kara J, Naorungroj S, Lomlim L. Antimicrobial and Antibiofilm Activities of Synthetic Lawsone Derivatives Containing N-Substituted 1,2,3-Triazole Against Dental Caries Pathogens. J Health Sci Med Res [Internet]. 2023 Apr. 21 [cited 2024 Jul. 18];41(2):1-13. Available from: https://he01.tci-thaijo.org/index.php/jhsmr/article/view/263107

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