CC BY-NC-ND 4.0 · Eur J Dent 2014; 08(02): 254-260
DOI: 10.4103/1305-7456.130626
Original Article
Dental Investigation Society

Antimicrobial activity of cationic peptides in endodontic procedures

Sofi Beaula Winfred
1   Department of Human Genetics, Sri Ramachandra University, Porur, Chennai, Tamil Nadu, India
,
Gowri Meiyazagan
1   Department of Human Genetics, Sri Ramachandra University, Porur, Chennai, Tamil Nadu, India
,
Jiban J. Panda
2   Malaria Research Laboratory, International Center for Genetic Engineering and Biotechnology, New Delhi, India
,
Venkateshbabu Nagendrababu
3   Department of Conservative Dentistry, Faculty of Dental Science, Sri Ramachandra University, Porur, Chennai, Tamil Nadu, India
,
Kandaswamy Deivanayagam
3   Department of Conservative Dentistry, Faculty of Dental Science, Sri Ramachandra University, Porur, Chennai, Tamil Nadu, India
,
Virander S. Chauhan
2   Malaria Research Laboratory, International Center for Genetic Engineering and Biotechnology, New Delhi, India
,
Ganesh Venkatraman
1   Department of Human Genetics, Sri Ramachandra University, Porur, Chennai, Tamil Nadu, India
› Author Affiliations
Further Information

Publication History

Publication Date:
25 September 2019 (online)

ABSTRACT

Objectives: The present study aimed to investigate the antimicrobial and biofilm inhibition activity of synthetic antimicrobial peptides (AMPs) against microbes such as Enterococcus faecalis, Staphylococcus aureus, and Candida albicans which are involved in endodontic infections. Materials and Methods: Agar diffusion test was done to determine the activity of peptides. The morphological changes in E. faecalis and reduction in biofilm formation after treatment with peptides were observed using scanning electron microscope. The efficacy of peptides using an ex vivo dentinal model was determined by polymerase chain reaction and confocal laser scanning microscopy. Platelet aggregation was done to determine the biocompatibility of peptides. Results: Among 11 peptides, two of the amphipathic cationic peptides were found to be highly active against E. faecalis, S. aureus, C. albicans. Efficacy results using dentinal tubule model showed significant reduction in microbial load at 400 μm depth. The peptides were also biocompatible. Conclusion: These results suggest that synthetic AMPs have the potential to be developed as antibacterial agents against microorganisms involved in dental infections and thus could prevent the spread and persistence of endodontic infections improving treatment outcomes and teeth preservation.

 
  • REFERENCES

  • 1 Andersson DI, Hughes D. Antibiotic resistance and its cost: Is it possible to reverse resistance?. Nat Rev Microbiol 2010; 8: 260-71
  • 2 Batoni G, Maisetta G, Brancatisano FL, Esin S, Campa M. Use of antimicrobial peptides against microbial biofilms: Advantages and limits. Curr Med Chem 2011; 18: 256-79
  • 3 Bystrom A, Claesson R, Sundqvist G. The antibacterial effect of camphorated paramonochlorophenol, camphorated phenol and calcium hydroxide in the treatment of infected root canals. Endod Dent Traumatol 1985; 1: 170-5
  • 4 Coates AR, Hu Y. Targeting non-multiplying organisms as a way to develop novel antimicrobials. Trends Pharmacol Sci 2008; 29: 143-50
  • 5 Feder R, Dagan A, Mor A. Structure-activity relationship study of antimicrobial dermaseptin S4 showing the consequences of peptide oligomerization on selective cytotoxicity. J Biol Chem 2000; 275: 4230-8
  • 6 Fernandez-Lopez S, Kim HS, Choi EC, Delgado M, Granja JR, Khasanov A. et al. Antibacterial agents based on the cyclic D, L-alpha-peptide architecture. Nature 2001; 412: 452-5
  • 7 Hancock RE, Brown KL, Mookherjee N. Host defence peptides from invertebrates: Emerging antimicrobial strategies. Immunobiology 2006; 211: 315-22
  • 8 Hancock RE, Chapple DS. Peptide antibiotics. Antimicrob Agents Chemother 1999; 43: 1317-23
  • 9 Hoiby N, Bjarnsholt T, Givskov M, Molin S, Ciofu O. Antibiotic resistance of bacterial biofilms. Int J Antimicrob Agents 2010; 35: 322-32
  • 10 Kawashima N, Wadachi R, Suda H, Yeng T, Parashos P. Root canal medicaments. Int Dent J 2009; 59: 5-11
  • 11 Kolembrander PE. Multispecies communities: Interspecies interactions influence growth on saliva as sole nutritional source. Int J Oral Sci 2011; 3: 49-54
  • 12 Krause TA, Liewehr FR, Hahn CL. The antimicrobial effect of MTAD, sodium hypochlorite, doxycycline, and citric acid on Enterococcus faecalis. J Endod 2007; 33: 28-30
  • 13 Lee MT, Chen FY, Huang HW. Energetics of pore formation induced by membrane active peptides. Biochemistry 2004; 43: 3590-9
  • 14 Mirhendi SH, Makimura K. PCR detection of Candida albicans in blood using a new primer pair to diagnosis of systemic candidiasis. Iran J Public Heath 2006; 32: 1-5
  • 15 Mohan KV, Rao SS, Atreya CD. Antiviral activity of selected antimicrobial peptides against vaccinia virus. Antiviral Res 2010; 86: 306-11
  • 16 Yallapu MM, Ebeling MC, Chauhan N, Jaggi M, Chauhan SC. Interaction of curcumin nanoformulations with human plasma protein and erythrocytes. Int J Nanomedicine 2011; 6: 2779-90
  • 17 O'Toole G, Kaplan HB, Kolter R. Biofilm formation as microbial development. Annu Rev Microbiol 2000; 54: 49-79
  • 18 Pathak S, Chauhan VS. Rationale-based, de novo design of dehydrophenylalanine-containing antibiotic peptides and systematic modification in sequence for enhanced potency. Antimicrob Agents Chemother 2011; 55: 2178-88
  • 19 Reddy KV, Yedery RD, Aranha C. Antimicrobial peptides: Premises and promises. Int J Antimicrob Agents 2004; 24: 536-47
  • 20 Rôças IN, Siqueira Jr JF, Santos KR. Association of Enterococcus faecalis with different forms of periradicular diseases. J Endod 2004; 30: 315-20
  • 21 Straus SK, Hancock RE. Mode of action of the new antibiotic for Gram-positive pathogens daptomycin: Comparison with cationic antimicrobial peptides and lipopeptides. Biochim Biophys Acta 2006; 1758: 1215-23
  • 22 Strøm MB, Haug BE, Skar ML, Stensen W, Stiberg T, Svendsen JS. The pharmacophore of short cationic antibacterial peptides. J Med Chem 2003; 46: 1567-70
  • 23 Tao R, Tong Z, Lin Y, Xue Y, Wang W, Kuang R. et al. Antimicrobial and antibiofilm activity of pleurocidin against cariogenic microorganisms. Peptides 2011; 32: 1748-54
  • 24 Vaara M. Agents that increase the permeability of the outer membrane. Microbiol Rev 1992; 256: 395-411
  • 25 Zasloff M. Antimicrobial peptides of multicellular organisms. Nature 2002; 415: 389-95
  • 26 Ringel AM, Patterson SS, Newton CW, Miller CH, Mulhern JM. In vivo evaluation of chlorhexidine gluconate solution and sodium hypochlorite solution as root canal irrigants. J Endod 1982; 8: 200-4
  • 27 Pashley EL, Birdsong NL, Bowman K, Pashley DH. Cytotoxic effects of NaOCl on vital tissue. J Endod 1985; 11: 525-8
  • 28 Williams JM, Trope M, Caplan DJ, Shugars DC. Detection and quantitation of E. faecalis by real-time PCR (qPCR), reverse transcription-PCR (RT-PCR), and cultivation during endodontic treatment. J Endod 2006; 32: 715-21
  • 29 Stewart PS, Costerton JW. Antibiotic resistance of bacteria in biofilms. Lancet 2001; 358: 135-8
  • 30 Endo MS, Ferraz CC, Zaia AA, Almeida JF, Gomes BP. Quantitative and qualitative analysis of microorganisms in root-filled teeth with persistent infection: Monitoring of the endodontic retreatment. Eur J Dent 2013; 7: 302-9
  • 31 Chai WL, Hamimah H, Cheng SC, Sallam AA, Abdullah M. Susceptibility of Enterococcus faecalis biofilm to antibiotics and calcium hydroxide. J Oral Sci 2007; 49: 161-6
  • 32 Weber M, Gerdsen F, Gutensohn K, Schoder V, Eifrig B, Hossfeld DK. Enhanced platelet aggregation with TRAP-6 and collagen in platelet aggregometry in patients with venous thromboembolism. Thromb Res 2002; 107: 325-8
  • 33 Poyart C, Pierre C, Quesne G, Pron B, Berche P, Trieu-Cuot P. Emergence of vancomycin resistance in the genus Streptococcus: Characterization of a vanB transferable determinant in Streptococcus bovis. Antimicrob Agents Chemother 1997; 41: 24-9