4.6 Article

Potential of two delivery systems for nisin topical application to dental plaque biofilms in dogs

Journal

BMC VETERINARY RESEARCH
Volume 14, Issue -, Pages -

Publisher

BMC
DOI: 10.1186/s12917-018-1692-9

Keywords

Dogs; Enterococci; Guar-gum gel; Nisin; Periodontal disease; Toothpaste

Funding

  1. Foundation for Science and Technology [SFRH/BD/131384/2017, SFRH/BD/100571/2014]
  2. CIISA - Centre for Interdisciplinary Research in Animal Health, Faculty of Veterinary Medicine, University of Lisbon [UID/CVT/276/2013]
  3. Virbac(R) Portugal

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BackgroundPeriodontal disease (PD) is caused by the development of a microbial biofilm (dental plaque) in the periodontium, affecting approximately 80% of dogs. Several bacterial species present in the canine oral cavity can be implicated in the development of this disease, including Enterococcus spp. To decrease antibiotic administration, a possible control strategy for dog's enterococcal PD may involve the use of the antimicrobial peptide (AMP) nisin.Nisin's inhibitory activity was evaluated against a collection of previously characterized enterococci obtained from the oral cavity of dogs with PD (n=20), as well as the potential of a guar-gum gel and a veterinary toothpaste as topical delivery systems for this AMP. The Minimum Inhibitory (MIC) and Bactericidal Concentrations (MBC) and the Minimum Biofilm Eradication (MBEC) and Inhibitory Concentrations (MBIC) were determined for nisin and for the supplemented guar-gum gel. For the supplemented veterinary toothpaste an agar-well diffusion assay was used to evaluate its inhibitory potential.ResultsNisin was effective against all isolates. Independently of being or not incorporated in the guar-gum gel, its inhibitory activity on biofilms was higher, with MBIC (12.465.16 and 13.60 +/- 4.31g/mL, respectively) and MBEC values (21.87 +/- 11.33 and 42.34 +/- 16.61g/mL) being lower than MIC (24.61 +/- 4.64 and 14.90 +/- 4.10g/mL) and MBC (63.09 +/- 13.22 and 66.63 +/- 19.55g/mL) values. The supplemented toothpaste was also effective, showing inhibitory activity against 95% of the isolates.Conclusions The inhibitory ability of nisin when incorporated in the two delivery systems was maintained or increased, demonstrating the potential of these supplemented vehicles to be applied to PD control in dogs.

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