Antagonism of Bacteria from Dog Dental Plaque against Human Cariogenic Bacteria

Martins, Káthia Santana; Magalhães, Lorena Tirza de Assis; Almeida, Jeferson Geison de; Pieri, Fábio Alessandro

doi:https://doi.org/10.1155/2018/2780948

BioMed Research International

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Volume 2018 | Article ID 2780948 | https://doi.org/10.1155/2018/2780948

Antagonism of Bacteria from Dog Dental Plaque against Human Cariogenic Bacteria

Káthia Santana Martins,¹Lorena Tirza de Assis Magalhães,¹Jeferson Geison de Almeida,¹and Fábio Alessandro Pieri¹

Guest Editor: Chedly Chouchani

Received04 May 2018

Accepted21 Oct 2018

Published04 Nov 2018

Abstract

Dental caries are a process of demineralization and destruction of human teeth. They originate through many factors and are associated with biofilm formation, which consists of bacteria adhered to the teeth that form a structurally and functionally organized mass called dental plaque. Both the presence of Streptococcus mutans and the frequent consumption of sucrose correlate with a higher prevalence of caries in humans. In dogs, however, the incidence of this disease is low, due to factors such as differences in dental microbiota and/or their low consumption of sucrose. This work evaluated the antagonism of bacteria from dog’s dental plaque against S. mutans, for the identification of producing strains of biotechnological products for use in preventing caries. This study used 95 bacterial isolates of canine dental plaque from the Veterinary Department at the Federal University of Viçosa, Minas Gerais, Brazil. A spot-on-the-lawn method was performed using Brain Heart Infusion agar with catalase for an initial identification of the antagonistic activity. Additional tests were conducted on the isolates classified as antagonists for confirmation of the activity, using modified Mann-Rogosa-Sharpe medium containing low dextrose concentration. These isolates were incubated at 37°C for 24 hours in anaerobiosis. The peptide nature of inhibition was evaluated using the following proteinases: proteinase K from Tritirachium album, bovine pancreatic trypsin, and type XII-A α-amylase from Bacillus licheniformis. In the initial identification of those strains exhibiting antimicrobial activity, 14 were classified as antagonists. One of the isolates (Bacillus sp.) indicated bacteriocinogenic activity, with a deformed inhibition halo on S. mutans by the addition of trypsin. These results suggest that this bacterial isolate may be applicable to biotechnological use to combat the main etiological agent of caries in humans. Further studies are needed to evaluate the bacteriocinogenic nature of the antimicrobial activities of the other 13 antagonistic bacterial isolates.

1. Introduction

Dental caries is a multifactorial disease, where microbial involvement and the host response are both of fundamental importance. The genesis of caries is associated with the formation of a biofilm consisting of bacteria that adhere to the surface of the tooth. These bacteria form a structurally and functionally organized mass called dental plaque [1–4]. Caries is the result of a chronic process that, according to Newbrun [5], appears after the interaction and presence of four factors: a susceptible teeth, microorganisms, diet, and time [6]. The aetiology of caries disease involves Streptococcus mutans, an acidophilic and acidogenic microorganism important in the production of acid in human dental plaque [7, 8]. The presence of S. mutans and the frequent consumption of sugars are directly correlated with a higher prevalence and incidence of caries [9].

In dogs, dental caries are somewhat unusual. The differences in a dog’s dental microbiota, their poor sucrose consumption [10, 11], or the possibility of microorganisms present in the oral cavity could establish antagonism on S. mutans and other cariogenic bacteria. This antagonism results from competition for nutrients or production of compounds inhibitory to these bacteria, bacteriocins, which would develop a critical barrier against colonization by pathogenic species [1]. Pieri and colleagues [12] investigated the microbiota of the dental plaque of dogs through isolating and identifying its bacterial components. They found that one of the most present genera in dog plaque is Streptococcus; however, none of the isolates presented genetic similarity of the 16S rDNA gene with Streptococcus mutans, indicating the absence of this species in dogs [12–14].

Bacteriocins are peptides produced by bacteria to give them a competitive advantage [1]. S. mutans may produce bacteriocins to antagonise other bacteria in the dental plaque of humans. The species of Streptococcus present in the dental plaque of dogs could perform this same mechanism against S. mutans in the dental plaque of humans [1, 12]. Numerous lactic acid bacteria are consistently found in the dental plaque of dogs; many of these have the capacity to produce bacteriocins against similar bacteria in order to establish their colonization sites [7–9]. This ability to inhibit target strains is potentially useful in food preservation and the production of alternative antimicrobial therapeutic agents for diseased sites [15–18].

The most effective way to prevent caries is the mechanical removal of biofilm by brushing and using dental floss. However, this physical removal of biofilm is typically not enough to control the disease for the majority of the population. It is important to identify additive resources to combat dental biofilm, such as chlorhexidine [4, 13]. Chlorhexidine is currently considered as an antiseptic reference in dentistry and is approved by the American Dental Association Council on Dental Therapeutics. However, the continuous use of this product in the oral cavity has numerous side effects, including burning in the oral cavity, ulcerations in the jugal mucosa, darkening of the dental enamel, and loss of taste [4, 19–21]. Consequently, there has recently been increased interest in the development of new antimicrobial chemotherapeutic agents with potential for incorporation into oral products that control cariogenic microbiota [1, 4, 9, 17, 22–26].

Caries is a major public health problem, reaching between 60 and 90% of school-age children and a large majority of adults in developed and developing countries [27, 28]. The work presented here furthers the development of anticaries products through evaluating the antagonism of bacterial isolates from canine dental plaques against S. mutans to identify strains that produce compounds with biotechnological potential.

2. Materials and Methods

All methods in this study were conducted at the Laboratory of Microbiology Studies, Institute of Life Sciences, Federal University of Juiz de Fora, Campus Governador Valadares (UFJF-GV). The antagonistic potential of 95 bacterial isolates from the dental plaque of 10 dogs was previously obtained by Pieri and colleagues [12], from January to December of 2009 (Table S1). These isolates were within the bacterial repository of the Veterinary Department at the Federal University of Viçosa, and were selected representing equal percentage of its genus in total isolates obtained from the dogs. Streptococcus mutans (ATCC UA159) was used as cariogenic target strain. Staphylococcus aureus (ATCC 25923) were used as the traditional target cultures for these assays. All cultures were stored in Brain Heart Infusion (BHI) broth, with 20% glycerol as cryoprotectant, at -80°C until use. The analysis of the antagonistic activity of the isolates was performed according to Moraes and colleagues [16], by using spot-on-the-lawn methodology for initial identification of antimicrobial activity.

Bacterial cultures of dog plaque were activated for 24 hours at 37°C. From these cultures, 2 μL were inoculated on the surface of Petri dishes containing BHI agar and a catalase solution (100 IU/mL) and subsequently incubated at 37°C for 24 hours [29, 30] (Figure 1(a)). After the formation of the colonies on the agar surface (Figure 1(b)), a 10 mL overlay of BHI semisolid agar was added (0.75% bacteriological agar), containing approximately 106 CFU/mL of the target bacteria: S. mutans (ATCC UA159) and S. aureus (ATCC 25923) (Figure 1(c)). After solidification of the overlayer, the plates were again incubated at 37°C for 24 hours. After that incubation step, the formation of any inhibition halo around the bacterial colony indicated antagonism (Figure 1(d)). All tests were conducted in triplicate.

Figure 1

Sequence of spot-on-the-lawn surface to establish antagonistic activity of one strain of bacteria against a target strain and to confirm the protein nature of this inhibition; (a) 2 μL of test strain is inoculated on the surface of Petri dishes containing agar; (b) formation of the colonies of test strain on the agar surface; (c) addition of a semisolid agar overlayer with the target bacteria; (d) inhibition halo after the incubation of target strain, confirming antagonistic activity; (e) four holes adjacent to the colonies made to inoculation of different proteinases; (f) interference of bovine pancreatic trypsin on inhibition halo of test strain against target strain, confirming the protein nature of antagonistic activity.

The cultures that presented antagonistic activity were subjected to additional tests to confirm the protein nature of the produced antimicrobial substances [16]. A modified Mann-Rogosa-Sharpe (MRS) agar plate containing dextrose at a low concentration (5 g/L) was used, where 2 μL of one of the cultures of active isolates of the dog dental plaque was inoculated in the centre of the plate and incubated anaerobically at 37°C for 24 hours (Figure 1(a)). After incubation, four holes adjacent to the colonies formed (Figure 1(e)) were inoculated with 30 μL of one of the following solutions: sterile distilled water (negative control), Tritirachium album proteinase K (Sigma-Aldrich, Saint Louis, MI, USA), bovine pancreas trypsin (Sigma-Aldrich, Saint Louis, MI, USA), and Bacillus licheniformis type XII-A α-amylase (Sigma-Aldrich, Saint Louis, MI, USA). All inoculated enzymes held concentrations of 20mg/mL. The plates were then incubated at 37°C for two hours to allow diffusion of the inoculated solutions into the agar. After diffusion, a 10 mL overlay of BHI semisolid agar, seeded with approximately one million CFU/mL of the target microorganism, was added, followed by incubation for 24 hours at 37°C. Sensitivity of the antagonistic culture to the proteolytic enzyme solutions was observed as interference in the inoculated regions (Figure 1(f)), thus confirming the protein nature of the inhibitory substance.

3. Results and Discussion

From the 95 isolates tested in the initial evaluation of the antagonistic activity, 14 formed inhibition halos around the colonies in the BHI agar medium containing a catalase solution. These isolates were initially classified as antagonists against S. mutans and/or S. aureus.

Of the 14 isolates initially classified as antagonists, only one did not show growth in the dextrose-modified MRS medium and was subsequently discarded. The other 13 strains showed growth and formation of inhibition halos around the colonies when incubated with the target strains. These 13 isolates which were confirmed as antagonists and the diameters of their inhibition halos were evaluated (Table 1).

Of the 13 isolates, only Bacillus sp. (HQ717211; Table 1) had an inhibition halo that was modified by proteolytic enzyme solution (bovine pancreas trypsin). These results indicated the sensitivity of the culture to the enzyme solution, thereby confirming the protein nature of the inhibitory substance.

The spot-on-the-lawn methodology is widely used to detect the protein character of antimicrobial substances produced from bacteria. It is considered advantageous, as proteins are distinguishable even in cultures that produce small inhibition halos [16, 30, 31]. This methodology was performed using BHI medium with catalase (100 IU/mL) incubated at 37°C for 24 hours for the initial identification of the antimicrobial activity. The catalase solution was added to hydrolyse any possible hydrogen peroxide produced by the cultures [16, 32, 33]. Hydrogen peroxide has antimicrobial potential and could thus interfere with the identification of isolates with antagonistic activity derived from the production of bacteriocins [16, 34]. The inhibition halos identified in the 14 isolates classified as antagonists had no relation to hydrogen peroxide production.

Although any one acidogenic bacterium may contribute to enamel demineralization that results in caries, the S. mutans strain presents additional characteristics that may initiate and exacerbate the disease [1, 35]. In addition to the fermentation of sucrose in organic acids, S. mutans hydrolyses substrate forming polymers, allowing them to coaggregate with other bacteria, thus forming an extracellular matrix with greater biodiversity [1, 35]. Although other human oral bacteria such as S. sanguis, S. salivarius, and S. gordonii, can synthesize these polysaccharides, only S. mutans presents a preference to the presence of sucrose in the infection site [1, 35]. In addition, S. mutans has the ability to store amylopectin intracellular polysaccharides for fermentation in the absence of extracellular carbohydrates, allowing continuous fermentation between host meals. S. mutans also shows greater release of acid when compared to other bacteria of the genus Streptococcus [1]. Therefore, the reduction of S. mutans levels in the plaque microbiota could become a desirable strategy for the prevention and treatment of the disease [9].

Streptococcus spp., obtained from dental plaques of dogs (supplementary data), were expected to act as potential inhibitors of S. mutans, as bacteriocins are produced by a microorganism to antagonise those with high genetic similarity [1, 29]. However, of the eight isolates of Streptococcus spp. tested in this study, none presented antagonistic activity. Our data showed a large variety of bacteria presenting antagonism against S. mutans. These species include Enterococcus faecalis, Actinomyces sp., Aerococcus viridans, Bacillus sp., and Lactococcus lactis. Among the isolates classified at the end of the second stage of the incubation, 53.9% of the antagonists were Enterococcus faecalis (Table 1). This bacterial species was previously classified as Streptococcus faecalis, due to its high genetic and phenotypic similarity with the Streptococcus genus [36]. Considering that similarity, the bacteria of the genus Enterococcus could potentially antagonise those species within the genus Streptococcus.

With regard to the second phase of evaluating antagonistic activity of the bacterial isolates, the use of the MRS medium under anaerobic conditions tends to inhibit the production of hydrogen peroxide [31, 33]. In addition to the exclusion of the possible hydrogen peroxide activity on target strains, this medium and culture condition caused an increase in the diameter of the halos of some test strains, indicating antagonistic activity.

Following the aim of this work, the protein character of the antagonist activity of isolates was evaluated against S. mutans. The S. aureus overlay was used as a comparison strain in the initial phase of evaluation of the antagonistic activity, as it is used often with the spot-on-the-lawn method. However, as S. aureus is a recognized pathogen for both human and animal health [24], new studies evaluating the protein nature of isolates from canine dental plaque should be carried out for a possible identification of bioproducts for the treatment of diseases caused by this pathogen.

While 13 strains showed the formation of an inhibition halo in the overlay of S. mutans, only one isolate (HQ717211, Bacillus sp.) showed deformation of the halo in the deposit site of proteolytic enzyme bovine pancreatic trypsin, suggesting the loss of antagonistic activity by the interaction of the enzyme and the protein-based bacteriocin produced by this isolate.

4. Conclusions

This study shows that the isolate of Bacillus sp. (HQ717211), obtained from canine dental plaque, has biotechnological potential in combatting a major etiologic agent of caries in humans. In addition, 13 other bacterial isolates were identified as potential antagonists of S. mutans. Future work confirming the bacteriocinogenic nature of these isolates should be considered for use in preventive therapy and treatment of caries in humans.

Data Availability

The 16S rDNA sequences for all isolates from canine dental plaque used to identify the bacteria involved on the findings of this study have been deposited in the Genbank repository, (Genbank access codes are located in Tables 1 and S1).

Conflicts of Interest

The authors declare that there are no conflicts of interest regarding the publication of this paper.

Acknowledgments

We acknowledge Professor Maria Aparecida Scatamburlo Moreira (Federal University of Viçosa) for granting us with the isolates from dog’s dental plaque. This work was funded by scholarship grant and financial support by FAPEMIG, CAPES, CNPq, and PROPP-UFJF.

Supplementary Materials

Table S1: all isolates from dog’s dental plaque used for the study of bacteriocinogenic activity against Streptococcus mutans and their respective Genbank access number for 16S rDNA sequences. (Supplementary Materials)

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Copyright © 2018 Káthia Santana Martins et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

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