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International Journal of Dentistry
Volume 2010 (2010), Article ID 824976, 5 pages
Genotypic Diversity of Streptococcus mutans in Caries-Free and Caries-Active Preschool Children
1School of Dentistry, University North of Parana, Londrina, 86041-100 Paraná, Brazil
2School of Biology, University Federal of Pernambuco, 55608-680 Vitória de Santo Antão, Brazil
Received 2 June 2009; Accepted 8 September 2009
Academic Editor: Alexandre R. Vieira
Copyright © 2010 F. J. S. Pieralisi 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.
Aim. The aim of the present paper was to evaluate the genotypic diversity of S. mutans in caries-free and caries-active preschool children in Brazil. Design. Twenty-eight preschool children were examined regarding caries experience by the dmft index. DNA from 280 isolates of S. mutans was extracted. S. mutans evaluated using to the PCR method, with primers for the glucosyltransferase gene. The genetic diversity of S. mutans isolates was analyzed by arbitrary primed-PCR (AP-PCR) reactions. The differences between the diversity genotypic and dmft/caries experience were evaluated by test and Spearman's correlation. Results. The Spearman correlation test showed a strong association between genotypic diversity and caries experience (; ). There were more S. mutans genotypes in the group of preschool children with dental caries, compared with the caries-free group. Among the children with more than 1 genotype, 13 had dental caries (2 to 5 genotypes) and 4 were caries-free (only 2 genotypes). Conclusion. Our results support the previous findings of genetic diversity of S. mutans in preschool children being associated with dental caries. The investigation of such populations may be important for directing the development of programs for caries prevention worldwide.
Streptococcus mutans is generally considered to be the principal aetiological agent for dental caries [1, 2], which possesses a variety of mechanisms to colonize tooth surfaces. Clinical isolates of S. mutans exhibit considerable variations in their genomes or genes . S. mutans species, under certain conditions, is numerically significant in cariogenic biofilms and forms biofilms with other organisms in the oral cavity  after the eruption and colonization of primary teeth . Furthermore, epidemiologic surveys have confirmed that higher levels of S. mutans organisms in children are associated with a higher incidence of decayed, missing, and filled (dmf) teeth [2, 6]. Conversely, it can be found in populations with no caries or with low caries experience [7, 8]. One possible explanation for their presence in subjects with low caries experience is that S. mutans virulence factors can differ between populations with contrasting caries prevalence .
Bowden  pointed out the necessity for understanding the clonality patterns of S. mutans in the caries-free subjects where it is important to ascertain whether S. mutans populations in subjects free of caries exhibit the same clonal diversity of caries-active groups or not .
Several studies have showed genetic heterogeneity among Streptococcus mutans strains [11–16]; however, the relationship between caries activity and the genetic diversity of S. mutans is still controversial. Alaluusua et al.  suggested that caries-active children with high sucrose consumption carried greater ribotype diversity of S. mutans compared with caries-free children. Napimoga et al.  found that caries-active subjects have more genotypes than caries-free subjects. On the other hand, Kreulen et al.  showed a negative correlation between caries activity and genotypic diversity.
The aim of the present paper was to evaluate the genotypic diversity of S. mutans in caries-free and caries-active preschool children in Brazil.
2. Material and Methods
Study participants consisted of 28 preschool children aged between 4 and 5 years old from low socioeconomic level families. They had similar lifestyle, dietary, and oral hygiene habits. The subjects were selected from a group of children attending a nursery located in a medium-sized city from Southern Brazil. All of them were from the day nursery, staying in the nursery for 5 days per week, 8 hours per day. During the sample selection, subjects who had any chronic disease and were using antibiotic in the last 3 months were excluded. The aim and details of the experiments were explained, and the informed consent was obtained from parents and guardians prior to the beginning of the research procedures. Experimental procedures were approved by the Ethical Committee of the University of North of Parana School of Dentistry.
2.2. Clinical Examination
The children were examined while sitting on a chair under natural light. Diagnosis was visual, using a mouth mirror and cotton rolls to assist visibility and a periodontal probe to remove any plaque or debris when necessary.
Caries experience was measured by the dmft (decayed, missing, and filled teeth) index, according to the World Health Organization . The caries experience was dichotomized into two groups: caries-free () and dental caries children (). The clinical examination was performed by the same examiner (F.J.S.P.). The intraexaminer agreement was high ().
2.3. Bacterial Strains and DNA Extraction
Streptococcus mutans clinical isolates were obtained from Mitis-Salivarius Agar with bacitracin and potassium telurite . About 10 colonies resembling S. mutans from each child were transferred to brain heart infusion broth—BHI (Difco, Detroit, USA) and incubated at for 48 hours in an anaerobic jar. DNA from 280 isolates were extracted by using a simple DNA preparation in which the cells were washed and boiled for 10 minutes with TE buffer (10 mM Tris/HCl, 1 mM EDTA, pH 8.0) modified from Saarela et al.  and Welsh and McClelland . The debris were pelleted and the supernatants were stored in a freezer at until use.
2.4. PCR Analyses
Isolates were confirmed for species identity in PCR reactions with primers specific for gtfB, encoding glucosyltransferase ACT ACA CTT TCG GGT GGC TTGG and CAG TAT AAG CGC CAG TTT CATC—(Invitrogen) , yielding an amplicon of 517 pb for S. mutans gtfB gene. Each reaction consisted of 5 L template DNA, 1 of each primer, 200 of each dNTP, 5 L 1x PCR buffer, 1.5 mM MgCl2, and 1 U Taq DNA polymerase (Invitrogen, São Paulo, Brazil) in a total volume of 25 L. The amplification reaction was performed in 30 cycles as follows: denaturation for 30 seconds, annealing at for 30 seconds, and extension at for 1 minute. One reference strain (ATCC 25175) was used as a positive control of S. mutans and distilled water was used as a negative control. Amplification products were analysed electrophoretically in 1% agarose gels using TBE buffer (89 mmol Tris borate, 89 mmol boric acid, 2 mmol EDTA; pH 8), stained with ethidium bromide and observed under UV light. A 100 bp DNA ladder served as molecular-size marker in each gel. All reactions were repeated at least twice.
2.5. AP-PCR Typing
Strains identified as S. mutans were genotyped. The genetic diversity of S. mutans isolates was analyzed by AP-PCR reactions. The sequences of the primers OPA 02 (TGCCGAGCTG) and OPA 13 (CAGCACCCAC) were used. The PCR reactions were performed as follows: 1X PCR buffer (200 mmol Tris-HCl pH 8.4; 500 mmol KCl) with 3.5 mM of , 0.2 mM of each dNTPs, 0.4 mM of primers, 2.5 U of Taq DNA polymerase, and 2.5 of DNA sample. The PCR conditions included 35 cycles of denaturation at for 1 minute, annealing at for 2 minutes, extension at for 2 minutes, with initial denaturation at for 5 minutes, and a final extension at for 5 minutes. The eletrophoresis was carried out as described previously; however amplification products were analysed in 2% agarose gel.
Individual AP-PCR amplicons were marked, and the individual bands were analyzed by using the Dice coefficient (95%) following Mitchell et al. . A dendrogram was constructed using the UPGMA cluster analysis with the aid of Numerical Taxonomy and Multivariate Analysis System (NTSYS) program (Exeter Software, Setauket, NY).
2.6. Statistical Analysis
The differences between the genotypic diversity and dmft/caries experience were evaluated by test and the Spearman’s coefficient of correlation. Statistical significance was considered to be at . The Software Statistical Package for Social Science, v. 11.5 (SSPS, Chicago, IL, USA) was used for the data analysis.
A total of 140 isolates of the preschool children with dental caries and 140 isolates of the caries-free preschool children were analyzed by AP-PCR, and 62 different amplitypes were identified. Figure 1 illustrates the AP-PCR patterns performed with OPA-02 and OPA-13, with each of these primers generating a different spectrum of amplicons, indicative of genetic polymorphism.
Characteristics of the children with colonization of S. mutans are presented in Table 1. No significant correlation of S. mutans was found between genotypic diversity of S. mutans and gender. The Spearman correlation test showed a strong association between genotypic diversity and caries experience (). There were more S. mutans genotypes in the group of preschool children with dental caries, compared with the caries-free group. Among the children with more than 1 genotype, 13 had dental caries (2 to 5 genotypes) and 4 were caries-free (only 2 genotypes).
Considering the whole population, some of the preschool children harbored just one genotype whereas others exhibited until five genotypes (Figure 2).
The dental biofilm consists of a complex bacterial community, and the ability of specific strains of Streptococcus mutans to compete with other strains may be essential for colonization . Studies of S. mutans virulence factors and their correlation with other species are fundamental to understand the role played by colonization of different genotypes in the same individual .
The knowledge of genotypic diversity of S. mutans may help in the development of new treatment strategies for caries, so as to prevent disease and promote health in addition to standard prevention treatments .
Although the findings of Kreulen et al.  have demonstrated a negative relationship between caries activity and genotype diversity and the results of Lembo et al.  have shown no significant differences in the number of genotypes detected in caries-free and caries-active children, the findings of the present study showed a positive relationship between caries activity and the genetic diversity of S. mutans. The preschool children with dental caries have more genotypes than the caries-free children, which is consistent with earlier reports [17, 18, 28, 29]. The existence of several genotypes in the biofilm could merely be a consequence of favorable circumstances for S. mutans. Moreover, it is possible that the simultaneous action of different genotypes, with distinct virulence potential, further increases the risk of caries .
In studies with young adults, Emanuelsson et al.  found a maximum of seven genotypes in subjects who had previously experienced dental caries. Napimoga et al.  also found a maximum of eight genotypes in caries-active subjects using AP-PCR. However, it has been observed that children harbor only one to five distinct genotypes of S. mutans [3, 11, 15–17, 19, 30]. The results of this research are consistent with previous studies reported in children. It was observed that in the caries-free group, 10 preschool children had only one genotype. On the other hand, in the dental caries group, 13 children had more than one genotype. Of these 13, only 2 harbored five distinct genotypes. This may be attributed to heavy colonization and growth of multiple genotypes in the same oral cavity is likely to be consequences of frequent consumption of fermentable carbohydrates . Different clonal types of S. mutans detected within the oral cavity of one subject may exhibit different phenotypic and genetic properties . In addition, the high clonal diversity of S. mutans can result in colonization by clones with different virulence attributes .
Our results support the previous findings of genetic diversity of S. mutans in preschool children being associated with dental caries. The investigation of such populations may be important for directing the development of programs for caries prevention worldwide.
- S. Hamada and H. D. Slade, “Biology, immunology, and cariogenicity of Streptococcus mutans,” Microbiological Reviews, vol. 44, no. 2, pp. 331–384, 1980.
- W. J. Loesche, “Role of Streptococcus mutans in human dental decay,” Microbiological Reviews, vol. 50, no. 4, pp. 353–380, 1986.
- P. W. Caufield and T. M. Walker, “Genetic diversity within Streptococcus mutans evident from chromosomal DNA restriction fragment polymorphisms,” Journal of Clinical Microbiology, vol. 27, no. 2, pp. 274–278, 1989.
- R. A. Burne, “Oral streptococci. . . products of their environment,” Journal of Dental Research, vol. 77, no. 3, pp. 445–452, 1998.
- R. J. Berkowitz and H. V. Jordan, “Similarity of bacteriocins of Streptococcus mutans from mother and infant,” Archives of Oral Biology, vol. 20, no. 11, pp. 725–730, 1975.
- L. Granath, P. Cleaton-Jones, L. P. Fatti, and E. S. Grossman, “Prevalence of dental caries in 4- to 5-year-old children partly explained by presence of salivary mutans streptococci,” Journal of Clinical Microbiology, vol. 31, no. 1, pp. 66–70, 1993.
- P. Carlsson, B. Olsson, and D. Bratthall, “The relationship between the bacterium Streptococcus mutans in the saliva and dental caries in children in Mozambique,” Archives of Oral Biology, vol. 30, no. 3, pp. 265–268, 1985.
- M. I. Matee, F. H. Mikx, J. S. de Soet, S. Y. Maselle, J. de Graaff, and W. H. van Palenstein Helderman, “Mutans streptococci in caries-active and caries-free infants in Tanzania,” Oral Microbiology and Immunology, vol. 8, no. 5, pp. 322–324, 1993.
- C. G. Emilson, P. Carlsson, and D. Bratthall, “Strains of mutans streptococci isolated in a population with extremely low caries prevalence are cariogenic in the hamster model,” Oral Microbiology and Immunology, vol. 2, no. 4, pp. 183–186, 1987.
- G. H. Bowden, “Does assessment of microbial composition of plaque/saliva allow for diagnosis of disease activity of individuals?” Community Dentistry and Oral Epidemiology, vol. 25, no. 1, pp. 76–81, 1997.
- G. V. Kulkarni, K. H. Chan, and H. J. Sandham, “An investigation into the use of restriction endonuclease analysis for the study of transmission of mutans streptococci,” Journal of Dental Research, vol. 68, no. 7, pp. 1155–1161, 1989.
- Y. Li and P. W. Caufield, “The fidelity of initial acquisition of mutans streptococci by infants from their mothers,” Journal of Dental Research, vol. 74, no. 2, pp. 681–685, 1995.
- M. Saarela, J. Hannula, J. Mattö, S. Asikainen, and S. Alaluusua, “Typing of mutans streptococci by arbitrarily primed polymerase chain reaction,” Archives of Oral Biology, vol. 41, no. 8-9, pp. 821–826, 1996.
- Y. Li and P. W. Caufield, “Arbitrarily primed polymerase chain reaction fingerprinting for the genotypic identification of mutans streptococci from humans,” Oral Microbiology and Immunology, vol. 13, no. 1, pp. 17–22, 1998.
- L. Grönroos and S. Alaluusua, “Site-specific oral colonization of mutans streptococci detected by arbitrarily primed PCR fingerprinting,” Caries Research, vol. 34, no. 6, pp. 474–480, 2000.
- R. O. Mattos-Graner, Y. Li, P. W. Caufield, M. Duncan, and D. J. Smith, “Genotypic diversity of mutans streptococci in Brazilian nursery children suggests horizontal transmission,” Journal of Clinical Microbiology, vol. 39, no. 6, pp. 2313–2316, 2001.
- S. Alaluusua, J. Mättö, L. Grönroos, et al., “Oral colonization by more than one clonal type of mutans streptococcus in children with nursing-bottle dental caries,” Archives of Oral Biology, vol. 41, no. 2, pp. 167–173, 1996.
- M. H. Napimoga, R. U. Kamiya, R. T. Rosa, et al., “Genotypic diversity and virulence traits of Streptococcus mutans in caries-free and caries-active individuals,” Journal of Medical Microbiology, vol. 53, no. 7, pp. 697–703, 2004.
- C. M. Kreulen, H. J. de Soet, R. Hogeveen, and J. S. Veerkamp, “Streptococcus mutans in children using nursing bottles,” Journal of Dentistry for Children, vol. 64, no. 3, pp. 107–111, 1997.
- World Health Organization, Oral Health Surveys—Basic Methods, WHO, Geneva, Switzerland, 4th edition, 1997.
- B. Kohler and D. Bratthall, “Practical method to facilitate estimation of Streptococcus mutans levels in saliva,” Journal of Clinical Microbiology, vol. 9, no. 5, pp. 584–588, 1979.
- J. Welsh and M. McClelland, “Fingerprinting genomes using PCR with arbitrary primers,” Nucleic Acids Research, vol. 18, no. 24, pp. 7213–7218, 1990.
- T. Oho, Y. Yamashita, Y. Shimazaki, M. Kushiyama, and T. Koga, “Simple and rapid detection of Streptococcus mutans and Streptococcus sobrinus in human saliva by polymerase chain reaction,” Oral Microbiology and Immunology, vol. 15, no. 4, pp. 258–262, 2000.
- S. C. Mitchell, J. D. Ruby, S. Moser, et al., “Maternal transmission of mutans streptococci in severe-early childhood caries,” Pediatric Dentistry, vol. 31, no. 3, pp. 193–201, 2009.
- R. U. Kamiya, M. H. Napimoga, J. F. Höfling, and R. B. Gonçalves, “Frequency of four different mutacin genes in Streptococcus mutans genotypes isolated from caries-free and caries-active individuals,” Journal of Medical Microbiology, vol. 54, no. 6, pp. 599–604, 2005.
- M. H. Napimoga, J. F. Höfling, M. I. Klein, R. U. Kamiya, and R. B. Gonçalves, “Tansmission, diversity and virulence factors of Sreptococcus mutans genotypes,” Journal of Oral Science, vol. 47, no. 2, pp. 59–64, 2005.
- F. L. Lembo, P. L. Longo, C. Ota-Tsuzuki, C. R. M. D. Rodrigues, and M. P. A. Mayer, “Genotypic and phenotypic analysis of Streptococcus mutans from different oral cavity sites of caries-free and caries-active children,” Oral Microbiology and Immunology, vol. 22, no. 5, pp. 313–319, 2007.
- H. Hirose, K. Hirose, E. Isogai, H. Miura, and I. Ueda, “Close association between Streptococcus sobrinus in the saliva of young children and smooth-surface caries increment,” Caries Research, vol. 27, no. 4, pp. 292–297, 1993.
- I.-M. Emanuelsson, P. Carlsson, K. Hamberg, and D. Bratthall, “Tracing genotypes of mutans streptococci on tooth sites by random amplified polymorphic DNA (RAPD) analysis,” Oral Microbiology and Immunology, vol. 18, no. 1, pp. 24–29, 2003.
- M. I. Klein, F. M. Florio, A. C. Pereira, J. F. Höfling, and R. B. Gonçalves, “Longitudinal study of transmission, diversity and stability of Streptococcus mutans and Streptococcus sobrinus genotypes in Brazilian nursery children,” Journal of Clinical Microbiology, vol. 42, no. 10, pp. 4620–4626, 2004.
- L. H. Guo, J. N. Shi, Y. Zhang, X. D. Liu, J. Duan, and S. Wei, “Identification of genetic differences between two clinical isolates of Streptococcus mutans by suppression subtractive hyridization,” Oral Microbiology and Immunology, vol. 21, no. 6, pp. 372–380, 2006.
- P. W. Caufield, “Dental caries—a transmissible and infectious disease revisited: a position paper,” Pediatric Dentistry, vol. 19, no. 8, pp. 491–498, 1997.