Oral microbiota carriage in patients with multibracket appliance in relation to the quality of oral hygiene

Ethical approval was granted by the ethical committee of the medical faculty of the Justus-Liebig-University of Giessen, Germany (No. 95/08).

Patients were selected from the Department of Orthodontics at Justus-Liebig-University Giessen, Germany. In general, after placement of a MB appliance, all patients of the department received the same standardized oral care instructions regarding frequency, technique, and duration of daily tooth brushing with fluoridated toothpaste, use of interdental brushes, and additional weekly fluoride gel application.

The inclusion criteria comprised patients aged 11 years or older without craniofacial anomalies, general diseases, or drug intake undergoing active MB appliance treatment in both jaws for at least three months. All selected patients were prospectively monitored for the quality of their oral hygiene at three consecutive regular appointments.

Dental plaque at selected index teeth (13, 21, 24, 33, 41, and 44) was visually inspected, and oral hygiene was categorized as follows:

Patients with consistent scorings of GOH or POH with/without WSL formation for three consecutive appointments were considered for possible inclusion in the present study. Patients with AOH were excluded. Written informed consent was obtained from the patients and their parents. For each group (GOH, POH, and POH/WSL), the first 25 patients fulfilling the abovementioned criteria were included.

The study appointment occurred during the next regular control appointment. Patients were instructed to stop oral hygiene for 24 h before the appointment (tooth brushing/antibacterial oral rinsing) to ensure a sufficient amount of plaque for sampling even in patients with GOH.

The dental status was checked using a slight modification of the DMF-T-index [26]. The index was modified to assess orthodontic patients. Tooth agenesis, extractions caused by orthodontic treatment plan, and impacted teeth were not scored as missing teeth.

The plaque samples were obtained by sterilized swabs (Nerbe plus, Winsen/Luhe, Germany) from the enamel surfaces along the gingival margin of the index teeth. In all patients of the POH/WSL group, a second plaque sample was obtained from the affected WSL surface regions with a probe tip and then applied on a second swab.

Saliva secretion was stimulated by chewing a paraffin wax pellet over a period of 5 min. The entire amount of saliva produced during that period was collected in a single-use plastic cup. From this sample, 2 ml of saliva was extracted using a sterile syringe (B. Braun, Melsungen, Germany) and used for further analysis.

Candida counts were identified with Sabouraud agar (Merck, Darmstadt, Germany) for the saliva samples. Depending on the number of colony forming units (CFU) per milliliter of saliva, counts were categorized into 0 (none), 1 (isolated, <10 CFU/ml), 2 (moderate, 10–10² CFU/ml), 3 (many, 10²–10³ CFU/ml), and 4 (massive, >10³ CFU/ml). Candida species were differentiated by an Auxacolor™ 2-Test (Bio-Rad, Marnes-la-Coquette, France). Furthermore, the amounts of S. mutans and Lactobacilli were counted using the CRT® bacteria test (Ivoclar Vivadent, Schaan, Liechtenstein). The number of CFU per milliliter of saliva was categorized as 0 (none), 1 (moderate, <10⁵ CFU/ml), and 2 (many, ≥10⁵ CFU/ml). For plaque samples, the test manufacturers recommended classifying the occurrence of S. mutans, Lactobacilli, and Candida in terms of a binary (yes/no) decision only, because the plaque samples have no defined volume.

Statistical analysis was performed by IBM SPSS Statistics 22 (IBM Company, Chicago, IL, USA). Descriptive data analysis was conducted by exploring means, standard deviations, minima, and maxima. The data were not normally distributed, and the differences between groups were assessed using the Chi-square and Mann–Whitney U tests.

The general descriptive characteristics of the final patient sample are given in Table 1. The mean age of the total sample was 14.4 ± 1.5 years and did not differ significantly among the three oral hygiene groups. The gender distribution was nearly equal in the total sample and in the POH/WSL group. Female predominance was found in the GOH group, whereas male predominance was noted in the POH group. The DMF-T-index was generally very low (mean range: 0–0.1) and did not differ among the oral hygiene groups.

Analysis of the saliva samples revealed that 73.4 % of the patient sample were Candida carriers. About half of the carrier samples (49.4 %, n = 37) showed isolated to moderate numbers of CFU, whereas 24 % (n = 18) presented many to massive CFU. CFU of Candida spp. were significantly lower in the GOH group than in the POH group (p = 0.045) and POH/WSL group (p = 0.011) (Fig. 1). Saliva samples of Candida carriers (n = 54) showed C. albicans in 83.3 % (n = 45), C. dubliniensis in 14.8 % (n = 8), and C. albicans II in 1.9 % (n = 1). No significant difference in the distribution of species was found among the different oral hygiene groups.

S. mutans and Lactobacilli were detected in the saliva samples of all patients. Patients with POH irrespective of WSL formation presented higher counts of S. mutans, but the difference was not statistically significant (Fig. 2). High Lactobacilli CFU were noted in 52 % of patients in the GOH group. A comparable amount of CFU was found in 60 % and 84 % of patients in the POH group and POH/WSL group, respectively. This difference was statistically significant (p = 0.047; Fig. 3). For the saliva samples, the null hypothesis regarding S. mutans was accepted but rejected in Candida and Lactobacilli.

Analysis of the plaque samples revealed a 60.9 % prevalence of Candida carriers in the total sample. In the POH/WSL patients, the plaque samples from the index teeth showed an insignificantly higher Candida prevalence (62.4 %). The second plaque samples from the affected white spot enamel regions exhibited only a slightly and insignificantly different prevalence of 64 %.

Among the Candida carriers (n = 46), 82.6 % (n = 38) of the carriers showed C. albicans, 15.2 % (n = 7) presented C. dubliniensis, and C. albicans II was found in 2.2 % (n = 1). As in the saliva samples, the distribution of Candida species revealed no statistically significant difference among the oral hygiene groups. Similar to the saliva samples, S. mutans was verified in the plaque samples of all patients, whereas Lactobacilli were found in 90.7 % (n = 68) of all plaque samples. For the plaque samples, the null hypothesis regarding all types of microbiota was accepted.

Counts of oral microbiota peak at about three months after insertion of a fixed appliance [3, 27‐30]. Although most studies [3, 28‐30] reported a slight decrease thereafter, Arslan et al. [27] found a consistent increase in Candida, S. mutans, and Lactobacilli counts up to 12 months of treatment. Despite the slight decrease reported by the other studies, patients showed consistently higher counts of oral microbiota compared with pre-treatment [28‐30]. In the present patient sample, the mean treatment duration at the study appointment ranged between 13.4 and 19.6 months with a significantly longer treatment time in the POH/WSL group, which was far longer than that in all other studies in the literature. For the POH/WSL group in the present study, the influence of oral microbiota or longer treatment duration on the development of WSL could not be clarified. However, given the cross-sectional design of the present study, the development of microbial counts in all the investigated groups during the treatment period remains unclear.

In the current literature, oral Candida carrier rates vary between 28.6 % and 57.2 %, depending on the age of the examined individuals and the microbiological sampling method [31‐36]. During orthodontic treatment, an even greater variation with prevalence rates between 8.3 % and 78.8 % was reported [1, 3, 27, 37]. The results of the present study corresponded to the top end of these data with Candida prevalence in dental plaque of 60.9 % and in saliva of 73.4 % of the patients.

Unfortunately, no standard currently exists for oral microbiological sampling. According to the literature, the most popular sampling methods are stimulated and unstimulated saliva samples, centrifuged saliva samples, swabs from oral mucosa, plaque samples, and imprint cultures from different sites in the oral cavity [20]. When comparing results achieved by different sampling methods and different culture media [38], centrifuged saliva samples and imprint cultures showed a significantly higher sensitivity in detecting oral yeasts [39] than cultures from the other sampling methods. In the current literature, studies with patient samples comparable with the present investigation [1, 3, 27, 37] used various sampling methods (Table 2). Hägg et al. [3] used three different sampling methods, and the method closest to the sampling collection in our study (pooled plaque) revealed a clearly lower Candida rate (22.2 %), in contrast to our study. Furthermore, 18.5 % of their patients became Candida carriers during treatment. In the present work, the incidence rates of Candida infection could not be revealed because of the cross-sectional design of the study.

In concordance with the present findings, the current literature on oral yeast carriage indicated C. albicans as the dominant species both in orthodontic-treated patients [3, 27, 37] and untreated individuals [31, 33]. In our sample, C. dubliniensis was the second most frequent species and one patient presented C. albicans II; the literature reported other additional Candida strains. Given that C. albicans and C. dubliniensis present pronounced morphological similarities and some common tests are unable to differentiate them reliably [16], C. dubliniensis was possibly undetected in other investigations.

In general, the current literature agreed that S. mutans and Lactobacilli are characteristic for deep carious lesions [14, 15, 40‐42] and therefore not for initial carious lesions such as WSL. Aas et al. [40] verified high concentrations of Actinomyces and non-S. mutans–Streptococci in initial lesions, but they additionally emphasized that bacterial profiles in initial lesions are more complex than in advanced destruction stages. Badet and Thebaud [41] revealed a strong correlation between the DMF-T-index and amount of Lactobacilli counts and furthermore showed that Lactobacilli are not isolated from initial carious lesions because of weak adherence potential; retentive niches for adherence are required by Lactobacilli. A fixed orthodontic appliance inevitably presents retentive niches, so whether the high Lactobacilli counts in the present study are associated with WSL development or simply caused by better possibilities for plaque accumulation remains unclear.

However, an in vivo study by Arneberg et al. [43] revealed higher bacterial counts for S. mutans and Lactobacilli at initial carious lesion surfaces compared with the unchanged control surfaces of neighboring teeth, suggesting the participation of these microorganisms even in initial enamel lesions.

The association of C. albicans with dental caries has been frequently investigated in patients with severe early childhood caries [17‐19, 44‐46]. Current in vitro and in vivo studies [12, 13] demonstrated a symbiosis between C. albicans and S. mutans in dental plaque, in which the two microbiota strains stick together because of extracellular polysaccharides. During the maturation of dental plaque, large microcolonies of S. mutans and C. albicans can be observed after 42 h [13]. Falsetta et al. [13] investigated the effect of S. mutans and C. albicans in rodents and showed that co-infected animals present significantly more severe carious lesions, whereas rodents infected with either S. mutans or C. albicans revealed initial carious lesions. In the present study, a statistically significant relationship between the quality of oral hygiene and Candida colonization could only be demonstrated for the saliva samples. Furthermore, the present patient sample showed high counts of S. mutans and Lactobacilli in POH or POH/WSL patients (significant for Lactobacilli in saliva only). In other words, all three microorganisms investigated in the present study influenced caries development, but the relative amount of their contribution and possible timing of their contribution remain unknown.

The first possible limiting factor of the present study is the lack of precise knowledge on the age and maturity of the dental plaque analyzed, because one cannot be sure that all patients followed the instructions to stop their oral hygiene for 24 h before the study appointment. Even if the patients followed this instruction, we are uncertain of the events that occurred during the previous days. Additionally, patients received no standardized information regarding eating or drinking between the appointments and before sample collection. Perhaps the comparability could have been improved slightly if all patients had a professional cleaning of their teeth, followed by the sampling appointment after a determined time period.

Furthermore, we cannot exclude the Hawthorne effect, because the knowledge about study participation and the special reminders about the study appointment given by the study team can evoke patient’s behavior modification [47]. Moreover, such knowledge and reminders possibly influenced oral hygiene and in turn the oral microbiota in the weeks before study sampling.

One could also question the categorization of the patients into the GOH and POH groups based on the subjective judgement of the treating orthodontists instead of an objective measurement. However, even with objective measurements, cut-off values for the groups have to be defined, which still provide ample space for large variations in the quality of oral hygiene. Nevertheless, a quantitative plaque assessment would have improved the comparability with the results of Hägg et al. [3] and Arslan et al. [27].

Given the present results, oral Candida counts and S. mutans or Lactobacilli counts showed no clear interrelation to the development of WSL. The current literature revealed that the abovementioned organisms participated in initial enamel caries formation. Further prospective longitudinal clinical trials concerning changes in oral microbiota during MB treatment are required to clarify the developmental process of WSL.

The investigated sample of patients showed a high carriage of oral Candida spp., S. mutans, and Lactobacilli. Patients with WSL formation during MB appliance treatment showed higher counts of Candida and Lactobacilli compared with patients with GOH. Independent of oral hygiene quality, S. mutans was detected in all patients.