Keywords clear aligners - copper–calcium–hydroxide - orthodontic therapy - microbial plaque
Introduction
Notoriously, the conventional orthodontic treatment with stainless appliances[1 ] is related to reduce patient's ability to maintain oral hygiene increasing the risk
of periodontal disease via accumulation of microbial plaque.[2 ]
[3 ]
[4 ] Plaque-embedded microorganisms activate several genes involved in virulence factors[5 ]
[6 ] reducing susceptibility to detergents or antibiotics as well as to host-mediated
immune defenses.[7 ]
[8 ]
[9 ]
[10 ]
Recently, clear aligners use in dentistry allows the gradual move of teeth into an
ideal position (computerized technology), minimizing microbial risk,[11 ]
[12 ] dental trauma, and apical resorptions.[4 ] The orthodontic protocol includes 20/24 hours aligners use, removal during meals
or sugar containing drinking beverages, followed by tooth and device brushing before
re-wearing.[11 ]
[12 ] A helpful method to visualize microbial and device-associated plaque is through
the use of disclosing agents, which stain microbial pellicle.[13 ]
[14 ]
Cupral (a copper–calcium–hydroxide based compound) is a dental paste clinically used
in periodontal infections, being endowed with antimicrobial activity.[15 ]
[16 ] Moreover, recent clinical experience demonstrates that Cupral efficiently counteracts
endodontic infections.[17 ]
[18 ] Yet, its mechanisms of action have not been investigated; neither data exist on
Cupral use in other dentistry fields.
The purpose of this pilot study was to investigate the ability of Cupral to remove
microbial plaque, naturally produced onto orthodontic aligners. Briefly, clear aligners,
regularly used by a healthy volunteer undergoing standard orthodontic therapy, were
exposed or not to Cupral and assessed for total and residual microbial population,
by quali-quantitative analysis.
Case Report
A healthy volunteer (female, 32-year old) undergoing orthodontic treatment for 12 months
with thermoplastic clear aligners was enrolled. She started treatment on December
2017 using the Nuvola (Rome, Italy) system, that included 8 months of active treatment
(replacing the aligners every 2 weeks) and 4 months of stabilization period (replacing
the aligners every 2 months), the latter known as limited retention before the fixed
retention applied from the clinical orthodontist. The volunteer was informed about
the nature of the study, performed on individual basis, that did not directly involve
her as a patient, but only the used aligners at the time of their disposal. She was
asked to provide the upper and lower aligners pieces, on winter and summer months
of 2018. In particular, at the times when the aligners had to be replaced with new
pairs, the used ones were carefully removed from the mouth using sterile gloves and
inserted in a bottle with sterile physiological saline solution (200 mL); then, the
bottle was delivered to the Microbiology Laboratory for microbiological analysis.
Totally, six couples (upper and lower) of 2-weeks-used aligners were provided, focusing
on winter and summer months (January–March and June–August).
Cupral
We used a commercially available compound (HUMANCHEMIE GmbH; Alfeld, Germany), containing
highly dispersed calcium and copper hydroxide. A starting solution of Cupral was prepared
by diluting 1 g of compound in 4 mL of distilled water (weight/volume 25%) sterilized
by autoclave, and stored at 4°C prior to be used in the study. Operationally, Cupral’s
solution was diluted in culture medium or microbial cultures up to the final working
conditions (1.25%).
Confocal Microscopy on Cupral-Treated and Untreated Aligners
The aligners were washed with phosphate-buffered saline (PBS) at room temperature
and then treated for 30 to 60 seconds with plaque disclosing tablets (MGS GAP Research
Co, Ltd, Northfleet, Kent, United Kingdom) containing erythrosine red, to stain microbial
plaque. Then, the aligners were further washed and brushed using running water, to
mimic the daily hygiene practice. After this step, the upper and lower aligner were
split in two equal pieces (right and left), transferred in two different bottles and
processed in parallel; the right half upper and lower aligners were maintained in
saline buffer (control group), while the left half upper and lower aligners were treated
with Cupral 1.25% (treated group), the procedure was done for 1 hour at room temperature.
Finally, all the pieces were brushed again, processed using standard procedures and
analyzed by transmitted illumination confocal microscopy (Nikon LV 150 Confovis Microscope,
Japan).
Microbiological Analysis on Clear Aligners Exposed or Not to Cupral
The procedure is detailed in [Fig. 1 ]. The clear aligners were split in two equal parts and inserted in two sterile bottles,
one containing saline buffer and the other Cupral 1.25%. After an hour at room temperature,
both bottles were sonicated at 3500HZ for 15 minutes to disaggregate microbial plaque.
Then, the suspension was seeded uniformly onto two series of tryptic soy agar (TSA;
Oxoid,Milan, Italy) and Sabouraud (SAB) plates (100 μL/plate in triplicates), to assess
total bacterial and fungal load, by colony-forming unit (CFU) assay. Two sets of TSA
and SAB plates were prepared to assess microbial growth in aerobiosis and anaerobiosis
conditions. Following 24 hours of incubation at 37°C, the number of colonies/plate
were counted and the results were expressed as mean of CFUx107 /aligner.
Fig. 1 Flowchart of the microbiological analysis performed on clear aligners. Two-weeks-used
clear aligners (upper and lower) were split in two equal parts. A part was maintained
in saline buffer (A ), while the other was exposed to Cupral 1.25% (B ); both groups were incubated for 1 hour and sonicated for 15 minutes. The supernatants
were harvested, diluted, and plated on TSA and SAB plates; each set of plates was
incubated, under aerobiosis or anaerobiosis conditions, for 24 hours. Total and residual
microbial loads were evaluated by colony-forming unit analysis; each group was tested
in triplicate plates.
According to macroscopic aspect, namely color, morphology and size, the colonies were
clustered and counted. Then, to identify the isolates, representative colonies from
each typology were subcultured in Columbia agar plates (OXOID; Milan, Italy); the
growing colonies were then Gram stained, observed by optical microscope and identified
by matrix-assisted laser desorption ionization-time of flight mass spectrometry (MALDI-TOF
MS, Biomerieux, France).
Optical Microscopy of the Isolated Colonies
Representative colonies, isolated after 24 hours incubation in TSA or SAB, were observed
and photographed by inverted light microscope (Nikon Eclipse TS 100, Japan).
Results
Cupral Effects on Microbial Plaque Produced onto Clear Aligners: Confocal Analysis
To investigate the structure of biofilm produced on the aligners, we performed a topographic
analysis (three-dimensional [3D] mapping) by transmitted-illumination confocal microscopy,
before and after Cupral treatment. [Figure 2 ] (upper panel) shows the overall architecture of biofilm on untreated aligner; microbial
plaque and polysaccharide matrix were easily detectable (A). To evaluate biofilm thickness,
a 3D reconstruction of biofilm structure was obtained from the same capture, by means
of a mathematical linearization of the sample (B ); according to the chromatic scale (C ), the plaque thickness in the untreated device varied from 4.5 to 8 µm, as indicated
by the yellow, red, and white colors. The lower panel shows an image from Cupral-treated
aligner (1 hour with 1.25%); only a scant 3D structure with minimal polysaccharide
matrix was detected on the surface of the device (A ). Furthermore, the 3D reconstruction (B ) indicated the predominance of peaks chromatically quite uniform (mostly green and
yellow colors), indicating a reduced thickness that, based on the reference scale
(C ), was around 1 to 1.5 μm, in several areas.
Fig. 2 Confocal microscopy of microbial plaque on orthodontic clear aligner. The upper panel shows a representative image of the untreated clear aligner; an abundant microbial
biofilm is observed (A ), as confirmed by the three-dimensional (3D) reconstruction of the same capture (B ), according to the thickness scale (C ). The lower panel shows a representative image of the Cupral-treated aligner; the device surface with
minimal residual cells is observed (A ), as confirmed by the 3D reconstruction of the same capture (B ), according to the thickness scale (C ).
Cupral Effects on Clear Aligners-Associated Microbial Load: CFU Evaluation and MALDI-TOF
Identification
Microbial load was quantified in clear aligners, used for 2 weeks, during winter [Fig. 3 ] and summer months [Fig. 4 ]. In particular, [Figure 3A ] indicates the total (untreated aligners) and residual (Cupral treated aligners)
microbial load, using TSA and SAB medium in aerobiosis and anaerobiosis conditions.
The colonies obtained in TSA ranged around 200 to 400 CFUx107 /aligner in both conditions. In contrast, no microbial growth was detected in SAB
plates in aerobiosis condition, while only few colonies were counted in anaerobiosis
condition. Following Cupral treatment, no residual microbial load was ever observed,
at any of the conditions tested. [Figure 3B ] depicts the isolated species, expressed in percent with respect to the total number
of colonies. While no growth occurred in SAB under aerobiosis conditions, few colonies
were detected in anaerobiosis and were identified as Rothia aeria and Streptococcus sanguinis . As detailed in [Fig. 3B ], Streptococcus mitis/oralis was the most common isolated species in TSA, both under aerobiosis and anaerobiosis
conditions (71% and 63%, respectively).
Fig. 3 TSA Total and residual microbial load detected on winter months. The clear aligners
were exposed or not to Cupral 1.25%. The colonies isolated after incubation in TSA
or SAB medium were counted and clustered. The upper table shows the total and residual
microbial load expressed as colony-forming units/aligners. The values represent the
mean of three independent analyses, where each sample had been assessed in triplicate.
The standard errors, less than 10%, are omitted. The lower pie graphs represent the
percent of species detected in aerobiosis and anaerobiosis conditions. n.d.: not detected.
Fig. 4 Total and residual microbial load detected on summer months. The clear aligners were
exposed or not to Cupral 1.25%. The colonies isolated after incubation in SAB medium
were counted and clustered. The upper table shows the total and residual microbial
load expressed as colony-forming units/aligners. The values represent the mean of
three independent analyses, where each sample had been assessed in triplicate. The
standard errors, less than 10%, are omitted. The lower pie graphs represent the percent
of species detected in aerobiosis and anaerobiosis conditions. n.d.: not detected.
[Figure 4A ] shows the data obtained analyzing the aligners during summer times. The CFU/aligner
in TSA ranged around 160 to 210 CFU x 107 /aligner, while in SAB, the CFU values varied from 1.5 to 23 CFU x 107 /aligner, in both conditions. Also, in this case, following Cupral treatment, no residual
microbial load was ever observed, at any of the conditions tested. [Figure 4B ] displays the isolated species, expressed in percent, with respect to the total number
of colonies. Here, once again Streptococcus mitis/oralis was found as the most abundant isolated species (96% of colonies in TSA aerobiosis
and 84% in TSA anaerobiosis, 99% in SAB aerobiosis and 100% in SAB anaerobiosis).
According to morphology, color and size, the isolated species were clustered in six
different types of colonies, as depicted in [Fig. 5 ]. In particular, the colonies grown on aligners used during winter months included
Gram-negative coccobacilli and diplococci, Gram-positive cocci and streptococci. On
aligners used during summer months, we observed a similar trend with the most representative
isolates being Gram-positive streptococci. By MALDI-TOF analysis, they were identified
as H. parainfluenzae , N. mucosa/sicca , S. aureus , S. mitis/oralis , S. sanguinis , and R. aeria .
Fig. 5 Morphological peculiarities of the isolated colonies observed by inverted light microscope.
Images (10x magnification) of the most representative colonies in TSA or SAB medium:
(A ) translucent white, coccobacilli Gram- (Haemophilus parainfluenzae ); (B ) wrinkled large yellow, diplococci Gram- (Neisseria mucosa/sicca ); (C ) large white, cocci Gram+ (Staphylococcus aureus ); (D ) small white, streptococci Gram+ (Streptococcus mitis/oralis ); (E ) irregular margins, streptococci Gram+ (Streptococcus sanguinis ); (F ) large beige, cocci Gram+ (Rothia aeria ).
Discussion
Here, we show that clear aligners, regularly worn for ~2 weeks by a healthy subject,
are abundantly contaminated by different bacterial species, with total microbial load
ranging around 109 per device. As predictable, microbial biofilm is naturally produced onto clear aligners;
despite daily washing and brushing, the presence of microbial plaque is easily detectable
by staining with plaque disclosing tablets (data not shown). According to culture-dependent
analysis, Gram staining/morphology, and MALDI-TOF identification of the isolates,
several bacterial species have been obtained, including Haemophilus parainfluenzae, N. mucosa/sicca, S. aureus, S. mitis/oralis , S. sanguinis , and R. aeria . In contrast, no cultivable fungal isolates have been detected, although SAB has
been used as a fungi-preferential medium. Unexpectedly, under anaerobic conditions,
SAB returns colonies belonging to the Streptococcus genus; likely, as facultative anaerobic species, streptococci easily grow in such
conditions, because of the large amount of dextrose present in such medium, as an
important element for their cellular metabolism.
It is well known that in orthodontic treatment, not only the active period but also
the retention time is important because the extended periodontium must be stabilized.[19 ] In our study, irrespective of the season time, Streptococcus mitis/oralis happens to be the most representative species on aligners. These findings are in
line with an extensive literature[20 ]
[21 ] describing such species as commonly found in oral cavity, among the early colonizers
of mucosa and dental surfaces.
In our hands, slight winter–summer variations occur. In particular, about one log
reduction is observed in terms of total microbial load/aligner, when using TSA in
aerobiosis conditions during summer months in comparison with winter months. Nevertheless,
it is worth noting that S. aureus , H. parainfluenzae, and N. mucosa/sicca are vice-versa more abundant on January–March sampling (108 CFU and 107 CFU/aligners on winter and summer season, respectively). This result may be explained
considering that such microorganisms are, indeed, easily found in the upper respiratory
tract (including oral cavity) during winter season. When considering summer season,
S. mitis/oralis represents the most detectable microbial species within the device-associated bacterial
plaque. Overall, the relative homogeneity in terms of microbial population observed
during the 1-year analysis argues on a good and regular hygiene of the oral cavity
and excludes a major impact of seasonal climate on aligners colonization.
Recently, we provided in vitro evidence on the efficacy of Cupral as antimicrobial
compound, being effective both against planktonic and biofilm communities.[16 ] Moreover, clinical evidence exists on the successful treatment of periodontal disease
patients by Cupral.[17 ]
[18 ] Here, we show that Cupral can be successfully employed to perform aligners hygiene;
microbial contamination is totally removed, even when Cupral is diluted up to 1.25%.
As shown by CFU assay, no residual viable cells have ever been detectable upon Cupral
treatment of the aligners. Moreover, confocal data document the abundant presence
of a biofilm on aligner’s surface, where microbial cells aggregate in a tridimensional
architecture of irregular peaks. Interestingly, Cupral profoundly affects such biofilm;
the 3D construction indicates residual material, related to debris and dead cells
according to the fact that no growth has ever been obtained by the CFU assay. It is
well known that not only oral hygiene but also the chemical composition of the aligners
plays an important role in conditioning microbial adhesion on the devices and, in
turn, persistence in the oral cavity; indeed, microcracks, abraded areas, and localized
hard deposits are often visible, likely facilitating microbial establishment and long-term
maintenance.[22 ] To our knowledge, this is the first evidence describing a novel usage of Cupral,
as a promising tool capable of eliminating aligner-associated microbial contamination.
Such present data encourage clinical studies to establish whether the regular use
of Cupral for clear aligners disinfection may allow amelioration of gingival health
and integrity during orthodontic treatment.
Conclusion
Cupral, a copper–calcium–hydroxide-based compound, exerts potent effects against microbial
plaque, naturally occurring on clear aligners; tridimensional biofilm structure appears
profoundly affected as well as no bacterial growth ever occurs following exposure
to Cupral. While expanding the knowledge on Cupral antimicrobial activity, our data
open to its use as a novel tool for clear aligners daily hygiene.
