Candida albicans enriched in orthodontic derived white spot lesions and shaped focal supragingival bacteriome.

White spot lesions (WSLs) are common enamel infectious diseases in fixed orthodontic treatment, which might attribute to the dysbiosis of oral microbiome. However, the correlation of Candida albicans with oral bacteriome in WSLs still remains unrevealed. This study investigated the carriage of C. albicans and how it shaped the bacterial community in disease or healthy supragingival plaque, to explore the potential role of interkingdom interaction in orthodontic WSLs. In this study, 31 patients with WSLs (WSLs) and 23 healthy patients (Health) undergoing fixed orthodontic treatment were enrolled. The supragingival microbiota in both groups were determined using 16S rRNA gene sequencing. Colonization and abundance of C. albicans in the plaque were determined via culture-dependent and -independent methods. Among WSLs patients, the correlation of C. albicans and bacteriome was analyzed under QIIME2-based bioinformatics and Spearman's correlation coefficient. The raw reads were deposited into the NCBI Sequence Read Archive (SRA) database (Accession Number: SRP404186). Significant differences in microbial diversity as well as composition were observed between WSLs and Health groups. Leptotrichia remarkably enriched in the WSLs group, while Neisseria and Cardiobacterium significantly enriched in the Health group. In addition, 45% of WSLs patients were C. albicans carriers but none in patients without WSLs. Among all WSLs patients, beta diversity and microbial composition were distinguished between C. albicans carriers and non-carriers. In C. albicans carriers, Corynebacterium matruchotii and Streptococcus mutans significantly enriched whereas Saccharibacteria_TM7_G-1 significantly depleted. The abundance of C. albicans was positively associated with bacteria such as Streptococcus mutans, while the negative correlation was detected between C. albicans and several bacteria such as Cardiobacterium hominis and Streptococcus sanguinis. Our study elucidated the distinguished supragingival plaque microbiome between orthodontic patients with and without WSLs. C. albicans frequently existed and enriched in orthodontic derived WSLs. The carriage of C. albicans shape plaque bacterial community in demineralized lesions and might play roles in WSLs pathogenesis.

Changes in mechanical properties, surface morphology, structure, and composition of Invisalign material in the oral environment.

INTRODUCTION: The mechanical properties of Invisalign material have rarely been explored because of the inaccessibility of the patent-protected raw material. The purpose of this study was to systematically evaluate the Invisalign thermoformed aligner material before and after clinical application, including mechanical properties, surface morphology, internal structure, and chemical composition changes. METHODS: Twenty sets of "as-received" (0-week) and retrieved (2-week; worn for 2 weeks, 20 ± 2 hours per day) Invisalign aligners were randomly collected from 4 different patients. Tensile tests, stress relaxation, and creep tests were carried out with a dynamic mechanical analyzer to characterize the changes in the mechanical properties of this material, Fourier transform infrared spectroscopy was used to capture the molecular changes on the surface of these aligners, scanning electron microscopy and transmission electron microscopy were used to observe the changes in surface morphology and internal structure, and scanning transmission electron microscopy-energy dispersive x-ray analysis was used to detect any changes in the chemical composition of this material before and after clinical application. RESULTS: The elastic modulus of 0-week and 2-week samples were 842 ± 63 MPa and 806 ± 19 MPa, respectively, with no significant difference. In addition, the relative stress after stress relaxation of 2 hours was 19.89 ± 2.25% and 15.91 ± 6.04% for 0-week and 2-week groups, respectively, with no significant difference. Scanning electron microscopy observations showed voids and signs of delamination on the surface of the 2-week samples, and scanning transmission electron microscopy-energy dispersive x-ray analysis indicated the possible release of trace elements during clinical use, such as aluminum. Results of Fourier transform infrared spectroscopy analysis, and transmission electron microscopy observations were quite stable, indicating that the molecular structure on the surface and the internal structure of this material were relatively stable under the oral environment. CONCLUSIONS: The surface morphology showed some defects after the clinical use of 2 weeks; however, there was no significant difference in mechanical properties. Trace elements may release out during clinical use and may pose a specific danger to allergic patients.

Dynamic stress relaxation of orthodontic thermoplastic materials in a simulated oral environment.

Mechanical properties are crucial for screening orthodontic thermoplastic materials for invisible aligners. However, most of previous studies were carried out within laboratory conditions which limit our understanding of the mechanical behaviors of aligners within oral environment. In this study, we studied the dynamic stress relaxation of thermoplastic materials by combination of Bose ElectroForce and a homemade temperature-controlled water bath. The 3-h stress relaxation curves of five orthodontic thermoplastic materials were measured within 37°C water bath as well as comparatively in ambient atmospheric environment (~20°C). The percentage residual stress at 0, 30, 60, 90, 120, 150, and 180 min was selected for statistical analyses. As expected, the experimental results showed that the residual stress within all five materials decreased with time, and that this process was significantly accelerated in the 37°C water bath (p<0.05). Compared with other materials, Erkodur and Masel exhibited slower relaxing rates in the 37°C water bath (p<0.05).

Note: Axially pull-up electrochemical etching method for fabricating tungsten nanoprobes with controllable aspect ratio.

A mathematical model representing the relation between pulling up speed, time and aspect ratio is reported, accordingly the axially pull-up electrochemical etching method for fabricating nanoprobes is proposed. The tungsten probes with predetermined shape and aspect ratio according to the model were successfully produced with this method. Then the probes were installed inside a micromanipulation system to manipulate the carbon nanotubes and measure their current-voltage (I-V) characteristics. The probe fabrication and application experiments demonstrated the reasonability and reliability of the model and method developed in this note.

[A comparative study of mechanical properties of commercialized dental thermoplastic materials].

OBJECTIVE: To compare the mechanical properties of different dental optimal material selection for orthodontic appliance. METHODS: Four commercialized thermoplastic products under different test conditions, and provide the suggestion of thermoplastic products were tested. The tear strength, elongation at break and stress relaxation of these materials were measured under different test conditions. RESULTS: The tear strength declined after thermoforming, and rose again after 2 weeks of distilled water immersion. The elongation at break rose after thermoforming, and declined after 2 weeks of distilled water immersion. No significant changes were observed for brand A under different test conditions. Brand A showed the slowest stress relaxation of 0.0148 N/s. CONCLUSIONS: The mechanical properties of thermoplastic materials were influenced by environmental factors. Brand A exhibited optimal comprehensive properties.

FGF-2 acts through an ERK1/2 intracellular pathway to affect osteoblast differentiation.

An abundance of genetic and experimental data have suggested that fibroblast growth factor (FGF) signaling plays a central role in physiological and pathological cranial suture fusion. Although alterations in the differentiation and proliferation of sutural osteoblasts may be a key mediator of this process, the mechanisms by which FGF signaling regulates osteoblast differentiation remain incompletely understood. In the current study, the authors show that recombinant human FGF-2 alters osteoblastic expression of bone morphogenetic protein-2 and Msx-2 in vitro to favor cellular differentiation and osteoinduction. The ERK1/2 intracellular signaling cascade was shown to be necessary for recombinant human FGF-2-mediated bone morphogenetic protein-2 transcriptional changes. Furthermore, the cellular production of an intermediate transcriptional modifier was found to be necessary for the recombinant human FGF-2-mediated gene expression changes in bone morphogenetic protein-2 and Msx-2. Together, these findings offer new insight into the mechanisms by which FGF-2 modulates osteoblast biology.