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1.
International Journal of Oral Science ; (4): 10-10, 2019.
Article in English | WPRIM | ID: wpr-772273

ABSTRACT

The oral microbiota is associated with oral diseases and digestive systemic diseases. Nevertheless, the causal relationship between them has not been completely elucidated, and colonisation of the gut by oral bacteria is not clear due to the limitations of existing research models. The aim of this study was to develop a human oral microbiota-associated (HOMA) mouse model and to investigate the ecological invasion into the gut. By transplanting human saliva into germ-free (GF) mice, a HOMA mouse model was first constructed. 16S rRNA gene sequencing was used to reveal the biogeography of oral bacteria along the cephalocaudal axis of the digestive tract. In the HOMA mice, 84.78% of the detected genus-level taxa were specific to the donor. Principal component analysis (PCA) revealed that the donor oral microbiota clustered with those of the HOMA mice and were distinct from those of specific pathogen-free (SPF) mice. In HOMA mice, OTU counts decreased from the stomach and small intestine to the distal gut. The distal gut was dominated by Streptococcus, Veillonella, Haemophilus, Fusobacterium, Trichococcus and Actinomyces. HOMA mice and human microbiota-associated (HMA) mice along with the GF mice were then cohoused. Microbial communities of cohoused mice clustered together and were significantly separated from those of HOMA mice and HMA mice. The Source Tracker analysis and network analysis revealed more significant ecological invasion from oral bacteria in the small intestines, compared to the distal gut, of cohoused mice. In conclusion, a HOMA mouse model was successfully established. By overcoming the physical and microbial barrier, oral bacteria colonised the gut and profiled the gut microbiota, especially in the small intestine.


Subject(s)
Animals , Humans , Mice , Bacteria , Gastrointestinal Microbiome , Germ-Free Life , Microbiota , RNA, Ribosomal, 16S
2.
International Journal of Oral Science ; (4): 9-9, 2018.
Article in English | WPRIM | ID: wpr-772307

ABSTRACT

The hyphal development of Candida albicans (C. albicans) has been considered as an essential virulent factor for host cell damage. However, the missing link between hyphae and virulence of C. albicans is also been discovered. Here, we identified that the null mutants of ERG3 and ERG11, two key genes in ergosterol biosynthesis pathway, can form typical hyphae but failed to cause the oral mucosal infection in vitro and in vivo for the first time. In particular, the erg3Δ/Δ and erg11Δ/Δ strains co-cultured with epithelial cells significantly reduced the adhesion, damage, and cytokine (interleukin-1α (IL-1α)) production, whereas the invasion was not affected in vitro. Importantly, they were incapable of extensive hyphal invasion, formation of micro-abscesses, and tongue epithelium damage compared to wild type due to the decrease of the colonization and epithelial infection area in a murine oropharyngeal candidiasis model. The fluconazole (FLC), an antifungal targeted at ergosterol biosynthesis, relieved the epithelial infection of C. albicansin vitro and in vivo even under non-growth inhibitory dosage confirming the virulent contribution of ergosterol biosynthesis pathway. The erg3Δ/Δ and erg11Δ/Δ strains were cleared by macrophages similar to wild type, whereas their virulence factors including agglutinin-like sequence 1 (Als1), secreted aspartyl proteinase 6 (Sap6), and hyphal wall protein-1 (Hwp1) were significantly reduced indicated that the non-toxicity might not result from the change on immune tolerance but the defective virulence. The incapacity of erg3Δ/Δ and erg11Δ/Δ in epithelial infection highlights the contribution of ergosterol biosynthesis pathway to C. albicans pathogenesis and fluconazole can not only eliminate the fungal pathogens but also reduced their virulence even at low dosage.


Subject(s)
Animals , Mice , Antifungal Agents , Pharmacology , Candida albicans , Genetics , Virulence , Candidiasis, Oral , Drug Therapy , Genetics , Microbiology , Fluconazole , Pharmacology , Genes, Fungal , Genetics , Microscopy, Electron, Scanning , Potassium Channels , Genetics , Virulence
3.
Chinese Journal of Microbiology and Immunology ; (12): 790-795, 2018.
Article in Chinese | WPRIM | ID: wpr-711455

ABSTRACT

Microbes are closely associated with tumor development. The interactions between mi-crobes and immune system contribute to tumor progression and metastasis. This review focused on the inter-actions between microbes and immune cells (macrophages, T cells, myeloid-derived suppressor cells and other immune cells) in the course of tumor growth, and summarized the roles of microbes in tumor immuno-therapies, aiming to improve the overall understanding of the mechanisms for microbes affecting tumors, and provide ideas for tumor prevention and future immunotherapies.

4.
Chinese Journal of Stomatology ; (12): 114-118, 2016.
Article in Chinese | WPRIM | ID: wpr-259433

ABSTRACT

Tooth bleaching agents contain powerful oxidizing agents, which serve as the main part of bleaching agents because of its release of effective bleaching component. It has been a hot topic whether tooth bleaching agents exert negative influence on oral health. In order to provide train of thoughts and reference for further clinical researches and treatments, this review paper focuses on bleaching agents' effects on the growth of oral microbes and the formation of biofilms.


Subject(s)
Humans , Bacteria , Biofilms , Hydrogen Peroxide , Mouth , Microbiology , Oral Health , Oxidants , Pharmacology , Tooth Bleaching , Tooth Bleaching Agents , Pharmacology
5.
Journal of Southern Medical University ; (12): 1710-1714, 2015.
Article in Chinese | WPRIM | ID: wpr-232541

ABSTRACT

<p><b>OBJECTIVE</b>To establish a systematic method for isolation and identification of aerobic and facultative anaerobic bacteria in the oral cavity.</p><p><b>METHODS</b>Samples of the saliva, dental plaque and periapical granulation tissue were collected from 20 subjects with healthy oral condition and from 8 patients with different oral diseases. The bacteria in the samples were identified by morphological identification, VITEK automatic microorganism identification and 16s rRNA gene sequencing.</p><p><b>RESULTS</b>VITEK automatic microorganism identification and 16s rRNA gene sequencing showed an agreement rate of 22.39% in identifying the bacteria in the samples. We identified altogether 63 bacterial genus (175 species), among which Streptococcus, Actinomyces and Staphylococcus were the most common bacterial genus, and Streptococcus anginosus, Actinomyces oris, Streptococcus mutans and Streptococcus mitis were the most common species. Streptococcus anginosus was commonly found in patients with chronic periapical periodontitis. Streptococcus intermedius and Staphylococcus aureus were common in patients with radiation caries, and in patients with rampant caries, Streptococcus mutans was found at considerably higher rate than other species.</p><p><b>CONCLUSION</b>Aerobic and facultative anaerobic bacteria are commonly found in the oral cavity, and most of them are gram-positive. 16s rRNA gene sequencing is more accurate than VITEK automatic microorganism identification in identifying the bacteria.</p>


Subject(s)
Humans , Actinomyces , Dental Caries , Dental Plaque , Microbiology , Mouth , Microbiology , RNA, Ribosomal, 16S , Genetics , Saliva , Microbiology , Staphylococcus aureus , Streptococcus
6.
West China Journal of Stomatology ; (6): 182-185, 2014.
Article in Chinese | WPRIM | ID: wpr-315847

ABSTRACT

<p><b>OBJECTIVE</b>To analyze the differences between the oral microbiota of monozygotic and dizygotic twins by polymerase chain reaction-denaturing gradient gel electrophoresis (PCR-DGGE).</p><p><b>METHODS</b>A total of 20 pairs of twin children were included in this study, in which 10 pairs were monozygotic (MZ) twins, and 10 pairs were dizygotic (DZ) twins. Of the 20 pairs, 10 pairs of twins had primary dentition, and 10 pairs had mixed dentition; 17 children had caries, and 23 children had no caries. Genomic DNA was extracted from saliva samples. The 16s rRNA was amplified and analyzed by PCR-DGGE. The PCR-DGGE band number and Shannon index were calculated.</p><p><b>RESULTS</b>Cluster analysis showed high similarity in the oral bacterial community seen in co-twins. However, no significant difference was seen between MZ and DZ twins. In the primary dentition, the PCR-DGGE band number and Shannon index of children with caries (11.00 +/- 1.56, 1.05 +/- 0.36) were lower than those of children without caries (14.00 +/- 2.74, 1.44 +/- 0.37) (P < 0.05). In mixed dentition, the PCR-DGGE band number and Shannon index of children with caries (11.88 +/- 4.05, 1.18 +/- 0.36) were lower than those of children without caries (14.31 +/- 5.71, 1.28 +/- 0.47), but the differences were not statistically significant (P > 0.05).</p><p><b>CONCLUSION</b>Environmental factors may have a stronger effect on the constitution of oral microbiota in children compared with genetic factors. Children without caries may have a richer microbial diversity compared with children with caries.</p>


Subject(s)
Child , Female , Humans , Male , Bacteria , Denaturing Gradient Gel Electrophoresis , Dental Caries , Microbiota , Mouth , Microbiology , Polymerase Chain Reaction , RNA, Ribosomal, 16S , Saliva , Twins, Monozygotic
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