The vicK gene of Streptococcus mutans mediates its cariogenicity via exopolysaccharides metabolism

来源 :国际口腔科学杂志(英文版) | 被引量 : 0次 | 上传用户:monorrch
下载到本地 , 更方便阅读
声明 : 本文档内容版权归属内容提供方 , 如果您对本文有版权争议 , 可与客服联系进行内容授权或下架
论文部分内容阅读
Streptococcus mutans (S. mutans) is generally regarded as a major contributor to dental caries because of its ability to synthesize extracellular polysaccharides (EPS) that aid in the formation of plaque biofilm. The VicRKX system of S. mutans plays an important role in biofilm formation. The aim of this study was to investigate the effects of vicK gene on specific characteristics of EPS in S. mutans biofilm. We constructed single-species biofilms formed by different mutants of vicK gene. Production and distribution of EPS were detected through atomic force microscopy, scanning electron microscopy and confocal laser scanning microscopy. Microcosmic structures of EPS were analyzed by gel permeation chromatography and gas chromatography-mass spectrometry. Cariogenicity of the vicK mutant was assessed in a specific pathogen-free rat model. Transcriptional levels of cariogenicity-associated genes were confirmed by quantitative real-time polymerase chain reaction. The results showed that deletion of vicK gene suppressed biofilm formation as well as EPS production, and EPS were synthesized mostly around the cells. Molecular weight and monosaccharide components underwent evident alterations. Biofilms formed in vivo were sparse and contributed a decreased degree of caries. Moreover, expressional levels of genes related to EPS synthesis were down-regulated, except for gtfB. Our report demonstrates that vicK gene enhances biofilm formation and subsequent caries development. And this may due to its regulations on EPS metabolism, like synthesis or microcosmic features of EPS. This study suggests that vicK gene and EPS can be considered as promising targets to modulate dental caries.
其他文献
RNA sequencing (RNAseq) can reveal gene fusions, splicing variants, mutations/indels in addition to differential gene expression, thus providing a more complete genetic picture than DNA sequencing. This most widely used technology in genomics tool box has
SAM pointed domain containing E26 transformation-specific transcription factor (SPDEF) plays dual roles in the initiation and development of human malignancies. However, the biological role of SPDEF in head and neck squamous cell carcinoma (HNSCC) remains
本文对慢性非癌痛患者实施姑息照护的必要性和影响因素进行综述,并提出慢性非癌痛姑息照护者应具备的核心能力,以期为我国开展慢性非癌痛患者姑息照护提供信息支持.
The first branchial arch (BA1), which is derived from cranial neural crest (CNC) cells, gives rise to various orofacial tissues. Cre mice are widely used for the determination of CNC and exploration of gene functions in orofacial development. However, the
通过查阅相关文献,对甘草梢的来源本草学考证、实地调研、甘草产地初加工、甘草梢的中医治病机理等方面进行综述,并对甘草梢作了全方位考证,对甘草的不同药用部位来替代“甘草梢”调配处方的乱象和甘草梢入药部位展开全方位探讨,明确甘草梢药用部位,确保临床疗效.明确了甘草梢资源现状,为今后制定甘草梢的饮片规格和质量标准提供理论依据,为甘草梢的有效药用部位、资源合理利用及今后发展的方向提供基础.
目的:依据国际妇产科联盟(FIGO)分期标准,对早期(ⅠA2~ⅡA2)宫颈小细胞神经内分泌癌(SCNECC)患者的临床特征及预后影响因素进行分析,为提高其治疗效果及预后提供临床依据.方法:回顾性分析我院2012年1月至2018年8月收治的41例FIGOⅠA2~ⅡA2期SCNECC患者的临床治疗及术后随访资料,采用免疫组化法检测神经元特异烯醇化酶(NSE)、神经细胞黏附分子(NCAM)、突触素(Syn)、嗜铬粒蛋白A(CgA)、胰岛素瘤相关蛋白1(INSM1)标志物的表达;采用生存分析法及多因素Cox回归模
寒是自然界正常的气候现象,当气候发生异常或人体自身正气不足时,寒气则成为病邪侵犯人体.本文通过对寒燥的临床表现及治疗进行相关文献挖掘,并结合现代研究,针对地域性和季节性的特点,探析寒燥之邪当以温润为先,辛甘助阳,散寒润燥予以施治.
Unrestrained inflammation is harmful to tissue repair and regeneration. Immune cell membrane-camouflaged nanoparticles have been proven to show promise as inflammation targets and multitargeted inflammation controls in the treatment of severe inflammation
目的:探讨股骨近端防旋髓内钉(PFNA)联合阿仑磷酸钠片治疗老年股骨粗隆间骨折的临床疗效及对骨密度的影响.方法:选取古浪县中医医院骨伤科自2015年11月至2019年11月收治的老年股骨粗隆间骨折患者70例,随机分为观察组和对照组,两组患者均接受股骨近端防旋髓内钉内固定手术,且术后两组患者均给予相同剂量的钙尔奇D片治疗,观察组在此基础治疗上再给予阿仑磷酸钠片治疗.比较两组患者术前、术后的骨密度情况和术后骨愈合、髋关节功能恢复情况等结果.结果:观察组患者手术时间、住院时间、术中出血量及骨折愈合时间与对照组相
目的:本研究探讨常规磁共振成像(MRI)联合磁共振弥散加权成像(DWI)在宫颈癌术前分期诊断中的应用价值.方法:选择我院2018年1月至2020年1月收治的宫颈癌患者130例,所有患者均进行MRI、DWI检查,以手术病理结果为金标准,观察所有患者MRI+DWI诊断情况,与病理结果进行对比,并分析ADC、eADC情况.结果:MRI+DWI诊断ⅠB期96.55%,ⅡA期93.94%,ⅡB期97.06%,ⅢA期92.31%,ⅢB期90.91%,ⅣA期90.00%.两组ⅢB、ⅣA分期诊断情况上无统计学差异(P>0