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The proteomic profile of the acquired enamel pellicle according to its location in the dental arches.根据其在牙弓中的位置,获得性釉质 pellicle 的蛋白质组学特征。
Arch Oral Biol. 2017 Jul;79:20-29. doi: 10.1016/j.archoralbio.2017.03.001. Epub 2017 Mar 3.
2
CDD/SPARCLE: functional classification of proteins via subfamily domain architectures.CDD/SPARCLE:通过亚家族结构域架构对蛋白质进行功能分类
Nucleic Acids Res. 2017 Jan 4;45(D1):D200-D203. doi: 10.1093/nar/gkw1129. Epub 2016 Nov 29.
3
Terminal complexes of the complement system: new structural insights and their relevance to function.补体系统的末端复合物:新的结构见解及其与功能的相关性。
Immunol Rev. 2016 Nov;274(1):141-151. doi: 10.1111/imr.12461.
4
CovR Regulates Streptococcus mutans Susceptibility To Complement Immunity and Survival in Blood.CovR调节变形链球菌对补体免疫的敏感性及在血液中的生存能力。
Infect Immun. 2016 Oct 17;84(11):3206-3219. doi: 10.1128/IAI.00406-16. Print 2016 Nov.
5
The road less traveled - defining molecular commensalism with Streptococcus sanguinis.少有人走的路——定义与血链球菌的分子共生关系
Mol Oral Microbiol. 2017 Jun;32(3):181-196. doi: 10.1111/omi.12170. Epub 2016 Sep 20.
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Salivary agglutinin is the major component in human saliva that modulates the lectin pathway of the complement system.唾液凝集素是人类唾液中的主要成分,可调节补体系统的凝集素途径。
Innate Immun. 2016 May;22(4):257-65. doi: 10.1177/1753425916642614. Epub 2016 Apr 4.
7
Can Pulp Fibroblasts Kill Cariogenic Bacteria? Role of Complement Activation.牙髓成纤维细胞能杀死致龋细菌吗?补体激活的作用。
J Dent Res. 2015 Dec;94(12):1765-72. doi: 10.1177/0022034515611074. Epub 2015 Oct 13.
8
Saliva as the Sole Nutritional Source in the Development of Multispecies Communities in Dental Plaque.唾液作为牙菌斑中多物种群落发展的唯一营养来源。
Microbiol Spectr. 2015 Jun;3(3). doi: 10.1128/microbiolspec.MBP-0013-2014.
9
Deletion analysis of Streptococcus pneumoniae late competence genes distinguishes virulence determinants that are dependent or independent of competence induction.肺炎链球菌晚期感受态基因的缺失分析可区分依赖或不依赖感受态诱导的毒力决定因素。
Mol Microbiol. 2015 Jul;97(1):151-65. doi: 10.1111/mmi.13016. Epub 2015 Apr 24.
10
Gingival crevicular fluid proteomes in health, gingivitis and chronic periodontitis.牙龈沟液蛋白质组学在健康、牙龈炎和慢性牙周炎中的研究。
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新型血链球菌双组份系统影响唾液中存活相关功能和生物膜形成。

Novel Two-Component System of Streptococcus sanguinis Affecting Functions Associated with Viability in Saliva and Biofilm Formation.

机构信息

Department of Oral Diagnosis, Piracicaba Dental School, University of Campinas-UNICAMP, SP, Brazil.

Department of Oral Diagnosis, Piracicaba Dental School, University of Campinas-UNICAMP, SP, Brazil

出版信息

Infect Immun. 2018 Mar 22;86(4). doi: 10.1128/IAI.00942-17. Print 2018 Apr.

DOI:10.1128/IAI.00942-17
PMID:29339459
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5865015/
Abstract

is a pioneer species of teeth and a common opportunistic pathogen of infective endocarditis. In this study, we identified a two-component system, SptRS (SptRS ), affecting survival in saliva and biofilm formation. Isogenic mutants of (SKsptR) and (SKsptS) showed reduced cell counts in assays of viability in saliva compared to those of parent strain SK36 and complemented mutants. Reduced counts of the mutants in saliva were associated with reduced growth rates in nutrient-poor medium (RPMI) and increased susceptibility to the deposition of C3b and the membrane attach complex (MAC) of the complement system, a defense component of saliva and serum. Conversely, and mutants showed increased biofilm formation associated with higher levels of production of HO and extracellular DNA. Reverse transcription-quantitative PCR (RT-qPCR) comparisons of strains indicated a global role of SptRS in repressing genes for HO production (2.5- to 15-fold upregulation of , , , , and in and mutants), biofilm formation, and/or evasion of host immunity (2.1- to 11.4-fold upregulation of , , , , and ). Compatible with the homology of SptR with AraC-type regulators, duplicate to multiple conserved repeats were identified in 1,000-bp regulatory regions of downstream genes, suggesting that SptR regulates transcription by DNA looping. Significant transcriptional changes in the regulatory genes , , , , and in the and mutants further indicated that SptRS is part of a regulatory network that coordinates cell wall homeostasis, HO production, and competence. This study reveals that SptRS is involved in the regulation of crucial functions for persistence in the oral cavity.

摘要

是一种牙齿的先驱物种,也是感染性心内膜炎常见的机会致病菌。在这项研究中,我们鉴定了一个双组分系统 SptRS(SptRS),它影响唾液中的生存能力和生物膜形成。与亲本菌株 SK36 和互补突变体相比,(SKsptR)和(SKsptS)的同工酶突变体在唾液中存活测定中的细胞计数减少。突变体在唾液中的计数减少与在营养贫瘠的培养基(RPMI)中生长速度降低以及对补体系统防御成分 C3b 和膜附着复合物(MAC)的沉积的易感性增加有关,补体系统是唾液和血清中的防御成分。相反,和突变体显示出与更高水平的 HO 和细胞外 DNA 产生相关的生物膜形成增加。对菌株的逆转录定量 PCR(RT-qPCR)比较表明 SptRS 在抑制 HO 产生基因(在和突变体中,2.5-15 倍上调,,,和)、生物膜形成和/或逃避宿主免疫方面具有全局作用(2.1-11.4 倍上调,,,和)。与 AraC 型调节剂的 SptR 同源性相兼容,在下游基因的 1000bp 调控区中鉴定出重复 2 次到多次的重复,表明 SptR 通过 DNA 环化调节转录。在和突变体中的调控基因、、、和的转录变化显著,进一步表明 SptRS 是协调细胞壁稳态、HO 产生和感受态的调控网络的一部分。这项研究揭示了 SptRS 参与了在口腔中持续存在的关键功能的调节。