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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.

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。

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