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葡萄糖水平改变 A 组链球菌的 mga 毒力调节子。

Glucose Levels Alter the Mga Virulence Regulon in the Group A Streptococcus.

机构信息

Department of Cell Biology & Molecular Genetics and Maryland Pathogen Research Institute, University of Maryland, College Park (UMCP), College Park, Maryland, USA.

Center for Bioinformatics and Computation Biology, UMCP, College Park, MD, USA.

出版信息

Sci Rep. 2018 Mar 21;8(1):4971. doi: 10.1038/s41598-018-23366-7.

Abstract

Many bacterial pathogens coordinately regulate genes encoding important metabolic pathways during disease progression, including the phosphoenolpyruvate (PEP)-phosphotransferase system (PTS) for uptake of carbohydrates. The Gram-positive Group A Streptococcus (GAS) is a pathogen that infects multiple tissues in the human host. The virulence regulator Mga in GAS can be phosphorylated by the PTS, affecting Mga activity based on carbohydrate availability. Here, we explored the effects of glucose availability on the Mga regulon. RNA-seq was used to identify transcriptomic differences between the Mga regulon grown to late log phase in the presence of glucose (THY) or after glucose has been expended (C media). Our results revealed a correlation between the genes activated in C media with those known to be repressed by CcpA, indicating that C media mimics a non-preferred sugar environment. Interestingly, we found very little overlap in the Mga regulon from GAS grown in THY versus C media beyond the core virulence genes. We also observed an alteration in the phosphorylation status of Mga, indicating that the observed media differences in the Mga regulon may be directly attributed to glucose levels. Thus, these results support an in vivo link between glucose availability and virulence regulation in GAS.

摘要

许多细菌病原体在疾病进展过程中协调调节编码重要代谢途径的基因,包括用于摄取碳水化合物的磷酸烯醇丙酮酸 (PEP) -磷酸转移酶系统 (PTS)。革兰氏阳性 A 组链球菌 (GAS) 是一种感染宿主多种组织的病原体。GAS 中的毒力调节因子 Mga 可以被 PTS 磷酸化,根据碳水化合物的可用性影响 Mga 活性。在这里,我们研究了葡萄糖可用性对 Mga 调控子的影响。使用 RNA-seq 来鉴定在存在葡萄糖 (THY) 或消耗葡萄糖后 (C 培养基) 生长到对数晚期的 Mga 调控子的转录组差异。我们的结果显示,C 培养基中激活的基因与已知被 CcpA 抑制的基因之间存在相关性,这表明 C 培养基模拟了非首选糖环境。有趣的是,我们发现 GAS 在 THY 中生长与在 C 培养基中生长的 Mga 调控子之间除了核心毒力基因之外几乎没有重叠。我们还观察到 Mga 的磷酸化状态发生改变,表明 Mga 调控子中观察到的培养基差异可能直接归因于葡萄糖水平。因此,这些结果支持 GAS 中葡萄糖可用性与毒力调节之间的体内联系。

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