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Transcriptomic data for analyzing global gene expression patterns in Methicillin-resistance Staphylococcus aureus in response to spermine and oxacillin stress

机译:转录组学数据用于分析抗精胺和奥沙西林胁迫的耐甲氧西林金黄色葡萄球菌总体基因表达模式

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摘要

Methicillin-resistant Staphylococcus aureus (MRSA) is a rapidly emerging bacteria causing infection, which has developed resistance to most of the beta-lactam antibiotics because of newly acquired low-affinity penicillin binding protein (PBP2a), which can continue to build the cell wall when other PBPs are blocked by beta-lactams. Exogenous spermine exerts a dose dependent inhibition effect on the growth of E. coli, Salmonella enterica serovar and Staphylococcus aureus. We have selected an MRSA Mu50 derivative which harbors mutation on PBP2 gene (named as MuM) showing spermine resistance and which confers a complete abolishment of spermine-beta-lactam synergy. A transcriptomic profiling of MuM against Mu50 (wild type) without any treatment, MuM and Mu50 in response to high dose spermine and Mu50 in response to spermine-beta-lactam synergy is provided in this article. These comparisons will enhance our current understanding of mechanisms of spermine-beta-lactam synergy sensitization effects on MRSA.
机译:耐甲氧西林金黄色葡萄球菌(MRSA)是一种引起感染的迅速出现的细菌,由于新获得的低亲和力青霉素结合蛋白(PBP2a)可以继续建立细胞壁,因此对大多数β-内酰胺抗生素产生了耐药性当其他PBP被β-内酰胺阻滞时。外源精胺对大肠杆菌,肠炎沙门氏菌和金黄色葡萄球菌的生长具有剂量依赖性的抑制作用。我们选择了一种MRSA Mu50衍生物,该衍生物在PBP2基因上具有突变(命名为MuM),显示出对精胺的抗性,并且完全废除了精胺-β-内酰胺的协同作用。本文提供了未经任何处理的MuM对Mu50(野生型)的转录组谱分析,MuM和Mu50对高剂量精胺的响应以及Mu50对精胺-β-内酰胺协同作用的响应。这些比较将增强我们目前对MRSA对精胺-β-内酰胺协同增敏作用机理的了解。

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