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首页> 外文期刊>MBio >Role of Fatty Acid Kinase in Cellular Lipid Homeostasis and SaeRS-Dependent Virulence Factor Expression in Staphylococcus aureus
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Role of Fatty Acid Kinase in Cellular Lipid Homeostasis and SaeRS-Dependent Virulence Factor Expression in Staphylococcus aureus

机译:脂肪酸激酶在金黄色葡萄球菌中细胞脂质稳态和SaeRS依赖性毒力因子表达中的作用

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ABSTRACT The SaeRS two-component system is a master activator of virulence factor transcription in Staphylococcus aureus , but the cellular factors that control its activity are unknown. Fatty acid (FA) kinase is a two-component enzyme system required for extracellular FA uptake and SaeRS activity. Here, we demonstrate the existence of an intracellular nonesterified FA pool in S.?aureus that is elevated in strains lacking FA kinase activity. SaeRS-mediated transcription is restored in FA kinase-negative strains when the intracellular FA pool is reduced either by growth with FA-depleted bovine serum albumin to extract the FA into the medium or by the heterologous expression of Neisseria gonorrhoeae acyl-acyl carrier protein synthetase to activate FA for phospholipid synthesis. These data show that FAs act as negative regulators of SaeRS signaling, and FA kinase activates SaeRS-dependent virulence factor production by lowering inhibitory FA levels. Thus, FA kinase plays a role in cellular lipid homeostasis by activating FA for incorporation into phospholipid, and it indirectly regulates SaeRS signaling by maintaining a low intracellular FA pool. IMPORTANCE The SaeRS two-component system is a master transcriptional activator of virulence factor production in response to the host environment in S.?aureus , and strains lacking FA kinase have severely attenuated SaeRS-dependent virulence factor transcription. FA kinase is required for the activation of exogenous FAs, and it plays a role in cellular lipid homeostasis by recycling cellular FAs into the phospholipid biosynthetic pathway. Activation of the sensor kinase, SaeS, is mediated by its membrane anchor domain, and the FAs which accumulate in FA kinase knockout strains are potent inhibitors of SaeS-dependent signaling. This work identifies FAs as physiological effectors for the SaeRS system and reveals a connection between cellular lipid homeostasis and the regulation of virulence factor transcription. FA kinase is widely distributed in Gram-positive bacteria, suggesting similar roles for FA kinase in these organisms.
机译:摘要SaeRS两组分系统是金黄色葡萄球菌中毒力因子转录的主要激活因子,但控制其活性的细胞因子尚不清楚。脂肪酸(FA)激酶是细胞外FA摄取和SaeRS活性所需的两组分酶系统。在这里,我们证明了在缺乏FA激酶活性的菌株中金黄色葡萄球菌存在细胞内非酯化FA池。当通过贫FA的牛血清白蛋白生长以将FA提取到培养基中或通过淋病奈瑟氏球菌酰基-酰基载体蛋白合成酶的异源表达来减少细胞内FA池时,FA激酶阴性菌株中的SaeRS介导的转录得以恢复。激活FA以合成磷脂。这些数据表明,FA充当SaeRS信号的负调节剂,而FA激酶通过降低抑制性FA的水平来激活SaeRS依赖性毒力因子的产生。因此,FA激酶通过激活FA并结合到磷脂中而在细胞脂质稳态中起作用,并且它通过维持低的细胞内FA池间接地调节SaeRS信号传导。重要SaeRS两组分系统是响应金黄色葡萄球菌宿主环境的毒力因子产生的主要转录激活因子,缺乏FA激酶的菌株已严重减弱了SaeRS依赖性毒力因子的转录。 FA激酶是激活外源性FA所必需的,并且它通过将细胞中的FAs循环到磷脂的生物合成途径中而在细胞脂质稳态中发挥作用。传感器激酶SaeS的激活是由其膜锚结构域介导的,在FA激酶敲除菌株中积累的FA是SaeS依赖性信号传导的有效抑制剂。这项工作确定FAs为SaeRS系统的生理效应,并揭示了细胞脂质稳态与毒力因子转录调控之间的联系。 FA激酶广泛分布于革兰氏阳性细菌中,表明FA激酶在这些生物体中的作用相似。

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