Park Sun-Yang, Groisman Eduardo A
Department of Microbial Pathogenesis, Yale School of Medicine, Boyer Center for Molecular Medicine, 295 Congress Avenue, New Haven, CT, 06536-0812, USA; Howard Hughes Medical Institute, New Haven, CT, USA; Yale Microbial Diversity Institute, PO Box 27389, West Haven, CT, 06516, USA.
Mol Microbiol. 2014 Jan;91(1):135-44. doi: 10.1111/mmi.12449. Epub 2013 Nov 20.
The two-component system PhoP/PhoQ controls a large number of genes responsible for a variety of physiological and virulence functions in Salmonella enterica serovar Typhimurium. Here we describe a mechanism whereby the transcriptional activator PhoP elicits expression of dissimilar gene sets when its cognate sensor PhoQ is activated by different signals in the periplasm. We determine that full transcription of over half of the genes directly activated by PhoP requires the Mg(2+) transporter MgtA when the PhoQ inducing signal is low Mg(2+) , but not when PhoQ is activated by mildly acidic pH or the antimicrobial peptide C18G. MgtA promotes the active (i.e. phosphorylated) form of PhoP by removing Mg(2+) from the periplasm, where it functions as a repressing signal for PhoQ. MgtA-dependent expression enhances resistance to the cationic antibiotic polymyxin B. Production of the MgtA protein requires cytoplasmic Mg(2+) levels to drop below a certain threshold, thereby creating a two-tiered temporal response among PhoP-dependent genes.
双组分系统PhoP/PhoQ控制着鼠伤寒沙门氏菌中大量负责多种生理和毒力功能的基因。在此,我们描述了一种机制,即当转录激活因子PhoP的同源传感器PhoQ在周质中被不同信号激活时,PhoP会引发不同基因集的表达。我们确定,当PhoQ诱导信号为低镁离子时,PhoP直接激活的基因中超过一半的基因的完全转录需要镁离子转运蛋白MgtA,但当PhoQ被轻度酸性pH或抗菌肽C18G激活时则不需要。MgtA通过从周质中去除镁离子来促进PhoP的活性(即磷酸化)形式,在周质中镁离子作为PhoQ的抑制信号发挥作用。依赖MgtA的表达增强了对阳离子抗生素多粘菌素B的抗性。MgtA蛋白的产生需要细胞质镁离子水平降至某个阈值以下,从而在依赖PhoP的基因中产生两级时间响应。