Barchiesi Julieta, Castelli María E, Soncini Fernando C, Véscovi Eleonora García
Departamento de Microbiología, Facultad de Ciencias Bioquímicas y Farmacéuticas (UNR), Instituto de Biología Molecular y Celular de Rosario (IBR-CONICET), Rosario, Argentina.
J Bacteriol. 2008 Jul;190(14):4951-8. doi: 10.1128/JB.00195-08. Epub 2008 May 16.
Rob is a member of the Sox/Mar subfamily of AraC/XylS-type transcriptional regulators implicated in bacterial multidrug, heavy metal, superoxide, and organic solvent resistance phenotypes. We demonstrate that, in Salmonella enterica, Rob overexpression upregulates the transcription of mgtA, which codes for the MgtA Mg2+ transporter. mgtA was previously characterized as a member of the Mg2+-modulated PhoPQ regulon. Here we demonstrate that Rob (but not its paralog protein SoxS or MarA) is able to induce mgtA transcription in a PhoP-independent fashion by binding to a conserved Mar/Sox/Rob motif localized downstream of the PhoP-box and overlapping the PhoP-dependent transcriptional start site. We found that Rob-induced mgtA expression confers low-level cyclohexane resistance on Salmonella. Because mgtA intactness is required for Rob-induced cyclohexane resistance, provided the AcrAB multidrug efflux pump can be expressed, we postulate that MgtA is involved in the AcrAB-mediated cyclohexane detoxification mechanism promoted by Rob in Salmonella.
罗布是AraC/XylS型转录调节因子的Sox/Mar亚家族成员,与细菌的多药、重金属、超氧化物和有机溶剂抗性表型有关。我们证明,在肠炎沙门氏菌中,罗布的过表达上调了mgtA的转录,mgtA编码MgtA镁离子转运蛋白。mgtA先前被鉴定为镁离子调节的PhoPQ调节子的成员。在这里,我们证明罗布(而非其旁系同源蛋白SoxS或MarA)能够通过结合位于PhoP框下游且与PhoP依赖的转录起始位点重叠的保守Mar/Sox/Rob基序,以不依赖PhoP的方式诱导mgtA转录。我们发现罗布诱导的mgtA表达赋予肠炎沙门氏菌低水平的环己烷抗性。由于罗布诱导的环己烷抗性需要mgtA完整,前提是AcrAB多药外排泵能够表达,我们推测MgtA参与了罗布在肠炎沙门氏菌中促进的AcrAB介导的环己烷解毒机制。