Publication | Open Access
<i>mexEF-oprN</i> Multidrug Efflux Operon of <i>Pseudomonas aeruginosa</i> : Regulation by the MexT Activator in Response to Nitrosative Stress and Chloramphenicol
136
Citations
45
References
2010
Year
BacteriologyMolecular BiologyBacterial PathogensRedox BiologyDrug ResistanceAntibacterial MechanismsAntimicrobial ResistanceMexs GeneBiochemistryMedicineVirulence FactorPseudomonas FluorescensNull MutationMolecular MicrobiologyGene ExpressionClinical MicrobiologyAntimicrobial Resistance GeneAntibioticsNatural SciencesMicrobiologyMext ActivatorNitrosative StressMicrobial Genetics
A null mutation in the mexS gene of Pseudomonas aeruginosa yielded an increased level of expression of a 3-gene operon containing a gene, xenB, whose product is highly homologous to a xenobiotic reductase in Pseudomonas fluorescens shown previously to remove nitro groups from trinitrotoluene and nitroglycerin (D. S. Blehert, B. G. Fox, and G. H. Chambliss, J. Bacteriol. 181:6254, 1999). This expression, which paralleled an increase in mexEF-oprN expression in the same mutant, was, like mexEF-oprN, dependent on the MexT LysR family positive regulator previously implicated in mexEF-oprN expression. As nitration is a well-known result of nitrosative stress, a role for xenB (and the coregulated mexEF-oprN) in a nitrosative stress response was hypothesized and tested. Using s-nitrosoglutathione (GSNO) as a source of nitrosative stress, the expression of xenB and mexEF-oprN was shown to be GSNO inducible, although in the case of xenB, this was seen only for a mutant lacking MexEF-OprN. In both instances, this GSNO-inducible expression was dependent upon MexT. Chloramphenicol, a nitroaromatic antimicrobial that is a substrate for MexEF-OprN, was shown to induce mexEF-oprN but not xenB, again dependent upon the MexT regulator, possibly because it resembles a nitrosated nitrosative stress product accommodated by MexEF-OprN.
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