@article{mbs:/content/journal/micro/10.1099/mic.0.2007/011577-0, author = "Ferrell, Evan and Carty, Nancy L. and Colmer-Hamood, Jane A. and Hamood, Abdul N. and West, Susan E. H.", title = "Regulation of Pseudomonas aeruginosa ptxR by Vfr", journal= "Microbiology", year = "2008", volume = "154", number = "2", pages = "431-439", doi = "https://doi.org/10.1099/mic.0.2007/011577-0", url = "https://www.microbiologyresearch.org/content/journal/micro/10.1099/mic.0.2007/011577-0", publisher = "Microbiology Society", issn = "1465-2080", type = "Journal Article", keywords = "CRP, cAMP receptor protein", keywords = "PQS, Pseudomonas quinolone signal", keywords = "EMSA, electrophoretic mobility shift assay", keywords = "QS, quorum sensing", keywords = "r-Vfr, recombinant Vfr", keywords = "Vfr-BS, Vfr-binding sequence", keywords = "ETA, exotoxin A", abstract = " Pseudomonas aeruginosa PtxR enhances the expression of the exotoxin A gene toxA. The expression of ptxR itself, which occurs from two promoters (P1 and P2), is not completely understood. We have recently demonstrated that the ptxR upstream region contains potential binding sites for multiple regulators, including the virulence factor regulator Vfr. In this study, we identified within the ptxR upstream region, a 25 bp sequence to which Vfr specifically binds. The sequence is located 20–44 (32.5) bp 5′ of the ptxR P2 promoter, and overlaps a potential binding site for the iron-starvation sigma factor PvdS. We also show that, throughout the growth cycle, deletion of vfr reduces ptxR expression from the P2 promoter in the P. aeruginosa strain PAO1 by four- to eightfold, but does not affect ptxR expression from P1. Further, loss of Vfr eliminates the PtxR-induced enhancement in the synthesis of exotoxin A and the metalloproteinase LasB. Our results suggest that Vfr modulates toxA and lasB expression in PAO1 through PtxR. A model defining the relationships between these different genes is presented.", }