ABSTRACTTheSalmonella entericaserovar Typhimurium RcsCDB system regulates the synthesis of colanic acid and the flagellum as well as the expression of virulence genes. We previously demonstrated that thercsC11mutant, which constitutively activates the RcsB regulator, attenuatesSalmonellavirulence in an animal model. This attenuated phenotype was also produced by deletion of theslyAgene. In this work, we investigated if this antagonistic behavior is produced by modulating the expression of both regulator-encoding genes. We demonstrated that SlyA overproduction negatively regulatesrcsBtranscription. A bioinformatics analysis enabled us to identify putative SlyA binding sites on both promoters, PrcsDBand PrcsB, which controlrcsBtranscriptional levels. We also determined that SlyA is able to recognize and bind to these predicted sites to modulate the activity of bothrcsBpromoters. According to these results, SlyA repressesrcsBtranscription by direct binding to specific sites located on thercsBpromoters, thus accounting for the attenuated/virulence antagonistic behaviors. Moreover, we showed that the opposite effect between both regulators also physiologically affects theSalmonellamotility phenotype. In this sense, we observed that under SlyA overproduction, PrcsBis repressed, and consequently, bacterial motility is increased. On the basis of these results, we suggest that during infection, the different RcsB levels produced act as a switch between the virulent and attenuated forms ofSalmonella. Thereby, we propose that higher concentrations of RcsB tilt the balance toward the attenuated form, while absence or low concentrations resulting from SlyA overproduction tilt the balance toward the virulent form.IMPORTANCEThe antagonistic behavior of RcsB and SlyA on virulence gene expression led us to hypothesize that there is interplay between both regulators in a regulatory network and these could be considered coordinators of this process. Here, we report that the SlyA virulence factor influences motility behavior by controllingrcsBtranscription from the PrcsBpromoter. We also demonstrate that SlyA negatively affects the expression of thercsBgene by direct binding to PrcsDBand PrcsBpromoters. We suggest that different levels of RcsB act as a switch between the virulent and attenuated forms ofSalmonella, where high concentrations of the regulator tend to tilt the balance toward the attenuated form and low concentrations or its absence tilt it toward the virulent form.