Mucoid strains of Pseudomonas aeruginosa isolated from the lungs of cystic fibrosis patients produce large amounts of the exopolysaccharide alginate. AlgR has long been considered a key regulator of alginate production, but its cognate sensor has not been identified. Here we show that AlgR is required for twitching motility, which is a form ofbacterial surface translocation mediated by type 4 fimbriae. Adjacent to algR we have identified a sensor gene (fimS), which is also required for twitching motility. However, FimS does not appear to be required for alginate production in mucoid strains. FimS and AlgR are representative of a new subclass of two-component transmitter-receiver regulatory systems. The alternative sigma factor AlgU also affects both alginate production and twitching motility. Therefore, these two virulence determinants appear to be closely associated and coordinately regulated.Pseudomonas aeruginosa is an opportunistic pathogen of humans and other species (1). It causes severe chronic infections in patients who are immunocompromised as a result of cancer chemotherapy or AIDS, or who are suffering from burns or cystic fibrosis. It produces an extensive suite of virulence factors including extracellular proteases and toxins, lipases, pyochelins, exopolysaccharides, and type 4 fimbriae. In cystic fibrosis, P. aeruginosa produces recurrent and chronic lung infections, which impose substantial morbidity and often mortality as a consequence of accumulated damage to the lung. Isolates from such chronic infections exhibit a "mucoid" colony phenotype due to the production of large amounts of the exopolysaccharide alginate, apparently as a means of evading immune responses (for reviews see refs. 2 and 3).