Pseudomonas aeruginosa Regulated Intramembrane Proteolysis: Protease MucP Can Overcome Mutations in the AlgO Periplasmic Protease To Restore Alginate Production in Nonmucoid Revertants

• Published in: Journal of bacteriology 2018-08, Vol.200 (16)
• Main Authors: Delgado, Camila, Florez, Laura, Lollett, Ivonne, Lopez, Christine, Kangeyan, Shiva, Kumari, Hansi, Stylianou, Marios, Smiddy, Robert J, Schneper, Lisa, Sautter, Robert T, Smith, David, Szatmari, George, Mathee, Kalai
• Format: Article
• Language: English
• Subjects: Alginates; Alginic acid; AlgT/U; anti-sigma factor; Bacteriology; Chronic illnesses; Complementation; Conversion; Cystic fibrosis; Exopolysaccharides; M form; Medical prognosis; mucoid conversion; Mutation; Opportunist infection; Pathogens; Phenotypes; Prc/AlgO/Tsp; Protease; Proteases; Proteinase; Proteolysis; Pseudomonas aeruginosa; Regulatory mechanisms (biology); Revertants; RseP/MucP/YaeL; sigma; Sigma factor; sigma factors; sigma(E); sigma-22; Tiling
• ISSN: 0021-9193; 1098-5530; 1098-5530
• DOI: 10.1128/jb.00215-18

The progression of cystic fibrosis (CF) from an acute to a chronic disease is often associated with the conversion of the opportunistic pathogen from a nonmucoid form to a mucoid form in the lung. This conversion involves the constitutive synthesis of the exopolysaccharide alginate, whose production is under the control of the AlgT/U sigma factor. This factor is regulated posttranslationally by an extremely unstable process and has been commonly attributed to mutations in the ( ) gene. By exploiting this unstable phenotype, we isolated 34 spontaneous nonmucoid variants arising from the mucoid strain PDO300, a PAO1 derivative containing the allele commonly found in mucoid CF isolates. Complementation analysis using a minimal tiling path cosmid library revealed that most of these mutants mapped to two protease-encoding genes, , also known as or , and Interestingly, our mutations were complemented by both and , leading us to delete, clone, and overexpress , , , and in both wild-type PAO1 and PDO300 backgrounds to better understand the regulation of this complex regulatory mechanism. Our findings suggest that the regulatory proteases follow two pathways for regulated intramembrane proteolysis (RIP), where both the AlgO/MucP pathway and MucE/AlgW pathway are required in the wild-type strain but where the AlgO/MucP pathway can bypass the MucE/AlgW pathway in mucoid strains with membrane-associated forms of MucA with shortened C termini, such as the MucA22 variant. This work gives us a better understanding of how alginate production is regulated in the clinically important mucoid variants of Infection by the opportunistic pathogen is the leading cause of morbidity and mortality seen in CF patients. Poor patient prognosis correlates with the genotypic and phenotypic change of the bacteria from a typical nonmucoid to a mucoid form in the CF lung, characterized by the overproduction of alginate. The expression of this exopolysaccharide is under the control an alternate sigma factor, AlgT/U, that is regulated posttranslationally by a series of proteases. A better understanding of this regulatory phenomenon will help in the development of therapies targeting alginate production, ultimately leading to an increase in the length and quality of life for those suffering from CF.