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ABSTRACT: Background
Pseudomonas aeruginosa is a grave nosocomial pathogen that persistently inhabits the lungs of patients with cystic fibrosis (CF) and causes various chronic infections. The bacterial toxin-antitoxin (TA) system is associated with latent and long-term infections, but the underlying mechanisms remain to be fully characterized.Methods
We here investigated the diversity and function of five genomic type II TA systems widely distributed among P. aeruginosa clinical isolates. We also examined the distinct structural features of the toxin protein from different TA systems and characterized their contributions to persistence, invasion ability, and intracellular infection caused by P. aeruginosa.Results
ParDE, PA1030/PA1029, and HigBA could mod
SUBMITTER: Song Y
PROVIDER: S-EPMC9948252 | biostudies-literature | 2023
REPOSITORIES: biostudies-literature