CRISPRi screen identifies FprB as a synergistic target for gallium therapy in Pseudomonas aeruginosa

Nat Commun. 2025 Jul 1;16(1):5870. doi: 10.1038/s41467-025-61208-z.

Abstract

With the rise of antibiotic-resistant bacteria, non-antibiotic therapies like gallium gain increasing attention. Intravenous gallium nitrate is under Phase II clinical trials to treat chronic Pseudomonas aeruginosa infections in cystic fibrosis patients. However, its clinical efficacy is constrained by the achievable peak concentration in human tissue. To address this limitation, we apply a genome-wide CRISPR interference approach (CRISPRi-seq) to identify potential synergistic targets with gallium. We classify the essential genes by response time and growth reduction, pinpointing the most vulnerable therapeutic targets in this species. In addition, we identify a highly conserved gene, fprB, encoding a ferredoxin-NADP⁺ reductase, whose deletion sensitizes P. aeruginosa to gallium, lowering its MIC by 32-fold and shifting mode of action from bacteriostatic to bactericidal. Further investigation reveals that FprB plays a critical role in modulating oxidative stress induced by gallium, via control of iron homeostasis and reactive oxygen species accumulation. Deleting fprB enhances gallium's efficacy against biofilm formation and improves outcomes in a murine lung infection model of P. aeruginosa, suggesting FprB is a promising drug target in combination with gallium. Overall, our data show CRISPRi-seq as a powerful tool for systematic genetic analysis of P. aeruginosa, advancing the identification of novel therapeutic targets.

MeSH terms

  • Animals
  • Anti-Bacterial Agents* / pharmacology
  • Bacterial Proteins* / genetics
  • Bacterial Proteins* / metabolism
  • Biofilms / drug effects
  • Biofilms / growth & development
  • CRISPR-Cas Systems
  • Female
  • Gallium* / pharmacology
  • Gallium* / therapeutic use
  • Humans
  • Iron / metabolism
  • Mice
  • Microbial Sensitivity Tests
  • Oxidative Stress / drug effects
  • Pseudomonas Infections* / drug therapy
  • Pseudomonas Infections* / microbiology
  • Pseudomonas aeruginosa* / drug effects
  • Pseudomonas aeruginosa* / genetics
  • Reactive Oxygen Species / metabolism

Substances

  • Gallium
  • Anti-Bacterial Agents
  • Reactive Oxygen Species
  • Bacterial Proteins
  • gallium nitrate
  • Iron