Using phage to drive selections toward restoring antibiotic sensitivity in Pseudomonas aeruginosa via chromosomal deletions

• Published in: Frontiers in microbiology 2024-05, Vol.15, p.1401234-1401234
• Main Authors: Fujiki, Jumpei, Nakamura, Keisuke, Ishiguro, Yuko, Iwano, Hidetomo
• Format: Article
• Language: English
• Subjects: AMR (antimicrobial resistance); ESKAPE bacteria; fluoroquinolones; galU; MexXY/OprM; Microbiology; phage-resistance
• ISSN: 1664-302X; 1664-302X
• DOI: 10.3389/fmicb.2024.1401234

Phage therapy has re-emerged in modern medicine as a robust antimicrobial strategy in response to the increasing prevalence of antimicrobial-resistant bacteria. However, bacterial resistance to phages can also arise via a variety of molecular mechanisms. In fact, several clinical studies on phage therapy have reported the occurrence of phage-resistant variants, representing a significant concern for the successful development of phage-based therapies. In this context, the fitness trade-offs between phage and antibiotic resistance have revealed new avenues in the field of phage therapy as a countermeasure against phage resistance. This strategy forces to restore the antibiotic susceptibility of antimicrobial-resistant bacteria as compensation for the development of phage resistance. Here, we present the key achievements of these fitness trade-offs, notably focusing on the enhancement of antibiotic sensitivity through the induction of large chromosomal deletions by bacteriophage infection. We also describe the challenges of this strategy that need to be overcome to promote favorable therapeutic outcomes and discuss future directions. The insights gained from the trade-offs between phage and antibiotic sensitivity will help maximize the potential of phage therapy for the treatment of infectious diseases.