Personalized Inhaled Bacteriophage Therapy Decreases Multidrug-ResistantPseudomonas aeruginosa

Author:

Chan BK,Stanley GL,Kortright KE,Modak M,Ott IM,Sun Y,Würstle S,Grun C,Kazmierczak B,Rajagopalan G,Harris Z,Britto CJ,Stewart J,Talwalkar JS,Appell C,Chaudary N,Jagpal SK,Jain R,Kanu A,Quon BS,Reynolds JM,Mai QA,Shabanova V,Turner PE,Koff JL

Abstract

AbstractBacteriophage therapy, which uses lytic viruses as antimicrobials, has received renewed interest to address the emerging antimicrobial resistance (AMR) crisis. Cystic fibrosis (CF), a disease complicated by recurrentP. aeruginosapulmonary infections that cause lung function decline, is an example where AMR is already a clinical problem. While bacteria evolve bacteriophage resistance, we developed a strategy to select bacteriophages that target bacterial cell surface receptors that contribute to antibiotic resistance or virulence. Thus, in addition to killing bacteria, these phages steer surviving, evolved bacteria to antibiotic re-sensitivity or attenuated virulence. Here, we present outcomes from nine CF adults treated with nebulized bacteriophage therapy for AMRP. aeruginosausing this personalized approach. Results showed that phage therapy: 1) reduced sputumP. aeruginosa, 2) showed evidence for predicted trade-offs in most subjects, and 3) improved lung function, which may reflect the combined effects of decreased bacterial sputum density and phage-driven evolved trade-offs.

Publisher

Cold Spring Harbor Laboratory

Reference35 articles.

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