Inhaled bacteriophage therapy in a porcine model of pneumonia caused by Pseudomonas aeruginosa during mechanical ventilation

铜绿假单胞菌 微生物学 噬菌体疗法 溶解循环 噬菌体 肺炎 抗菌剂 抗生素 体内 细菌 医学 化学 生物 病毒学 病毒 大肠杆菌 内科学 生物技术 基因 生物化学 遗传学
作者
Antoine Guillon,Jeoffrey Pardessus,Guillaume L’Hostis,Cindy Fèvre,Céline Barc,Emilie Dalloneau,Youenn Jouan,Elsa Bodier-Montagutelli,Yonatan Perez,Camille Thorey,Laurent Méreghetti,Montserrat Cabrera,Mickaël Riou,Laurent Vecellio,Sandrine Le Guellec,Nathalie Heuzé-Vourc’h
出处
期刊:British Journal of Pharmacology [Wiley]
卷期号:178 (18): 3829-3842 被引量:14
标识
DOI:10.1111/bph.15526
摘要

BACKGROUND AND PURPOSE 255: Pseudomonas aeruginosa is a main cause of ventilator-associated pneumonia (VAP) with drug-resistant bacteria. Bacteriophage therapy has experienced resurgence to compensate for the limited development of novel antibiotics. However, phage therapy is limited to a compassionate use so far, resulting from lack of adequate studies in relevant pharmacological models. We used a pig model of pneumonia caused by P. aeruginosa that recapitulates essential features of human disease to study the antimicrobial efficacy of nebulized-phage therapy.(i) Lysis kinetic assays were performed to evaluate in vitro phage antibacterial efficacy against P. aeruginosa and select relevant combinations of lytic phages. (ii) The efficacy of the phage combinations was investigated in vivo (murine model of P. aeruginosa lung infection). (iii) We determined the optimal conditions to ensure efficient phage delivery by aerosol during mechanical ventilation. (iv) Lung antimicrobial efficacy of inhaled-phage therapy was evaluated in pigs, which were anaesthetized, mechanically ventilated and infected with P. aeruginosa.By selecting an active phage cocktail and optimizing aerosol delivery conditions, we were able to deliver high phage concentrations in the lungs, which resulted in a rapid and marked reduction in P. aeruginosa density (1.5-log reduction, p < .001). No infective phage was detected in the sera and urines throughout the experiment.Our findings demonstrated (i) the feasibility of delivering large amounts of active phages by nebulization during mechanical ventilation and (ii) rapid control of in situ infection by inhaled bacteriophage in an experimental model of P. aeruginosa pneumonia with high translational value.
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