Journal
APPLIED AND ENVIRONMENTAL MICROBIOLOGY
Volume 85, Issue 9, Pages -Publisher
AMER SOC MICROBIOLOGY
DOI: 10.1128/AEM.02900-18
Keywords
Galleria mellonella infection; Pseudomonas aeruginosa; Siphoviridae; bacteriophage; biofilm; mouse acute pneumonia; phage therapy
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Funding
- Basic Science Research Program through the National Research Foundation of Korea (NRF) - Ministry of Education [NRF-2017R1D1A1B03034730]
- Korea Institute of Planning and Evaluation for Technology in Food, Agriculture, Forestry and Fisheries (IPET) through the Agricultural Microbiome RD Program
- Nano Material Technology Development Program through the National Research Foundation of Korea (NRF) - Ministry of Science and ICT [2017M3A7B4039936]
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Extensively drug-resistant Pseudomonas aeruginosa (XDR-PA) is a life-threatening pathogen that causes serious global problems. Here, we investigated two novel P. aeruginosa bacteriophages (phages), B phi-R656 and B phi-R1836, in vitro, in silico, and in vivo to evaluate the potential of phage therapy to control XDR-PA clinical strains. B phi-R656 and B phi-R1836 belong to the Siphoviridae family and exhibited broad host ranges which could lyse 18 (64%) and 14 (50%) of the 28 XDR-PA strains. In addition, the two phages showed strong bacteriolytic activity against XDR-PA host strains from pneumonia patients. The whole genomes of B phi-R656 and B phi-R1836 have linear double-stranded DNA of 60,919 and 37,714 bp, respectively. The complete sequence of B phi-R656 had very low similarity to the previously discovered P. aeruginosa phages in GenBank, but phage B phi-R1836 exhibited 98% and 91% nucleotide similarity to Pseudomonas phages YMC12/01/R24 and PA1/KOR/2010, respectively. In the two in vivo infection models, treatment with B phi-R656 and B phi-R1836 enhanced the survival of Galleria mellonella larvae (50% and 60%, respectively) at 72 h postinfection and pneumonia-model mice (66% and 83%, respectively) at 12 days postinfection compared with untreated controls. Treatment with B phi-R656 or B phi-R1836 also significantly decreased the bacterial load in the lungs of the mouse pneumonia model (>6 log(10) CFU and >4 log(10) CFU, respectively) on day 5. IMPORTANCE In this study, two novel P. aeruginosa phages, B phi-R656 and B phi-R1836, were evaluated in vitro, in silico, and in vivo for therapeutic efficacy and safety as an alternative antibacterial agent to control XDR-PA strains collected from pneumonia patients. Both phages exhibited potent bacteriolytic activity and greatly improved survival in G. mellonella larva infection and a mouse acute pneumonia model. Based on these results, we strongly predict that these two new phages could be used as fast-acting and safe alternative biological weapons against XDR-PA infections.
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