Kinetics of Targeted Phage Rescue in a Mouse Model of Systemic Escherichia coli K1

• Published in: BioMed research international 2018-01, Vol.2018 (2018), p.1-8
• Main Authors: Kovács, Tamás, Rákhely, Gábor, Doffkay, Zsolt, Nagy, Gábor, Cox, A., Dorn, Á., Horváth, Marianna, Szentes, Nikolett, Schneider, György, Maróti, Gergely
• Format: Article
• Language: English
• Subjects: Analysis; Animal models; Animals; Antimicrobial agents; Bacteria; Bacterial infections; Bacteriophages; Capsular polysaccharides; Chemical compounds; Disease Models, Animal; E coli; Escherichia coli; Escherichia coli - pathogenicity; Escherichia coli Infections - drug therapy; Health aspects; Infections; Kinetics; Meningitis; Mice; Neonates; Phages; Pharmacology; Polysaccharides; Sepsis; Spleen
• ISSN: 2314-6133; 2314-6141
• DOI: 10.1155/2018/7569645

Escherichia (E.) coli K1 strains remain common causative agents of neonatal sepsis and meningitis. We have isolated a lytic bacteriophage (ΦIK1) against E. coli strain IHE3034 and tested its specificity in vitro, as well as distribution and protective efficacy in vivo. The phage was shown to be specific to the K1 capsular polysaccharide. In the lethal murine model, a high level of protection was afforded by the phage with strict kinetics. A single dose of 1 x 108 phage particles administered 10 and 60 minutes following the bacterial challenge elicited 100 % and 95 % survival, respectively. No mice could be rescued if phage administration occurred 3 hours postinfection. Tissue distribution surveys in the surviving mice revealed that the spleen was the primary organ in which accumulation of active ΦIK1 phages could be detected two weeks after phage administration. These results suggest that bacteriophages have potential as therapeutic agents in the control of systemic infections.