Prostatitis caused by antibiotic-resistant Escherichia coli pose a significant treatment challenge. Phage therapy is emerging as a promising antibacterial strategy. We report the case of a patient with a prostatitis caused by an ESBL-producing E. coli successfully treated with with oral doxycycline and two phage cocktails. The use of doxycycline was supported by the detection of Mycoplasma spp. in the patient's urine. We also tested the same phage-antibiotic combination against a panel of different E. coli strains in vitro.
A patient received oral SES and PYO phage cocktails alongside oral doxycycline for 30 days. The MIC values of doxycycline and phages alone and in combination were evaluated by checkboard assay versus five E. coli isolates, including the patient's strain. Synergy was assessed using a modified fractional inhibitory concentration (FIC) index. Data were analysed by synogram and interaction plot based on the percentage reduction of the absorbance values (OD570) between untreated control and treated samples. Growth curves were performed over 24 hours to monitor bacterial replication in presence/absence of phage and/or antibiotic.
After treatment, microbiological cultures were negative, and symptoms remitted. In vitro, synergy/additive effect between doxycycline and phages was observed in three out of five E. coli isolates. Synogram analysis showed the synergistic effect versus one strain, while an additive effect was observed for the other four isolates. Growth curve analysis demonstrated enhanced bacterial growth inhibition for up to 12 hours with the combined treatment compared to either therapy alone.
Although the E. coli strain was resistant to doxycycline, the antibiotic was administered specifically to target the Mycoplasma infection. Interestingly, the enhanced in vitro activity observed when the antibiotic was combined with phages versus E. coli suggests that this combination may be effective in eradicating chronic prostatitis caused by ESBL-producing E. coli.
International journal of antimicrobial agents. 2025 Jul 03 [Epub ahead of print]
Novella Cesta, Alessandro Fusco, Caterina Ferretti, Alessandro Materazzi, Anna Altieri, Cartesio D'Agostini, Marco Iannetta, Massimo Andreoni, Arianna Tavanti, Loredana Sarmati, Mariagrazia Di Luca
PhD course in Microbiology, Immunology, Infectious Diseases, and Transplants (MIMIT), University of Tor Vergata, Rome, Italy. Present adress/affiliation: Infectious Diseases Unit, Department of Clinical and Experimental Medicine, Azienda Ospedaliero Universitaria Pisana, University of Pisa, Pisa, Italy. Electronic address: ., Department of Biology, University of Pisa, Pisa Italy., Department of Experimental Medicine and Surgery, Unit of Microbiology and Virology, Policlinic of Tor Vergata, Rome, Italy., Infectious Diseases Clinic, Policlinic of Tor Vergata, Rome, Italy and Department of Systems Medicine, University of Rome Tor Vergata, Rome, Italy., Department of Biology, University of Pisa, Pisa Italy. Electronic address: .