TY - JOUR
T1 - Case report
T2 - Analysis of phage therapy failure in a patient with a Pseudomonas aeruginosa prosthetic vascular graft infection
AU - Merabishvili, Maya
AU - Pirnay, Jean Paul
N1 - Publisher Copyright:
Copyright © 2023 Blasco, López-Hernández, Rodríguez-Fernández, Pérez-Florido, Casimiro-Soriguer, Djebara, Merabishvili, Pirnay, Rodríguez-Baño, Tomás and López Cortés.
PY - 2023
Y1 - 2023
N2 - Clinical case of a patient with a Pseudomonas aeruginosa multidrug-resistant prosthetic vascular graft infection which was treated with a cocktail of phages (PT07, 14/01, and PNM) in combination with ceftazidime-avibactam (CZA). After the application of the phage treatment and in absence of antimicrobial therapy, a new P. aeruginosa bloodstream infection (BSI) with a septic residual limb metastasis occurred, now involving a wild-type strain being susceptible to ß-lactams and quinolones. Clinical strains were analyzed by microbiology and whole genome sequencing techniques. In relation with phage administration, the clinical isolates of P. aeruginosa before phage therapy (HE2011471) and post phage therapy (HE2105886) showed a clonal relationship but with important genomic changes which could be involved in the resistance to this therapy. Finally, phenotypic studies showed a decrease in Minimum Inhibitory Concentration (MIC) to ß-lactams and quinolones as well as an increase of the biofilm production and phage resistant mutants in the clinical isolate of P. aeruginosa post phage therapy.
AB - Clinical case of a patient with a Pseudomonas aeruginosa multidrug-resistant prosthetic vascular graft infection which was treated with a cocktail of phages (PT07, 14/01, and PNM) in combination with ceftazidime-avibactam (CZA). After the application of the phage treatment and in absence of antimicrobial therapy, a new P. aeruginosa bloodstream infection (BSI) with a septic residual limb metastasis occurred, now involving a wild-type strain being susceptible to ß-lactams and quinolones. Clinical strains were analyzed by microbiology and whole genome sequencing techniques. In relation with phage administration, the clinical isolates of P. aeruginosa before phage therapy (HE2011471) and post phage therapy (HE2105886) showed a clonal relationship but with important genomic changes which could be involved in the resistance to this therapy. Finally, phenotypic studies showed a decrease in Minimum Inhibitory Concentration (MIC) to ß-lactams and quinolones as well as an increase of the biofilm production and phage resistant mutants in the clinical isolate of P. aeruginosa post phage therapy.
KW - Pseudomonas aeruginosa
KW - antibiotic resistance
KW - bypass
KW - phage
KW - phage therapy
KW - prosthetic vascular graft infection
UR - http://www.scopus.com/inward/record.url?scp=85161064959&partnerID=8YFLogxK
U2 - 10.3389/fmed.2023.1199657
DO - 10.3389/fmed.2023.1199657
M3 - Article
AN - SCOPUS:85161064959
SN - 2296-858X
VL - 10
JO - Frontiers in Medicine
JF - Frontiers in Medicine
M1 - 1199657
ER -