Abstract

Post-operative bacterial infections are a leading cause of mortality and morbidity after ongoing liver transplantation. Bacteria causing these infections in the hospital setting can exhibit high degrees of resistance to multiple types of antibiotics, which leads to major therapeutic hurdles. Alternate ways of treating these antibiotic-resistant infections are thus urgently needed. Phage therapy is one of them and consists in using selected bacteriophage viruses – viruses who specifically prey on bacteria, naturally found in various environmental samples – as bactericidal agents in replacement or in combination with antibiotics. The use of phage therapy raises various research questions to further characterize what determines therapeutic success or failure. In this work, we report the story of a toddler who suffered from extensively drug-resistant Pseudomonas aeruginosa sepsis after liver transplantation. He was treated by a bacteriophage-antibiotic intravenous combination therapy for 86 days. This salvage therapy was well tolerated, without antibody-mediated phage neutralization. It was associated with objective clinical and microbiological improvement, eventually allowing for liver retransplantation and complete resolution of all infections. Clear in vitro phage-antibiotic synergies were observed. The occurrence of bacterial phage resistance did not result in therapeutic failure, possibly due to phage-induced virulence tradeoffs, which we investigated in different experimental models.

In this study, authors use combinatory bacteriophage-antibiotic therapy, as treatment for extensively drug-resistant Pseudomonas aeruginosa infection in a toddler post liver transplantation. They report on the clinical and microbiological improvement, and present their investigation on how bacterial phage resistance did not result in therapeutic failure.

Details

Title
Bacteriophage-antibiotic combination therapy against extensively drug-resistant Pseudomonas aeruginosa infection to allow liver transplantation in a toddler
Author
Van Nieuwenhuyse, Brieuc 1   VIAFID ORCID Logo  ; Van der Linden, Dimitri 2 ; Chatzis, Olga 3 ; Lood, Cédric 4   VIAFID ORCID Logo  ; Wagemans, Jeroen 5   VIAFID ORCID Logo  ; Lavigne, Rob 5   VIAFID ORCID Logo  ; Schroven, Kaat 5   VIAFID ORCID Logo  ; Paeshuyse, Jan 6 ; de Magnée, Catherine 7 ; Sokal, Etienne 8 ; Stéphenne, Xavier 8 ; Scheers, Isabelle 8 ; Rodriguez-Villalobos, Hector 9   VIAFID ORCID Logo  ; Djebara, Sarah 10 ; Merabishvili, Maya 11 ; Soentjens, Patrick 12 ; Pirnay, Jean-Paul 11   VIAFID ORCID Logo 

 Université catholique de Louvain - UCLouvain, Institute of Experimental and Clinical Research, Pediatric Department (IREC/PEDI), Brussels, Belgium (GRID:grid.7942.8) (ISNI:0000 0001 2294 713X) 
 Université catholique de Louvain - UCLouvain, Institute of Experimental and Clinical Research, Pediatric Department (IREC/PEDI), Brussels, Belgium (GRID:grid.7942.8) (ISNI:0000 0001 2294 713X); Université catholique de Louvain - UCLouvain, Pediatric Infectious Diseases, General Pediatrics Department, Cliniques universitaires Saint-Luc, Brussels, Belgium (GRID:grid.7942.8) (ISNI:0000 0001 2294 713X) 
 Université catholique de Louvain - UCLouvain, Pediatric Infectious Diseases, General Pediatrics Department, Cliniques universitaires Saint-Luc, Brussels, Belgium (GRID:grid.7942.8) (ISNI:0000 0001 2294 713X) 
 Laboratory of Gene Technology, KU Leuven, Department of Biosystems, Leuven, Belgium (GRID:grid.5596.f) (ISNI:0000 0001 0668 7884); Laboratory of Computational Systems Biology, KU Leuven, Department of Microbial and Molecular Systems, Centre of Microbial and Plant Genetics, Leuven, Belgium (GRID:grid.5596.f) (ISNI:0000 0001 0668 7884) 
 Laboratory of Gene Technology, KU Leuven, Department of Biosystems, Leuven, Belgium (GRID:grid.5596.f) (ISNI:0000 0001 0668 7884) 
 KU Leuven, Department of Biosystems, Laboratory of Host Pathogen Interactions, Leuven, Belgium (GRID:grid.5596.f) (ISNI:0000 0001 0668 7884) 
 Cliniques universitaires Saint-Luc, Pediatric and Transplantation Surgery, Brussels, Belgium (GRID:grid.48769.34) (ISNI:0000 0004 0461 6320) 
 Cliniques universitaires Saint-Luc, Pediatric Hepatology and Gastroenterology, Brussels, Belgium (GRID:grid.48769.34) (ISNI:0000 0004 0461 6320) 
 Cliniques universitaires Saint-Luc / Université catholique de Louvain - UCLouvain, Department of Microbiology, Brussels, Belgium (GRID:grid.48769.34) (ISNI:0000 0004 0461 6320) 
10  Queen Astrid Military Hospital, Center for Infectious Diseases, Brussels, Belgium (GRID:grid.415475.6) (ISNI:0000 0004 0610 4943) 
11  Queen Astrid Military Hospital, Laboratory for Molecular and Cellular Technology, Brussels, Belgium (GRID:grid.415475.6) (ISNI:0000 0004 0610 4943) 
12  Queen Astrid Military Hospital, Center for Infectious Diseases, Brussels, Belgium (GRID:grid.415475.6) (ISNI:0000 0004 0610 4943); Institute of Tropical Medicine, Department of Clinical Sciences, Antwerp, Belgium (GRID:grid.11505.30) (ISNI:0000 0001 2153 5088) 
Publication year
2022
Publication date
2022
Publisher
Nature Publishing Group
e-ISSN
20411723
Source type
Scholarly Journal
Language of publication
English
ProQuest document ID
2719248399
Copyright
© The Author(s) 2022. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.