Successful Bacteriophage-Antibiotic Combination Therapy against Multidrug-Resistant Pseudomonas aeruginosa Left Ventricular Assist Device Driveline Infection

Author:

Racenis Karlis123ORCID,Lacis Janis45,Rezevska Dace16,Mukane Laima1ORCID,Vilde Aija7,Putnins Ints5,Djebara Sarah8,Merabishvili Maya9ORCID,Pirnay Jean-Paul9ORCID,Kalnina Marika10,Petersons Aivars23,Stradins Peteris45,Maurins Sandis1ORCID,Kroica Juta1ORCID

Affiliation:

1. Department of Biology and Microbiology, Riga Stradins University, LV-1007 Riga, Latvia

2. Department of Internal Diseases, Riga Stradins University, LV-1007 Riga, Latvia

3. Center of Nephrology, Pauls Stradins Clinical University Hospital, LV-1002 Riga, Latvia

4. Department of Surgery, Riga Stradins University, LV-1007 Riga, Latvia

5. Centre of Cardiac Surgery, Pauls Stradins Clinical University Hospital, LV-1002 Riga, Latvia

6. Joint Laboratory, Pauls Stradins Clinical University Hospital, LV-1002 Riga, Latvia

7. Department of Infection Prevention and Control, Pauls Stradins Clinical University Hospital, LV-1002 Riga, Latvia

8. Center for Infectious Diseases, Queen Astrid Military Hospital, B-1120 Brussels, Belgium

9. Laboratory for Molecular and Cellular Technology, Queen Astrid Military Hospital, B-1120 Brussels, Belgium

10. Institute of Radiology, Pauls Stradins Clinical University Hospital, LV-1002 Riga, Latvia

Abstract

There is considerable interest in the use of bacteriophages (phages) to treat Pseudomonas aeruginosa infections associated with left ventricular assist devices (LVADs). These infections are often challenging to manage due to high rates of multidrug resistance and biofilm formation, which could potentially be overcome with the use of phages. We report a case of a 54-year-old man with relapsing multidrug-resistant P. aeruginosa LVAD driveline infection, who was treated with a combination of two lytic antipseudomonal phages administered intravenously and locally. Treatment was combined with LVAD driveline repositioning and systemic antibiotic administration, resulting in a successful outcome with clinical cure and eradication of the targeted bacteria. However, laboratory in vitro models showed that phages alone could not eradicate biofilms but could prevent biofilm formation. Phage-resistant bacterial strains evolved in biofilm models and showed decreased susceptibility to the phages used. Further studies are needed to understand the complexity of phage resistance and the interaction of phages and antibiotics. Our results indicate that the combination of phages, antibiotics, and surgical intervention can have great potential in treating LVAD-associated infections. More than 21 months post-treatment, our patient remains cured of the infection.

Publisher

MDPI AG

Subject

Virology,Infectious Diseases

Reference30 articles.

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