Phage therapy in a lung transplant recipient with cystic fibrosis infected with multidrug‐resistant Burkholderia multivorans

Author:

Haidar Ghady1ORCID,Chan Benjamin K.2,Cho Shu‐Ting1ORCID,Hughes Kramer Kailey1ORCID,Nordstrom Hayley R.1,Wallace Nathan R.1,Stellfox Madison E.1ORCID,Holland Mische1ORCID,Kline Ellen G.1,Kozar Jennifer M.3,Kilaru Silpa D.4,Pilewski Joseph M.4ORCID,LiPuma John J.5ORCID,Cooper Vaughn S.67ORCID,Shields Ryan K.1ORCID,Van Tyne Daria17ORCID

Affiliation:

1. Division of Infectious Diseases University of Pittsburgh School of Medicine Pittsburgh Pennsylvania USA

2. Department of Ecology and Evolutionary Biology, and Yale Center for Phage Biology and Therapy Yale University New Haven Connecticut USA

3. Investigational Drug Service University of Pittsburgh Medical Center Pittsburgh Pennsylvania USA

4. Division of Pulmonary Allergy, and Critical Care Medicine, University of Pittsburgh School of Medicine Pittsburgh Pennsylvania USA

5. Department of Pediatrics University of Michigan School of Medicine Ann Arbor Michigan USA

6. Department of Microbiology and Molecular Genetics University of Pittsburgh School of Medicine Pittsburgh Pennsylvania USA

7. Center for Evolutionary Biology and Medicine University of Pittsburgh School of Medicine Pittsburgh Pennsylvania USA

Abstract

AbstractBackgroundThere is increased interest in bacteriophage (phage) therapy to treat infections caused by antibiotic‐resistant bacteria. A lung transplant recipient with cystic fibrosis and Burkholderia multivorans infection was treated with inhaled phage therapy for 7 days before she died.MethodsPhages were given via nebulization through the mechanical ventilation circuit. Remnant respiratory specimens and serum were collected. We quantified phage and bacterial deoxyribonucleic acid (DNA) using quantitative polymerase chain reaction, and tested phage neutralization in the presence of patient serum. We performed whole genome sequencing and antibiotic and phage susceptibility testing on 15 B. multivorans isolates. Finally, we extracted lipopolysaccharide (LPS) from two isolates and visualized their LPS using gel electrophoresis.ResultsPhage therapy was temporally followed by a temporary improvement in leukocytosis and hemodynamics, followed by worsening leukocytosis on day 5, deterioration on day 7, and death on day 8. We detected phage DNA in respiratory samples after 6 days of nebulized phage therapy. Bacterial DNA in respiratory samples decreased over time, and no serum neutralization was detected. Isolates collected between 2001 and 2020 were closely related but differed in their antibiotic and phage susceptibility profiles. Early isolates were not susceptible to the phage used for therapy, while later isolates, including two isolates collected during phage therapy, were susceptible. Susceptibility to the phage used for therapy was correlated with differences in O‐antigen profiles of an early versus a late isolate.ConclusionsThis case of clinical failure of nebulized phage therapy highlights the limitations, unknowns, and challenges of phage therapy for resistant infections. image

Funder

Cystic Fibrosis Foundation

National Institute of Allergy and Infectious Diseases

Publisher

Wiley

Subject

Infectious Diseases,Transplantation

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