Repetitive Exposure to Bacteriophage Cocktails against Pseudomonas aeruginosa or Escherichia coli Provokes Marginal Humoral Immunity in Naïve Mice

Author:

Weissfuss Chantal1ORCID,Wienhold Sandra-Maria1,Bürkle Magdalena1ORCID,Gaborieau Baptiste234ORCID,Bushe Judith5ORCID,Behrendt Ulrike1,Bischoff Romina1ORCID,Korf Imke H. E.6ORCID,Wienecke Sarah6,Dannheim Antonia6,Ziehr Holger6,Rohde Christine7,Gruber Achim D.5ORCID,Ricard Jean-Damien34ORCID,Debarbieux Laurent2ORCID,Witzenrath Martin18ORCID,Nouailles Geraldine1ORCID

Affiliation:

1. Charité–Universitätsmedizin Berlin, Corporate Member of Freie Universität Berlin and Humboldt-Universität zu Berlin, Department of Infectious Diseases, Respiratory Medicine and Critical Care, 10117 Berlin, Germany

2. Institut Pasteur, Université Paris Cité, CNRS UMR6047, Department of Microbiology, Bacteriophage Bacteria Host, 75015 Paris, France

3. Université Paris Cité, INSERM UMR1137, IAME, 75018 Paris, France

4. APHP, Hôpital Louis Mourier, DMU ESPRIT, Service de Médecine Intensive Réanimation, 92700 Colombes, France

5. Department of Veterinary Pathology, Freie Universität Berlin, 14163 Berlin, Germany

6. Department of Pharmaceutical Biotechnology, Fraunhofer Institute for Toxicology and Experimental Medicine (ITEM), 38124 Braunschweig, Germany

7. Department of Microorganisms, Leibniz Institute DSMZ, German Collection of Microorganisms and Cell Cultures GmbH, 38124 Braunschweig, Germany

8. German Center for Lung Research (DZL), Partner Site Charité, 10117 Berlin, Germany

Abstract

Phage therapy of ventilator-associated pneumonia (VAP) is of great interest due to the rising incidence of multidrug-resistant bacterial pathogens. However, natural or therapy-induced immunity against therapeutic phages remains a potential concern. In this study, we investigated the innate and adaptive immune responses to two different phage cocktails targeting either Pseudomonas aeruginosa or Escherichia coli—two VAP-associated pathogens—in naïve mice without the confounding effects of a bacterial infection. Active or UV-inactivated phage cocktails or buffers were injected intraperitoneally daily for 7 days in C57BL/6J wild-type mice. Blood cell analysis, flow cytometry analysis, assessment of phage distribution and histopathological analysis of spleens were performed at 6 h, 10 days and 21 days after treatment start. Phages reached the lungs and although the phage cocktails were slightly immunogenic, phage injections were well tolerated without obvious adverse effects. No signs of activation of innate or adaptive immune cells were observed; however, both active phage cocktails elicited a minimal humoral response with secretion of phage-specific antibodies. Our findings show that even repetitive injections lead only to a minimal innate and adaptive immune response in naïve mice and suggest that systemic phage treatment is thus potentially suitable for treating bacterial lung infections.

Funder

Federal Ministry of Education and Research

Agence Nationale de la Recherche

DFG

Publisher

MDPI AG

Subject

Virology,Infectious Diseases

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