Nature Communications (Apr 2024)

Phage-specific immunity impairs efficacy of bacteriophage targeting Vancomycin Resistant Enterococcus in a murine model

  • Julia D. Berkson,
  • Claire E. Wate,
  • Garrison B. Allen,
  • Alyxandria M. Schubert,
  • Kristin E. Dunbar,
  • Michael P. Coryell,
  • Rosa L. Sava,
  • Yamei Gao,
  • Jessica L. Hastie,
  • Emily M. Smith,
  • Charlotte R. Kenneally,
  • Sally K. Zimmermann,
  • Paul E. Carlson

DOI
https://doi.org/10.1038/s41467-024-47192-w
Journal volume & issue
Vol. 15, no. 1
pp. 1 – 14

Abstract

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Abstract Bacteriophage therapy is a promising approach to address antimicrobial infections though questions remain regarding the impact of the immune response on clinical effectiveness. Here, we develop a mouse model to assess phage treatment using a cocktail of five phages from the Myoviridae and Siphoviridae families that target Vancomycin-Resistant Enterococcus gut colonization. Phage treatment significantly reduces fecal bacterial loads of Vancomycin-Resistant Enterococcus. We also characterize immune responses elicited following administration of the phage cocktail. While minimal innate responses are observed after phage administration, two rounds of treatment induces phage-specific neutralizing antibodies and accelerate phage clearance from tissues. Interestingly, the myophages in our cocktail induce a more robust neutralizing antibody response than the siphophages. This anti-phage immunity reduces the effectiveness of the phage cocktail in our murine model. Collectively, this study shows phage-specific immune responses may be an important consideration in the development of phage cocktails for therapeutic use.