Pharmacodynamic individualization of phage therapy against a KPC-5-producing <i>Pseudomonas aeruginosa</i>
This highlights the potential of reverse translational pharmacokinetic/pharmacodynamic-driven approaches to guide rational phage selection strategies against individual clinical isolates while identifying potential antagonistic phage-phage interactions.
Authors
- Chen Liang (ORCID: https://orcid.org/0000-0002-0023-1066)
- Brian M. Ho (ORCID: https://orcid.org/0000-0003-1533-6263)
- Thomas D. Nguyen (ORCID: https://orcid.org/0009-0000-1069-1720)
- Nicholas M. Smith (ORCID: https://orcid.org/0000-0002-0212-2787)
- Dwayne R. Roach (ORCID: https://orcid.org/0000-0002-2069-8915)
- Tiffany Luong (ORCID: https://orcid.org/0000-0002-7694-277X)
- Jacob T. Sanborn
- Wood Troy
Institutions
- San Diego State University (US)
- University at Buffalo, State University of New York (US)
Publication Details
- Journal
- JAC-Antimicrobial Resistance
- Published
- 2025-12-19
- DOI
- https://doi.org/10.1093/jacamr/dlaf257
- Primary Topic
- Bacteriophages and microbial interactions
- Type
- article
- Field-Weighted Citation Impact
- 0.00