# Timely bespoke phage-antibiotic combination to treat refractory Pseudomonas aeruginosa mediastinitis and vascular graft infection

**Authors:** Shimin Jasmine Chung, Yang Liu, Shuhua Thong, Yang Zhong, Zhi Soon Chong, Zhining Lim, Sabrina Tan, Jia Hao Yeo, Ming Guang Koh, Nathalie Grace Sy Chua, Dorothy Hui Lin Ng, Winnie Hui-Ling Lee, Tze Peng Lim, Limin Wijaya, Boon Huan Tan, Peng Huat Eric Yap, Thet Tun Aung, Rick Twee-Hee Ong, Karrie Kwan Ki Ko, Tse Hua Nicholas Wong, Yu Lin Charlene Tang, Yee Jim Loh, Teing Ee Tan, Thuan Tong Tan, Sandra Kolundzija, Wilfried Moreira, Andrea Lay-Hoon Kwa

PMC · DOI: 10.1038/s41467-025-68136-y · Nature Communications · 2026-01-09

## TL;DR

A combination of phage therapy and antibiotics successfully treated a difficult-to-cure Pseudomonas infection in a vascular graft.

## Contribution

A systematic phage-antibiotic combination strategy was used to treat a refractory Pseudomonas aeruginosa vascular graft infection.

## Key findings

- Phage therapy sensitized Pseudomonas aeruginosa to antibiotics like levofloxacin and piperacillin-tazobactam.
- The phages used the MexAB-OprM efflux pump as a receptor, contributing to antibiotic sensitization.
- The treatment led to radiological improvement and no recurrence of infection after one year.

## Abstract

Biofilm-related vascular graft infections (VGIs) pose major therapeutic challenges due to persistent, antibiotic-resistant bacteria often residing in retained grafts. Phage therapy offers a promising alternative treatment strategy against biofilm-associated infections, though its use remains mostly ad hoc and typically considered a last-resort intervention. We report here the treatment of a refractory, fluoroquinolone non-susceptible Pseudomonas aeruginosa VGI using a systematically planned and synergistic phage-antibiotic combination approach. Adjunctive phage therapy led to radiological improvement, as seen by reduced 18F-FDG PET/CT tracer uptake around the graft. The patient was transitioned to oral fluoroquinolone suppression therapy with no recurrence of bacteremia to-date, after a year. Our workflow led to the selection of phages that sensitized Pseudomonas aeruginosa to killing by levofloxacin and piperacillin-tazobactam. We established that this phage-driven antibiotic sensitization was due to the ability of our phages to use the MexAB-OprM efflux pump as a receptor. We also showed that our phages had potent anti-biofilm activity. We advocate a systematic, multi-pronged management strategy for refractory VGIs, including early therapeutic drug monitoring (TDM), in vitro antibiotic combination testing (iACT), and timely adjunctive phage therapy. This case illustrates the utility of individualized, strategic approaches and highlights adjunctive phage therapy’s potential in treating complex biofilm-related infections.

Phage therapy is an alternative treatment against biofilm-associated infections. In this case report, phage-antibiotic therapy was used to treat a vascular graft infection caused by a refractory fluoroquinolone non-susceptible Pseudomonas aeruginosa.

## Linked entities

- **Chemicals:** levofloxacin (PubChem CID 149096), piperacillin-tazobactam (PubChem CID 461573)
- **Species:** Pseudomonas aeruginosa (taxon 287)

## Full-text entities

- **Diseases:** infections (MESH:D007239), bacteremia (MESH:D016470), Pseudomonas aeruginosa mediastinitis (MESH:D011552), VGIs (MESH:D006083)
- **Chemicals:** piperacillin-tazobactam (MESH:D000077725), fluoroquinolone (MESH:D024841), 18F-FDG (MESH:D019788), levofloxacin (MESH:D064704)
- **Species:** Pseudomonas aeruginosa (species) [taxon 287], Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

5 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12877064/full.md

## References

6 references — full list in the complete paper: https://tomesphere.com/paper/PMC12877064/full.md

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Source: https://tomesphere.com/paper/PMC12877064