# Antibiotic-sparing strategies for multidrug-resistant organism (MDRO) infections

**Authors:** Shuai Geng, Qing Tang, Ning Shi

PMC · DOI: 10.3389/fphar.2025.1653424 · Frontiers in Pharmacology · 2025-09-29

## TL;DR

This paper reviews strategies to reduce antibiotic use for treating drug-resistant infections, focusing on alternatives like phages, antibodies, and improved stewardship to combat rising resistance.

## Contribution

The paper introduces a comprehensive framework of antibiotic-sparing interventions, including novel therapies and stewardship innovations, to address multidrug-resistant infections.

## Key findings

- Non-antibiotic therapies like bacteriophages and monoclonal antibodies show promise in targeting MDROs.
- Antimicrobial stewardship with rapid diagnostics and short-course regimens reduces unnecessary antibiotic use.
- Transmission prevention strategies, such as UV-C and microbiota modulation, help curb resistance spread.

## Abstract

The global rise of multidrug-resistant organisms (MDROs), such as carbapenem-resistant Enterobacteriaceae (CRE) and methicillin-resistant Staphylococcus aureus (MRSA), has rendered conventional antibiotics increasingly ineffective, particularly in intensive care units (ICUs) where mortality rates exceed 50% in severe infections. Overuse of broad-spectrum antibiotics accelerates resistance while disrupting host microbiota, necessitating innovative “antibiotic-sparing” strategies. This review synthesizes three pillars of intervention: (1) non-antibiotic therapies, including bacteriophages for targeted pathogen lysis, monoclonal antibodies (e.g., BiS4αPa against Pseudomonas aeruginosa), and nanotechnology-enhanced antimicrobial peptides (AMPs) for biofilm disruption; (2) antimicrobial stewardship integrating rapid diagnostics (MALDI-TOF, mNGS), PK/PD-guided dosing, and short-course regimens (7-day therapy validated by RCTs); and (3) transmission prevention through UV-C disinfection, AI-driven hygiene compliance, and gut microbiota modulation. Key innovations include phage-antibiotic synergies, bispecific antibody engineering, and dynamic PK/PD-TDM frameworks. Despite challenges in clinical translation and cost-effectiveness, these strategies collectively reduce antibiotic reliance, mitigate resistance evolution, and offer a paradigm shift toward precision infection control. Future directions emphasize combinatorial therapies, regulatory harmonization, and scalable environmental-behavioral interventions to address the post-antibiotic era crisis.

## Linked entities

- **Species:** Pseudomonas aeruginosa (taxon 287)

## Full-text entities

- **Diseases:** multidrug-resistant organism (MDRO) infections (MESH:D018088), infection (MESH:D007239)
- **Chemicals:** carbapenem (MESH:D015780), methicillin (MESH:D008712), BiS4alphaPa (-)
- **Species:** Pseudomonas aeruginosa (species) [taxon 287], Enterobacteriaceae (enterobacteria, family) [taxon 543], Staphylococcus aureus (species) [taxon 1280]

## Full text

_Full body text omitted from this summary view._ Fetch the complete paper as Markdown: https://tomesphere.com/paper/PMC12515910/full.md

## Figures

2 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12515910/full.md

## References

58 references — full list in the complete paper: https://tomesphere.com/paper/PMC12515910/full.md

---
Source: https://tomesphere.com/paper/PMC12515910