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Phage Therapy in Combating Multidrug-Resistant Gram-Negative Pathogens: A Scoping Review
Asif Sukri1, Bruno Silvester Lopes2,3, Alfizah Hanafiah4
1Department of Biological Sciences and Biotechnology, Faculty of Science and Technology, Universiti Kebangsaan Malaysia, Bangi 43600, Selangor, Malaysia.
Abstract:
Background: The emergence of multidrug-resistant (MDR) Gram-negative pathogens, namely Klebsiella pneumoniae, Pseudomonas aeruginosa, Acinetobacter baumannii and Helicobacter pylori, necessitates urgent therapeutic alternatives. This scoping review aimed to summarize the current evidence on the efficacy of lytic bacteriophages against these critical MDR pathogens, and to identify existing research gaps and implementation challenges. Methods: The literature search was conducted by searching PubMed, Web of Science, and Scopus AI for studies published from 2015 to 2025. The inclusion criteria focused on experimental and human studies evaluating phage therapy against MDR, extensively drug-resistant (XDR), or pan-drug-resistant (PDR) strains in the four target species. A total of 172 articles were included. Results: A number of studies showed an increasing trend (2015-2025), focusing mainly on K. pneumoniae (n = 65), P. aeruginosa (n = 55), and A. baumannii (n = 48). No eligible studies for MDR H. pylori were found. All 172 studies confirmed lytic activity, with phage cocktails showing superior antibacterial activity than single phages in four studies. Phages also demonstrated antibiofilm activity (n = 44). Most animal studies reported successful bacterial reduction in animals treated with phages, and 87.5% of 23 human case studies reported patient improvement or infection clearance. However, heterogeneity in the types of animal models used and in dosage and administration routes in human studies was notable. Conclusions: Lytic bacteriophages exhibit strong potential as a new therapeutic option. Key challenges include the lack of data for MDR H. pylori, heterogeneity in animal models, and a paucity of large-scale human clinical trials. Future research must prioritize standardization, mechanistic studies, and conducting robust human trials to enable clinical translation and regulatory acceptance.
Insights
Lytic bacteriophages show promise against multidrug-resistant Gram-negative bacteria like Klebsiella pneumoniae and Pseudomonas aeruginosa. However, more research is needed for Helicobacter pylori and larger human trials are crucial for clinical use.
Area of Science:
- * Microbiology
- * Infectious Diseases
- * Pharmacology
Background:
- * Rising threat of multidrug-resistant (MDR) Gram-negative pathogens: Klebsiella pneumoniae, Pseudomonas aeruginosa, Acinetobacter baumannii, and Helicobacter pylori.
- * Urgent need for novel therapeutic alternatives to combat these resistant infections.
Purpose of the Study:
- * To review current evidence on the efficacy of lytic bacteriophages against critical MDR Gram-negative pathogens.
- * To identify research gaps and challenges in the implementation of phage therapy.
Main Methods:
- * Scoping review of literature from 2015-2025, searching PubMed, Web of Science, and Scopus AI.
- * Inclusion of experimental and human studies on phage therapy for MDR, extensively drug-resistant (XDR), or pan-drug-resistant (PDR) strains.
- * Analysis of 172 selected articles.
Main Results:
- * Increasing research trend from 2015-2025, predominantly on K. pneumoniae, P. aeruginosa, and A. baumannii.
- * No eligible studies found for MDR H. pylori.
- * All studies confirmed lytic activity; phage cocktails were superior to single phages in some cases.
- * Demonstrated antibiofilm activity and successful bacterial reduction in animal models.
- * 87.5% of human case studies reported patient improvement or infection clearance.
Conclusions:
- * Lytic bacteriophages present a strong potential as a novel therapeutic strategy.
- * Significant challenges remain: lack of data for MDR H. pylori, heterogeneity in animal models, and limited large-scale human trials.
- * Future research should focus on standardization, mechanistic studies, and robust clinical trials for regulatory acceptance.
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