Reprogramming resistance: phage-antibiotic synergy targets efflux systems in ESKAPEE pathogens

ABSTRACT Multidrug-resistant (MDR) and extensively drug-resistant (XDR) ESKAPE pathogens pose a significant global health threat due to their ability to evade antibiotics through intrinsic and acquired mechanisms. These bacteria, including Enterococcus faecium, Staphylococcus aureus, Klebsiella pneu...

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Published in:mBio
Main Authors: Anita Tarasenko, Bhavya N. Papudeshi, Susanna R. Grigson, Vijini Mallawaarachchi, Abbey L. K. Hutton, Morgyn S. Warner, Jeremy J. Barr, Jon Iredell, Bart Eijkelkamp, Robert A. Edwards
Format: Article
Language:English
Published: American Society for Microbiology 2025-10-01
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Online Access:https://journals.asm.org/doi/10.1128/mbio.01822-25
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author Anita Tarasenko
Bhavya N. Papudeshi
Susanna R. Grigson
Vijini Mallawaarachchi
Abbey L. K. Hutton
Morgyn S. Warner
Jeremy J. Barr
Jon Iredell
Bart Eijkelkamp
Robert A. Edwards
author_facet Anita Tarasenko
Bhavya N. Papudeshi
Susanna R. Grigson
Vijini Mallawaarachchi
Abbey L. K. Hutton
Morgyn S. Warner
Jeremy J. Barr
Jon Iredell
Bart Eijkelkamp
Robert A. Edwards
author_sort Anita Tarasenko
collection DOAJ
container_title mBio
description ABSTRACT Multidrug-resistant (MDR) and extensively drug-resistant (XDR) ESKAPE pathogens pose a significant global health threat due to their ability to evade antibiotics through intrinsic and acquired mechanisms. These bacteria, including Enterococcus faecium, Staphylococcus aureus, Klebsiella pneumoniae, Acinetobacter baumannii, Pseudomonas aeruginosa, Escherichia coli, and Enterobacter species, evade antibiotics through intrinsic and adaptive mechanisms. Common strategies include capsule formation, biofilm, β-lactamase production, and efflux activity. Using these mechanisms, bacteria can evade the effects of antibiotics, leading to persistent and difficult-to-treat infections. Understanding the mechanisms of resistance is crucial in developing effective strategies to combat MDR and XDR ESKAPEE pathogens. A promising approach is the development of alternative treatments targeting specific resistance mechanisms in these pathogens. Bacteriophages (phages), which co-evolve with bacterial hosts, offer a dynamic therapeutic alternative by targeting pathogenic bacteria using precision-based strategies. This targeted approach can overcome antibiotic resistance and reduce the risk of damaging the beneficial microbiota. Phages can restore susceptibility in previously untreatable infections by enhancing antibiotic uptake and imposing fitness costs on resistant strains. However, therapeutic deployment faces challenges such as rapid evolution of phage resistance, inconsistent production standards, and limited regulatory pathways. This review examines the mechanistic insights into phage-antibiotic synergy, with a focus on efflux pump-mediated resistance. It discusses emerging therapeutic strategies, current clinical applications, and the translational frameworks needed to integrate phage therapy into mainstream medicine and transform the clinical management of drug-resistant ESKAPEE infections.
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spelling doaj-art-a2fbb72404c94df39bd2dafef3e7d2fb2025-10-08T13:01:25ZengAmerican Society for MicrobiologymBio2150-75112025-10-01161010.1128/mbio.01822-25Reprogramming resistance: phage-antibiotic synergy targets efflux systems in ESKAPEE pathogensAnita Tarasenko0Bhavya N. Papudeshi1Susanna R. Grigson2Vijini Mallawaarachchi3Abbey L. K. Hutton4Morgyn S. Warner5Jeremy J. Barr6Jon Iredell7Bart Eijkelkamp8Robert A. Edwards9Flinders Accelerator for Microbiome Exploration, College of Science and Engineering, Flinders University, Adelaide, South Australia, AustraliaFlinders Accelerator for Microbiome Exploration, College of Science and Engineering, Flinders University, Adelaide, South Australia, AustraliaFlinders Accelerator for Microbiome Exploration, College of Science and Engineering, Flinders University, Adelaide, South Australia, AustraliaFlinders Accelerator for Microbiome Exploration, College of Science and Engineering, Flinders University, Adelaide, South Australia, AustraliaFlinders Accelerator for Microbiome Exploration, College of Science and Engineering, Flinders University, Adelaide, South Australia, AustraliaMicrobiology & Infectious Diseases Directorate, SA Pathology, Central Adelaide Local Health Network, Adelaide, South Australia, AustraliaSchool of Biological Sciences, Monash University, Melbourne, Victoria, AustraliaCentre for Infectious Diseases and Microbiology, The Westmead Institute for Medical Research, Westmead, New South Wales, AustraliaCollege of Science and Engineering, Flinders University, Bedford Park, South Australia, AustraliaFlinders Accelerator for Microbiome Exploration, College of Science and Engineering, Flinders University, Adelaide, South Australia, AustraliaABSTRACT Multidrug-resistant (MDR) and extensively drug-resistant (XDR) ESKAPE pathogens pose a significant global health threat due to their ability to evade antibiotics through intrinsic and acquired mechanisms. These bacteria, including Enterococcus faecium, Staphylococcus aureus, Klebsiella pneumoniae, Acinetobacter baumannii, Pseudomonas aeruginosa, Escherichia coli, and Enterobacter species, evade antibiotics through intrinsic and adaptive mechanisms. Common strategies include capsule formation, biofilm, β-lactamase production, and efflux activity. Using these mechanisms, bacteria can evade the effects of antibiotics, leading to persistent and difficult-to-treat infections. Understanding the mechanisms of resistance is crucial in developing effective strategies to combat MDR and XDR ESKAPEE pathogens. A promising approach is the development of alternative treatments targeting specific resistance mechanisms in these pathogens. Bacteriophages (phages), which co-evolve with bacterial hosts, offer a dynamic therapeutic alternative by targeting pathogenic bacteria using precision-based strategies. This targeted approach can overcome antibiotic resistance and reduce the risk of damaging the beneficial microbiota. Phages can restore susceptibility in previously untreatable infections by enhancing antibiotic uptake and imposing fitness costs on resistant strains. However, therapeutic deployment faces challenges such as rapid evolution of phage resistance, inconsistent production standards, and limited regulatory pathways. This review examines the mechanistic insights into phage-antibiotic synergy, with a focus on efflux pump-mediated resistance. It discusses emerging therapeutic strategies, current clinical applications, and the translational frameworks needed to integrate phage therapy into mainstream medicine and transform the clinical management of drug-resistant ESKAPEE infections.https://journals.asm.org/doi/10.1128/mbio.01822-25multidrug resistance (MDR)ESKAPEE pathogensphage therapyefflux pump inhibitionphage-antibiotic synergy
spellingShingle Anita Tarasenko
Bhavya N. Papudeshi
Susanna R. Grigson
Vijini Mallawaarachchi
Abbey L. K. Hutton
Morgyn S. Warner
Jeremy J. Barr
Jon Iredell
Bart Eijkelkamp
Robert A. Edwards
Reprogramming resistance: phage-antibiotic synergy targets efflux systems in ESKAPEE pathogens
multidrug resistance (MDR)
ESKAPEE pathogens
phage therapy
efflux pump inhibition
phage-antibiotic synergy
title Reprogramming resistance: phage-antibiotic synergy targets efflux systems in ESKAPEE pathogens
title_full Reprogramming resistance: phage-antibiotic synergy targets efflux systems in ESKAPEE pathogens
title_fullStr Reprogramming resistance: phage-antibiotic synergy targets efflux systems in ESKAPEE pathogens
title_full_unstemmed Reprogramming resistance: phage-antibiotic synergy targets efflux systems in ESKAPEE pathogens
title_short Reprogramming resistance: phage-antibiotic synergy targets efflux systems in ESKAPEE pathogens
title_sort reprogramming resistance phage antibiotic synergy targets efflux systems in eskapee pathogens
topic multidrug resistance (MDR)
ESKAPEE pathogens
phage therapy
efflux pump inhibition
phage-antibiotic synergy
url https://journals.asm.org/doi/10.1128/mbio.01822-25
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