Isolation and Characterization of a Lytic Phage vB_EcoS_GZMU_E2010: A Promising Candidate against Clinical Multidrug-Resistant <i>Escherichia coli</i>

The global escalation of bacterial antimicrobial resistance, particularly in <i>Escherichia coli</i>, constitutes an urgent public health threat. Bacteriophages represent a promising therapeutic arsenal against multidrug-resistant pathogens, underscoring the necessity of acquiring additional phages to expand phage libraries. In response to multidrug-resistant <i>E. coli</i>, this study isolated a lytic phage, designated <i>E. coli</i> phage vB_EcoS_GZMU_E2010. This phage demonstrated effective lytic activity against pathogenic <i>E. coli</i> strains, that included Extended-Spectrum β-Lactamase-producing <i>E. coli</i> (ESBL-<i>E. coli</i>) strains. The time-kill kinetics and terminal growth suppression data illustrate that, bacteriophage vB_EcoS_GZMU_E2010 exhibits potent antimicrobial action across a wide range of MOIs (from 0.001 to 1000). Transmission electron microscopy revealed that phage exhibits a siphovirus-like morphology within class <i>Caudoviricetes</i>, featuring a long noncontractile tail and icosahedral capsid. Whole-genome sequencing identified a 44,255 bp circular double-stranded DNA genome with 50.81% GC content. Comparative genomics revealed <95% whole-genome nucleotide identity to all reported phages, with the closest relative (<i>Escherichia</i> phage hz69, GenBank accession: ON556632.1) sharing only 90.7% identity, establishing its taxonomic novelty. Following a 60 min latent period, the phage entered a rapid burst phase characterized by exponential titer increase. Viral progeny release plateaued at 80 min postinfection. Bacteriophage vB_EcoS_GZMU_E2010 exhibited high stability across temperature (4-50 °C) and pH (4-10) gradients. Comprehensive screening confirmed the absence of antibiotic resistance genes and virulence factors. Besides, the maximum inhibition rate of this bacteriophage on biofilm reached 73.5%. Collectively, these findings position phage vB_EcoS_GZMU_E2010 as a promising candidate for combating drug-resistant infections, providing a potential strategy against multidrug-resistant <i>E. coli</i> pathogenesis.

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Publication Details

Journal
ACS Infectious Diseases
Published
2026-03-24
DOI
https://doi.org/10.1021/acsinfecdis.5c01070
Primary Topic
Bacteriophages and microbial interactions
Type
article
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article

Isolation and Characterization of a Lytic Phage vB_EcoS_GZMU_E2010: A Promising Candidate against Clinical Multidrug-Resistant Escherichia coli

ACS Infectious Diseases
Bacteriophages and microbial interactions
article

Isolation and Characterization of a Lytic Phage vB_EcoS_GZMU_E2010: A Promising Candidate against Clinical Multidrug-Resistant Escherichia coli

article en

Abstract

The global escalation of bacterial antimicrobial resistance, particularly in <i>Escherichia coli</i>, constitutes an urgent public health threat. Bacteriophages represent a promising therapeutic arsenal against multidrug-resistant pathogens, underscoring the necessity of acquiring additional phages to expand phage libraries. In response to multidrug-resistant <i>E. coli</i>, this study isolated a lytic phage, designated <i>E. coli</i> phage vB_EcoS_GZMU_E2010. This phage demonstrated effective lytic activity against pathogenic <i>E. coli</i> strains, that included Extended-Spectrum β-Lactamase-producing <i>E. coli</i> (ESBL-<i>E. coli</i>) strains. The time-kill kinetics and terminal growth suppression data illustrate that, bacteriophage vB_EcoS_GZMU_E2010 exhibits potent antimicrobial action across a wide range of MOIs (from 0.001 to 1000). Transmission electron microscopy revealed that phage exhibits a siphovirus-like morphology within class <i>Caudoviricetes</i>, featuring a long noncontractile tail and icosahedral capsid. Whole-genome sequencing identified a 44,255 bp circular double-stranded DNA genome with 50.81% GC content. Comparative genomics revealed <95% whole-genome nucleotide identity to all reported phages, with the closest relative (<i>Escherichia</i> phage hz69, GenBank accession: ON556632.1) sharing only 90.7% identity, establishing its taxonomic novelty. Following a 60 min latent period, the phage entered a rapid burst phase characterized by exponential titer increase. Viral progeny release plateaued at 80 min postinfection. Bacteriophage vB_EcoS_GZMU_E2010 exhibited high stability across temperature (4-50 °C) and pH (4-10) gradients. Comprehensive screening confirmed the absence of antibiotic resistance genes and virulence factors. Besides, the maximum inhibition rate of this bacteriophage on biofilm reached 73.5%. Collectively, these findings position phage vB_EcoS_GZMU_E2010 as a promising candidate for combating drug-resistant infections, providing a potential strategy against multidrug-resistant <i>E. coli</i> pathogenesis.

ACS Infectious Diseases
Hunan University (CN), Hunan Normal University (CN), Third Affiliated Hospital of Southern Medical University (CN), Second Affiliated Hospital of Zhengzhou University (CN), Zhujiang Hospital (CN), State Key Laboratory of Respiratory Disease (CN), Pulmonary and Critical Care Associates (US), Southern Medical University (CN), Guangzhou Medical University (CN)
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Bacteriophages and microbial interactions
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