Physicochemical, genomic, and phenotypic characterization of <i>Escherichia</i> phage BME3

Infections caused by pathogenic <i>Escherichia coli</i> strains are increasing, and with the rising of antimicrobial resistance among bacterial pathogens, alternative therapeutic options are being actively explored, including phage therapy. In this research, a new bacteriophage, provisionally named BME3, with lytic activity against <i>Escherichia coli</i> was identified and characterized at the physicochemical, morphological, and genetic levels. BME3 was isolated from the tropical estuarine waters of Estero Salado, Guayaquil, Ecuador. Subsequently, it was purified and amplified, followed by a series of tests that included host range, stability studies, morphological characterization by transmission electron microscopy (TEM), and whole genome sequencing. The genomic analysis revealed that BME3 is closely related to members of the genus <i>Justusliebigvirus</i>, with a double-stranded DNA genome of 147,371 bp in length, a GC content of 37.5%, and 16 tRNA genes. In addition, BME3 lacks genes associated with lysogenesis, antibiotic resistance, or virulence. BME3 infected approximately 48% (13/27) of environmental <i>E. coli</i> strains. Among these, the infection rate was higher for antibiotic-resistant strains (67%) compared to intermediate and sensitive strains (33%). The phage infected <i>E. coli</i> and <i>Salmonella</i> sp. strains but did not affect <i>Bacillus</i> sp., <i>Pseudomonas</i> sp., or <i>Vibrio</i> sp. Moreover, BME3 was found to be stable at temperatures below 60°C, in pH ranges between 5 and 9, and was not sensitive to chloroform. TEM analysis supported the genetic sequence that assigned BME3 to the class <i>Caudoviricetes</i>. Phenotypic, genomic, and physicochemical characterization suggests that BME3 represents a promising option for phage therapy, with the potential to control antibiotic-resistant bacteria.IMPORTANCEAlthough metagenomics offers a wealth of information, not all microorganisms can be isolated and cultivated in the laboratory. In this study, we successfully isolated and characterized a phage belonging to the <i>Justusliebigvirus</i> genus. This group has been poorly studied regarding its physicochemical properties and lysis profile against antibiotic-resistant environmental bacteria. These bacteriophages have received less attention compared to well-studied models such as phage T4. The isolation and characterization of the indigenous polyvalent bacteriophage BME3, obtained from tropical estuarine waters in Ecuador, provide valuable insights into its potential applications for environmental control of <i>Escherichia coli</i> and for mitigating the spread of bacterial resistance.

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Journal
Microbiology Spectrum
Published
2025-05-22
DOI
https://doi.org/10.1128/spectrum.01301-24
Citations
2
Primary Topic
Bacteriophages and microbial interactions
Type
article
Field-Weighted Citation Impact
3.43
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article

Physicochemical, genomic, and phenotypic characterization of Escherichia phage BME3

Marynés Montiel, Omar Ruíz-Barzola, diego fernando quito-avila, Alexis Debut et al.
2 citations
Microbiology Spectrum
Bacteriophages and microbial interactions
3.43
article

Physicochemical, genomic, and phenotypic characterization of Escherichia phage BME3

Marynés Montiel, Omar Ruíz-Barzola, diego fernando quito-avila, Alexis Debut, Pedro Maldonado‐Alvarado, Belén Toaquiza-Vilca
article en
2 citations

Abstract

Infections caused by pathogenic <i>Escherichia coli</i> strains are increasing, and with the rising of antimicrobial resistance among bacterial pathogens, alternative therapeutic options are being actively explored, including phage therapy. In this research, a new bacteriophage, provisionally named BME3, with lytic activity against <i>Escherichia coli</i> was identified and characterized at the physicochemical, morphological, and genetic levels. BME3 was isolated from the tropical estuarine waters of Estero Salado, Guayaquil, Ecuador. Subsequently, it was purified and amplified, followed by a series of tests that included host range, stability studies, morphological characterization by transmission electron microscopy (TEM), and whole genome sequencing. The genomic analysis revealed that BME3 is closely related to members of the genus <i>Justusliebigvirus</i>, with a double-stranded DNA genome of 147,371 bp in length, a GC content of 37.5%, and 16 tRNA genes. In addition, BME3 lacks genes associated with lysogenesis, antibiotic resistance, or virulence. BME3 infected approximately 48% (13/27) of environmental <i>E. coli</i> strains. Among these, the infection rate was higher for antibiotic-resistant strains (67%) compared to intermediate and sensitive strains (33%). The phage infected <i>E. coli</i> and <i>Salmonella</i> sp. strains but did not affect <i>Bacillus</i> sp., <i>Pseudomonas</i> sp., or <i>Vibrio</i> sp. Moreover, BME3 was found to be stable at temperatures below 60°C, in pH ranges between 5 and 9, and was not sensitive to chloroform. TEM analysis supported the genetic sequence that assigned BME3 to the class <i>Caudoviricetes</i>. Phenotypic, genomic, and physicochemical characterization suggests that BME3 represents a promising option for phage therapy, with the potential to control antibiotic-resistant bacteria.IMPORTANCEAlthough metagenomics offers a wealth of information, not all microorganisms can be isolated and cultivated in the laboratory. In this study, we successfully isolated and characterized a phage belonging to the <i>Justusliebigvirus</i> genus. This group has been poorly studied regarding its physicochemical properties and lysis profile against antibiotic-resistant environmental bacteria. These bacteriophages have received less attention compared to well-studied models such as phage T4. The isolation and characterization of the indigenous polyvalent bacteriophage BME3, obtained from tropical estuarine waters in Ecuador, provide valuable insights into its potential applications for environmental control of <i>Escherichia coli</i> and for mitigating the spread of bacterial resistance.

Microbiology SpectrumVol. 13(7)
Universidad de las Fuerzas Armadas ESPE (EC), Universidad de Salamanca (ES), Escuela Superior Politecnica del Litoral (EC), National Polytechnic School (EC)
Life below water
Openalex Percentile: Top 9%
Bacteriophages and microbial interactions
3.43
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