# Isolation, characterization and genomic analysis of a novel lytic bacteriophage EcoPhCCP1, capable of infecting multiple strains of multidrug-resistant Escherichia coli recovered from urinary tract infections

**Authors:** Boris Parra, Maximiliano Sandoval, Maximiliano Matus-Köhler, Dácil Rivera, Mathias I. Hepp, Andrés Opazo-Capurro, Gerardo González-Rocha

PMC · DOI: 10.1099/jgv.0.002198 · The Journal of General Virology · 2026-02-19

## TL;DR

This paper describes a new bacteriophage that can infect drug-resistant E. coli causing urinary tract infections and may be useful for phage therapy.

## Contribution

The study isolates and characterizes a novel lytic phage, EcoPhCCP1, effective against multidrug-resistant E. coli strains.

## Key findings

- EcoPhCCP1 infects multiple multidrug-resistant E. coli strains from urinary tract infections.
- The phage genome is 44,482 bp long with no antimicrobial resistance or virulence genes.
- EcoPhCCP1 belongs to the Kagunavirus genus and contains putative anti-CRISPR proteins.

## Abstract

There is an urgent need for alternative solutions to combat multidrug-resistant (MDR) E. coli infections. In recent years, there has been an increase in MDR strains causing urinary tract infections (UTIs), which has resulted in more challenging treatment options, increased healthcare costs and prolonged hospital stays. The utilization of bacteriophages as a prospective modality for the management of bacterial infections has garnered significant attention. The objective of this study was to isolate and describe a phage capable of infecting MDR E. coli strains isolated from the urine of patients affected with UTI. The phage EcoPhCCP1 was isolated using the plaque assay from the influent of a wastewater treatment plant. The phage was characterized by phenotypic and genomic features. Morphological characteristics such as shape and size were determined using electron microscopy, and its host range was determined against multiple MDR strains. The complete genome of the phage was subjected to whole-genome sequencing and then assembled and annotated to search for virulence or antimicrobial resistance gene (ARG). VIRIDIC was employed to compare the closest phage genomes, while VICTOR and taxMyPhage were used to construct its phylogeny. EcoPhCCP1 is a tailed phage capable of infecting and propagating in multiple MDR E. coli strains recovered from UTI. The phage genome is 44,482 bp in length, with a GC content of 50.7 mol%, and encodes 87 ORFs, 33 of which have been previously functionally annotated. Phage EcoPhCCP1 is a Kagunavirus, in the recently created Sarkviridae family. Notably, phage EcoPhCCP1 does not harbour ARGs or virulence genes, thus rendering it a promising candidate for phage therapy against clinically significant MDR E. coli strains. Moreover, phage EcoPhCCP1 possesses putative anti-CRISPR proteins.

## Linked entities

- **Species:** Escherichia coli (taxon 562)

## Full-text entities

- **Diseases:** Antibiotic (MESH:D004761), MDR (MESH:D018088), AMR (MESH:D060467), gastrointestinal imbalances (MESH:D005767), infection (MESH:D007239), UTIs (MESH:D014552), E. coli infections (MESH:D004927), bacterial infections (MESH:D001424), allergies (MESH:D004342)
- **Chemicals:** NaCl (MESH:D012965), FEP (MESH:D011138), EDTA (MESH:D004492), lactose (MESH:D007785), TGC (MESH:D000078304), CIP (MESH:D002939), agar (MESH:D000362), sialic acid (MESH:D019158), SM (MESH:D012493), water (MESH:D014867), ETP (MESH:D000077727), cefepime (MESH:D000077723), MEM (MESH:D000077731), LEV (MESH:D064704), carbapenems (MESH:D015780), CAZ (MESH:D002442), GEN (MESH:D005839), copper (MESH:D003300), CaCl2 (MESH:D002122), TSA (MESH:C481298), CTX (MESH:D002439), LB (-), NIT (MESH:D009582), FOS (MESH:D005578), glycerol (MESH:D005990), ATM (MESH:D001398), CZA (MESH:C000595613), Magnesium sulphate (MESH:D008278), CRO (MESH:D002443), cephalosporins (MESH:D002511), NDM (MESH:C052821), Quinolones (MESH:D015363), uranyl acetate (MESH:C005460), AMK (MESH:D000583), citrate (MESH:D019343), AMP (MESH:D000667), IPM (MESH:D015378), SAM (MESH:C035444), agarose (MESH:D012685), SXT (MESH:D015662), beta-lactam (MESH:D047090), glutaraldehyde (MESH:D005976), indole (MESH:C030374), PEG8000 (MESH:C000595216)
- **Species:** Staphylococcus saprophyticus (species) [taxon 29385], Escherichia coli (E. coli, species) [taxon 562], Pseudomonas aeruginosa (species) [taxon 287], Escherichia coli K1 (strain) [taxon 1392869], Kagunavirus (genus) [taxon 1910992], Klebsiella pneumoniae (species) [taxon 573], Salmonella enterica (species) [taxon 28901], Enterobacterales (order) [taxon 91347], Salmonella enterica subsp. enterica (subspecies) [taxon 59201], Klebsiella oxytoca (species) [taxon 571], Raoultella sp. (species) [taxon 1873496], Bacteria Latreille et al. 1825 (Bacteria stick insect, genus) [taxon 629395], Staphylococcus aureus (species) [taxon 1280], Homo sapiens (human, species) [taxon 9606], Staphylococcus epidermidis (species) [taxon 1282], Acinetobacter baumannii (species) [taxon 470], Bacteriophage sp. (species) [taxon 38018]
- **Cell lines:** ATCC 25922 — Homo sapiens (Human), Lung adenocarcinoma, Cancer cell line (CVCL_0023), UCO-452 — Homo sapiens (Human), Melanoma, Cancer cell line (CVCL_C264), EC-377 — Homo sapiens (Human), Lesch-Nyhan syndrome, Finite cell line (CVCL_L481), EC-421 — Cricetulus griseus (Chinese hamster), Spontaneously immortalized cell line (CVCL_7054)

## Full text

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## Figures

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## References

102 references — full list in the complete paper: https://tomesphere.com/paper/PMC12919940/full.md

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Source: https://tomesphere.com/paper/PMC12919940