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Updated: Jul 28, 2025

Phage Phenomics: Physiological Approaches to Characterize Novel Viral Proteins
Published on: June 11, 2015
Characterization of a novel phage vB_Pae_HB2107-3I that infects Pseudomonas aeruginosa
Jiuna Kong1, Guanhua Xuan1, Hong Lin1
1Food Safety Laboratory, College of Food Science and Engineering, Ocean University of China, Qingdao, 266003, China.
Abstract:
Bacteriophages are potential antibiotic substitutes for the treatment of antibiotic resistant bacteria. Here, we report the genome sequences of a double-stranded DNA podovirus vB_Pae_HB2107-3I against clinical multi-drug resistant Pseudomonas aeruginosa. Phage vB_Pae_HB2107-3I remained stable over a wide range of temperatures (37-60 °C) and pH values (pH 4-12). At MOI of 0.01, the latent period of vB_Pae_HB2107-3I was 10 min, and the final titer reached about 8.1 × 109 PFU/mL. The vB_Pae_HB2107-3I genome is 45,929 bp, with an average G + C content of 57%. A total of 72 open reading frames (ORFs) were predicted, of which 22 ORFs have a predicted function. Genome analyses confirmed the lysogenic nature of this phage. Phylogenetic analysis revealed that phage vB_Pae_HB2107-3I was a novel member of Caudovirales infecting P. aeruginosa. The characterization of vB_Pae_HB2107-3I enrich the research on Pseudomonas phages and provide a promising biocontrol agent against P. aeruginosa infections.
Insights
Bacteriophages, or phages, are promising alternatives to antibiotics for treating drug-resistant bacteria. This study details a novel phage, vB_Pae_HB2107-3I, effective against multi-drug resistant Pseudomonas aeruginosa.
Area of Science:
- Microbiology
- Virology
- Genomics
Background:
- Antibiotic resistance in bacteria, particularly Pseudomonas aeruginosa, poses a significant global health threat.
- Bacteriophages (phages) are viruses that infect bacteria and are being explored as alternatives to conventional antibiotics.
- Developing novel phages with broad host ranges and stability is crucial for phage therapy.
Purpose of the Study:
- To sequence and characterize the genome of a novel double-stranded DNA podovirus, vB_Pae_HB2107-3I.
- To evaluate the stability and lytic activity of vB_Pae_HB2107-3I against multi-drug resistant Pseudomonas aeruginosa.
- To determine the phylogenetic relationship of vB_Pae_HB2107-3I within the Caudovirales order.
Main Methods:
- Whole-genome sequencing of bacteriophage vB_Pae_HB2107-3I.
- Stability assays across a range of temperatures (37-60 °C) and pH values (pH 4-12).
- One-step growth curve analysis to determine latent period and burst size.
- Bioinformatic analysis including open reading frame (ORF) prediction, functional annotation, and phylogenetic analysis.
Main Results:
- The genome of vB_Pae_HB2107-3I is 45,929 bp with 57% G+C content, encoding 72 ORFs (22 with predicted functions).
- Phage vB_Pae_HB2107-3I demonstrated stability across tested temperatures and pH ranges, with a latent period of 10 min and a final titer of 8.1 × 10^9 PFU/mL at MOI 0.01.
- Genome analysis confirmed the lysogenic nature of the phage, and phylogenetic analysis identified it as a novel Caudovirales member infecting P. aeruginosa.
Conclusions:
- Phage vB_Pae_HB2107-3I is a stable, novel phage with potential as a biocontrol agent against Pseudomonas aeruginosa infections.
- The characterization of this phage expands the knowledge of Pseudomonas phages and supports their development for therapeutic applications.
- This research contributes to the growing body of evidence supporting bacteriophage therapy as a viable alternative to antibiotics for resistant bacterial infections.
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