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New Bacteriophage Pseudomonas Phage Ka2 from a Tributary Stream of Lake Baikal
Valeriya Ilyina1, Alina Gatina1, Elena Trizna1
1Institute of Fundamental Biology and Medicine, Kazan Federal University, 420012 Kazan, Russia.
Abstract:
Pseudomonas aeruginosa, an opportunistic pathogen, causes various biofilm-associated infections like pneumonia, infections in cystic fibrosis patients, and urinary tract and burn infections with high morbidity and mortality, as well as low treatment efficacy due to the extremely wide spread of isolates with multidrug resistance. Here, we report the new bacteriophage Pseudomonas phage Ka2 isolated from a tributary stream of Lake Baikal and belonging to the Pbunavirus genus. Transmission electron microscopy resolved that Pseudomonas phage Ka2 has a capsid of 57 ± 9 nm and a contractile and inflexible tail of 115 ± 10 nm in the non-contracted state. The genome consists of 66,310 bp with a GC content of 55% and contains 96 coding sequences. Among them, 52 encode proteins have known functions, and none of them are potentially associated with lysogeny. The bacteriophage lyses 21 of 30 P. aeruginosa clinical isolates and decreases the MIC of amikacin, gentamicin, and cefepime up to 16-fold and the MIC of colistin up to 32-fold. When treating the biofilms with Ka2, the biomass was reduced by twice, and up to a 32-fold decrease in the antibiotics MBC against biofilm-embedded cells was achieved by the combination of Ka2 with cefepime for the PAO1 strain, along with a decrease of up to 16-fold with either amikacin or colistin for clinical isolates. Taken together, these data characterize the new Pseudomonas phage Ka2 as a promising tool for the combined treatment of infections associated with P. aeruginosa biofilms.
Insights
A novel bacteriophage, Pseudomonas phage Ka2, effectively combats Pseudomonas aeruginosa infections. This phage reduces bacterial load and enhances antibiotic efficacy against multidrug-resistant strains and biofilms.
Area of Science:
- Microbiology
- Virology
- Infectious Diseases
Background:
- Pseudomonas aeruginosa is an opportunistic pathogen causing severe biofilm-associated infections.
- Multidrug resistance in P. aeruginosa leads to low treatment efficacy and high mortality.
- Bacteriophage therapy offers a potential alternative for treating resistant bacterial infections.
Purpose of the Study:
- To isolate and characterize a novel bacteriophage targeting Pseudomonas aeruginosa.
- To evaluate the efficacy of the isolated bacteriophage, Pseudomonas phage Ka2, against P. aeruginosa clinical isolates and biofilms.
- To assess the potential of phage Ka2 as an adjunct therapy to antibiotics.
Main Methods:
- Isolation and characterization of Pseudomonas phage Ka2 from Lake Baikal.
- Transmission electron microscopy for phage morphology analysis.
- Genome sequencing and analysis of coding sequences.
- In vitro testing against P. aeruginosa clinical isolates and biofilms, including antibiotic susceptibility testing.
Main Results:
- Pseudomonas phage Ka2, a novel Pbunavirus, was isolated and characterized with specific morphological and genomic features.
- The bacteriophage lysed 70% of tested P. aeruginosa clinical isolates.
- Phage Ka2 significantly reduced antibiotic minimum inhibitory concentrations (MICs) and minimum bactericidal concentrations (MBCs) against planktonic and biofilm-embedded P. aeruginosa, especially in combination with antibiotics like cefepime, amikacin, and colistin.
Conclusions:
- Pseudomonas phage Ka2 is a promising lytic bacteriophage with potential for treating P. aeruginosa infections.
- Combined therapy with phage Ka2 and antibiotics demonstrates enhanced efficacy against multidrug-resistant P. aeruginosa and its biofilms.
- Further research into phage Ka2 could lead to novel therapeutic strategies for challenging P. aeruginosa infections.
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