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Published on: September 28, 2022
Genome sequence of lytic phage phi1_164023 targeting ST23 KL1-type carbapenem-resistant Klebsiella pneumoniae
Huan Kuang1, Qingqing Fang1,2, Yu Feng3,4
1Center of Infectious Diseases, West China Hospital, Sichuan University, Chengdu, China.
Abstract:
We report the genome of a phage that belongs to the Przondovirus genus, which was isolated from sewage, and is capable of lysing ST23 KL1-type carbapenem-resistant Klebsiella pneumoniae strains. The genome is 39,059 bp in length, with a GC content of 53.11%, consisting of 55 protein-coding sequences and no tRNAs.
Insights
We sequenced a novel phage genome from sewage, belonging to the Przondovirus genus. This phage effectively lyses carbapenem-resistant Klebsiella pneumoniae strains, offering potential for combating antibiotic resistance.
Area of Science:
- Microbiology
- Genomics
- Bacteriophage research
Background:
- Carbapenem-resistant Klebsiella pneumoniae (CRKP) poses a significant global health threat.
- Bacteriophages are viruses that infect bacteria and are being explored as alternatives to antibiotics.
- The Przondovirus genus is a group of bacteriophages with limited genomic characterization.
Purpose of the Study:
- To characterize the genome of a novel phage with potential lytic activity against CRKP.
- To provide genomic insights into the Przondovirus genus.
Main Methods:
- Isolation of a bacteriophage from sewage.
- Whole-genome sequencing and analysis of the phage.
- Identification of protein-coding sequences and genomic features.
Main Results:
- The complete genome of a Przondovirus phage was sequenced (39,059 bp, 53.11% GC content).
- The genome encodes 55 protein-coding sequences and lacks tRNA genes.
- The isolated phage demonstrated the capability to lyse ST23 KL1-type carbapenem-resistant Klebsiella pneumoniae strains.
Conclusions:
- The characterized phage represents a potential candidate for phage therapy against CRKP infections.
- Genomic data contributes to the understanding of the Przondovirus genus and phage-host interactions.
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