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Published on: November 2, 2021
Novel Acinetobacter baumannii Bacteriophage Aristophanes Encoding Structural Polysaccharide Deacetylase
Olga Yu Timoshina1,2, Mikhail M Shneider1, Peter V Evseev1
1Shemyakin-Ovchinnikov Institute of Bioorganic Chemistry, Miklukho-Maklaya 16/10, 117997 Moscow, Russia.
A novel bacteriophage, Aristophanes, was discovered that targets drug-resistant Acinetobacter baumannii. This phage possesses a unique tailspike deacetylase enzyme, offering potential for new antimicrobial therapies against nosocomial infections.
Area of Science:
- Microbiology
- Virology
- Genomics
Background:
- Acinetobacter baumannii is a critical nosocomial pathogen, frequently exhibiting extreme drug resistance.
- Lytic bacteriophages and their enzymes are potential antimicrobial agents against multidrug-resistant bacteria.
Purpose of the Study:
- To characterize a novel virulent bacteriophage, Aristophanes, isolated against Acinetobacter baumannii.
- To investigate its biological features, genomic organization, and host interaction mechanisms.
Main Methods:
- Isolation and characterization of bacteriophage Aristophanes on Acinetobacter baumannii K26.
- Genomic sequencing and phylogenetic analysis.
- Identification of phage-encoded enzymes, specifically tailspike deacetylase.
Main Results:
- Phage Aristophanes was identified as a novel virulent bacteriophage.
- Phylogenetic analysis places Aristophanes within a new genus of the Autographiviridae family.
- Aristophanes is the first reported Acinetobacter baumannii phage encoding a tailspike deacetylase, responsible for O-acetylation of K26 capsular polysaccharide.
Conclusions:
- Phage Aristophanes represents a new genus within the Autographiviridae family.
- The unique tailspike deacetylase activity of Aristophanes offers a novel mechanism for targeting Acinetobacter baumannii.
- This discovery holds promise for developing phage-based therapies against difficult-to-treat Acinetobacter baumannii infections.
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