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Updated: Jan 27, 2026

Rapid and Specific Detection of Acinetobacter baumannii Infections Using a Recombinase Polymerase Amplification/Cas12a-based System
Published on: April 25, 2025
Characterization of myophage AM24 infecting Acinetobacter baumannii of the K9 capsular type
Anastasia V Popova1,2,3, Mikhail M Shneider4,5, Vera P Myakinina6
1Moscow Institute of Physics and Technology (State University), Dolgoprudny, Moscow Region, Russia. popova_av@mipt.ru.
Abstract:
In the present study, we investigate the biological properties and genomic organization of virulent bacteriophage AM24, which specifically infects multidrug-resistant clinical Acinetobacter baumannii strains with a K9 capsular polysaccharide structure. The phage was identified as a member of the family Myoviridae by transmission electron microscopy. The AM24 linear double-stranded DNA genome of 97,177 bp contains 167 open reading frames. Putative functions were assigned for products of 40 predicted genes, including proteins involved in nucleotide metabolism and DNA replication, packaging of DNA into the capsid, phage assembly and structural proteins, and bacterial cell lysis. The gene encoding the tailspike, which possesses depolymerase activity towards the corresponding capsular polysaccharides, is situated in the phage genome outside of the structural module, upstream of the genes responsible for packaging of DNA into the capsid. The data on characterization of depolymerase-carrying phage AM24 contributes to our knowledge of the diversity of viruses infecting different capsular types of A. baumannii.
Insights
This study characterizes bacteriophage AM24, a virulent virus targeting multidrug-resistant Acinetobacter baumannii. Its genome analysis reveals key genes for bacterial cell lysis and infection, enhancing our understanding of phage diversity.
Area of Science:
- Microbiology
- Virology
- Genomics
Background:
- Acinetobacter baumannii is a multidrug-resistant pathogen.
- Bacteriophages offer potential therapeutic alternatives.
- Understanding phage-host interactions is crucial for phage therapy development.
Purpose of the Study:
- To investigate the biological properties and genomic organization of bacteriophage AM24.
- To determine the host range and infection mechanism of AM24.
- To contribute to the knowledge of Acinetobacter baumannii phages.
Main Methods:
- Transmission electron microscopy for phage morphology.
- Genome sequencing and analysis of bacteriophage AM24.
- Bioinformatic analysis to identify open reading frames and predict gene functions.
Main Results:
- Bacteriophage AM24 belongs to the Myoviridae family.
- The phage has a linear double-stranded DNA genome of 97,177 bp with 167 open reading frames.
- The tailspike depolymerase gene is located outside the structural module, upstream of DNA packaging genes.
Conclusions:
- Bacteriophage AM24 is a virulent phage targeting specific Acinetobacter baumannii strains.
- Genomic analysis provides insights into phage replication, assembly, and lysis mechanisms.
- The characterization of AM24 expands our understanding of phage diversity against Acinetobacter baumannii.
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