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Updated: May 20, 2026

Phage Phenomics: Physiological Approaches to Characterize Novel Viral Proteins
Published on: June 11, 2015
Complete genome sequences of two Pseudomonas aeruginosa temperate phages, MP29 and MP42, which lack the phage-host
1Department of Pharmacy, College of Pharmacy, CHA University, Gyeonggi-do, South Korea.
Abstract:
We report the complete genome sequence of two Pseudomonas aeruginosa phages MP29 and MP42. Their genomes are similar to those of P. aeruginosa temperate phages DMS3 and MP22, whose lysogens are impaired in swarming motilities, involving the host CRISPR loci. Both MP29 and MP42 lysogens, however, were proficient in swarming, suggesting the absence of the phage-host CRISPR interaction.
Insights
We sequenced two Pseudomonas aeruginosa phages, MP29 and MP42. Unlike similar phages, their lysogens maintained swarming ability, indicating no phage-host CRISPR interaction.
Area of Science:
- Microbiology
- Virology
- Genomics
Background:
- Pseudomonas aeruginosa temperate phages can influence host bacterial behavior.
- Some phages, like DMS3 and MP22, impair bacterial swarming motility through interactions with host CRISPR systems.
Purpose of the Study:
- To determine the complete genome sequences of Pseudomonas aeruginosa phages MP29 and MP42.
- To investigate the impact of MP29 and MP42 lysogeny on P. aeruginosa swarming motility.
- To explore potential phage-host CRISPR interactions.
Main Methods:
- Whole genome sequencing of phages MP29 and MP42.
- Bacteriophage lysogen construction.
- Swarming motility assays for lysogenic bacterial strains.
Main Results:
- The complete genome sequences of phages MP29 and MP42 were determined.
- Lysogens of MP29 and MP42 exhibited proficient swarming motility.
- Genomic comparison revealed similarities to phages DMS3 and MP22, but functional differences in host interaction.
Conclusions:
- Phages MP29 and MP42 do not impair P. aeruginosa swarming motility.
- The absence of swarming impairment suggests that these phages do not engage in the same CRISPR-mediated host interaction as phages DMS3 and MP22.
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