Transduction of antibiotic resistance in Pseudomomas aeruginosa: relationship between lytic and transducing activity

J Blahová1, K Králiková, V Krcméry

  • 1Institute of Preventive and Clinical Medicine, Bratislava, Slovak Republic. blahova@upkm.sk

Acta Virologica
|May 29, 2000
PubMed

Insights

Researchers isolated a Pseudomonas aeruginosa phage, AP-423, from an antibiotic-resistant strain. This phage was used to transfer antibiotic resistance genes between bacteria, demonstrating host-specific transduction capabilities.

Area of Science:

  • Microbiology
  • Bacteriology
  • Virology

Background:

  • Pseudomonas aeruginosa is an opportunistic pathogen known for its antibiotic resistance.
  • Bacteriophages (phages) are viruses that infect bacteria and can be utilized for gene transfer.
  • Lysogenic conversion can alter bacterial phenotypes, including antibiotic resistance.

Purpose of the Study:

  • To isolate and characterize a wild-type phage from a lysogenic Pseudomonas aeruginosa strain.
  • To investigate the phage's ability to transduce antibiotic resistance determinants.
  • To assess the host range and transduction efficiency of the isolated phage.

Main Methods:

  • Isolation of bacteriophage AP-423 from a lysogenic Pseudomonas aeruginosa strain.
  • Propagation and titration of the phage on various P. aeruginosa recipient strains.
  • Transduction experiments to transfer antibiotic resistance genes.

Main Results:

  • Phage isolate AP-423 was successfully isolated and propagated.
  • The phage exhibited host restriction, lysogenizing only specific recipient strains.
  • Transduction capacity (gene sets and frequency) varied significantly between different P. aeruginosa recipient strains.
  • Phage propagation titers were also restricted to certain recipient strains.

Conclusions:

  • Phage AP-423 can be used to transduce antibiotic resistance determinants in Pseudomonas aeruginosa.
  • The phage displays significant host specificity in lysogenization, propagation, and transduction.
  • Understanding phage host range is crucial for effective phage therapy and genetic manipulation in P. aeruginosa.

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