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Published on: April 2, 2013
Investigating the phenotypic alterations associated with hypermucoviscous hypervirulent Klebsiella pneumoniae during
Ramya Juliet1, Ramesh Nachimuthu2
1Antibiotic Resistance and Phage Therapy Laboratory, Centre for Advanced Research in Bacteriophage and Infectious Diseases, School of Bio Sciences and Technology, Vellore Institute of Technology (VIT), Vellore, 632014, Tamil Nadu, India.
Abstract:
Phage therapy has been explored and used compassionately in the post-antibiotic era, though phage resistance might pose a serious challenge. The advent of hypervirulent and hypermucoviscous traits in Klebsiella pneumoniae limits therapeutic choices. This study investigated the phage resistance in hypermucoviscous hypervirulent Klebsiella pneumoniae clinical strain Kleb_53. A Klebsiella phage Disc against the Kleb_53 strain was isolated from sewage. The phage exhibited stability between - 20 °C and 60 °C and within the pH range of 3 to 11. The phage adsorption time was 15 min, with a latent period of 30 min and a burst size of 354 virions. The phage-resistant Kleb_53 variants were screened and examined for their phenotypic variations, antibiotic susceptibility, and biofilm formation. Colony morphotype variants were observed, including smooth, rough, and small colony variants. String, aggregation, and wetness tests confirmed reduced mucoviscosity. The plaque morphology differed between the wild and variants. Additionally, resistance to meropenem and third-generation cephalosporins was reversed, whereas the biofilm-forming ability varied among the recovered variants. This study demonstrates that ongoing phage-host interactions drive phenotypic changes and the emergence of phage-resistant variants with altered antibiotic susceptibility and biofilm-forming capacity. It also underscores the need for further research on phage resistance and strategies to overcome it for the effective application of phage therapy.
Insights
Phage therapy faces challenges from bacterial resistance. This study shows Klebsiella pneumoniae can develop phage resistance, altering its traits and antibiotic susceptibility, impacting therapeutic options.
Area of Science:
- Microbiology
- Bacteriology
- Virology
Background:
- Phage therapy is a promising alternative in the post-antibiotic era.
- Hypervirulent and hypermucoviscous Klebsiella pneumoniae presents significant therapeutic challenges.
- Bacterial resistance to phages is a critical concern for therapeutic efficacy.
Purpose of the Study:
- To investigate phage resistance in a hypermucoviscous, hypervirulent Klebsiella pneumoniae clinical strain (Kleb_53).
- To characterize the phenotypic and genotypic changes in phage-resistant Kleb_53 variants.
- To assess the impact of phage resistance on antibiotic susceptibility and biofilm formation.
Main Methods:
- Isolation and characterization of a Klebsiella phage (Phage Disc) effective against Kleb_53.
- Determination of phage stability across temperature and pH ranges.
- Screening and examination of phage-resistant Kleb_53 variants for phenotypic variations, antibiotic susceptibility, and biofilm formation.
Main Results:
- Phage Disc demonstrated stability between -20°C and 60°C and pH 3-11.
- Phage-resistant Kleb_53 variants exhibited reduced mucoviscosity and altered colony morphotypes.
- Reversal of resistance to meropenem and cephalosporins was observed in some variants, with varied biofilm formation.
Conclusions:
- Phage-host interactions drive phenotypic changes and the emergence of phage-resistant variants.
- Phage resistance in Klebsiella pneumoniae can lead to altered antibiotic susceptibility and biofilm capacity.
- Further research is needed to overcome phage resistance for effective phage therapy.
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