The Potential Roles of Prophages in the Pathogenicity of Klebsiella pneumoniae Strains from Kenya

Juliah K Akhwale1, Ivy J Mutai2,3, Janet Y Nale4

  • 1School of Biological Sciences, Jomo Kenyatta University of Agriculture and Technology, Nairobi P.O. Box 62000-00200, Kenya.

PubMed

Insights

Prophages within Klebsiella pneumoniae genomes in Kenya carry virulence genes, contributing to pathogenicity. This research highlights their role in antimicrobial resistance and potential for horizontal gene transfer, aiding control strategies.

Area of Science:

  • Microbiology
  • Genomics
  • Infectious Diseases

Background:

  • Antimicrobial resistance (AMR) in Klebsiella pneumoniae is a significant healthcare concern, particularly in sub-Saharan Africa.
  • Understanding the genetic factors contributing to K. pneumoniae pathogenicity is crucial for effective infection control.

Purpose of the Study:

  • To investigate the presence and characteristics of prophages in Kenyan K. pneumoniae clinical and environmental genomes.
  • To determine the potential role of these prophages in K. pneumoniae pathogenicity and virulence.

Main Methods:

  • Extraction and analysis of prophages from 89 Kenyan K. pneumoniae genomes.
  • Examination of intact prophages for virulence gene carriage.
  • Phylogenetic analysis of identified prophages.

Main Results:

  • Nearly all (99%) K. pneumoniae genomes contained at least one prophage, with an average of four per strain.
  • 30% of intact prophages encoded 38 distinct virulence genes, including those for iron uptake, adherence, and immune modulation.
  • Phylogenetic analysis revealed three distinct prophage clades, indicating potential for horizontal gene transfer.

Conclusions:

  • This study presents the first evidence of diverse prophages in K. pneumoniae from sub-Saharan Africa, specifically Kenyan strains.
  • Prophages likely contribute to K. pneumoniae pathogenicity and success, offering insights for regional and global control strategies.
  • Further research is needed to confirm gene expression via lysogenization.

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