Comparative Analyses Suggest Genome Stability and Plasticity in Stenotrophomonas maltophilia

Danny Khar Chen Sum1, Yee Yee Chong1, Joon Liang Tan1,2

  • 1Faculty of Information Science and Technology, Multimedia University, Melaka 75450, Malaysia.

Insights

Stenotrophomonas maltophilia (S. maltophilia) infections are a growing public health concern. Mobile genetic elements drive diversity and drug resistance in S. maltophilia populations, impacting genomic stability and plasticity.

Area of Science:

  • Microbiology
  • Genomics
  • Evolutionary Biology

Background:

  • Stenotrophomonas maltophilia (S. maltophilia) is an opportunistic pathogen known for multidrug resistance.
  • Increasing S. maltophilia infections highlight its public health significance.
  • Previous research focused on S. maltophilia pangenomes, antibiotic resistance, and virulence, but neglected mobile genetic elements (MGEs).

Purpose of the Study:

  • To investigate the role of MGEs in S. maltophilia population structure, diversity, and evolution.
  • To analyze the impact of MGEs on virulence and drug resistance gene distribution.
  • To assess evolutionary trends in S. maltophilia core genomes and accessory regions.

Main Methods:

  • Downloaded and analyzed 20 S. maltophilia genomes from NCBI.
  • Profiled MGEs and their distribution within the genomes.
  • Evaluated MGEs' impact on chromosomal rearrangements and linkage disequilibrium in core genomes.

Main Results:

  • Catalogued MGEs revealed active horizontal gene transfer in S. maltophilia.
  • Virulence and drug resistance genes were identified within and outside MGEs.
  • Observed significant chromosomal rearrangements (up to 50% of a genome) attributed to MGEs.
  • Detected high levels of linkage disequilibrium in core genomes.

Conclusions:

  • MGEs significantly contribute to the plasticity of the accessory genome in S. maltophilia.
  • MGEs are implicated in chromosomal instability and the spread of resistance and virulence factors.
  • The study elucidates the interplay between core genome stability and accessory genome plasticity in S. maltophilia.