Evolution and host-specific adaptation of Pseudomonas aeruginosa

Aaron Weimann1,2,3,4, Adam M Dinan1,2,3, Christopher Ruis1,2,3,4

  • 1Victor Phillip Dahdaleh Heart & Lung Research Institute, University of Cambridge, Cambridge, UK.

Science (New York, N.Y.)
|July 4, 2024
PubMed

Insights

Dominant clones of Pseudomonas aeruginosa have evolved over 200 years through gene acquisition and host adaptation, causing multidrug-resistant infections. Global surveillance is crucial to prevent future epidemic strains.

Area of Science:

  • Microbiology
  • Evolutionary Biology
  • Infectious Diseases

Background:

  • Pseudomonas aeruginosa is a major bacterial pathogen causing multidrug-resistant infections.
  • These infections disproportionately affect individuals with immunodeficiencies or structural lung diseases, such as cystic fibrosis (CF).

Purpose of the Study:

  • To investigate the evolutionary pathways and emergence of dominant epidemic clones of Pseudomonas aeruginosa.
  • To understand the genetic and adaptive mechanisms driving the pathogenicity and transmission of P. aeruginosa.

Main Methods:

  • Genomic analysis of environmental and clinical isolates of P. aeruginosa.
  • Phylogenetic analysis to reconstruct global transmission networks and evolutionary history.
  • Comparative transcriptomics to identify host-specific adaptation mechanisms.

Main Results:

  • A few environmental P. aeruginosa isolates have become dominant epidemic clones through horizontal gene acquisition over the past 200 years.
  • These clones exhibit varying abilities to infect CF and non-CF individuals, linked to transcriptional changes enabling macrophage survival.
  • Convergent, host-specific adaptations have occurred, leading to a loss of transmission ability between different patient groups.

Conclusions:

  • Horizontal gene acquisition and host-specific adaptation explain the pathogenic evolution of P. aeruginosa.
  • Global surveillance and cross-infection prevention are vital to mitigate the emergence of future epidemic clones.