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Updated: Jun 5, 2026

Replication of the Ordered, Nonredundant Library of Pseudomonas aeruginosa strain PA14 Transposon Insertion Mutants
Published on: May 4, 2018
Genetic characterization indicates that a specific subpopulation of Pseudomonas aeruginosa is associated with
Rosalind M K Stewart1, Lutz Wiehlmann, Kevin E Ashelford
1Institute of Infection and Global Health, University of Liverpool, Duncan Building, Daulby Street, Liverpool, L69 3GA, United Kingdom.
Abstract:
Pseudomonas aeruginosa is a common opportunistic bacterial pathogen that causes a variety of infections in humans. Populations of P. aeruginosa are dominated by common clones that can be isolated from diverse clinical and environmental sources. To determine whether specific clones are associated with corneal infection, we used a portable genotyping microarray system to analyze a set of 63 P. aeruginosa isolates from patients with corneal ulcers (keratitis). We then used population analysis to compare the keratitis isolates to a wider collection of P. aeruginosa from various nonocular sources. We identified various markers in a subpopulation of P. aeruginosa associated with keratitis that were in strong disequilibrium with the wider P. aeruginosa population, including oriC, exoU, katN, unmodified flagellin, and the carriage of common genomic islands. The genome sequencing of a keratitis isolate (39016; representing the dominant serotype O11), which was associated with a prolonged clinical healing time, revealed several genomic islands and prophages within the accessory genome. The PCR amplification screening of all 63 keratitis isolates, however, provided little evidence for the shared carriage of specific prophages or genomic islands between serotypes. P. aeruginosa twitching motility, due to type IV pili, is implicated in corneal virulence. We demonstrated that 46% of the O11 keratitis isolates, including 39016, carry a distinctive pilA, encoding the pilin of type IV pili. Thus, the keratitis isolates were associated with specific characteristics, indicating that a subpopulation of P. aeruginosa is adapted to cause corneal infection.
Insights
Specific Pseudomonas aeruginosa clones are adapted for corneal infections. Researchers identified unique genetic markers and type IV pili in these bacterial strains, suggesting a specialized subpopulation causes keratitis.
Area of Science:
- Microbiology
- Genetics
- Ophthalmology
Background:
- Pseudomonas aeruginosa is an opportunistic pathogen causing diverse human infections.
- Common clones of P. aeruginosa are found in both clinical and environmental settings.
- Understanding clonal associations is crucial for targeting specific infections like keratitis.
Purpose of the Study:
- To investigate if specific P. aeruginosa clones are associated with corneal infections (keratitis).
- To compare genetic characteristics of keratitis isolates with non-ocular P. aeruginosa strains.
- To identify genetic markers linked to adaptation for corneal pathogenesis.
Main Methods:
- Utilized a portable genotyping microarray to analyze 63 P. aeruginosa keratitis isolates.
- Conducted population analysis comparing keratitis isolates to non-ocular strains.
- Performed whole-genome sequencing on a representative keratitis isolate (serotype O11).
- Employed PCR screening to assess the carriage of specific genetic elements.
Main Results:
- Identified unique genetic markers (oriC, exoU, katN, unmodified flagellin, genomic islands) in keratitis-associated P. aeruginosa subpopulations.
- Genome sequencing revealed genomic islands and prophages in a keratitis isolate.
- Found limited evidence of shared prophages or genomic islands across different serotypes in keratitis isolates.
- Demonstrated that 46% of O11 keratitis isolates possess a distinct pilA gene, associated with type IV pili and twitching motility.
Conclusions:
- A distinct subpopulation of P. aeruginosa is associated with corneal infections.
- Specific genetic markers and the presence of type IV pili contribute to P. aeruginosa's adaptation for keratitis.
- These findings highlight clonal adaptation in bacterial pathogenesis.
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