The broad host range pathogen Pseudomonas aeruginosa strain PA14 carries two pathogenicity islands harboring plant and animal virulence genes
Related Experiment Video
Updated: Aug 26, 2026

Replication of the Ordered, Nonredundant Library of Pseudomonas aeruginosa strain PA14 Transposon Insertion Mutants
Published on: May 4, 2018
Jianxin He1, Regina L Baldini, Eric Déziel
1Department of Surgery, Harvard Medical School and Massachusetts General Hospital, Boston, MA 02114, USA.
Abstract:
The ubiquitous bacterium Pseudomonas aeruginosa is the quintessential opportunistic pathogen. Certain isolates infect a broad range of host organisms, from plants to humans. The pathogenic promiscuity of particular variants may reflect an increased virulence gene repertoire beyond the core P. aeruginosa genome. We have identified and characterized two P. aeruginosa pathogenicity islands (PAPI-1 and PAPI-2) in the genome of PA14, a highly virulent clinical isolate. The 108-kb PAPI-1 and 11-kb PAPI-2, which are absent from the less virulent reference strain PAO1, exhibit highly modular structures, revealing their complex derivations from a wide array of bacterial species and mobile elements. Most of the genes within these islands that are homologous to known genes occur in other human and plant bacterial pathogens. For example, PAPI-1 carries a complete gene cluster predicted to encode a type IV group B pilus, a well known adhesin absent from strain PAO1. However, >80% of the PAPI-1 DNA sequence is unique, and 75 of its 115 predicted ORF products are unrelated to any known proteins or functional domains. Significantly, many PAPI-1 ORFs also occur in several P. aeruginosa cystic fibrosis isolates. Twenty-three PAPI ORFs were mutated, and 19 were found to be necessary for full plant or animal virulence, with 11 required for both. The large set of "extra" virulence functions encoded by both PAPIs may contribute to the increased promiscuity of highly virulent P. aeruginosa strains, by directing additional pathogenic functions.
Insights
Highly virulent Pseudomonas aeruginosa strains possess unique pathogenicity islands (PAPI-1 and PAPI-2). These islands contain novel genes essential for both plant and animal infections, explaining the bacterium's broad host range.
Area of Science:
- Microbiology
- Genomics
- Pathogenesis
Background:
- Pseudomonas aeruginosa is an opportunistic pathogen infecting diverse hosts.
- Virulence variation may stem from expanded gene content beyond the core genome.
Purpose of the Study:
- Identify and characterize novel pathogenicity islands in a highly virulent P. aeruginosa strain (PA14).
- Investigate the role of these islands in bacterial virulence across different hosts.
Main Methods:
- Genomic analysis of P. aeruginosa PA14 and PAO1 strains.
- Identification and characterization of PAPI-1 and PAPI-2.
- Gene mutation and virulence assays in plant and animal models.
Main Results:
- Discovered PAPI-1 (108-kb) and PAPI-2 (11-kb) in PA14, absent in PAO1.
- PAPI-1 and PAPI-2 exhibit modular structures with genes from diverse bacterial sources.
- Over 80% of PAPI-1 DNA is unique; 75 ORFs have no known homologs.
- 19 of 23 mutated PAPI ORFs were essential for virulence in plants or animals, with 11 required for both.
Conclusions:
- PAPI-1 and PAPI-2 contribute significantly to P. aeruginosa virulence and host promiscuity.
- These pathogenicity islands encode novel virulence factors, expanding the bacterium's pathogenic potential.
- The unique genetic content of PAPIs likely drives the adaptation of P. aeruginosa to various hosts, including humans.
More Related Videos
08:34Generation of In-Frame Gene Deletion Mutants in Pseudomonas aeruginosa and Testing for Virulence Attenuation in a Simple Mouse Model of Infection
Published on: January 8, 2020
08:57Identification of Novel Genes Associated with Alginate Production in Pseudomonas aeruginosa Using Mini-himar1 Mariner Transposon-mediated Mutagenesis
Published on: March 10, 2014
Related Concept Videos
Determinants of Bacterial Pathogenicity and Virulence
Regulation of Bacterial Virulence
Gene Regulation in Microbial Communities: Quorum Sensing
Diversity of Protists II
Inhalation Anthrax
Colonisation of Pathogens