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Updated: Aug 25, 2026

Qualitative and Quantitative Analysis of Siderophore Production from Pseudomonas aeruginosa
Published on: March 15, 2024
Burkholderia spp. alter Pseudomonas aeruginosa physiology through iron sequestration
Valerie B Weaver1, Roberto Kolter
1Department of Microbiology and Molecular Genetics, Harvard Medical School, Boston, Massachusetts 02115, USA.
Abstract:
Pseudomonas aeruginosa and members of the Burkholderia cepacia complex often coexist in both the soil and the lungs of cystic fibrosis patients. To gain an understanding of how these different species affect each other's physiology when coexisting, we performed a screen to identify P. aeruginosa genes that are induced in the presence of Burkholderia: A random gene fusion library was constructed in P. aeruginosa PA14 by using a transposon containing a promoterless lacZ gene. Fusion strains were screened for their ability to be induced in the presence of Burkholderia strains in a cross-streak assay. Three fusion strains were induced specifically by Burkholderia species; all three had transposon insertions in genes known to be iron regulated. One of these fusion strains, containing a transposon insertion in gene PA4467, was used to characterize the inducing activity from Burkholderia: Biochemical and genetic evidence demonstrate that ornibactin, a siderophore produced by nearly all B. cepacia strains, can induce P. aeruginosa PA4467. Significantly, PA4467 is induced early in coculture with an ornibactin-producing but not an ornibactin-deficient B. cepacia strain, indicating that ornibactin can be produced by B. cepacia and detected by P. aeruginosa when the two species coexist.
Insights
Pseudomonas aeruginosa gene expression is altered by Burkholderia species. Ornibactin, a siderophore from Burkholderia, triggers a specific P. aeruginosa gene response during co-colonization.
Area of Science:
- Microbiology
- Bacterial Interactions
- Gene Regulation
Background:
- Pseudomonas aeruginosa and Burkholderia cepacia complex bacteria frequently co-occur in environments like soil and cystic fibrosis patient lungs.
- Understanding interspecies interactions is crucial for managing polymicrobial infections.
Purpose of the Study:
- To identify Pseudomonas aeruginosa genes induced by the presence of Burkholderia species.
- To elucidate the molecular mechanisms of P. aeruginosa response to Burkholderia co-colonization.
Main Methods:
- Construction of a random P. aeruginosa PA14 gene-lacZ fusion library.
- Screening of fusion strains for induction by Burkholderia species using a cross-streak assay.
- Biochemical and genetic analysis to identify the inducing molecule and its target gene.
Main Results:
- Three P. aeruginosa gene fusions were specifically induced by Burkholderia species, all linked to iron-regulated genes.
- Transposon insertion in gene PA4467 identified as responsive to Burkholderia.
- Ornibactin, a Burkholderia siderophore, was confirmed to induce P. aeruginosa PA4467 expression.
Conclusions:
- Ornibactin produced by Burkholderia cepacia directly induces the P. aeruginosa PA4467 gene.
- This interaction demonstrates that P. aeruginosa can detect and respond to Burkholderia-derived siderophores during co-colonization.
- The findings provide insight into the physiological adaptations during polymicrobial infections involving these species.
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