Phage-Mediated Iron Acquisition by <i>Pseudomonas aeruginosa</i>

Iron acquisition is critical to bacterial growth and pathogenesis. Here, we describe a previously unrecognized mechanism by which the major human pathogen <i>Pseudomonas aeruginosa</i> acquires iron through a unique partnership with bacteriophages (phages). Pf is a filamentous phage that infects <i>P. aeruginosa</i> and is associated with chronic infections. We reveal that Pf contributes to <i>P. aeruginosa</i> pathogenesis by promoting iron uptake. We demonstrate that Pf phage is highly induced under iron-deplete growth conditions and that once induced, Pf virions directly bind and locally concentrate free iron. Pf-bound iron is more efficiently utilized by <i>P. aeruginosa</i> than unbound iron, enhancing bacterial growth. We further demonstrate that Pf-mediated iron acquisition depends on type IV pili, which facilitate Pf attachment and confers strain selective uptake of phage-bound iron, providing a competitive fitness advantage in polymicrobial settings. Together, these findings identify an unrecognized role for filamentous phages in mediating iron acquisition and reveal a novel phage-bacterium partnership that operates through selective kin cooperation.

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Publication Details

Journal
bioRxiv (Cold Spring Harbor Laboratory)
Published
2026-01-26
DOI
https://doi.org/10.64898/2026.01.26.700923
Primary Topic
Bacteriophages and microbial interactions
Type
article
Field-Weighted Citation Impact
0.00

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article

Phage-Mediated Iron Acquisition by Pseudomonas aeruginosa

Saumel P Rodriguez, Paul L Bollyky, Elizabeth B Burgener, Arya Khosravi et al.
bioRxiv (Cold Spring Harbor Laboratory)
Bacteriophages and microbial interactions
article

Phage-Mediated Iron Acquisition by Pseudomonas aeruginosa

Saumel P Rodriguez, Paul L Bollyky, Elizabeth B Burgener, Arya Khosravi, Aditi Gupta, Carlos E Milla, Maryam Hajfathalian
article en

Abstract

Iron acquisition is critical to bacterial growth and pathogenesis. Here, we describe a previously unrecognized mechanism by which the major human pathogen <i>Pseudomonas aeruginosa</i> acquires iron through a unique partnership with bacteriophages (phages). Pf is a filamentous phage that infects <i>P. aeruginosa</i> and is associated with chronic infections. We reveal that Pf contributes to <i>P. aeruginosa</i> pathogenesis by promoting iron uptake. We demonstrate that Pf phage is highly induced under iron-deplete growth conditions and that once induced, Pf virions directly bind and locally concentrate free iron. Pf-bound iron is more efficiently utilized by <i>P. aeruginosa</i> than unbound iron, enhancing bacterial growth. We further demonstrate that Pf-mediated iron acquisition depends on type IV pili, which facilitate Pf attachment and confers strain selective uptake of phage-bound iron, providing a competitive fitness advantage in polymicrobial settings. Together, these findings identify an unrecognized role for filamentous phages in mediating iron acquisition and reveal a novel phage-bacterium partnership that operates through selective kin cooperation.

bioRxiv (Cold Spring Harbor Laboratory)
New Jersey Institute of Technology (US), Children's Hospital of Los Angeles (US), Stanford Medicine (US), Stanford University (US)
National Institutes of Health, Stanford Woods Institute for the Environment
Partnerships for the goals
Openalex Percentile: Top 79%
Bacteriophages and microbial interactions
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